Post by kickingfrog on Jan 31, 2011 12:19:02 GMT
Bones and Coeliac Disease
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The Institute of Genetics and Molecular Medicine
The University of Edinburgh
Osteoporosis and coeliac disease link
9 October 2009
People with coeliac disease may develop osteoporosis because their immune system attacks their bone tissue, a new study has shown.
It is the first time an autoimmune response - a condition whereby the body can attack itself - has been shown to cause damage to bones directly.
IGMM researchers studied a protein called osteoprotegerin (OPG) in people with coeliac disease - a digestive condition that affects 1 in 100 people.
In healthy people, OPG plays a crucial role in maintaining bone health by controlling the rate at which bone tissue is removed.
The latest research shows that 20 per cent of coeliac patients produce antibodies that attack the OPG protein and stop it working properly. This results in rapid bone destruction and severe osteoporosis.
It was previously thought that osteoporosis - a known complication of coeliac disease - develops in coeliac patients because they cannot properly absorb calcium and vitamin D from their diet. Both nutrients are essential for healthy bone development.
The team found that although this new form of osteoporosis did not respond to calcium and vitamin D supplements, it can be easily treated with drugs that prevent bone loss.
The research is published in the New England Journal of Medicine.
Professor Stuart Ralston, of the Institute of Genetics and Molecular Medicine, who led the team, said: “This is a very exciting step forward. Not only have we discovered a new reason to explain why osteoporosis occurs in coeliac disease, but we have also found that it responds very well to drugs that prevent bone tissue removal.
Testing for these antibodies could make a real and important difference to the lives of people with coeliac disease by alerting us to the risk of osteoporosis and helping us find the correct treatment for them.”
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Osteoporosis and Osteomalacia in Patients with Celiac Disease
Elizabeth Shane, M.D., Endocrinologist
The incidence of osteoporosis in patients with Celiac Disease varies somewhat. The incidence is higher with more severe disease and older age at diagnosis. When children present with Celiac Disease, they usually have evidence of delayed or poor growth, and bone density, if measured, is low.
When a gluten-free diet is maintained, there is usually an increase in bone mass, and the growth rate usually improves.
Some studies suggest that children with Celiac Disease who are diagnosed at a young age and treated effectively will have normal bone mass when they reach adulthood.
Adults who have had lifelong undiagnosed Celiac Disease are more likely to have lower bone density than the average person their age. They are significantly more likely to already have had broken bones than are age and se x matched controls.
Patients with Celiac Disease may also have a different bone disorder called osteomalacia. Osteomalacia differs in several respects from osteoporosis.
In osteomalacia, the amount of bone may be normal, but there is less mineral in the bone. Bone formation is a two-step process. Bone is first made as soft tissue; after the bone has been laid down, calcium and phosphorus are deposited in the tissue, and it hardens.
In osteomalacia, less calcium and phosphorus are deposited into bone. This makes the bone soft and more pliable. In children, the long bones of the legs will bend and bow, which is called rickets.
In contrast to osteoporosis, there are usually symptoms with osteomalacia. The bones may ache and feel sore to the touch. For example, it is common to have hip or heel pain when you stand.
Fractures do occur, but they tend to be a little different from osteoporatic fractures. It is important for the physician and the patient to know whether they’re dealing with osteoporosis or osteomalacia, because they are treated differently, and certain therapies that might make osteoporosis better might make osteomalacia worse.
The definitive diagnosis of osteomalacia is made by bone biopsy, where excess unmineralized bone can be seen, although tests of blood and urine may also be helpful.
www.enabling.org/ia/celiac/osteopo.html#index
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Bone Mass and Gastrointestinal Disease
CAROL E. SEMRAD
Department of Medicine, Columbia University, College of Physicians and Surgeons, New York, New York 10032, USA
Address for correspondence: Carol E. Semrad, Department of Medicine, Columbia University, College of Physicians and Surgeons, 630 West 168th Street, New York, NY 10032. Voice: 212-305-8156; fax: 212-305-6443.
"mailto:ces2@columbia.edu"
Several gastrointestinal and liver diseases impair the absorption of calcium, phosphate, and/or vitamin D, and are associated with an increased incidence of bone disease. Changes in bone mineral density (BMD) using dual-energy X-ray absorptiomety (DXA) have been best studied in the malabsorptive disorder, celiac disease. Celiac disease is an inflammatory condition of the small intestine triggered by ingesting gluten present in wheat, rye, or barley. Chronic inflammation leads to intestinal atrophy and nutrient malabsorption.
The disease affects the proximal small bowel; the site where calcium is best absorbed. About 70% of adults with celiac disease have abnormally low BMD values.
Treatment with a gluten-free diet increases BMD, but not to normal values. As celiac disease may not be detected until adult life, the failure to reach normal BMD on a gluten-free diet can be explained, at least in part, by the failure to reach peak bone mass.
All individuals with malabsorptive disorders should be screened for secondary bone disease. The development of easier and less expensive methods to assess BMD will facilitate screening those at risk for bone disease.
Annals of the New York Academy of Sciences 904:564-570 (2000)
© 2000 "/misc/terms.shtml"
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Bone and bone health
In adults, poor compliance to their gluten-free diet, and persistent villous atrophy are both associated with low bone mineral density. In a study by Mora et al, lumbar spine and whole body bone mineral density values in children and adolescents, at the diagnosis of coeliac disease, were found to be significantly lower than in control subjects. However, a gluten-free
www.coeliaccentre.org/en/
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Magnesium deficiency: possible role in osteoporosis associated with gluten-sensitive enteropathy.
Rude RK, Olerich M.
…This study demonstrates that GSE patients have reduction in intracellular free Mg2+, despite being clinically asymptomatic on a gluten-free diet. Bone mass also appears to be reduced. Mg therapy resulted in a rise in PTH, suggesting that the intracellular Mg deficit was impairing PTH secretion in these patients. The increase in bone density in response to Mg therapy suggests that Mg depletion may be one factor contributing to osteoporosis in GSE. ….
www.ncbi.nlm.nih.gov/pubmed/9116391
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Osteoporosis in people with coeliac disease
I have been sent a booklet from National Osteoporosis Society called 'Osteoporosis in people with coeliac disease: recommendations'.
This is very helpful, telling you about osteoporosis & CD, bone & bone health, treatment & prevention of osteoporosis in people with CD.
It points out that research re people with CD on GFD 'with daily calcium intake of 860mg/day were shown to have osteoporosis, whilst those with an intake of 1054mg/day were shown to have normal BMD' (bone mineral density).
You can get the booklet from NOS.
www.nos.org.uk/
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Silent Coeliac Disease (and increase of bone density on a gluten free diet)
acta.uta.fi/pdf/951-44-5721-8.pdf
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International Osteoporosis Foundation
Osteoporosis in the EC
www.iofbonehealth.org/
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What is osteoporosis?
C Christodoulou and C Cooper
MRC Environmental Epidemiology Unit, University of Southampton, Southampton General Hospital, Southampton
Correspondence to:
Professor C Cooper, MRC Environmental Epidemiology Unit, Southampton General Hospital, Southampton SO16 6YD, UK;
cc@mrc.soton.ac.uk
…Osteoporosis is a very common disorder, which results in an increase in fracture risk. The annual cost attributable to hip, vertebral, and wrist fractures in England and Wales is £1.7 billion.
Significant mortality and morbidity are associated with osteoporotic fractures.
The method that is most widely used for the diagnosis of osteoporosis is dual energy x-ray absorptiometry.
The aim of prevention and treatment of osteoporosis is to prevent the occurrence of future fractures.
Lifestyle changes should be encouraged in high risk patients.
Pharmacological treatments include the bisphosphonates, hormone replacement therapy, selective oestrogen receptor modulators calcitonin, the 1–34 fragment of parathyroid hormone, calcium and vitamin D supplements…
pmj.bmj.com/content/79/929/133.abstract
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Bone mass and metabolism in patients with celiac disease
BACKGROUND & AIMS: Several aspects of the pathogenesis of osteopenia in celiac disease are still unclear. Therefore, bone mass and metabolism were evaluated in adults with celiac disease in a cross-sectional study.
METHODS: Bone mineral density (BMD), assessed by total body dual- photon absorptiometry, and serum indices of bone metabolism and remodeling were evaluated in 17 patients with untreated celiac disease, 14 with celiac disease on a gluten-free diet, and 24 healthy volunteers.
RESULTS: BMD, expressed as a z score, was significantly lower in patients with untreated celiac disease than in patients with treated celiac disease and volunteers and lower in patients with treated celiac disease than in volunteers. Similar changes were observed in serum calcium level, whereas intact parathyroid hormone level was significantly higher in untreated than in treated patients with celiac disease and volunteers, and no difference was found between the latter two groups. 25-Vitamin D level was significantly lower and 1,25-vitamin D level significantly higher in untreated celiac disease than in treated celiac disease and volunteers. Indices of bone remodeling were significantly higher in untreated than in treated patients and volunteers and significantly and positively correlated with iPTH in untreated patients with celiac disease.
CONCLUSIONS: BMD is almost invariably low in patients with untreated celiac disease. Results in treated patients suggest that gluten-free diet improves but does not normalize BMD. Untreated celiac disease is characterized by high levels of 1,25-vitamin D and by increased bone turnover, caused by the increase in intact parathyroid hormone level.
(Gastroenterology 1995 Jul;109(1):122-8)
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Osteoporosis treatment and prevention
…Preventing osteoporosis by maintaining a health diet rich in calcium and vitamin D and exercising regularly can help many women avoid the serious effects of osteoporosis. Women who have low bone mineral density or osteoporosis may also benefit from taking hormone replacement therapy or other drug therapies…
imaginis.com/osteoporosis/osteo_treatment.asp
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......How can osteoporosis in men be prevented and treated?
The medical research on osteoporosis in men has been inadequate. However, experts agree that all persons should take the following steps to preserve bone health.
· Recognize and treat any underlying medical conditions that affect bone health. Identify and evaluate the use of medications that are known to cause bone loss.
· Change unhealthy habits, such as smoking, excessive alcohol intake, and inactivity.
· Ensure a daily calcium intake of 1000 mg/day to age 50 and 1200 mg/day over age 51 and over.
· Ensure adequate vitamin D intake. Normally, we make enough vitamin D from exposure to as little as 10 minutes of sunlight a day. If exposure to sunlight is inadequate, then vitamin D intake from supplements should be at least 400 IU but not more than 800 IU/day.
· Engage in a regular regimen of weight-bearing exercises where bone and muscles work against gravity. This includes walking, jogging, racquet sports, stair climbing, and team sports. Also, lifting weights or using resistance machines appears to help preserve bone density. Exercise also improves balance and muscle tone and imparts a sense of well-being. If you have already been diagnosed with osteoporosis, any exercise program should be evaluated for safety by your doctor before you begin. Twisting motions and impact activities may need to be curtailed depending on the severity of your condition.
What medications can slow or stop bone loss in men?
Alendronate (brand name Fosamax®) is approved as a treatment for osteoporosis in men.
Alendronate and risedronate (brand name Actonel®), medications from the class of drugs called bisphosphonates, are approved for use in steroid-induced osteoporosis that occurs in men and women as a result of long term use of steroids such as prednisone or cortisone.
Currently, none of the other osteoporosis medications that have been approved by the Food and Drug Administration (FDA) for postmenopausal women have been approved for men. However, to help men with osteoporosis, physicians may prescribe the following:
· Testosterone replacement therapy may be prescribed for a man with a low testosterone level.
