| Literature DB >> 20045497 |
Somlak Chuengsamarn1, Suthee Rattanamongkoulgul, Somponge Suwanwalaikorn, Somkiat Wattanasirichaigoon, Larry Kaufman.
Abstract
INTRODUCTION: The 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitors, named statins, are well-established cholesterol-lowering drugs able to reduce cardiovascular risk in hypercholesterolemic patients. The possible effect of statin on bone tissue, so-called pleiotropic effects has received particular attention. Studies reported a positive effect of statin on bone tissue in both of animal and human study by enhancing the expression of the bone morphogenetic proteins (BMPs), in particular of BMP2, which in turn leads to osteoblast differentiation and bone formation including interfering with osteoclastic activity. In a systematic review, the lipophilic statin as simvastatin had positive effect to bone mineral density (BMD) better than the more hydrophilic statin such as atorvastatin and fluvastatin. This study was aimed to compare efficacy of medical therapy between HMG-CoA reductase inhibitor and non-HMG-CoA reductase inhibitor group to changing of bone mineral density and bone markers in the patients with hyperlipidemia.Entities:
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Year: 2010 PMID: 20045497 DOI: 10.1016/j.bone.2009.12.023
Source DB: PubMed Journal: Bone ISSN: 1873-2763 Impact factor: 4.398