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全球和局部遗传背景对非裔美国人氯吡格雷反应的作用。

The Role of Global and Local Ancestry on Clopidogrel Response in African Americans.

机构信息

Department of Pharmacology, Center for Pharmacogenomics, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.

出版信息

Pac Symp Biocomput. 2023;28:221-232.

Abstract

Pharmacogenomics has long lacked dedicated studies in African Americans, resulting in a lack of indepth data in this populations. The ACCOuNT consortium has collected a cohort of 167 African American patients on steady state clopidogrel with the goal of discovering population specific variation that may contribute to the response of this anti-platelet agent. Here we analyze the role of both global and local ancestry on the clinical phenotypes of P2Y12 reaction units (PRU) and high on-treatment platelet reactivity (HTPR) in this cohort. We found that local ancestry at the TSS of three genes, IRS-1, ABCB1 and KDR were nominally associated with PRU, and local ancestry-adjusted SNP association identified variants in ITGA2 associated to increased PRU. These finding help to explain the variability in drug response seen in African Americans, especially as few studies on genes outside of CYP2C19 has been conducted in this population.

摘要

药物基因组学在非裔美国人中缺乏专门的研究,导致该人群缺乏深入的数据。ACCOuNT 联盟收集了 167 名稳定服用氯吡格雷的非裔美国患者队列,旨在发现可能导致这种抗血小板药物反应的人群特异性变异。在这里,我们分析了全球和局部祖源在该队列中 P2Y12 反应单位(PRU)和高治疗后血小板反应性(HTPR)的临床表型中的作用。我们发现,三个基因 IRS-1、ABCB1 和 KDR 的 TSS 处的局部祖源与 PRU 呈名义相关,并且局部祖源调整后的 SNP 关联确定了与 PRU 增加相关的 ITGA2 中的变体。这些发现有助于解释非裔美国人中药物反应的可变性,特别是因为在该人群中很少对 CYP2C19 以外的基因进行研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dcd/9782753/f904ccb0b186/nihms-1852991-f0001.jpg

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