Statins decrease bone turnover in postmenopausal women: a cross-sectional study
Background Statins have been suggested as potential agents in the management of osteoporosis. Reviews of medical records have shown an increased bone mass and some studies have shown a reduced occurrence of fractures in subjects on long‐term treatment with statins. We studied the effects of treatmen...
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Published in: | European journal of clinical investigation Vol. 32; no. 8; pp. 581 - 589 |
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Language: | English |
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Blackwell Science Ltd
01-08-2002
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Abstract | Background Statins have been suggested as potential agents in the management of osteoporosis. Reviews of medical records have shown an increased bone mass and some studies have shown a reduced occurrence of fractures in subjects on long‐term treatment with statins. We studied the effects of treatment with statins on calcium homeostasis, bone turnover and bone mineral density.
Design In a cross‐sectional design, plasma levels of parathyroid hormone (PTH) and biochemical markers of bone turnover, bone mineral density (BMD) and body composition (fat‐ and lean tissue‐mass) were measured in 140 postmenopausal women who had been treated with a statin for more than 2 years (median 4 years) and compared to 140 age‐ and gender‐matched, population‐based controls.
Results Plasma levels of bone turnover markers were lower in the statin‐treated subjects than in the controls: osteocalcin (−9%, P = 0·03), bone‐specific alkaline phosphatase (−14%, P < 0·01), and C‐terminal telopeptide of type I collagen (−11%, P < 0·01). On the other hand, plasma PTH levels were 16% higher in the statin‐treated subjects than in the controls (P < 0·01). However, body composition and BMD at the lumbar spine, hip, forearm and whole body did not differ between the two groups. No correlation could be demonstrated between changes in biochemical quantities and dose or duration of statin use.
Conclusion Our data show that statins affect the function of bone cells. Most likely, the effect is antiresorptive. |
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AbstractList | Background
Statins have been suggested as potential agents in the management of osteoporosis. Reviews of medical records have shown an increased bone mass and some studies have shown a reduced occurrence of fractures in subjects on long‐term treatment with statins. We studied the effects of treatment with statins on calcium homeostasis, bone turnover and bone mineral density.
Design
In a cross‐sectional design, plasma levels of parathyroid hormone (PTH) and biochemical markers of bone turnover, bone mineral density (BMD) and body composition (fat‐ and lean tissue‐mass) were measured in 140 postmenopausal women who had been treated with a statin for more than 2 years (median 4 years) and compared to 140 age‐ and gender‐matched, population‐based controls.
Results
Plasma levels of bone turnover markers were lower in the statin‐treated subjects than in the controls: osteocalcin (−9%,
P
= 0·03), bone‐specific alkaline phosphatase (−14%,
P
< 0·01), and C‐terminal telopeptide of type I collagen (−11%,
P
< 0·01). On the other hand, plasma PTH levels were 16% higher in the statin‐treated subjects than in the controls (
P
< 0·01). However, body composition and BMD at the lumbar spine, hip, forearm and whole body did not differ between the two groups. No correlation could be demonstrated between changes in biochemical quantities and dose or duration of statin use.
Conclusion
Our data show that statins affect the function of bone cells. Most likely, the effect is antiresorptive. Background Statins have been suggested as potential agents in the management of osteoporosis. Reviews of medical records have shown an increased bone mass and some studies have shown a reduced occurrence of fractures in subjects on long‐term treatment with statins. We studied the effects of treatment with statins on calcium homeostasis, bone turnover and bone mineral density. Design In a cross‐sectional design, plasma levels of parathyroid hormone (PTH) and biochemical markers of bone turnover, bone mineral density (BMD) and body composition (fat‐ and lean tissue‐mass) were measured in 140 postmenopausal women who had been treated with a statin for more than 2 years (median 4 years) and compared to 140 age‐ and gender‐matched, population‐based controls. Results Plasma levels of bone turnover markers were lower in the statin‐treated subjects than in the controls: osteocalcin (−9%, P = 0·03), bone‐specific alkaline phosphatase (−14%, P < 0·01), and C‐terminal telopeptide of type I collagen (−11%, P < 0·01). On the other hand, plasma PTH levels were 16% higher in the statin‐treated subjects than in the controls (P < 0·01). However, body composition and BMD at the lumbar spine, hip, forearm and whole body did not differ between the two groups. No correlation could be demonstrated between changes in biochemical quantities and dose or duration of statin use. Conclusion Our data show that statins affect the function of bone cells. Most likely, the effect is antiresorptive. BACKGROUNDStatins