· Calcitonin is a medication that slows or stops bone loss and may relieve the pain of fractures in some patients. Calcitonin is approved by the FDA for the treatment of osteoporosis in postmenopausal women. While its effect in men has not been studied, evidence suggests that it may work the same in men as in women. Calcitonin is available as an injection and as a nasal spray.
www.nof.org/men/index.htm
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Bone mass & CD
…Osteoporosis was shown in 47% of patients with treated adult coeliac disease.
www.ncbi.nlm.nih.gov/pubmed/7797121?dopt=Abstract
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…Celiac patients had a lower bone mass than controls despite early diagnosis and good compliance with the gluten-free diet. These differences could not be atributed entirely to the lower height of celiac patients. These results suggest that celiac patients constitute a risk group for development of osteoporosis later in life. This fact should be taken into consideration in the treatment of this condition.
www.ncbi.nlm.nih.gov/pubmed/9239290?dopt=Abstract
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…CONCLUSIONS: Treatment of coeliac disease with a gluten free diet is associated with a significant increase in bone mineral density, although patients still had lower bone mineral density than controls.
www.ncbi.nlm.nih.gov/pubmed/8991855?dopt=Abstract
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Associated Medical Conditions in Individuals with Celiac Disease
.... Sixty-two percent of respondents said they had their bone density measured. Twenty-seven percent of respondents had been diagnosed with osteoporosis and 10% with osteopenia. Forty-four percent (n = 116) had a history of a previous fracture and of these individuals, 36% had previously broken their wrist. Five percent were taking calcium and 5% vitamin D after diagnosis of osteoporosis/osteopenia. Thirteen percent were taking an anti-osteoporosis medication such as alendronate, risedronate, HRT or raloxifene.
www.biomedcentral.com/1471-230X/3/8#IDAGEMLP
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…The most important treatment is the gluten-free diet. The available evidence suggests that if children or adults adhere to a gluten-free diet, bone density will improve, especially during the first year or two of treatment. If you’re an adult at age 30, who has just discovered that you have Celiac Disease and low bone density, your bone density may increase anywhere between 5-10% over the first year or two on a gluten-free diet. There are no good studies looking beyond 1-2 years.
Calcium supplements are important, and may be necessary even in those patients who have a good response to the gluten-free diet. Celiac Disease patients lose more calcium in bowel movements than normal people do, and there is a certain amount of calcium that is lost in the urine whether you have Celiac Disease or not. Calcium is necessary for a myriad of body processes, and if it doesn’t come from the diet or supplements, it is taken from the bones.
Women with Celiac Disease who go through menopause should strongly consider taking estrogen, which will protect them from the additional bone loss that occurs with estrogen deficiency.
There are other newer therapies for osteoporosis. None of them have been evaluated in patients with Celiac Disease. The new Merck drug, Fosamax (Alendronate), is absorbed mainly in the stomach, and should be absorbed in the patient with Celiac Disease. It does not contain gluten, but does contain lactose. The decision to institute Fosamax therapy is a very individual one that should be reached between the Celiac Disease patient and their doctor after a careful evaluation to make sure that there is no evidence of osteomalacia. Fosamax may make osteomalacia worse. Moreover, at this time we don’t really know if Fosamax is effective. The other agent that is approved for osteoporosis is calcitonin, which is available in a nasal spray. Calcitonin probably won’t hurt anybody, but there is no information available about whether it helps. Newer agents that act by different mechanisms to increase bone density are now in clinical trials.
www.enabling.org/ia/celiac/osteopo.html#TREATMENT%20FOR%20CELIAC%20PATIENTS%20WITH%20LOW%20BONE%20DENSITY
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Severe osteopenia in symptom-free adults with a childhood diagnosis of coeliac disease.
Cellier C, Flobert C, Cormier C, Roux C, Schmitz J.
Lancet. 2000 Mar 4;355(9206):806.
The frequency of osteopenia in symptom-free adults diagnosed with coeliac disease during childhood and who resumed a normal diet during adolescence is unknown.
Severe osteopenia (a bone mineral density below two standard deviations of the mean) was found in up to a third of symptom-free young adults on a normal diet.
These patients should not be thought to be disease-free but should receive long-term follow-up and most of them should be advised to resume a gluten-free diet.
www.ncbi.nlm.nih.gov/pubmed/10711931?dopt=Abstract
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strategy for osteoporosis in gastroenterology
Reference
EM Scott and BB Scott. Eur Journal of Gastroenterology and Hepatology 1998; 10: 689-698
Osteoporotic fractures are a major public health problem. The estimated total cost of osteoporotic fractures in England and Wales is £742 million per annum. With an increasing elderly population the costs are likely to rise. Osteoporosis can be reliably detected by the measurement of Bone Mineral Density (BMD) using Dual energy X-ray absorptiometry (DEXA). A BMD more than two standard deviations below the mean for a young adult is generally taken as an indication of osteoporosis.
Gastroenterologists have a large proportion of patients who are at increased risk of osteoporosis. One of the main groups is that with coeliac disease (CD). One study showed that 47% of women and 50% of men on a gluten-free diet had osteoporosis. BMD was positively related to calcium intake, body mass index (BMI) and menopausal age. Other studies have shown significant improvement a year after starting a gluten-free diet, normal BMD in patients who had had a gluten-free diet since childhood and improved bone mineralisation on a gluten free diet in childhood and adolescence.
The mechanism of osteoporosis in CD is likely to be related to calcium malabsorption, leading to increased parathormone secretion, which increases bone turnover and cortical bone loss. The following points summarize the strategy for prevention and treatment of osteoporosis in CD as suggested in 1998:
General advice
· Strict gluten-free diet
· 1500mg calcium/day
· Exercise
· No smoking
· No excess alcohol
· Seek and treat Vitamin D deficiency
· Measure BMD at diagnosis – if low reinforce above advice
Post-menopausal women
· Measure BMD at menopause or when first seen
· If osteoporotic offer either HRT, preferably by skin patch, bisphosphonate orally or by calcitonin
Men over 55 years
· Measure BMD
· If osteoporotic offer bisphosphonate or calcitonin
All with fragility fracture
· Measure BMD
· If osteoporotic offer HRT (if post menopausal) bisphosphonate or calcitonin. If already on HRT consider adding bisphosphonate or calcitonin.
Duration of drug treatment
· For bisphosphonate and calcitonin measure BMD yearly
· If BMD falls below 4% per year in 2 successive years change to another drug
· If no fall continue drug for at least 3 years, possibly long term.
· Restart drug if, on stopping, yearly BMD falls below 4%
· For HRT check BMD after 10 years and continue HRT if osteoporosis persists
www.cdrc.org.uk/en/article.asp?chco_id=427
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Bone mineral density and importance of a gluten-free diet in patients with celiac disease in childhood
Posted by Charlotte, Oxford on 10/2/2005
GF board
Came across this very interesting study from Turkey ........
Abstract:
www.ncbi.nlm.nih.gov/pubmed/11694673?dopt=Abstract
Bone mineral density and importance of a gluten-free diet in patients with celiac disease in childhood.
Kalayci AG, Kansu A, Girgin N, Kucuk O, Aras G.
Department of Pediatric Gastroenterology, School of Medicine, Ondokuz Mayis University, Samsun, Turkey. ayhangk@omu.edu.tr
"OBJECTIVES: Celiac disease (CD), a common cause of malabsorption, is known to be associated with disorders of the skeleton, but there are conflicting data about the effect of diet on bone metabolism. The aims of this study were to investigate the prevalence of osteopenia; to identify the relationship between bone mineral density (BMD), serum calcium, and parathyroid hormone levels; and to determine the effect of gluten-free diet on BMD in children with celiac disease.....
CONCLUSIONS: BMD is almost invariably low in newly diagnosed celiac patients in childhood. We therefore recommend that BMD should be evaluated in patients with CD. Strict gluten avoidance promoted a significant increase in BMD. However, values still remained markedly low after 1 year of follow-up in some patients. These patients should be followed for longer periods of time with yearly BMD evaluation, as 1 year of diet therapy was found to be insufficient for osteopenia to be resolved."
pediatrics.aappublications.org/cgi/content/full/108/5/e89
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Increased prevalence of CD among patients with osteoporosis
Stenson WF, Newberry R, Lorenz R, Baldus C, Civitelli R.
Increased prevalence of celiac disease and need for routine screening among patients with osteoporosis. Archives of Internal Medicine; vol. 165, pp. 393-399, Feb. 28, 2005.
"Our results suggest that as many as three to four percent of patients who have osteoporosis have the bone disease as a consequence of having celiac disease, which makes them unable to absorb normal amounts of calcium and vitamin D," says principal investigator William F. Stenson, M.D., a Washington University physician at Barnes-Jewish Hospital. The study is reported in the Feb. 28 issue of the Archives of Internal Medicine’’
www.medicalnewstoday.com/articles/20501.php
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Recommendations for the treatment of osteoporosis in CD
Recommendations for the treatment of osteoporosis in coeliac disease and prevention of osteoporosis in people with coeliac disease have been produced in conjunction with a diverse panel of healthcare specialists.
www.cdrc.org.uk/en/article.asp?chco_id=466
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Bisphosphonates.
Drug for Bone Disease Linked to 'Jaw Death'
Researchers Report Cases of Osteonecrosis of Jaw in Patients Who Had Teeth Pulled
WebMD Medical News
Oct. 3, 2005 -- Millions of people treated for bone diseases such as osteoporosis may be at risk for developing a potentially serious jawbone condition that seems to be triggered by having teeth pulled.
More than a thousand cases of osteonecrosis of the jaw, or jaw death, have been reported in patients taking a class of drugs known as bisphosphonates. Osteonecrosis indicates that part of the bone is no longer alive; unlike normal bone it cannot regenerate itself because of a lack of blood supply.
Most cases occurred in cancer patients taking the intravenous bisphosphonates Aredia and Zometa to prevent cancer-related bone loss. But osteonecrosis of the jaw has also been reported in women who had teeth pulled while taking the widely prescribed osteoporosis pill Fosamax, dentistry professor Ken Hargreaves, DDS, PhD, tells WebMD.
"Even if this is a rare condition, so many women now take bisphosphonates to prevent bone loss that the numbers could grow," he says. "We just became aware of this a few years ago, and it has been called a growing epidemic."
The study appeared in the October issue of the Journal of Endodontics.
Saving Teeth Lowers Risk
A newly published report edited by Hargreaves outlines two cases of osteonecrosis of the jaw in cancer patients on monthly doses of intravenous bisphosphonates.
He says it is clear from these and other published cases that patients taking bisphosphonates should be warned that they may be at risk if they have teeth pulled. Osteonecrosis of the jaw is very painful and can lead to serious complications, including ulcerations within the lining of the mouth, infection, and breakdown of the jawbone with disfigurement.
"People taking these drugs need to see their dentist regularly, and they need to recognize the importance of preventive dental care," he says. "And when there is a problem, we need to do everything we can to save teeth."
That means performing root canals on patients taking these drugs rather than tooth extractions, he says.
my.webmd.com/content/article/113/110591.htm
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PREVENTION AND MANAGEMENT OF OSTEOPOROSIS
Report of a WHO Scientific Group World Health Organization Geneva ...
whqlibdoc.who.int/trs/WHO_TRS_921.pdf
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Re: Bone Scan/Dexa scan
Posted by Eileen on 16/11/2005
GF board
I arranged it through my Gp using the Fast Track system (NHS), and the cost was £62. I waited 2 weeks for the appointment. If you don't have time to visit the Gp, perhaps you could drop him a line instead requesting one.
