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
Main Authors: Rejnmark, L., Buus, N. H., Vestergaard, P., Andreasen, F., Larsen, M. L., Mosekilde, L.
Format: Journal Article
Language:English
Published: Oxford, UK 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.
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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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.
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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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https://onlinelibrary.wiley.com/doi/abs/10.1046%2Fj.1365-2362.2002.01024.x
https://www.ncbi.nlm.nih.gov/pubmed/12190958
https://www.proquest.com/docview/199127293
https://search.proquest.com/docview/72024800
Volume 32
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