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直接肾素抑制剂阿利吉仑对健康受试者心脏复极化和传导的影响。

Effects of aliskiren, a direct Renin inhibitor, on cardiac repolarization and conduction in healthy subjects.

作者信息

Ayalasomayajula Surya, Yeh Ching-Ming, Vaidyanathan Sujata, Flannery Brian, Dieterich Hans Armin, Howard Dan, Bedigian Martin P, Dole William P

机构信息

Novartis Pharmaceuticals Corporation, East Hanover, NJ, USA.

出版信息

J Clin Pharmacol. 2008 Jul;48(7):799-811. doi: 10.1177/0091270008319330. Epub 2008 May 19.

Abstract

This multicenter, double-blind study evaluated the effects of aliskiren, a direct renin inhibitor approved for hypertension, on cardiac repolarization and conduction. Healthy volunteers (n = 298) were randomized to aliskiren 300 mg, aliskiren 1200 mg, moxifloxacin 400 mg (positive control), or placebo once daily for 7 days. Digitized electrocardiograms were obtained at baseline and day 7 of treatment over 23 hours postdose. Placebo-adjusted mean changes from baseline in QTcF (Fridericia corrected), QTcI (individualized correction), PR, and QRS intervals were compared at each time point (time-matched analysis) and for values averaged across the dosing period (baseline-averaged analysis). In time-matched analysis, mean changes in QTcF with aliskiren were below predefined limits for QTc prolongation (mean increase <5 milliseconds; upper 90% confidence interval [CI] <10 milliseconds) except aliskiren 1200 mg at 23 hours (5.2 milliseconds; 90% CI 2.2, 8.1). With moxifloxacin, significant QTcF prolongation occurred at most time points, confirming the sensitivity of the assay. Baseline-averaged analysis was consistent with time-matched analysis. Instances of QTcF interval >450 milliseconds or a >30-millisecond increase from baseline with aliskiren (< or = 1%) were similar or lower than placebo (< or = 4%). Results were similar for QTcI. Aliskiren had no effect on PR or QRS duration. In conclusion, aliskiren at the highest approved dose (300 mg) and a 4-fold higher dose had no effect on cardiac repolarization or conduction in healthy volunteers.

摘要

这项多中心、双盲研究评估了已获批准用于治疗高血压的直接肾素抑制剂阿利吉仑对心脏复极化和传导的影响。健康志愿者(n = 298)被随机分为每日一次服用300毫克阿利吉仑、1200毫克阿利吉仑、400毫克莫西沙星(阳性对照)或安慰剂,共7天。在给药后23小时的基线期和治疗第7天获取数字化心电图。在每个时间点(时间匹配分析)以及整个给药期的平均值(基线平均分析),比较了QTcF(弗里德里西亚校正)、QTcI(个体化校正)、PR和QRS间期相对于基线的安慰剂校正平均变化。在时间匹配分析中,除了23小时时的1200毫克阿利吉仑(5.2毫秒;90%置信区间2.2, 8.1)外,阿利吉仑组QTcF的平均变化低于QTc延长的预定义限值(平均增加<5毫秒;90%置信区间上限<10毫秒)。使用莫西沙星时,在大多数时间点出现了显著的QTcF延长,证实了该检测方法的敏感性。基线平均分析与时间匹配分析一致。阿利吉仑组QTcF间期>450毫秒或相对于基线增加>30毫秒的情况(≤1%)与安慰剂组(≤4%)相似或更低。QTcI的结果相似。阿利吉仑对PR或QRS时限无影响。总之,已批准的最高剂量(300毫克)阿利吉仑以及4倍高剂量对健康志愿者的心脏复极化或传导无影响。

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