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Osteoporosis guide
A guide to osteoporosis for all ages
actnowosteoporosis.co.uk/index.html
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osteoporosis and coeliac disease
Question: I read your answer to a question on osteoporosis and coeliac disease in Oct 2002. Is there any evidence to suggest that adults with coeliac disease need dexa scanning? What is the start age and how frequently should they be investigated?
Answer:
ATTRACT found a few documents discussing this issue which differ slightly in their recommendations.
A position statement from the American Gastroenterological Association (2003)(1) states:
“DXA scans are likely unnecessary in patients with newly diagnosed uncomplicated pediatric celiac disease, but should be considered for adults with newly diagnosed celiac disease 1 year after initiation of a gluten-free diet, to allow for stabilization of bone density (level D evidence).”
The British Society of Gastroenterology produced interim guidelines on the management of patients with coeliac disease in April 2002 (2). This guideline states:
“It is usual practice to consider bone densitometry scanning on presentation which may be repeated after one to two years of dietary therapy if the initial value is low.”
The Primary Care Society for Gastroenterology published a document entitled Follow-up care of adult coeliac disease in August 2001 (3). This states:
“Osteoporosis risk assessment and management
DEXA at menopause for women, at 55 years for men, at any age following fragility fracture.”
The British Society of Gastroenterology guidelines for osteoporosis in coeliac disease and inflammatory bowel disease published in 2000 state:
“The timing of densitometry presents a problem. In women, postmenopausal densitometry will be more sensitive at detecting osteoporosis but the delay will give less scope for achieving a higher bone density with treatment, despite evidence that bisphosphonates may produce some reversal of osteoporosis.
Conversely, screening at presentation may reveal osteoporosis at a young age when intervention would theoretically have greater potential …
On balance, one could recommend that all patients have densitometry at diagnosis. This would allow reinforcement of general advice if BMD is low.
However, we can appreciate that the burden on both the clinician and the densitometry service might be counter-productive and deter any screening.
A simpler strategy, omitting BMD at presentation in younger patients and restricting BMD measurement to the older patients who are more likely to benefit, could therefore be more effective in IBD.
In any case, patients with IBD at presentation are unlikely to have osteoporosis as a result of their disease. There is more reason for measuring BMD at diagnosis in patients with coeliac disease because they will already have suffered malabsorption for many years.
In women, if the diagnosis is made earlier the BMD should be measured at the menopause.
It is debateable whether a single measurement at the menopause is adequate because there is considerable variation in the rate and duration of rapid perimenopausal bone loss. For this reason it would be sensible to repeat the BMD after perhaps two years in those whose BMD does not suggest osteoporosis.
Similarly, in men the BMD should be measured at about 55 years of age if they presented at an earlier age. BMD should be done at any age if there has been a fragility fracture, namely one which is atraumatic or follows a simple fall.”
American Gastroenterological Association. American Gastroenterological Association medical position statement: guidelines on osteoporosis in gastrointestinal diseases. Gastroenterology 2003 Mar;124(3):791-4.
www.bsg.org.uk/pdf_word_docs/coeliac.doc
www.bsg.org.uk/pdf_word_docs/osteo.pdf
Date Posted : 22/08/2005
Evidence:
Evidence 1:- 0
Evidence 2:- 0
Evidence 3:- 0
Evidence 4:- 2
Evidence G:- 2
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Osteomalacia causes bone pain
Posted by Charlotte, Oxford on 6/3/2007
GF board
Bone pain is caused by osteomalacia which is common in (mainly younger) coeliacs. It's known as rickets in children. You should not continue in pain. Your doctors should be treating you for this - you may need quite aggresive treatment with Vitamin D and calcium:
www.nhsdirect.nhs.uk/en
In the majority of cases, treatment will cure osteomalacia, although it may be several months before you have any relief from bone pain and muscle weakness. The increased vitamin D must be taken regularly otherwise the condition will come back.
www.netdoctor.co.uk/diseases/fac ... ickets.htm
What treatment is available?
Regular daily supplements of vitamin D and calcium, eg Calcichew D3 or Adcal D3, are usually used for people with simple vitamin D deficiency, but some people have a single injection vitamin D, in the form of calciferol (vitamin D2). This is stored in the body and can last up to a year before another injection may be needed.
People with vitamin D deficiency due to intestinal problems are best treated with calciferol. Most people with osteomalacia find their pain is reduced about two weeks after the injection. Extra calcium may also be needed while bone is healing.
bone-muscle.health-cares.net/ost ... atment.php
What's the treatment for osteomalacia?
Oral supplements of vitamin D, calcium and phosphorus may be given depending on the underlying cause of the disorder.
Larger doses of vitamin D and calcium may be needed for people with intestinal malabsorption. Monitoring of blood levels of phosphorus and calcium may be indicated for people with certain underlying conditions. Regular daily supplements of vitamin D and calcium are usually used for people with simple vitamin D deficiency, but some people have a single injection vitamin D, in the form of calciferol (vitamin D2). This is stored in the body and can last up to a year before another injection may be needed. People with vitamin D deficiency due to intestinal problems are best treated with calciferol. Most people with osteomalacia find their pain is reduced about two weeks after the injection. Extra calcium may also be needed while bone is healing. Direct exposure of the skin (i.e., hands, face, arms, etc.) to sunlight stimulates the body to manufacture vitamin D. However, both clothing and use of a sunscreen prevent the ultraviolet light that triggers the formation of vitamin D from reaching the skin. Depending on latitude, sunlight during the winter may not provide enough ultraviolet light to promote adequate vitamin D production. At other times during the year, even 30 minutes of exposure per day will usually lead to large increases in the amount of vitamin D made. If it is difficult to get sunlight exposure, full-spectrum lighting can be used to stimulate vitamin D production.
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….differences between osteomalacia (soft bones) and osteoporosis (bone loss).
Both are common in coeliacs: the former tends to affect young coeliacs and the latter older ones:
…..
In children, this is also known as rickets; in grown-ups, it is sometimes known as 'adult rickets'. This condition is caused by a deficiency in Vitamin D. Osteomalacia is more common than most physicians realize and should always be considered in patients with unexplained pain -especially the kind you describe.
The pain of osteomalacia is typically difficult to localize. All the bones are tender - especially the long ones in the legs and arms- because of inflammation of the nerve fibers imbedded in the lining of the bone (called the periosteum). When Vitamin D is deficient, the lining of the bone becomes activated, causing more bone to be absorbed and replaced at an accelerated rate. This is similar to the 'growing pains' experienced by adolescents who are going through the growth spurt.
In diagnosed cases of osteomalacia, 94% of patients complain of pain; 94% complain of muscle weakness; 88% complain of bone tenderness with pressure on touch; 24% complain of a waddling gait and muscle cramps; and, there is a higher incidence of fracture than expected for age- even in bones that test 'normal'on the DEXA bone density test.
It is very difficult these days to become deficient in Vitamin D because it is frequently supplemented in foods. Most vitamin preparations also contain Vitamin D. The most common cause of osteomalacia with apparently normal nutrition is bowel disorders, as in your case. Your bowel was bypassed, which can cause malabsorption of nutrients, including vitamins. The most common bowel disorder is celiac sprue, also known as gluten sensitivity. Gluten is present in wheat. Celiac disease may be present in as much as 5% of the population and is often confused with irritable bowel syndrome.
Researchers at the Henry Ford Health System reporting in The American Journal of Medicine, Vol. 108, 296 -300, looked at the causes of osteomalacia in patients they have seen with stomach surgery (for ulcers), gastric stapling, intestinal bypass, intestinal removal, removal of the pancreas and pancreatitis, and celiac disease. Most of these patients had their symptoms for more than two years. The average time for symptoms to develop from diagnosing the intestinal problem was 14 years! It is easy to see how physicians could overlook this condition, as these changes develop slowly over time. Additionally, these patients get passed on from physician to physician and often get labeled as chronic complainers or malingerers. The 'label' itself, like fibromyalgia, can mislead subsequent physicians.
Simple blood tests should help the doctor make the diagnosis. The bone density test you've had reveals bone loss, but that deficiency is not due to osteoporosis. Unfortunately, though, doctors often mistakenly treat patients for osteoporosis based on test results such as yours. Indeed, people who take this test may have osteomalacia and osteoporosis. However, the osteomalacia 'accidentally' gets better when Vitamin D and calcium are prescribed for the osteoporosis. Osteoporosis does not usually cause generalized bone pain or tenderness.
Doctors in the 'good ole days' would probably have made the diagnosis of osteomalacia very quickly. Rickets was common prior to 1940, as were nutritional diseases. Today, osteomalacia and rickets are relatively rare, so some of us doctors who are 'youngsters' (age 40 or so) may not have seen many cases.
If you have unexplained bone pain, ask your doctor to check for osteomalacia or adult rickets.
...
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Coeliac Disease and the Risk of Fractures - A General Population-based Cohort Study
Posted by Charlotte, Oxford on 16/3/2007
GF board
This new study (full text available in link) confirms earlier findings by Joe West but also suggests that the risk remains even after years on the diet and that coeliac children are at particular risk. It suggests (to me) that all coeliacs need to be particularly careful to maximise their bone health with calcium, vitamin D, sunlight, weight-bearing exercise etc.
From the Discussion:
"We found a statistically significantly positive association of CD with hip fracture or any fracture, irrespective of whether the fracture occurred prior to or after the diagnosis of CD. The overall risk estimates for subsequent hip fracture and any fracture were almost identical to those of West et al.[14] Individuals with CD diagnosed in childhood were at increased risk of subsequent hip fracture and may also be at increased risk of fracture of any type. The duration to and after diagnosis of CD did not notably influence the risk of hip fracture. Hence, this study found no evidence that a gluten-free diet lowers the risk of hip fracture. Even 20 years after diagnosis of CD were individuals with CD at increased risk of hip fracture."
Coeliac Disease and the Risk of Fractures - A General Population-based Cohort Study
J. F. Ludvigsson; K. Michaelsson; A. Ekbom; S. M. Montgomery
Aliment Pharmacol Ther. 2007;25(3):273-285. �2007 Blackwell Publishing
Posted 03/08/2007
Summary and Introduction
Summary
Background: Earlier studies have suggested that untreated coeliac disease may be associated with osteoporosis, but results are contradictory for the risk of long-term fractures.
Aim: To study the association between coeliac disease and fractures.
Methods: We used Cox regresson to examine the future risk of hip fracture and fracture of any type in more than 13 000 individuals with coeliac disease and 65 000 age- and sex-matched reference individuals in a general population-based cohort.
Results: During follow-up, 1365 first hip fractures and 4847 fractures of any type occurred. Coeliac disease was positively associated with subsequent hip fracture (hazard ratio = 2.1; 95% CI = 1.8-2.4) (in children: hazard ratio = 2.6; 95% CI = 1.1-6.2) and fractures of any type (hazard ratio = 1.4; 95% CI = 1.3-1.5) (in children: hazard ratio = 1.1; 95% CI = 1.0-1.2). The absolute excess risk of hip fractures in children with coeliac disease was 4/100 000 person-years. Incidence ratios for hip fracture in individuals with CD were around two both prior to diagnosis of coeliac disease and afterwards; this risk increase remained 20 years after diagnosis of coeliac disease.
