首页> 外文期刊>Journal of clinical densitometry >Effect of HMG-CoA reductase inhibitors (statins) on bone mineral density.
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Effect of HMG-CoA reductase inhibitors (statins) on bone mineral density.

机译:HMG-COA还原酶抑制剂(汀类汀类)对骨密度的影响。

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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.
机译:最近的研究表明,3-羟基-3-甲基谷族 - 辅酶A(HMG-COA)还原酶抑制剂(他汀类药物)可以增加骨密度(BMD)。我们的目标是确定他汀类药物上的患者是否更容易具有更大的骨矿物质密度和骨质疏松症的风险低于未服用这些药物的患者。计算机化药房系统为983名患者(697名男性和286名女性)提供了完整的药物分配记录,在一名退伍军人事务医疗中心提到骨矿物密度测试。在调整年龄,体重指数,种族和维生素使用的调整调整的协方差模型中,使用他汀类药物的男性更可能具有更大的脊柱BMD(P <0.005)。平均差异(效果尺寸)为0.05g / cm 2([Cl] 0.02-0.09的95%置信区间),BMD大约5.3%。在女性中,协会并不重要。使用逻辑回归分析进行调整后,确定骨质疏松症的风险(定义为T-Score <或= -2.5),调整潜在的混杂变量。虽然没有统计学意义,接受他汀类药物超过2年的人的男性大约发育骨质疏松症的一半(差异[或] = .55,95%CI = 0.28-1.08)。在服用他汀类药物的女性中观察到类似的效果(或= 0.36,95%CI = 0.12-1.07)。该研究表明,他汀类药物可能会降低骨质疏松症风险,需要随机对照试验。

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