General Toxicology Sciences, Safety Assessment UK, AstraZeneca R&D, Alderley Park, Macclesfield, Cheshire, SK10 4TG, UK.
Trends Pharmacol Sci. 2010 Mar;31(3):108-14. doi: 10.1016/j.tips.2009.12.001. Epub 2010 Feb 1.
Clinical data suggest that gender dimorphic profiles are emerging in terms of both drug efficacy and adverse drug reactions (ADRs). With an increasing emphasis on individualised therapies and the need to prevent drug attrition there is a compelling need to understand the molecular basis for gender dimorphic profiles in ADRs and the consequences. Classes of agents exhibiting gender-based variation in pharmaceutical efficacy and toxicity include anaesthetics, HIV-1 therapies and antiarrhythmic drugs. Body weight differences are often cited as a reason for differences in drug pharmacokinetics and subsequent toxicity. However, some studies accounted for these factors and still found significance suggesting that dosage versus body weight does not explain the outcome. Here, we present an overview of current understanding of gender-specific drug toxicity and present rational molecular explanations for these adverse events. There is mounting evidence in support of hormonal effects underpinning the majority of the ADR differences observed between the sexes.
临床数据表明,在药物疗效和药物不良反应(ADR)方面,性别二态性特征正在显现。鉴于人们越来越重视个体化治疗以及需要防止药物淘汰,因此迫切需要了解 ADR 中性别二态性特征的分子基础及其后果。在药物疗效和毒性方面具有性别差异的药物类别包括麻醉剂、HIV-1 治疗药物和抗心律失常药物。体重差异通常被认为是药物药代动力学和随后毒性差异的原因。然而,一些研究考虑了这些因素,仍然发现了具有统计学意义的结果,这表明剂量与体重并不能解释结果。在这里,我们概述了目前对性别特异性药物毒性的理解,并对这些不良事件提出了合理的分子解释。越来越多的证据支持激素对大多数性别间观察到的 ADR 差异的基础作用。