Pharmacological response depends on multiple factors and one of them is sex-gender. Data on the specific effects of sex-gender on pharmacokinetics, as well as the safety and efficacy of numerous medications, are beginning to emerge. Nevertheless, the recruitment of women for clinical research is inadequate, especially during the first phases. In general, pharmacokinetic differences between males and females are more numerous and consistent than disparities in pharmacodynamics. However, sex-gender pharmacodynamic differences are now increasingly being identified at the molecular level. It is now even becoming apparent that sex-gender influences pharmacogenomics and pharmacogenetics. Sex-related differences have been reported for several parameters, and it is consistently shown that women have a worse safety profile, with drug adverse reactions being more frequent and severe in women than in men. Overall, the pharmacological status of women is less well studied than that of men and deserves much more attention. The design of clinical and preclinical studies should have a sex-gender-based approach with the aim of tailoring therapies to an individual's needs and concerns.

译文

药理反应取决于多种因素,其中之一是性别。有关性别对药代动力学的特定影响以及许多药物的安全性和有效性的数据开始出现。然而,招募女性进行临床研究是不够的,尤其是在第一阶段。通常,男性和女性之间的药代动力学差异比药效学差异更多且一致。然而,性别-性别药效学差异现在越来越多地在分子水平上被发现。现在甚至变得很明显,性别会影响药物基因组学和药物遗传学。已经报告了几个参数的性别相关差异,并且一直显示女性的安全性较差,女性的药物不良反应比男性更为频繁和严重。总体而言,女性的药理状况比男性研究得少,值得更多关注。临床和临床前研究的设计应采用基于性别的方法,目的是根据个人的需求和关注点定制疗法。

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