Rejnmark Lars, Olsen Mette Lena, Johnsen Søren Paaske, Vestergaard Peter, Sørensen Henrik Toft, Mosekilde Leif
Department of Endocrinology and Metabolism C, Aarhus Amtssygehus, Aarhus University Hospital, Tage-Hansens Gade 2, 8000 Aarhus C, Denmark.
Osteoporos Int. 2004 Jun;15(6):452-8. doi: 10.1007/s00198-003-1568-z. Epub 2004 Feb 17.
Based on animal studies, statins (3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitors) have been suggested as potential agents in the treatment of osteoporosis. In some epidemiological studies, statins have been associated with a reduced fracture risk. Our objective was to examine associations between statin treatment and risk of hip fracture in a population-based case-control study. A total of 6660 subjects with hip fracture and 33,274 gender- and age-matched population controls were identified from 1 January 1994 to 31 December 2001 using the Hospital Patient Register in North Jutland County, Denmark, and the Danish Central Personal Registry, respectively. Data on redeemed prescriptions for statins within the last 5 years before the index date were retrieved from a population-based prescription database. We used conditional logistic regression to estimate odds ratios (OR) for hip fracture according to use of statin prescriptions adjusted for potential confounding factors, i.e. gender, other diseases, and use of other drugs known to affect bone metabolism and fracture risk. After adjustment for potential confounders, statin treatment was associated with a reduced risk of hip fracture (OR=0.68; 95% confidence interval: 0.50-0.93) for those who had redeemed more than three prescriptions for a statin drug. We found that risk of hip fracture decreased with the number of statin prescriptions. Stratified analyses on gender and age did not reveal any major differences between men and women or among different age groups on the estimates between use of statins and hip fracture risk. Our findings support an association between statin treatment and a reduced hip fracture risk. However, it is unclear whether this association is causal.
基于动物研究,他汀类药物(3-羟基-3-甲基戊二酰辅酶A还原酶抑制剂)被认为是治疗骨质疏松症的潜在药物。在一些流行病学研究中,他汀类药物与降低骨折风险有关。我们的目的是在一项基于人群的病例对照研究中,检验他汀类药物治疗与髋部骨折风险之间的关联。1994年1月1日至2001年12月31日期间,分别使用丹麦北日德兰郡的医院患者登记册和丹麦中央个人登记册,确定了6660例髋部骨折患者和33274例性别和年龄匹配的人群对照。从一个基于人群的处方数据库中检索索引日期前最后5年内他汀类药物的赎回处方数据。我们使用条件逻辑回归来估计根据他汀类药物处方使用情况调整潜在混杂因素(即性别、其他疾病以及已知影响骨代谢和骨折风险的其他药物使用情况)后的髋部骨折比值比(OR)。在对潜在混杂因素进行调整后,对于赎回超过三张他汀类药物处方的患者,他汀类药物治疗与降低髋部骨折风险相关(OR=0.68;95%置信区间:0.50-0.93)。我们发现髋部骨折风险随着他汀类药物处方数量的增加而降低。按性别和年龄进行的分层分析未显示在他汀类药物使用与髋部骨折风险估计值方面,男性和女性之间或不同年龄组之间存在任何重大差异。我们的研究结果支持他汀类药物治疗与降低髋部骨折风险之间存在关联。然而,尚不清楚这种关联是否具有因果关系