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QT和TRIaD在心脏安全性研究中的应用与滥用:研究设计与实施的重要性

Use and abuse of QT and TRIaD in cardiac safety research: importance of study design and conduct.

作者信息

Hondeghem Luc M

机构信息

Catholic University Leuven, Westlaan 85, B-8400 OOSTENDE, Belgium.

出版信息

Eur J Pharmacol. 2008 Apr 14;584(1):1-9. doi: 10.1016/j.ejphar.2008.01.016. Epub 2008 Jan 26.

Abstract

Triangulation, reverse use dependence, instability and dispersion of ventricular repolarization (TRIaD), together with the cardiac wavelength (lambda), are powerful proarrhythmic predictors. QT interval prolongation as such is not, as it provides false positives as well as false negatives. This has been established in various preclinical experiments on isolated tissues, perfused hearts and experimental animals, as well as in the clinic. Numerous risk factors including female gender, low serum potassium and magnesium, bradycardia and genetic predisposition, further promote arrhythmogenesis. Reliable quantitative preclinical cardiac safety studies using any experimental approach always require (1) rigorous adherence to Good Laboratory Practices (GLP), (2) collection of data only after complete drug equilibration has been established, (3) adequate resolution, (4) analysis based upon suitably powered statistical tests, (5) a sufficient number of experiments and (6) validated experimental protocols. Genesis of data not in accord with such standards and reported in an incorrect fashion confounds the significance of preclinical results for eventual clinical studies and elicits confusion regarding important drug effects. In this context, establishing a preclinical research consortium is suggested. This to assure: (1) the use of standardized experimental protocols and animal models; (2) data analysis with appropriately powered statistical tests; (3) correct testing and reporting and (4) elimination of some of the errors and abuses outlined in this paper.

摘要

心室复极的三角测量、反向使用依赖性、不稳定性和离散度(TRIaD),以及心脏波长(λ),都是强大的促心律失常预测指标。QT间期延长本身并非如此,因为它会产生假阳性和假阴性结果。这已在离体组织、灌注心脏和实验动物的各种临床前实验以及临床中得到证实。包括女性性别、低血钾和低血镁、心动过缓和遗传易感性在内的众多风险因素,会进一步促进心律失常的发生。使用任何实验方法进行可靠的临床前心脏安全性研究始终需要:(1)严格遵守良好实验室规范(GLP);(2)仅在药物完全平衡后收集数据;(3)足够的分辨率;(4)基于有足够效力的统计检验进行分析;(5)足够数量的实验;以及(6)经过验证的实验方案。不符合此类标准且报告方式不正确的数据生成,会混淆临床前结果对最终临床研究的意义,并引发对重要药物效应的困惑。在此背景下,建议建立一个临床前研究联盟。这是为了确保:(1)使用标准化的实验方案和动物模型;(2)用有足够效力的统计检验进行数据分析;(3)正确的测试和报告;以及(4)消除本文所述的一些错误和滥用情况。

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