Conclusions: Individuals with coeliac disease, including children with coeliac disease, may be at increased risk of hip fracture and fracture of any type. Coeliac disease may be positively associated with long-term hip fracture risk.
Link: www.medscape.com:80/viewarticle/552626_print
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CD and bones
From Pubmed:
Endocr Pract. 2004 May-Jun;10(3):203-7.
Celiac disease manifesting as isolated hypocalcemia.
Rickels MR, Mandel SJ.
Division of Endocrinology, Diabetes and Metabolism, Department of Medicine, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104, USA.
OBJECTIVE: To describe a patient who presented with hypocalcemia and hypocalciuria as the initial manifestations of celiac disease, despite a normal vitamin D status.
METHODS: We review the diagnostic evaluation, treatment, and biochemical and bone mineral density responses of a patient with asymptomatic celiac disease, which was initially suggested because of a low serum calcium level that became attributable to isolated malabsorption of calcium.
RESULTS: A 36-year-old woman presented with hypocalcemia in the presence of normal serum 25-hydroxyvitamin D and high serum 1,25-dihydroxyvitamin D levels. She had hypocalciuria and secondary hyperparathyroidism that were refractory to pharmacologic calcium and cholecalciferol supplementation. Fecal calcium excretion indicated malabsorption of calcium, and biopsy of the small intestine demonstrated pathologic changes characteristic of celiac disease. Bone mineral density, determined by dual-energy x-ray absorptiometry, was in the osteopenic range at the femoral neck. The initiation of a gluten-free diet resulted in correction of all biochemical abnormalities and a substantial increase in bone mineral density.
CONCLUSION: Primary intestinal malabsorption of calcium without concomitant vitamin D deficiency is possible in celiac disease because of the preferential involvement of the proximal small intestine early in the disease process. Our patient had hypocalcemia caused by celiac disease and values for serum 25-hydroxyvitamin D and 1,25-dihydroxyvitamin D that were normal and elevated, respectively. Correction was demonstrated after dietary gluten withdrawal.
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Osteoporos Int. 1996;6(6):453-61.
Magnesium deficiency: possible role in osteoporosis associated with gluten-sensitive enteropathy.
Rude RK, Olerich M.
Department of Medicine, University of Southern California School of Medicine, Los Angeles, USA.
Osteoporosis and magnesium (Mg) deficiency often occur in malabsorption syndromes such as gluten-sensitive enteropathy (GSE). Mg deficiency is known to impair parathyroid hormone (PTH) secretion and action in humans and will result in osteopenia and increased skeletal fragility in animal models. We hypothesize that Mg depletion may contribute to the osteoporosis associated with malabsorption. It was our objective to determine Mg status and bone mass in GSE patients who were clinically asymptomatic and on a stable gluten-free diet, as well as their response to Mg therapy. Twenty-three patients with biopsy-proven GSE on a gluten-free diet were assessed for Mg deficiency by determination of the serum Mg, red blood cell (RBC) and lymphocyte free Mg2+, and total lymphocyte Mg. Fourteen subjects completed a 3-month treatment period in which they were given 504-576 mg MgCl2 or Mg lactate daily. Serum PTH, 25-hydroxyvitamin D, 1,25-dihydroxyvitamin D and osteocalcin were measured at baseline and monthly thereafter. Eight patients who had documented Mg depletion (RBC Mg2+ < 150 microM) underwent bone density measurements of the lumbar spine and proximal femur, and 5 of these patients were followed for 2 years on Mg therapy. The mean serum Mg, calcium, phosphorus and alkaline phosphatase concentrations were in the normal range. Most serum calcium values fell below mean normal and the baseline serum PTH was high normal or slightly elevated in 7 of the 14 subjects who completed the 3-month treatment period. No correlation with the serum calcium was noted, however. Mean serum 25-hydroxyvitamin D, 1,25-dihydroxyvitamin D and osteocalcin concentrations were also normal. Despite only 1 patient having hypomagnesemia, the RBC Mg2+ (153 +/- 6.2 microM; mean +/- SEM) and lymphocyte Mg2+ (182 +/- 5.5 microM) were significantly lower than normal (202 +/- 6.0 microM, p < 0.001, and 198 +/- 6.8 microM, p < 0.05, respectively). Bone densitometry revealed that 4 of 8 patients had osteoporosis of the lumbar spine and 5 of 8 had osteoporosis of the proximal femur (T-scores < or = -2.5). Mg therapy resulted in a significant rise in the mean serum PTH concentration from 44.6 +/- 3.6 pg/ml to 55.9 +/- 5.6 pg/ml (p < 0.05). In the 5 patients given Mg supplements for 2 years, a significant increased in bone mineral density was observed in the femoral neck and total proximal femur. This increase in bone mineral density correlated positively with a rise in RBC Mg2+. This study demonstrates that GSE patients have reduction in intracellular free Mg2+, despite being clinically asymptomatic on a gluten-free diet. Bone mass also appears to be reduced. Mg therapy resulted in a rise in PTH, suggesting that the intracellular Mg deficit was impairing PTH secretion in these patients. The increase in bone density in response to Mg therapy suggests that Mg depletion may be one factor contributing to osteoporosis in GSE.
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J Pediatr Gastroenterol Nutr. 2003 Oct;37(4):434-6.
Bone mineral density in children with untreated and treated celiac disease.
Kavak US, Yüce A, Koçak N, Demir H, Saltik IN, Gürakan F, Ozen H.
Hacettepe University, Department of Pediatrics, Ankara, Turkey.
OBJECTIVES: Osteopenia is a common complication in adults with celiac disease. The effect of a gluten-free diet on bone mineral density is a matter of controversy. The aim of this study was to investigate bone mineral density in children with celiac disease at diagnosis and in patients treated for 1 year.
METHODS: Bone mineral density and bone mineral content were measured in 34 children with untreated celiac disease at diagnosis and in 28 patients on a gluten-free diet for 1 year. The results were compared with those of 64 gender- and age-matched healthy control subjects. Serum calcium, phosphate, alkaline phosphatase, 25 -hydroxy vitamin D, and intact parathormone levels were determined in treated and untreated patients.
RESULTS: The mean values of bone mineral density and bone mineral content of untreated patients with celiac were significantly lower than the control group (P = 0.006 and P = 0.005, respectively) and treated patients (P = 0.015 and P = 0.011 respectively). Treated patients had mean bone mineral density and bone mineral content values not significantly different from those of healthy control subjects. Minor hypocalcemia was detected in 17.6% of the patients with new diagnoses and 3.6% of the treated patients. Of the untreated patients, 29.4% had high intact parathormone concentrations; in untreated patients, the total was 14.3%. Untreated patients had significantly lower serum calcium and significantly higher intact parathormone levels than did treated patients. The other bone metabolism parameters were similar in the two celiac groups.
CONCLUSION: Children with celiac disease are at risk for reduced bone mineral density. A strict gluten-free diet improves bone mineralization, even in 1 year. Early diagnosis and treatment of celiac disease during childhood will protect the patient from osteoporosis
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Nobody looks for osteoporosis in males
From:
Men's Osteoporosis Support Group
…"I have never had any symptoms of sprue and never suspected it until my daughter's gastroenterologist suggested that my wife and I have blood tests. My wife's were negative, while both of mine (I think they tested for two antibodies) were positive for sprue. I then went in for a gastroscopy, which was also positive. I spoke with my gastroenterologist earlier this week and he told me that based on the severe nature of my osteoporosis I've probably had celiac sprue for a long time. Unfortunately, the long-term osteoporosis also went undiagnosed until I had a bone
density test after breaking my arm and then my leg within the span of a month a couple of years ago. My primary care physician did some research and found that osteoporosis is a common result of untreated celiac disease. Of course, now that we know about celiac disease and osteoporosis, I've been reading all kinds of information about it on the Web.
Unfortunately, nobody looks for osteoporosis in a fairly young male--or any male--for that matter. (My Fosamax packages still say the drug is for post-menopausal women!) It was apparently so uncommon in my immediate area that the only place with a bone density machine was a local women's health center….
maleosteoporosis.citywebshop.com ... celiac.htm
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Adrian S on 2/4/2010
GF board
…
Any decent GP should know the facts before refusing a DEXA. CD is associated with low bone density regardless of age and sex. Many of us here are do not meet the normal criteria for a DEXA but have to take supplements or meds to treat low bone density. I am male and was diagnosed with osteopenia at 39, I asked for a scan.
…
This should be the most useful reference.
"Dual energy x-ray absorptiometry (DXA) is the most widely used test to assess bone mineral density. Bone densitometry should be checked at diagnosis with a DXA scan." - British society of Gastroenterology - The Management of Adults with Coeliac Disease.
www.bsg.org.uk/images/stories/cl ... iac_10.pdf
www.bsg.org.uk/clinical-guidelin ... sease.html
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Osteoporosis Associated with Neutralizing Autoantibodies against Osteoprotegerin
N Engl J Med. 2009 Oct 8;361(15):1459-65.
Osteoporosis associated with neutralizing autoantibodies against osteoprotegerin.
Riches PL, McRorie E, Fraser WD, Determann C, van't Hof R, Ralston SH.
Rheumatic Diseases Unit, Institute of Genetics and Molecular Medicine, University of Edinburgh, Western General Hospital, Edinburgh, United Kingdom.
Abstract
Autoantibodies against osteoprotegerin, which block the inhibitory effect of osteoprotegerin on signaling by the receptor activator of nuclear factor (NF)-kappaB (RANK), were identified in a man with celiac disease who presented with severe osteoporosis and high bone turnover.
The osteoporosis did not respond to the treatment of his celiac disease but was completely reversed by bisphosphonate therapy.
Autoantibodies against osteoprotegerin were detected in three additional patients with celiac disease.
Such autoantibodies may be associated with the development of high-turnover osteoporosis, but whether autoantibodies against osteoprotegerin commonly contribute to the pathogenesis of osteoporosis in patients with celiac disease remains to be determined.
2009 Massachusetts Medical Society
PMID: 19812402 [PubMed - indexed for MEDLINE]
maleosteoporosis.citywebshop.com/maleosteo/celiac.htm
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Proximal myopathy and bone
pain as the presenting features
of coeliac disease
It is rare for coeliac disease to present only
with symptoms of osteomalacia, without the
classic symptoms of diarrhoea, steatorrhoea,
and abdominal discomfort....
A 22 year old woman presented with 18
months of a waddling gait disturbance. Hip
and back x rays were normal. She experienced
bone pain when being hugged, when laughing,
or coughing, and had difficulty standing
up from a low chair and holding her arms up
to blow-dry her hair.
She had extreme
tiredness and thought she might have lost
some weight, but there were no gastrointestinal
symptoms.
On examination, she was pale and had difficulty
squatting and holding her arms above
her head.
www.ncbi.nlm.nih.gov/pmc/articles/PMC1753868/pdf/v061p00087.pdf
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Prevention of conditions associated with coeliac disease
Osteoporosis
If you are diagnosed with coeliac disease you should also have a DEXA scan. This is to check the density of your bones. You should also have this scan again when you reach the menopause if you are a woman, or at 55 if you are a man. If you have a fragility fracture, which is linked to osteoporosis, at any point during your life you should have a DEXA scan.
