HMG-CoA Reductase Inhibitors in OsteoporosisDo They Reduce the Risk of Fracture?

被引:0
作者
Raymond G. Schlienger
Christoph R. Meier
机构
[1] University Hospital,Basel Pharmacoepidemiology Unit, Division of Clinical Pharmacology & Toxicology
[2] University of Basel,Department of Pharmacy, Institute of Clinical Pharmacy
[3] Boston University Medical Center,Boston Collaborative Drug Surveillance Program
来源
Drugs & Aging | 2003年 / 20卷
关键词
Bone Mineral Density; Simvastatin; Fracture Risk; Atorvastatin; Pravastatin;
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摘要
Osteoporosis affects a large number of people in industrialised countries. It has clinical and public-health impacts, most importantly due to subsequent fractures. Osteoporotic fractures are one of the most common causes of disability and are associated with enormous healthcare expenditure. The majority of existing treatment options for osteoporosis only inhibit bone resorption and prevent excessive bone loss but are not capable of stimulating bone formation. However, several recent in vitro and in vivo studies in animals demonstrated that HMG-CoA reductase inhibitors stimulate the production of bone morphogenetic protein (BMP-2), which is a potent regulating protein in osteoblast differentiation and activity. This suggests that HMG-CoA reductase inhibitors may have an anabolic effect on bones, making them a potentially interesting treatment option for osteoporosis. Additionally, several studies in humans showed that some HMG-CoA reductase inhibitors may have a beneficial effect on bone turnover and may lead to an increase in bone mineral density.
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页码:321 / 336
页数:15
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