have been suggested as potential agents in the management of osteoporosis. Reviews of medical records have shown an increased bone mass and some studies have shown a reduced occurrence of fractures in subjects on long-term treatment with statins. We studied the effects of treatment with statins on calcium homeostasis, bone turnover and bone mineral density. DESIGNIn a cross-sectional design, plasma levels of parathyroid hormone (PTH) and biochemical markers of bone turnover, bone mineral density (BMD) and body composition (fat- and lean tissue-mass) were measured in 140 postmenopausal women who had been treated with a statin for more than 2 years (median 4 years) and compared to 140 age- and gender-matched, population-based controls. RESULTSPlasma levels of bone turnover markers were lower in the statin-treated subjects than in the controls: osteocalcin (-9%, P = 0.03), bone-specific alkaline phosphatase (-14%, P < 0.01), and C-terminal telopeptide of type I collagen (-11%, P < 0.01). On the other hand, plasma PTH levels were 16% higher in the statin-treated subjects than in the controls (P < 0.01). However, body composition and BMD at the lumbar spine, hip, forearm and whole body did not differ between the two groups. No correlation could be demonstrated between changes in biochemical quantities and dose or duration of statin use. CONCLUSIONOur data show that statins affect the function of bone cells. Most likely, the effect is antiresorptive. Statins have been suggested as potential agents in the management of osteoporosis. Reviews of medical records have shown an increased bone mass and some studies have shown a reduced occurrence of fractures in subjects on long-term treatment with statins. We studied the effects of treatment with statins on calcium homeostasis, bone turnover and bone mineral density. In a cross-sectional design, plasma levels of parathyroid hormone (PTH) and biochemical markers of bone turnover, bone mineral density (BMD) and body composition (fat- and lean tissue-mass) were measured in 140 postmenopausal women who had been treated with a statin for more than 2 years (median 4 years) and compared to 140 age- and gender-matched, population-based controls. Plasma levels of bone turnover markers were lower in the statin-treated subjects than in the controls: osteocalcin (-9%, P = 0.03), bone-specific alkaline phosphatase (-14%, P < 0.01), and C-terminal telopeptide of type I collagen (-11%, P < 0.01). On the other hand, plasma PTH levels were 16% higher in the statin-treated subjects than in the controls (P < 0.01). However, body composition and BMD at the lumbar spine, hip, forearm and whole body did not differ between the two groups. No correlation could be demonstrated between changes in biochemical quantities and dose or duration of statin use. Our data show that statins affect the function of bone cells. Most likely, the effect is antiresorptive. |
Author | Buus, N. H. Vestergaard, P. Rejnmark, L. Larsen, M. L. Mosekilde, L. Andreasen, F. |
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BackLink | https://www.ncbi.nlm.nih.gov/pubmed/12190958$$D View this record in MEDLINE/PubMed |
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Notes | ArticleID:ECI1024 istex:98F66E7EBD782A2C96629FE57CBBDF2FF8B67FF3 ark:/67375/WNG-X705R2C1-6 Department of Endocrinology and Metabolism C, Aarhus Amtssygehus, Aarhus University Hospital (L. Rejnmark, N. H. Buus, P. Vestergaard, L. Mosekilde); Centre for Clinical Pharmacology, Faculty of Health Sciences, Aarhus University (L. Rejnmark, N. H. Buus, F. Andreasen); Department of Medicine and Cardiology, Aarhus Amtssygehus, Aarhus University Hospital (M. L. Larsen); Faculty of Health Sciences, Aarhus University (P. Vestergaard, L. Mosekilde); Aarhus, DenmarkAarhus, Denmark. ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
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Snippet | Background Statins have been suggested as potential agents in the management of osteoporosis. Reviews of medical records have shown an increased bone mass and... Statins have been suggested as potential agents in the management of osteoporosis. Reviews of medical records have shown an increased bone mass and some... Background Statins have been suggested as potential agents in the management of osteoporosis. Reviews of medical records have shown an increased bone mass and... BACKGROUNDStatins have been suggested as potential agents in the management of osteoporosis. Reviews of medical records have shown an increased bone mass and... |
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SubjectTerms | Aged Alkaline Phosphatase - blood Biochemical bone markers Biomarkers - blood bone Bone Density Bone Remodeling - drug effects Calcium - metabolism Collagen - blood Collagen Type I Cross-Sectional Studies Female Humans Hydroxymethylglutaryl-CoA Reductase Inhibitors - therapeutic use Hypercholesterolemia - drug therapy Hypercholesterolemia - metabolism Linear Models Middle Aged Osteocalcin - blood osteoporosis Parathyroid Hormone - blood Peptides - blood postmenopausal women Postmenopause - metabolism Simvastatin - therapeutic use statins |
Title | Statins decrease bone turnover in postmenopausal women: a cross-sectional study |
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