..…
www.bupa.co.uk/individuals/health-information/directory/c/coeliac-disease
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The Institute of Genetics and Molecular Medicine
The University of Edinburgh
Osteoporosis and coeliac disease link
9 October 2009
People with coeliac disease may develop osteoporosis because their immune system attacks their bone tissue, a new study has shown.
It is the first time an autoimmune response - a condition whereby the body can attack itself - has been shown to cause damage to bones directly.
IGMM researchers studied a protein called osteoprotegerin (OPG) in people with coeliac disease - a digestive condition that affects 1 in 100 people.
In healthy people, OPG plays a crucial role in maintaining bone health by controlling the rate at which bone tissue is removed.
The latest research shows that 20 per cent of coeliac patients produce antibodies that attack the OPG protein and stop it working properly. This results in rapid bone destruction and severe osteoporosis.
It was previously thought that osteoporosis - a known complication of coeliac disease - develops in coeliac patients because they cannot properly absorb calcium and vitamin D from their diet. Both nutrients are essential for healthy bone development.
The team found that although this new form of osteoporosis did not respond to calcium and vitamin D supplements, it can be easily treated with drugs that prevent bone loss.
The research is published in the New England Journal of Medicine.
Professor Stuart Ralston, of the Institute of Genetics and Molecular Medicine, who led the team, said: “This is a very exciting step forward. Not only have we discovered a new reason to explain why osteoporosis occurs in coeliac disease, but we have also found that it responds very well to drugs that prevent bone tissue removal.
Testing for these antibodies could make a real and important difference to the lives of people with coeliac disease by alerting us to the risk of osteoporosis and helping us find the correct treatment for them.”
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Osteoporosis and Osteomalacia in Patients with Celiac Disease
Elizabeth Shane, M.D., Endocrinologist
The incidence of osteoporosis in patients with Celiac Disease varies somewhat. The incidence is higher with more severe disease and older age at diagnosis. When children present with Celiac Disease, they usually have evidence of delayed or poor growth, and bone density, if measured, is low.
When a gluten-free diet is maintained, there is usually an increase in bone mass, and the growth rate usually improves.
Some studies suggest that children with Celiac Disease who are diagnosed at a young age and treated effectively will have normal bone mass when they reach adulthood.
Adults who have had lifelong undiagnosed Celiac Disease are more likely to have lower bone density than the average person their age. They are significantly more likely to already have had broken bones than are age and se x matched controls.
Patients with Celiac Disease may also have a different bone disorder called osteomalacia. Osteomalacia differs in several respects from osteoporosis.
In osteomalacia, the amount of bone may be normal, but there is less mineral in the bone. Bone formation is a two-step process. Bone is first made as soft tissue; after the bone has been laid down, calcium and phosphorus are deposited in the tissue, and it hardens.
In osteomalacia, less calcium and phosphorus are deposited into bone. This makes the bone soft and more pliable. In children, the long bones of the legs will bend and bow, which is called rickets.
In contrast to osteoporosis, there are usually symptoms with osteomalacia. The bones may ache and feel sore to the touch. For example, it is common to have hip or heel pain when you stand.
Fractures do occur, but they tend to be a little different from osteoporatic fractures. It is important for the physician and the patient to know whether they’re dealing with osteoporosis or osteomalacia, because they are treated differently, and certain therapies that might make osteoporosis better might make osteomalacia worse.
The definitive diagnosis of osteomalacia is made by bone biopsy, where excess unmineralized bone can be seen, although tests of blood and urine may also be helpful.
www.enabling.org/ia/celiac/osteopo.html#index
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Bone Mass and Gastrointestinal Disease
CAROL E. SEMRAD
Department of Medicine, Columbia University, College of Physicians and Surgeons, New York, New York 10032, USA
Address for correspondence: Carol E. Semrad, Department of Medicine, Columbia University, College of Physicians and Surgeons, 630 West 168th Street, New York, NY 10032. Voice: 212-305-8156; fax: 212-305-6443.
"mailto:ces2@columbia.edu"
Several gastrointestinal and liver diseases impair the absorption of calcium, phosphate, and/or vitamin D, and are associated with an increased incidence of bone disease. Changes in bone mineral density (BMD) using dual-energy X-ray absorptiomety (DXA) have been best studied in the malabsorptive disorder, celiac disease. Celiac disease is an inflammatory condition of the small intestine triggered by ingesting gluten present in wheat, rye, or barley. Chronic inflammation leads to intestinal atrophy and nutrient malabsorption.
The disease affects the proximal small bowel; the site where calcium is best absorbed. About 70% of adults with celiac disease have abnormally low BMD values.
Treatment with a gluten-free diet increases BMD, but not to normal values. As celiac disease may not be detected until adult life, the failure to reach normal BMD on a gluten-free diet can be explained, at least in part, by the failure to reach peak bone mass.
All individuals with malabsorptive disorders should be screened for secondary bone disease. The development of easier and less expensive methods to assess BMD will facilitate screening those at risk for bone disease.
Annals of the New York Academy of Sciences 904:564-570 (2000)
© 2000 "/misc/terms.shtml"
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Bone and bone health
In adults, poor compliance to their gluten-free diet, and persistent villous atrophy are both associated with low bone mineral density. In a study by Mora et al, lumbar spine and whole body bone mineral density values in children and adolescents, at the diagnosis of coeliac disease, were found to be significantly lower than in control subjects. However, a gluten-free
www.coeliaccentre.org/en/
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Magnesium deficiency: possible role in osteoporosis associated with gluten-sensitive enteropathy.
Rude RK, Olerich M.
…This study demonstrates that GSE patients have reduction in intracellular free Mg2+, despite being clinically asymptomatic on a gluten-free diet. Bone mass also appears to be reduced. Mg therapy resulted in a rise in PTH, suggesting that the intracellular Mg deficit was impairing PTH secretion in these patients. The increase in bone density in response to Mg therapy suggests that Mg depletion may be one factor contributing to osteoporosis in GSE. ….
www.ncbi.nlm.nih.gov/pubmed/9116391
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Osteoporosis in people with coeliac disease
I have been sent a booklet from National Osteoporosis Society called 'Osteoporosis in people with coeliac disease: recommendations'.
This is very helpful, telling you about osteoporosis & CD, bone & bone health, treatment & prevention of osteoporosis in people with CD.
It points out that research re people with CD on GFD 'with daily calcium intake of 860mg/day were shown to have osteoporosis, whilst those with an intake of 1054mg/day were shown to have normal BMD' (bone mineral density).
You can get the booklet from NOS.
www.nos.org.uk/
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Silent Coeliac Disease (and increase of bone density on a gluten free diet)
acta.uta.fi/pdf/951-44-5721-8.pdf
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International Osteoporosis Foundation
Osteoporosis in the EC
www.iofbonehealth.org/
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What is osteoporosis?
C Christodoulou and C Cooper
MRC Environmental Epidemiology Unit, University of Southampton, Southampton General Hospital, Southampton
Correspondence to:
Professor C Cooper, MRC Environmental Epidemiology Unit, Southampton General Hospital, Southampton SO16 6YD, UK;
cc@mrc.soton.ac.uk
…Osteoporosis is a very common disorder, which results in an increase in fracture risk. The annual cost attributable to hip, vertebral, and wrist fractures in England and Wales is £1.7 billion.
Significant mortality and morbidity are associated with osteoporotic fractures.
The method that is most widely used for the diagnosis of osteoporosis is dual energy x-ray absorptiometry.
The aim of prevention and treatment of osteoporosis is to prevent the occurrence of future fractures.
Lifestyle changes should be encouraged in high risk patients.
Pharmacological treatments include the bisphosphonates, hormone replacement therapy, selective oestrogen receptor modulators calcitonin, the 1–34 fragment of parathyroid hormone, calcium and vitamin D supplements…
pmj.bmj.com/content/79/929/133.abstract
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Bone mass and metabolism in patients with celiac disease
BACKGROUND & AIMS: Several aspects of the pathogenesis of osteopenia in celiac disease are still unclear. Therefore, bone mass and metabolism were evaluated in adults with celiac disease in a cross-sectional study.
METHODS: Bone mineral density (BMD), assessed by total body dual- photon absorptiometry, and serum indices of bone metabolism and remodeling were evaluated in 17 patients with untreated celiac disease, 14 with celiac disease on a gluten-free diet, and 24 healthy volunteers.
RESULTS: BMD, expressed as a z score, was significantly lower in patients with untreated celiac disease than in patients with treated celiac disease and volunteers and lower in patients with treated celiac disease than in volunteers. Similar changes were observed in serum calcium level, whereas intact parathyroid hormone level was significantly higher in untreated than in treated patients with celiac disease and volunteers, and no difference was found between the latter two groups. 25-Vitamin D level was significantly lower and 1,25-vitamin D level significantly higher in untreated celiac disease than in treated celiac disease and volunteers. Indices of bone remodeling were significantly higher in untreated than in treated patients and volunteers and significantly and positively correlated with iPTH in untreated patients with celiac disease.
CONCLUSIONS: BMD is almost invariably low in patients with untreated celiac disease. Results in treated patients suggest that gluten-free diet improves but does not normalize BMD. Untreated celiac disease is characterized by high levels of 1,25-vitamin D and by increased bone turnover, caused by the increase in intact parathyroid hormone level.
(Gastroenterology 1995 Jul;109(1):122-8)
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Osteoporosis treatment and prevention
…Preventing osteoporosis by maintaining a health diet rich in calcium and vitamin D and exercising regularly can help many women avoid the serious effects of osteoporosis. Women who have low bone mineral density or osteoporosis may also benefit from taking hormone replacement therapy or other drug therapies…
imaginis.com/osteoporosis/osteo_treatment.asp
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......How can osteoporosis in men be prevented and treated?
The medical research on osteoporosis in men has been inadequate. However, experts agree that all persons should take the following steps to preserve bone health.
· Recognize and treat any underlying medical conditions that affect bone health. Identify and evaluate the use of medications that are known to cause bone loss.
· Change unhealthy habits, such as smoking, excessive alcohol intake, and inactivity.
· Ensure a daily calcium intake of 1000 mg/day to age 50 and 1200 mg/day over age 51 and over.
· Ensure adequate vitamin D intake. Normally, we make enough vitamin D from exposure to as little as 10 minutes of sunlight a day. If exposure to sunlight is inadequate, then vitamin D intake from supplements should be at least 400 IU but not more than 800 IU/day.
· Engage in a regular regimen of weight-bearing exercises where bone and muscles work against gravity. This includes walking, jogging, racquet sports, stair climbing, and team sports. Also, lifting weights or using resistance machines appears to help preserve bone density. Exercise also improves balance and muscle tone and imparts a sense of well-being. If you have already been diagnosed with osteoporosis, any exercise program should be evaluated for safety by your doctor before you begin. Twisting motions and impact activities may need to be curtailed depending on the severity of your condition.
What medications can slow or stop bone loss in men?
Alendronate (brand name Fosamax®) is approved as a treatment for osteoporosis in men.
Alendronate and risedronate (brand name Actonel®), medications from the class of drugs called bisphosphonates, are approved for use in steroid-induced osteoporosis that occurs in men and women as a result of long term use of steroids such as prednisone or cortisone.
Currently, none of the other osteoporosis medications that have been approved by the Food and Drug Administration (FDA) for postmenopausal women have been approved for men. However, to help men with osteoporosis, physicians may prescribe the following:
· Testosterone replacement therapy may be prescribed for a man with a low testosterone level.
