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The impact of vitamin D status on changes in bone mineral density during treatment with bisphosphonates and after discontinuation following long-term use in post-menopausal osteoporosis.

作者信息

Deane Andrew, Constancio Leonor, Fogelman Ignac, Hampson Geeta

机构信息

Department of Chemical Pathology and metabolic bone clinic, St Thomas' Hospital campus, Kings College London, London, UK.

出版信息

BMC Musculoskelet Disord. 2007 Jan 10;8:3. doi: 10.1186/1471-2474-8-3.


DOI:10.1186/1471-2474-8-3
PMID:17214897
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1781939/
Abstract

BACKGROUND: It is still unclear whether addition of calcium/vitamin D supplements leads to an incremental benefit in patients taking bisphosphonates and whether achievement of serum level of 25 (OH) vitamin D of at least 70 nmol/L has an impact on the skeletal response to bisphosphonates. Moreover the maintenance of BMD after bisphosphonates withdrawal with the continuation of calcium/vitamin D supplements only, remains uncertain. The aims were to assess the impact of vitamin D status on changes in bone mineral density (BMD) in firstly patients with post-menopausal osteoporosis on bisphosphonates and secondly following discontinuation of bisphosphonates after long-term use. METHODS: Two patient groups were recruited. The first study population comprised of 112 women treated with a bisphosphonate. The second study population consisted of 35 women who had been on bisphosphonates for > 5 years in whom the treatment agent was discontinued. Baseline BMD, changes in BMD following treatment, duration of treatment, serum 25 (OH) vitamin D, parathyroid hormone (PTH), urine C-terminal telopeptides of type 1 collagen (CTX) were obtained on the study participants. RESULTS: In the first study group, subjects with serum vitamin D concentrations (> 70 nmol/L) had a significantly lower serum PTH level (mean [SEM] 41 2 ng/L). PTH concentrations of 41 ng/L or less was associated with a significantly higher increase in BMD at the hip following treatment with bisphosphonates compared to patients with PTH > 41 ng/L (2.5% [0.9] v/s -0.2% [0.9], P = 0.04). In the second study group, discontinuation of bisphosphonate for 15 months after long-term treatment did not result in significant bone loss at the lumbar spine and total hip, although a trend towards gradual decline in BMD at the femoral neck was observed. CONCLUSION: the data suggest that optimal serum 25 (OH) vitamin D concentration may lead to further reduction in bone loss at the hip in patients on bisphosphonates. A prospective controlled trial is needed to evaluate whether the response to bisphosphonates is influenced by vitamin D status. BMD is preserved at the lumbar spine and total hip following discontinuation of bisphosphonate for a short period following long-term treatment, although a gradual loss occurs at the femoral neck.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/52a9/1781939/07e3516ecc96/1471-2474-8-3-7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/52a9/1781939/a636e9362b4b/1471-2474-8-3-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/52a9/1781939/cbb2a74e490e/1471-2474-8-3-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/52a9/1781939/aa751b090032/1471-2474-8-3-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/52a9/1781939/1b6b655c1777/1471-2474-8-3-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/52a9/1781939/8acf1387224e/1471-2474-8-3-5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/52a9/1781939/e0944ee8d604/1471-2474-8-3-6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/52a9/1781939/07e3516ecc96/1471-2474-8-3-7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/52a9/1781939/a636e9362b4b/1471-2474-8-3-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/52a9/1781939/cbb2a74e490e/1471-2474-8-3-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/52a9/1781939/aa751b090032/1471-2474-8-3-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/52a9/1781939/1b6b655c1777/1471-2474-8-3-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/52a9/1781939/8acf1387224e/1471-2474-8-3-5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/52a9/1781939/e0944ee8d604/1471-2474-8-3-6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/52a9/1781939/07e3516ecc96/1471-2474-8-3-7.jpg

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The impact of vitamin D status on changes in bone mineral density during treatment with bisphosphonates and after discontinuation following long-term use in post-menopausal osteoporosis.

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[3]
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[4]
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Transl Clin Pharmacol. 2022-9

[5]
Clinical characteristics associated with bone mineral density improvement after 1-year alendronate/vitamin d3 or calcitriol treatment: Exploratory results from a phase 3, randomized, controlled trial on postmenopausal osteoporotic women in China.

Medicine (Baltimore). 2018-8

[6]
Vitamin D assays and the definition of hypovitaminosis D: results from the First International Conference on Controversies in Vitamin D.

Br J Clin Pharmacol. 2018-7-17

[7]
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[8]
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[9]
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本文引用的文献

[1]
Prevalence of vitamin D inadequacy in Scottish adults with non-vertebral fragility fractures.

Curr Med Res Opin. 2005-9

[2]
Vitamin D concentrations among people aged 65 years and over living in private households and institutions in England: population survey.

Age Ageing. 2005-9

[3]
The role of vitamin D in the prevention of osteoporosis.

Ann Med. 2005

[4]
Vitamin D insufficiency does not affect bone mineral density response to raloxifene.

J Clin Endocrinol Metab. 2005-8

[5]
The high prevalence of inadequate serum vitamin D levels and implications for bone health.

Curr Med Res Opin. 2005-4

[6]
Fracture prevention with vitamin D supplementation: a meta-analysis of randomized controlled trials.

JAMA. 2005-5-11

[7]
Oral vitamin D3 and calcium for secondary prevention of low-trauma fractures in elderly people (Randomised Evaluation of Calcium Or vitamin D, RECORD): a randomised placebo-controlled trial.

Lancet. 2005

[8]
Randomised controlled trial of calcium and supplementation with cholecalciferol (vitamin D3) for prevention of fractures in primary care.

BMJ. 2005-4-30

[9]
Estimates of optimal vitamin D status.

Osteoporos Int. 2005-7

[10]
Severely suppressed bone turnover: a potential complication of alendronate therapy.

J Clin Endocrinol Metab. 2005-3

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