艾滋病毒和代谢综合征患者的药物相互作用分析。

Jessica Tuan, Grace Igiraneza, Onyema Ogbuagu
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引用次数: 0

摘要

背景:艾滋病病毒感染者(PWH)寿命的延长与高效的抗逆转录病毒疗法(ART)直接相关。然而,在寿命延长的同时,新陈代谢合并症的发病率和死亡率也在不断上升。新陈代谢紊乱的治疗方法越来越多。因此,临床医生必须了解抗逆转录病毒疗法与代谢紊乱治疗之间的药物相互作用(DDIs):本综述将讨论当代抗逆转录病毒疗法与用于治疗代谢综合征(糖尿病、血脂异常、肥胖症和高血压)的药物之间的 DDIs。我们从以下来源对已发表和未发表的手稿、会议记录、监管文件和药物处方信息中的数据进行了文献综述:专家意见:艾滋病病毒感染者的代谢紊乱发病率很高。大多数抗逆转录病毒疗法与代谢紊乱治疗之间的重大 DDI 是单向的,抗逆转录病毒疗法是肇事者,而不是受害者,因此谨慎选择 DDI 倾向低的抗逆转录病毒疗法可以解决这一问题。然而,长效抗逆转录病毒疗法以及治疗糖尿病和减肥的新型口服注射药物的 DDI 数据还存在空白。基于纳米技术的给药平台有望解决一些 DDI 问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Analysis of drug-drug interactions in patients with HIV and metabolic syndrome.

Background: People with HIV (PWH) are living longer directly related to benefits of highly effective antiretroviral therapy (ART). However, concurrent with improved longevity is the growing prevalence of metabolic comorbidities that drive morbidity and mortality among PWH. There is an increasing repertoire of treatment options for metabolic disorders. Thus, it is important for clinicians to understand the drug-drug interactions (DDIs) between ART and treatments for metabolic disorders.

Areas covered: This review will discuss DDIs between contemporary ART and agents used to treat metabolic syndrome (diabetes, dyslipidemia, obesity and hypertension). Literature review of published and unpublished data from manuscripts, conference proceedings, regulatory submissions, and drug prescribing information were conducted from the following sources: PubMed, Google, and Google Scholar through January 2024.

Expert opinion: People with HIV have a high prevalence of metabolic disorders. Most significant DDIs between ART and treatments for metabolic disorders are unidirectional with ART as perpetrators, rather than victims, such that careful selection of ART with low DDI propensity can address the concern. However, there are data gaps with DDI data for long-acting ART as well as newer oral and injectable medications for diabetes and weight loss. Nanotechnology-based drug delivery platforms hold promise to address some problematic DDIs.

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