· Calcitonin is a medication that slows or stops bone loss and may relieve the pain of fractures in some patients. Calcitonin is approved by the FDA for the treatment of osteoporosis in postmenopausal women. While its effect in men has not been studied, evidence suggests that it may work the same in men as in women. Calcitonin is available as an injection and as a nasal spray.
www.nof.org/men/index.htm
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Bone mass & CD
…Osteoporosis was shown in 47% of patients with treated adult coeliac disease.
www.ncbi.nlm.nih.gov/pubmed/7797121?dopt=Abstract
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…Celiac patients had a lower bone mass than controls despite early diagnosis and good compliance with the gluten-free diet. These differences could not be atributed entirely to the lower height of celiac patients. These results suggest that celiac patients constitute a risk group for development of osteoporosis later in life. This fact should be taken into consideration in the treatment of this condition.
www.ncbi.nlm.nih.gov/pubmed/9239290?dopt=Abstract
*******************************************************
…CONCLUSIONS: Treatment of coeliac disease with a gluten free diet is associated with a significant increase in bone mineral density, although patients still had lower bone mineral density than controls.
www.ncbi.nlm.nih.gov/pubmed/8991855?dopt=Abstract
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Associated Medical Conditions in Individuals with Celiac Disease
.... Sixty-two percent of respondents said they had their bone density measured. Twenty-seven percent of respondents had been diagnosed with osteoporosis and 10% with osteopenia. Forty-four percent (n = 116) had a history of a previous fracture and of these individuals, 36% had previously broken their wrist. Five percent were taking calcium and 5% vitamin D after diagnosis of osteoporosis/osteopenia. Thirteen percent were taking an anti-osteoporosis medication such as alendronate, risedronate, HRT or raloxifene.
www.biomedcentral.com/1471-230X/3/8#IDAGEMLP
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…The most important treatment is the gluten-free diet. The available evidence suggests that if children or adults adhere to a gluten-free diet, bone density will improve, especially during the first year or two of treatment. If you’re an adult at age 30, who has just discovered that you have Celiac Disease and low bone density, your bone density may increase anywhere between 5-10% over the first year or two on a gluten-free diet. There are no good studies looking beyond 1-2 years.
Calcium supplements are important, and may be necessary even in those patients who have a good response to the gluten-free diet. Celiac Disease patients lose more calcium in bowel movements than normal people do, and there is a certain amount of calcium that is lost in the urine whether you have Celiac Disease or not. Calcium is necessary for a myriad of body processes, and if it doesn’t come from the diet or supplements, it is taken from the bones.
Women with Celiac Disease who go through menopause should strongly consider taking estrogen, which will protect them from the additional bone loss that occurs with estrogen deficiency.
There are other newer therapies for osteoporosis. None of them have been evaluated in patients with Celiac Disease. The new Merck drug, Fosamax (Alendronate), is absorbed mainly in the stomach, and should be absorbed in the patient with Celiac Disease. It does not contain gluten, but does contain lactose. The decision to institute Fosamax therapy is a very individual one that should be reached between the Celiac Disease patient and their doctor after a careful evaluation to make sure that there is no evidence of osteomalacia. Fosamax may make osteomalacia worse. Moreover, at this time we don’t really know if Fosamax is effective. The other agent that is approved for osteoporosis is calcitonin, which is available in a nasal spray. Calcitonin probably won’t hurt anybody, but there is no information available about whether it helps. Newer agents that act by different mechanisms to increase bone density are now in clinical trials.
www.enabling.org/ia/celiac/osteopo.html#TREATMENT%20FOR%20CELIAC%20PATIENTS%20WITH%20LOW%20BONE%20DENSITY
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Severe osteopenia in symptom-free adults with a childhood diagnosis of coeliac disease.
Cellier C, Flobert C, Cormier C, Roux C, Schmitz J.
Lancet. 2000 Mar 4;355(9206):806.
The frequency of osteopenia in symptom-free adults diagnosed with coeliac disease during childhood and who resumed a normal diet during adolescence is unknown.
Severe osteopenia (a bone mineral density below two standard deviations of the mean) was found in up to a third of symptom-free young adults on a normal diet.
These patients should not be thought to be disease-free but should receive long-term follow-up and most of them should be advised to resume a gluten-free diet.
www.ncbi.nlm.nih.gov/pubmed/10711931?dopt=Abstract
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strategy for osteoporosis in gastroenterology
Reference
EM Scott and BB Scott. Eur Journal of Gastroenterology and Hepatology 1998; 10: 689-698
Osteoporotic fractures are a major public health problem. The estimated total cost of osteoporotic fractures in England and Wales is £742 million per annum. With an increasing elderly population the costs are likely to rise. Osteoporosis can be reliably detected by the measurement of Bone Mineral Density (BMD) using Dual energy X-ray absorptiometry (DEXA). A BMD more than two standard deviations below the mean for a young adult is generally taken as an indication of osteoporosis.
Gastroenterologists have a large proportion of patients who are at increased risk of osteoporosis. One of the main groups is that with coeliac disease (CD). One study showed that 47% of women and 50% of men on a gluten-free diet had osteoporosis. BMD was positively related to calcium intake, body mass index (BMI) and menopausal age. Other studies have shown significant improvement a year after starting a gluten-free diet, normal BMD in patients who had had a gluten-free diet since childhood and improved bone mineralisation on a gluten free diet in childhood and adolescence.
The mechanism of osteoporosis in CD is likely to be related to calcium malabsorption, leading to increased parathormone secretion, which increases bone turnover and cortical bone loss. The following points summarize the strategy for prevention and treatment of osteoporosis in CD as suggested in 1998:
General advice
· Strict gluten-free diet
· 1500mg calcium/day
· Exercise
· No smoking
· No excess alcohol
· Seek and treat Vitamin D deficiency
· Measure BMD at diagnosis – if low reinforce above advice
Post-menopausal women
· Measure BMD at menopause or when first seen
· If osteoporotic offer either HRT, preferably by skin patch, bisphosphonate orally or by calcitonin
Men over 55 years
· Measure BMD
· If osteoporotic offer bisphosphonate or calcitonin
All with fragility fracture
· Measure BMD
· If osteoporotic offer HRT (if post menopausal) bisphosphonate or calcitonin. If already on HRT consider adding bisphosphonate or calcitonin.
Duration of drug treatment
· For bisphosphonate and calcitonin measure BMD yearly
· If BMD falls below 4% per year in 2 successive years change to another drug
· If no fall continue drug for at least 3 years, possibly long term.
· Restart drug if, on stopping, yearly BMD falls below 4%
· For HRT check BMD after 10 years and continue HRT if osteoporosis persists
www.cdrc.org.uk/en/article.asp?chco_id=427
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Bone mineral density and importance of a gluten-free diet in patients with celiac disease in childhood
Posted by Charlotte, Oxford on 10/2/2005
GF board
Came across this very interesting study from Turkey ........
Abstract:
www.ncbi.nlm.nih.gov/pubmed/11694673?dopt=Abstract
Bone mineral density and importance of a gluten-free diet in patients with celiac disease in childhood.
Kalayci AG, Kansu A, Girgin N, Kucuk O, Aras G.
Department of Pediatric Gastroenterology, School of Medicine, Ondokuz Mayis University, Samsun, Turkey. ayhangk@omu.edu.tr
"OBJECTIVES: Celiac disease (CD), a common cause of malabsorption, is known to be associated with disorders of the skeleton, but there are conflicting data about the effect of diet on bone metabolism. The aims of this study were to investigate the prevalence of osteopenia; to identify the relationship between bone mineral density (BMD), serum calcium, and parathyroid hormone levels; and to determine the effect of gluten-free diet on BMD in children with celiac disease.....
CONCLUSIONS: BMD is almost invariably low in newly diagnosed celiac patients in childhood. We therefore recommend that BMD should be evaluated in patients with CD. Strict gluten avoidance promoted a significant increase in BMD. However, values still remained markedly low after 1 year of follow-up in some patients. These patients should be followed for longer periods of time with yearly BMD evaluation, as 1 year of diet therapy was found to be insufficient for osteopenia to be resolved."
pediatrics.aappublications.org/cgi/content/full/108/5/e89
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Increased prevalence of CD among patients with osteoporosis
Stenson WF, Newberry R, Lorenz R, Baldus C, Civitelli R.
Increased prevalence of celiac disease and need for routine screening among patients with osteoporosis. Archives of Internal Medicine; vol. 165, pp. 393-399, Feb. 28, 2005.
"Our results suggest that as many as three to four percent of patients who have osteoporosis have the bone disease as a consequence of having celiac disease, which makes them unable to absorb normal amounts of calcium and vitamin D," says principal investigator William F. Stenson, M.D., a Washington University physician at Barnes-Jewish Hospital. The study is reported in the Feb. 28 issue of the Archives of Internal Medicine’’
www.medicalnewstoday.com/articles/20501.php
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Recommendations for the treatment of osteoporosis in CD
Recommendations for the treatment of osteoporosis in coeliac disease and prevention of osteoporosis in people with coeliac disease have been produced in conjunction with a diverse panel of healthcare specialists.
www.cdrc.org.uk/en/article.asp?chco_id=466
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Bisphosphonates.
Drug for Bone Disease Linked to 'Jaw Death'
Researchers Report Cases of Osteonecrosis of Jaw in Patients Who Had Teeth Pulled
WebMD Medical News
Oct. 3, 2005 -- Millions of people treated for bone diseases such as osteoporosis may be at risk for developing a potentially serious jawbone condition that seems to be triggered by having teeth pulled.
More than a thousand cases of osteonecrosis of the jaw, or jaw death, have been reported in patients taking a class of drugs known as bisphosphonates. Osteonecrosis indicates that part of the bone is no longer alive; unlike normal bone it cannot regenerate itself because of a lack of blood supply.
Most cases occurred in cancer patients taking the intravenous bisphosphonates Aredia and Zometa to prevent cancer-related bone loss. But osteonecrosis of the jaw has also been reported in women who had teeth pulled while taking the widely prescribed osteoporosis pill Fosamax, dentistry professor Ken Hargreaves, DDS, PhD, tells WebMD.
"Even if this is a rare condition, so many women now take bisphosphonates to prevent bone loss that the numbers could grow," he says. "We just became aware of this a few years ago, and it has been called a growing epidemic."
The study appeared in the October issue of the Journal of Endodontics.
Saving Teeth Lowers Risk
A newly published report edited by Hargreaves outlines two cases of osteonecrosis of the jaw in cancer patients on monthly doses of intravenous bisphosphonates.
He says it is clear from these and other published cases that patients taking bisphosphonates should be warned that they may be at risk if they have teeth pulled. Osteonecrosis of the jaw is very painful and can lead to serious complications, including ulcerations within the lining of the mouth, infection, and breakdown of the jawbone with disfigurement.
"People taking these drugs need to see their dentist regularly, and they need to recognize the importance of preventive dental care," he says. "And when there is a problem, we need to do everything we can to save teeth."
That means performing root canals on patients taking these drugs rather than tooth extractions, he says.
my.webmd.com/content/article/113/110591.htm
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PREVENTION AND MANAGEMENT OF OSTEOPOROSIS
Report of a WHO Scientific Group World Health Organization Geneva ...
whqlibdoc.who.int/trs/WHO_TRS_921.pdf
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Re: Bone Scan/Dexa scan
Posted by Eileen on 16/11/2005
GF board
I arranged it through my Gp using the Fast Track system (NHS), and the cost was £62. I waited 2 weeks for the appointment. If you don't have time to visit the Gp, perhaps you could drop him a line instead requesting one.
