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普萘洛尔与住院肌病风险:将化学基因组学研究结果转化为人群假说。

Propranolol and the risk of hospitalized myopathy: translating chemical genomics findings into population-level hypotheses.

机构信息

Department of Medicine, Brigham and Women's Hospital, Boston, MA, USA.

出版信息

Am Heart J. 2010 Mar;159(3):428-33. doi: 10.1016/j.ahj.2009.12.008.

Abstract

BACKGROUND

A recent large-scale, chemical screening study raised the hypothesis that propranolol may increase the risk of myopathy. We tested this hypothesis in a large population to assess whether (1) propranolol use is associated with an increased risk of myopathy and (2) the concurrent use of propranolol with a statin may further increase risk of myopathy.

METHODS

New users of propranolol and other beta-blockers (BBs) aged >/=65 were identified using data from Medicare and drug benefit programs in 2 states (1994-2005). The primary end point studied was hospitalization for myopathy or rhabdomyolysis. We used stratified Cox proportional hazards regression to estimate the multivariate-adjusted effect of propranolol compared to other BBs and controlled for demographic variables, risk factors for myopathy, other comorbidities, and health service use measures. We also assessed whether co-use of propranolol and statin further increases the risk, by including an interaction term for use of propranolol and statins.

RESULTS

We identified 9,304 initiators of propranolol and 130,070 initiators of other BBs and found 30 cases of hospitalized myopathy in 15,477 person-years (PYs) of propranolol use and 523 in 343,132 PYs of other BB use. Comparing propranolol with other BB users, the adjusted hazard ratio was 1.45 (95% CI 1.00-2.11) for myopathy and 1.48 (95% CI 0.82-2.67) for rhabdomyolysis. We could not detect interaction between propranolol and statins due to limited power. Similar results were observed when propranolol users were compared to other antihypertensive drug users.

CONCLUSIONS

Propranolol may be associated with a 45% increased risk of hospitalized myopathy in the elderly. Our study illustrates how results from in vitro chemical screens can be translated into hypotheses about drug toxicity at the population level.

摘要

背景

最近一项大规模的化学筛选研究提出了普萘洛尔可能会增加肌病风险的假设。我们在一个大人群中检验了这一假设,以评估(1)普萘洛尔的使用是否与肌病风险增加有关,以及(2)普萘洛尔与他汀类药物同时使用是否会进一步增加肌病风险。

方法

使用来自 2 个州的医疗保险和药物福利计划的数据(1994-2005 年),确定年龄≥65 岁的新普萘洛尔和其他β受体阻滞剂(BB)使用者。主要研究终点为因肌病或横纹肌溶解症住院。我们使用分层 Cox 比例风险回归来估计与其他 BB 相比普萘洛尔的多变量调整后效果,并控制了人口统计学变量、肌病风险因素、其他合并症和卫生服务使用措施。我们还通过包含普萘洛尔和他汀类药物同时使用的交互项,评估了普萘洛尔和他汀类药物同时使用是否会进一步增加风险。

结果

我们确定了 9304 名普萘洛尔的起始使用者和 130070 名其他 BB 的起始使用者,在 15477 人年(PYs)的普萘洛尔使用中发现了 30 例住院肌病病例,在 343132PYs 的其他 BB 使用中发现了 523 例。与其他 BB 使用者相比,普萘洛尔的调整后风险比为 1.45(95%CI 1.00-2.11),肌病为 1.48(95%CI 0.82-2.67),横纹肌溶解症为 1.48(95%CI 0.82-2.67)。由于效力有限,我们无法检测到普萘洛尔和他汀类药物之间的相互作用。当将普萘洛尔使用者与其他降压药物使用者进行比较时,也观察到了类似的结果。

结论

普萘洛尔可能与老年人住院肌病风险增加 45%有关。我们的研究说明了如何将体外化学筛选的结果转化为人群水平的药物毒性假设。

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