Literature DB >> 12110758

Effect of HMG-CoA reductase inhibitors (statins) on bone mineral density.

Holly L Funkhouser1, Tilahun Adera, Robert A Adler.   

Abstract

Recent studies have suggested that 3-hydroxy-3-methylglutaryl - coenzyme A (HMG-CoA) reductase inhibitors (statins) can increase the bone mineral density (BMD). Our objective was to determine if patients on statin drugs were more likely to have a greater bone mineral density and lower risk of osteoporosis than patients not taking these drugs. A computerized pharmacy system provided complete medication dispensing records for the 983 patients (697 men and 286 women) referred for bone mineral density testing at a single Veterans Affairs Medical Center. In an analysis of covariance model that adjusted for age, body mass index, race, and vitamin use, men using statin drugs were more likely to have a greater BMD of the spine (p < 0.005). The mean difference (effect size) was 0.05 g/cm2 (95% confidence interval of [CL] 0.02-0.09), about 5.3% greater BMD. In women, the association was not significant. The risk of osteoporosis (defined as a T-score < or = -2.5) was determined using logistic regression analysis after adjustment for potential confounding variables. Although not statistically significant, men who received statin drugs for more than 2 yr were approximately half as likely to develop osteoporosis (odds ratio [OR] =.55, 95% CI = 0.28-1.08). A similar effect was observed in women taking statins for any length of time (OR = 0.36, 95% CI = 0.12-1.07). This study suggests that statin drugs may decrease osteoporosis risk, warranting a randomized controlled trial.

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Year:  2002        PMID: 12110758     DOI: 10.1385/jcd:5:2:151

Source DB:  PubMed          Journal:  J Clin Densitom        ISSN: 1094-6950            Impact factor:   2.963


  8 in total

Review 1.  Efficacy of statins for osteoporosis: a systematic review and meta-analysis.

Authors:  T An; J Hao; S Sun; R Li; M Yang; G Cheng; M Zou
Journal:  Osteoporos Int       Date:  2016-11-25       Impact factor: 4.507

2.  Modified electrospun chitosan membranes for controlled release of simvastatin.

Authors:  Vishnu Priya Murali; Tomoko Fujiwara; Caleb Gallop; Yongmei Wang; Jack A Wilson; Matthew Thomas Atwill; Mallesh Kurakula; Joel D Bumgardner
Journal:  Int J Pharm       Date:  2020-05-17       Impact factor: 5.875

3.  Simvastatin induces estrogen receptor-alpha expression in bone, restores bone loss, and decreases ERα expression and uterine wet weight in ovariectomized rats.

Authors:  Xu Li; Quan-Sheng Song; Jing-Ying Wang; Hui-jie Leng; Zhong-Qiang Chen; Zhong-Jun Liu; Geng-Ting Dang; Chun-Li Song
Journal:  J Bone Miner Metab       Date:  2010-11-10       Impact factor: 2.626

Review 4.  HMG-CoA reductase inhibitors in osteoporosis: do they reduce the risk of fracture?

Authors:  Raymond G Schlienger; Christoph R Meier
Journal:  Drugs Aging       Date:  2003       Impact factor: 3.923

5.  Novel applications of statins for bone regeneration.

Authors:  Sarita R Shah; Caroline A Werlang; F Kurtis Kasper; Antonios G Mikos
Journal:  Natl Sci Rev       Date:  2014-08-16       Impact factor: 17.275

6.  Local low-dose lovastatin delivery improves the bone-healing defect caused by Nf1 loss of function in osteoblasts.

Authors:  Weixi Wang; Jeffry S Nyman; Heather E Moss; Gloria Gutierrez; Gregory R Mundy; Xiangli Yang; Florent Elefteriou
Journal:  J Bone Miner Res       Date:  2010-07       Impact factor: 6.741

7.  The Interleukin-6 inflammation pathway from cholesterol to aging--role of statins, bisphosphonates and plant polyphenols in aging and age-related diseases.

Authors:  Sota Omoigui
Journal:  Immun Ageing       Date:  2007-03-20       Impact factor: 6.400

Review 8.  Role of Metabolism in Bone Development and Homeostasis.

Authors:  Akiko Suzuki; Mina Minamide; Chihiro Iwaya; Kenichi Ogata; Junichi Iwata
Journal:  Int J Mol Sci       Date:  2020-11-26       Impact factor: 5.923

  8 in total

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