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Osteoporosis guide
A guide to osteoporosis for all ages
actnowosteoporosis.co.uk/index.html
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osteoporosis and coeliac disease
Question: I read your answer to a question on osteoporosis and coeliac disease in Oct 2002. Is there any evidence to suggest that adults with coeliac disease need dexa scanning? What is the start age and how frequently should they be investigated?
Answer:
ATTRACT found a few documents discussing this issue which differ slightly in their recommendations.
A position statement from the American Gastroenterological Association (2003)(1) states:
“DXA scans are likely unnecessary in patients with newly diagnosed uncomplicated pediatric celiac disease, but should be considered for adults with newly diagnosed celiac disease 1 year after initiation of a gluten-free diet, to allow for stabilization of bone density (level D evidence).”
The British Society of Gastroenterology produced interim guidelines on the management of patients with coeliac disease in April 2002 (2). This guideline states:
“It is usual practice to consider bone densitometry scanning on presentation which may be repeated after one to two years of dietary therapy if the initial value is low.”
The Primary Care Society for Gastroenterology published a document entitled Follow-up care of adult coeliac disease in August 2001 (3). This states:
“Osteoporosis risk assessment and management
DEXA at menopause for women, at 55 years for men, at any age following fragility fracture.”
The British Society of Gastroenterology guidelines for osteoporosis in coeliac disease and inflammatory bowel disease published in 2000 state:
“The timing of densitometry presents a problem. In women, postmenopausal densitometry will be more sensitive at detecting osteoporosis but the delay will give less scope for achieving a higher bone density with treatment, despite evidence that bisphosphonates may produce some reversal of osteoporosis.
Conversely, screening at presentation may reveal osteoporosis at a young age when intervention would theoretically have greater potential …
On balance, one could recommend that all patients have densitometry at diagnosis. This would allow reinforcement of general advice if BMD is low.
However, we can appreciate that the burden on both the clinician and the densitometry service might be counter-productive and deter any screening.
A simpler strategy, omitting BMD at presentation in younger patients and restricting BMD measurement to the older patients who are more likely to benefit, could therefore be more effective in IBD.
In any case, patients with IBD at presentation are unlikely to have osteoporosis as a result of their disease. There is more reason for measuring BMD at diagnosis in patients with coeliac disease because they will already have suffered malabsorption for many years.
In women, if the diagnosis is made earlier the BMD should be measured at the menopause.
It is debateable whether a single measurement at the menopause is adequate because there is considerable variation in the rate and duration of rapid perimenopausal bone loss. For this reason it would be sensible to repeat the BMD after perhaps two years in those whose BMD does not suggest osteoporosis.
Similarly, in men the BMD should be measured at about 55 years of age if they presented at an earlier age. BMD should be done at any age if there has been a fragility fracture, namely one which is atraumatic or follows a simple fall.”
American Gastroenterological Association. American Gastroenterological Association medical position statement: guidelines on osteoporosis in gastrointestinal diseases. Gastroenterology 2003 Mar;124(3):791-4.
www.bsg.org.uk/pdf_word_docs/coeliac.doc
www.bsg.org.uk/pdf_word_docs/osteo.pdf
Date Posted : 22/08/2005
Evidence:
Evidence 1:- 0
Evidence 2:- 0
Evidence 3:- 0
Evidence 4:- 2
Evidence G:- 2
***********************************************
Osteomalacia causes bone pain
Posted by Charlotte, Oxford on 6/3/2007
GF board
Bone pain is caused by osteomalacia which is common in (mainly younger) coeliacs. It's known as rickets in children. You should not continue in pain. Your doctors should be treating you for this - you may need quite aggresive treatment with Vitamin D and calcium:
www.nhsdirect.nhs.uk/en
In the majority of cases, treatment will cure osteomalacia, although it may be several months before you have any relief from bone pain and muscle weakness. The increased vitamin D must be taken regularly otherwise the condition will come back.
www.netdoctor.co.uk/diseases/fac ... ickets.htm
What treatment is available?
Regular daily supplements of vitamin D and calcium, eg Calcichew D3 or Adcal D3, are usually used for people with simple vitamin D deficiency, but some people have a single injection vitamin D, in the form of calciferol (vitamin D2). This is stored in the body and can last up to a year before another injection may be needed.
People with vitamin D deficiency due to intestinal problems are best treated with calciferol. Most people with osteomalacia find their pain is reduced about two weeks after the injection. Extra calcium may also be needed while bone is healing.
bone-muscle.health-cares.net/ost ... atment.php
What's the treatment for osteomalacia?
Oral supplements of vitamin D, calcium and phosphorus may be given depending on the underlying cause of the disorder.
Larger doses of vitamin D and calcium may be needed for people with intestinal malabsorption. Monitoring of blood levels of phosphorus and calcium may be indicated for people with certain underlying conditions. Regular daily supplements of vitamin D and calcium are usually used for people with simple vitamin D deficiency, but some people have a single injection vitamin D, in the form of calciferol (vitamin D2). This is stored in the body and can last up to a year before another injection may be needed. People with vitamin D deficiency due to intestinal problems are best treated with calciferol. Most people with osteomalacia find their pain is reduced about two weeks after the injection. Extra calcium may also be needed while bone is healing. Direct exposure of the skin (i.e., hands, face, arms, etc.) to sunlight stimulates the body to manufacture vitamin D. However, both clothing and use of a sunscreen prevent the ultraviolet light that triggers the formation of vitamin D from reaching the skin. Depending on latitude, sunlight during the winter may not provide enough ultraviolet light to promote adequate vitamin D production. At other times during the year, even 30 minutes of exposure per day will usually lead to large increases in the amount of vitamin D made. If it is difficult to get sunlight exposure, full-spectrum lighting can be used to stimulate vitamin D production.
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….differences between osteomalacia (soft bones) and osteoporosis (bone loss).
Both are common in coeliacs: the former tends to affect young coeliacs and the latter older ones:
…..
In children, this is also known as rickets; in grown-ups, it is sometimes known as 'adult rickets'. This condition is caused by a deficiency in Vitamin D. Osteomalacia is more common than most physicians realize and should always be considered in patients with unexplained pain -especially the kind you describe.
The pain of osteomalacia is typically difficult to localize. All the bones are tender - especially the long ones in the legs and arms- because of inflammation of the nerve fibers imbedded in the lining of the bone (called the periosteum). When Vitamin D is deficient, the lining of the bone becomes activated, causing more bone to be absorbed and replaced at an accelerated rate. This is similar to the 'growing pains' experienced by adolescents who are going through the growth spurt.
In diagnosed cases of osteomalacia, 94% of patients complain of pain; 94% complain of muscle weakness; 88% complain of bone tenderness with pressure on touch; 24% complain of a waddling gait and muscle cramps; and, there is a higher incidence of fracture than expected for age- even in bones that test 'normal'on the DEXA bone density test.
It is very difficult these days to become deficient in Vitamin D because it is frequently supplemented in foods. Most vitamin preparations also contain Vitamin D. The most common cause of osteomalacia with apparently normal nutrition is bowel disorders, as in your case. Your bowel was bypassed, which can cause malabsorption of nutrients, including vitamins. The most common bowel disorder is celiac sprue, also known as gluten sensitivity. Gluten is present in wheat. Celiac disease may be present in as much as 5% of the population and is often confused with irritable bowel syndrome.
Researchers at the Henry Ford Health System reporting in The American Journal of Medicine, Vol. 108, 296 -300, looked at the causes of osteomalacia in patients they have seen with stomach surgery (for ulcers), gastric stapling, intestinal bypass, intestinal removal, removal of the pancreas and pancreatitis, and celiac disease. Most of these patients had their symptoms for more than two years. The average time for symptoms to develop from diagnosing the intestinal problem was 14 years! It is easy to see how physicians could overlook this condition, as these changes develop slowly over time. Additionally, these patients get passed on from physician to physician and often get labeled as chronic complainers or malingerers. The 'label' itself, like fibromyalgia, can mislead subsequent physicians.
Simple blood tests should help the doctor make the diagnosis. The bone density test you've had reveals bone loss, but that deficiency is not due to osteoporosis. Unfortunately, though, doctors often mistakenly treat patients for osteoporosis based on test results such as yours. Indeed, people who take this test may have osteomalacia and osteoporosis. However, the osteomalacia 'accidentally' gets better when Vitamin D and calcium are prescribed for the osteoporosis. Osteoporosis does not usually cause generalized bone pain or tenderness.
Doctors in the 'good ole days' would probably have made the diagnosis of osteomalacia very quickly. Rickets was common prior to 1940, as were nutritional diseases. Today, osteomalacia and rickets are relatively rare, so some of us doctors who are 'youngsters' (age 40 or so) may not have seen many cases.
If you have unexplained bone pain, ask your doctor to check for osteomalacia or adult rickets.
...
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Coeliac Disease and the Risk of Fractures - A General Population-based Cohort Study
Posted by Charlotte, Oxford on 16/3/2007
GF board
This new study (full text available in link) confirms earlier findings by Joe West but also suggests that the risk remains even after years on the diet and that coeliac children are at particular risk. It suggests (to me) that all coeliacs need to be particularly careful to maximise their bone health with calcium, vitamin D, sunlight, weight-bearing exercise etc.
From the Discussion:
"We found a statistically significantly positive association of CD with hip fracture or any fracture, irrespective of whether the fracture occurred prior to or after the diagnosis of CD. The overall risk estimates for subsequent hip fracture and any fracture were almost identical to those of West et al.[14] Individuals with CD diagnosed in childhood were at increased risk of subsequent hip fracture and may also be at increased risk of fracture of any type. The duration to and after diagnosis of CD did not notably influence the risk of hip fracture. Hence, this study found no evidence that a gluten-free diet lowers the risk of hip fracture. Even 20 years after diagnosis of CD were individuals with CD at increased risk of hip fracture."
Coeliac Disease and the Risk of Fractures - A General Population-based Cohort Study
J. F. Ludvigsson; K. Michaelsson; A. Ekbom; S. M. Montgomery
Aliment Pharmacol Ther. 2007;25(3):273-285. �2007 Blackwell Publishing
Posted 03/08/2007
Summary and Introduction
Summary
Background: Earlier studies have suggested that untreated coeliac disease may be associated with osteoporosis, but results are contradictory for the risk of long-term fractures.
Aim: To study the association between coeliac disease and fractures.
Methods: We used Cox regresson to examine the future risk of hip fracture and fracture of any type in more than 13 000 individuals with coeliac disease and 65 000 age- and sex-matched reference individuals in a general population-based cohort.
Results: During follow-up, 1365 first hip fractures and 4847 fractures of any type occurred. Coeliac disease was positively associated with subsequent hip fracture (hazard ratio = 2.1; 95% CI = 1.8-2.4) (in children: hazard ratio = 2.6; 95% CI = 1.1-6.2) and fractures of any type (hazard ratio = 1.4; 95% CI = 1.3-1.5) (in children: hazard ratio = 1.1; 95% CI = 1.0-1.2). The absolute excess risk of hip fractures in children with coeliac disease was 4/100 000 person-years. Incidence ratios for hip fracture in individuals with CD were around two both prior to diagnosis of coeliac disease and afterwards; this risk increase remained 20 years after diagnosis of coeliac disease.
