利托那韦增强阿扎那韦对HIV患者的剂量:基于东南亚遗传多态性流行病学的重新评估。

International journal of physiology, pathophysiology and pharmacology Pub Date : 2022-08-15 eCollection Date: 2022-01-01
Rujittika Mungmunpuntipantip, Viroj Wiwanitkit
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引用次数: 0

摘要

目前有几种抗艾滋病毒药物可供使用,并用于世界各地艾滋病毒阳性患者的医疗保健。耐药性是一个全球性问题,需要开发一种新的治疗方案来解决它。在一些国家,现在使用利托那韦(RTV)增强的阿扎那韦(ATV)。有证据表明,定期接受rtv增强ATV的患者有较高的ATV暴露,增加了毒性风险。最近的一项理论表明,较小剂量的ATV/r可能就足够了。在本文中,作者根据CYP3A5 6986 A > G遗传流行病学的现有数据重新评估了HIV患者的ATV/r剂量。根据研究,个体通过各种ATV/r方案的浓度达到ATV治疗范围的可能性取决于基线性别和CYP3A5 6986 A > G型。除了男性受试者的正常给药方案外,所有受试者都有机会通过浓度达到ATV的治疗范围(总概率大于1)。因此,应主要考虑对男性HIV感染者降低ATV/r剂量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dose of ritonavir-boosted atazanavir for HIV patient: a reappraisal based on genetic polymorphism epidemiology in Southeast Asia.

Several anti-HIV medications are currently available and used in medical care for HIV-positive people all over the world. Drug resistance is a global problem that necessitates the development of a new treatment regimen to address it. In several countries, ritonavir (RTV)-boosted atazanavir (ATV) is now used. There is evidence that patients taking RTV-boosted ATV on a regular basis have a higher ATV exposure, increasing the risk of toxicity. A recent theory suggests that a smaller dose of ATV/r may be sufficient. In this article, the authors reevaluate the dose of ATV/r for HIV patients based on existing data on the genetic epidemiology of CYP3A5 6986 A > G. According to the research, the likelihood of an individual achieving the therapeutic range of ATV through concentrations in various ATV/r regimens differs depending on baseline sex and CYP3A5 6986 A > G type. With the exception of a normal dosing regimen for male subjects, all have a chance of reaching the therapeutic range of ATV through concentrations (overall probability greater than 1). As a result, the lowering of the ATV/r dose should be considered primarily for male HIV infected patients.

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