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临床药物基因组学 MT-RNR1 筛查氨基糖苷类药物诱导的耳毒性及其检测后咨询难题。

Clinical Pharmacogenomic MT-RNR1 Screening for Aminoglycoside-Induced Ototoxicity and the Post-Test Counseling Conundrum.

机构信息

GeneDx, Gaithersburg, Maryland, USA.

Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, New York, USA.

出版信息

Clin Pharmacol Ther. 2023 Aug;114(2):262-265. doi: 10.1002/cpt.2910. Epub 2023 May 4.

Abstract

Aminoglycoside antibiotic exposure can result in ototoxicity and irreversible hearing loss among individuals that harbor the m.1555A>G variant in the mitochondrial 12S rRNA gene, MT-RNR1. Importantly, pre-emptive m.1555A>G screening has been shown to reduce the prevalence of pediatric aminoglycoside-induced ototoxicity; however, professional guidelines to support and guide post-test pharmacogenomic counseling in this context are not currently available. This Perspective highlights key issues with delivering MT-RNR1 results, including longitudinal familial care considerations and communicating m.1555A>G heteroplasmy.

摘要

氨基糖苷类抗生素的使用可能导致携带线粒体 12S rRNA 基因(MT-RNR1)m.1555A>G 变异的个体发生耳毒性和不可逆转的听力损失。重要的是,预防性 m.1555A>G 筛查已被证明可降低儿科氨基糖苷类药物诱导的耳毒性的发生率;然而,目前尚缺乏支持和指导这种情况下的药物基因组学咨询的专业指南。本观点强调了提供 MT-RNR1 结果的关键问题,包括纵向家庭护理考虑因素和 m.1555A>G 异质性的沟通。

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