Conclusions: Individuals with coeliac disease, including children with coeliac disease, may be at increased risk of hip fracture and fracture of any type. Coeliac disease may be positively associated with long-term hip fracture risk.
Link: www.medscape.com:80/viewarticle/552626_print
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CD and bones
From Pubmed:
Endocr Pract. 2004 May-Jun;10(3):203-7.
Celiac disease manifesting as isolated hypocalcemia.
Rickels MR, Mandel SJ.
Division of Endocrinology, Diabetes and Metabolism, Department of Medicine, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104, USA.
OBJECTIVE: To describe a patient who presented with hypocalcemia and hypocalciuria as the initial manifestations of celiac disease, despite a normal vitamin D status.
METHODS: We review the diagnostic evaluation, treatment, and biochemical and bone mineral density responses of a patient with asymptomatic celiac disease, which was initially suggested because of a low serum calcium level that became attributable to isolated malabsorption of calcium.
RESULTS: A 36-year-old woman presented with hypocalcemia in the presence of normal serum 25-hydroxyvitamin D and high serum 1,25-dihydroxyvitamin D levels. She had hypocalciuria and secondary hyperparathyroidism that were refractory to pharmacologic calcium and cholecalciferol supplementation. Fecal calcium excretion indicated malabsorption of calcium, and biopsy of the small intestine demonstrated pathologic changes characteristic of celiac disease. Bone mineral density, determined by dual-energy x-ray absorptiometry, was in the osteopenic range at the femoral neck. The initiation of a gluten-free diet resulted in correction of all biochemical abnormalities and a substantial increase in bone mineral density.
CONCLUSION: Primary intestinal malabsorption of calcium without concomitant vitamin D deficiency is possible in celiac disease because of the preferential involvement of the proximal small intestine early in the disease process. Our patient had hypocalcemia caused by celiac disease and values for serum 25-hydroxyvitamin D and 1,25-dihydroxyvitamin D that were normal and elevated, respectively. Correction was demonstrated after dietary gluten withdrawal.
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Osteoporos Int. 1996;6(6):453-61.
Magnesium deficiency: possible role in osteoporosis associated with gluten-sensitive enteropathy.
Rude RK, Olerich M.
Department of Medicine, University of Southern California School of Medicine, Los Angeles, USA.
Osteoporosis and magnesium (Mg) deficiency often occur in malabsorption syndromes such as gluten-sensitive enteropathy (GSE). Mg deficiency is known to impair parathyroid hormone (PTH) secretion and action in humans and will result in osteopenia and increased skeletal fragility in animal models. We hypothesize that Mg depletion may contribute to the osteoporosis associated with malabsorption. It was our objective to determine Mg status and bone mass in GSE patients who were clinically asymptomatic and on a stable gluten-free diet, as well as their response to Mg therapy. Twenty-three patients with biopsy-proven GSE on a gluten-free diet were assessed for Mg deficiency by determination of the serum Mg, red blood cell (RBC) and lymphocyte free Mg2+, and total lymphocyte Mg. Fourteen subjects completed a 3-month treatment period in which they were given 504-576 mg MgCl2 or Mg lactate daily. Serum PTH, 25-hydroxyvitamin D, 1,25-dihydroxyvitamin D and osteocalcin were measured at baseline and monthly thereafter. Eight patients who had documented Mg depletion (RBC Mg2+ < 150 microM) underwent bone density measurements of the lumbar spine and proximal femur, and 5 of these patients were followed for 2 years on Mg therapy. The mean serum Mg, calcium, phosphorus and alkaline phosphatase concentrations were in the normal range. Most serum calcium values fell below mean normal and the baseline serum PTH was high normal or slightly elevated in 7 of the 14 subjects who completed the 3-month treatment period. No correlation with the serum calcium was noted, however. Mean serum 25-hydroxyvitamin D, 1,25-dihydroxyvitamin D and osteocalcin concentrations were also normal. Despite only 1 patient having hypomagnesemia, the RBC Mg2+ (153 +/- 6.2 microM; mean +/- SEM) and lymphocyte Mg2+ (182 +/- 5.5 microM) were significantly lower than normal (202 +/- 6.0 microM, p < 0.001, and 198 +/- 6.8 microM, p < 0.05, respectively). Bone densitometry revealed that 4 of 8 patients had osteoporosis of the lumbar spine and 5 of 8 had osteoporosis of the proximal femur (T-scores < or = -2.5). Mg therapy resulted in a significant rise in the mean serum PTH concentration from 44.6 +/- 3.6 pg/ml to 55.9 +/- 5.6 pg/ml (p < 0.05). In the 5 patients given Mg supplements for 2 years, a significant increased in bone mineral density was observed in the femoral neck and total proximal femur. This increase in bone mineral density correlated positively with a rise in RBC Mg2+. This study demonstrates that GSE patients have reduction in intracellular free Mg2+, despite being clinically asymptomatic on a gluten-free diet. Bone mass also appears to be reduced. Mg therapy resulted in a rise in PTH, suggesting that the intracellular Mg deficit was impairing PTH secretion in these patients. The increase in bone density in response to Mg therapy suggests that Mg depletion may be one factor contributing to osteoporosis in GSE.
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J Pediatr Gastroenterol Nutr. 2003 Oct;37(4):434-6.
Bone mineral density in children with untreated and treated celiac disease.
Kavak US, Yüce A, Koçak N, Demir H, Saltik IN, Gürakan F, Ozen H.
Hacettepe University, Department of Pediatrics, Ankara, Turkey.
OBJECTIVES: Osteopenia is a common complication in adults with celiac disease. The effect of a gluten-free diet on bone mineral density is a matter of controversy. The aim of this study was to investigate bone mineral density in children with celiac disease at diagnosis and in patients treated for 1 year.
METHODS: Bone mineral density and bone mineral content were measured in 34 children with untreated celiac disease at diagnosis and in 28 patients on a gluten-free diet for 1 year. The results were compared with those of 64 gender- and age-matched healthy control subjects. Serum calcium, phosphate, alkaline phosphatase, 25 -hydroxy vitamin D, and intact parathormone levels were determined in treated and untreated patients.
RESULTS: The mean values of bone mineral density and bone mineral content of untreated patients with celiac were significantly lower than the control group (P = 0.006 and P = 0.005, respectively) and treated patients (P = 0.015 and P = 0.011 respectively). Treated patients had mean bone mineral density and bone mineral content values not significantly different from those of healthy control subjects. Minor hypocalcemia was detected in 17.6% of the patients with new diagnoses and 3.6% of the treated patients. Of the untreated patients, 29.4% had high intact parathormone concentrations; in untreated patients, the total was 14.3%. Untreated patients had significantly lower serum calcium and significantly higher intact parathormone levels than did treated patients. The other bone metabolism parameters were similar in the two celiac groups.
CONCLUSION: Children with celiac disease are at risk for reduced bone mineral density. A strict gluten-free diet improves bone mineralization, even in 1 year. Early diagnosis and treatment of celiac disease during childhood will protect the patient from osteoporosis
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Nobody looks for osteoporosis in males
From:
Men's Osteoporosis Support Group
…"I have never had any symptoms of sprue and never suspected it until my daughter's gastroenterologist suggested that my wife and I have blood tests. My wife's were negative, while both of mine (I think they tested for two antibodies) were positive for sprue. I then went in for a gastroscopy, which was also positive. I spoke with my gastroenterologist earlier this week and he told me that based on the severe nature of my osteoporosis I've probably had celiac sprue for a long time. Unfortunately, the long-term osteoporosis also went undiagnosed until I had a bone
density test after breaking my arm and then my leg within the span of a month a couple of years ago. My primary care physician did some research and found that osteoporosis is a common result of untreated celiac disease. Of course, now that we know about celiac disease and osteoporosis, I've been reading all kinds of information about it on the Web.
Unfortunately, nobody looks for osteoporosis in a fairly young male--or any male--for that matter. (My Fosamax packages still say the drug is for post-menopausal women!) It was apparently so uncommon in my immediate area that the only place with a bone density machine was a local women's health center….
maleosteoporosis.citywebshop.com ... celiac.htm
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Adrian S on 2/4/2010
GF board
…
Any decent GP should know the facts before refusing a DEXA. CD is associated with low bone density regardless of age and sex. Many of us here are do not meet the normal criteria for a DEXA but have to take supplements or meds to treat low bone density. I am male and was diagnosed with osteopenia at 39, I asked for a scan.
…
This should be the most useful reference.
"Dual energy x-ray absorptiometry (DXA) is the most widely used test to assess bone mineral density. Bone densitometry should be checked at diagnosis with a DXA scan." - British society of Gastroenterology - The Management of Adults with Coeliac Disease.
www.bsg.org.uk/images/stories/cl ... iac_10.pdf
www.bsg.org.uk/clinical-guidelin ... sease.html
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Osteoporosis Associated with Neutralizing Autoantibodies against Osteoprotegerin
N Engl J Med. 2009 Oct 8;361(15):1459-65.
Osteoporosis associated with neutralizing autoantibodies against osteoprotegerin.
Riches PL, McRorie E, Fraser WD, Determann C, van't Hof R, Ralston SH.
Rheumatic Diseases Unit, Institute of Genetics and Molecular Medicine, University of Edinburgh, Western General Hospital, Edinburgh, United Kingdom.
Abstract
Autoantibodies against osteoprotegerin, which block the inhibitory effect of osteoprotegerin on signaling by the receptor activator of nuclear factor (NF)-kappaB (RANK), were identified in a man with celiac disease who presented with severe osteoporosis and high bone turnover.
The osteoporosis did not respond to the treatment of his celiac disease but was completely reversed by bisphosphonate therapy.
Autoantibodies against osteoprotegerin were detected in three additional patients with celiac disease.
Such autoantibodies may be associated with the development of high-turnover osteoporosis, but whether autoantibodies against osteoprotegerin commonly contribute to the pathogenesis of osteoporosis in patients with celiac disease remains to be determined.
2009 Massachusetts Medical Society
PMID: 19812402 [PubMed - indexed for MEDLINE]
maleosteoporosis.citywebshop.com/maleosteo/celiac.htm
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Proximal myopathy and bone
pain as the presenting features
of coeliac disease
It is rare for coeliac disease to present only
with symptoms of osteomalacia, without the
classic symptoms of diarrhoea, steatorrhoea,
and abdominal discomfort....
A 22 year old woman presented with 18
months of a waddling gait disturbance. Hip
and back x rays were normal. She experienced
bone pain when being hugged, when laughing,
or coughing, and had difficulty standing
up from a low chair and holding her arms up
to blow-dry her hair.
She had extreme
tiredness and thought she might have lost
some weight, but there were no gastrointestinal
symptoms.
On examination, she was pale and had difficulty
squatting and holding her arms above
her head.
www.ncbi.nlm.nih.gov/pmc/articles/PMC1753868/pdf/v061p00087.pdf
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Prevention of conditions associated with coeliac disease
Osteoporosis
If you are diagnosed with coeliac disease you should also have a DEXA scan. This is to check the density of your bones. You should also have this scan again when you reach the menopause if you are a woman, or at 55 if you are a man. If you have a fragility fracture, which is linked to osteoporosis, at any point during your life you should have a DEXA scan.
..…
www.bupa.co.uk/individuals/health-information/directory/c/coeliac-disease
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