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针对男性和女性的药物——性别作为尖端扭转型室性心动过速的风险因素有多重要?

Drugs for men and women - how important is gender as a risk factor for TdP?

作者信息

Coker Susan J

机构信息

Strathclyde Institute of Pharmacy and Biomedical Sciences, University of Strathclyde, 27 Taylor Street, Glasgow G4 0NR, United Kingdom.

出版信息

Pharmacol Ther. 2008 Aug;119(2):186-94. doi: 10.1016/j.pharmthera.2008.03.005. Epub 2008 Apr 7.

Abstract

The cardiac arrhythmia known as torsade de pointes (TdP), which is a very rare but potentially lethal side effect of a variety of drugs, occurs approximately twice as often in women as it does in men. Most drugs that have this adverse effect prolong the repolarization phase of the cardiac action potential which can be detected by a lengthening of the QT interval on the ECG. The gender difference in susceptibility to TdP only appears after puberty suggesting that sex hormones are contributory factors. Studies in patients indicate that testosterone-induced shortening of action potential duration may account for the shorter rate-corrected QT interval in men rather than any effect of estradiol in women, whereas drug-induced QT prolongation can be potentiated by estradiol. Experimental investigations suggest that sex hormones may alter either Ca2+ currents, K+ currents, or both and that actions on these ionic currents may account for the gender differences in cardiac repolarization. Although estradiol exacerbated drug-induced TdP in an in vivo model, no similar information is available for progesterone or testosterone. Further studies are required to clarify the influence of these sex hormones and to investigate the importance of the balance between sex hormones in both genders. Such information would assist in risk:benefit analysis and may allow the development of "drugs for men" and "drugs for women".

摘要

被称为尖端扭转型室性心动过速(TdP)的心律失常是多种药物非常罕见但可能致命的副作用,其在女性中的发生率约为男性的两倍。大多数具有这种不良反应的药物会延长心脏动作电位的复极期,这可以通过心电图上QT间期的延长来检测。对TdP易感性的性别差异仅在青春期后出现,这表明性激素是促成因素。对患者的研究表明,睾酮诱导的动作电位持续时间缩短可能是男性心率校正QT间期较短的原因,而不是雌二醇对女性有任何影响,而药物诱导的QT延长可被雌二醇增强。实验研究表明,性激素可能会改变钙电流、钾电流或两者,并且对这些离子电流的作用可能解释了心脏复极中的性别差异。尽管在体内模型中雌二醇会加剧药物诱导的TdP,但关于孕酮或睾酮的类似信息尚无。需要进一步研究以阐明这些性激素的影响,并研究两性中性激素平衡的重要性。此类信息将有助于进行风险效益分析,并可能促进“男性用药”和“女性用药”的开发。

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