在加勒比海西班牙裔中发现与氯吡格雷反应相关的祖先特异性变异。

IF 4.7 2区 医学 Q1 GENETICS & HEREDITY
Guang Yang, Pablo González, Mariangeli Moneró, Kelvin Carrasquillo, Jessicca Y Renta, Dagmar F Hernandez-Suarez, Mariana R Botton, Kyle Melin, Stuart A Scott, Gualberto Ruaño, Abiel Roche-Lima, Cristina Alarcon, Marylyn D Ritchie, Minoli A Perera, Jorge Duconge
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引用次数: 0

摘要

氯吡格雷治疗时的高血小板反应性(HTPR)可预测成人冠状动脉疾病患者的缺血事件,虽然HTPR因种族而异,但尚未在加勒比海西班牙裔人群中进行氯吡格雷反应的全基因组关联研究(GWAS)。本研究旨在确定511名接受氯吡格雷治疗的波多黎各心血管患者HTPR的遗传预测因子,按P2Y12反应单位(PRU)分为反应者和无反应者(HTPR)。本地祖先推断(LAI)和传统的GWAS发现了与HTPR相关的CYP2C19区域的变异,主要发生在欧洲血统的个体中。三个变异(OSBPL10 rs1376606, DERL3 rs5030613, RGS6 rs9323567)显示了提示意义,UNC5C的一个变异与HTPR风险增加有关。这些发现突出了加勒比海西班牙裔人独特的遗传景观,并挑战了CYP2C19*2在预测高非欧洲血统患者氯吡格雷反应中的重要性。需要进一步的研究来在其他不同的队列中复制这些结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Discovery of ancestry-specific variants associated with clopidogrel response among Caribbean Hispanics.

High on-treatment platelet reactivity (HTPR) with clopidogrel predicts ischemic events in adults with coronary artery disease, and while HTPR varies by ethnicity, no genome-wide association study (GWAS) of clopidogrel response has been conducted in Caribbean Hispanics. This study aimed to identify genetic predictors of HTPR in a cohort of 511 Puerto Rican cardiovascular patients treated with clopidogrel, stratified by P2Y12 reaction units (PRU) into responders and non-responders (HTPR). Local ancestry inference (LAI) and traditional GWAS identified variants in the CYP2C19 region associated with HTPR, primarily in individuals with European ancestry. Three variants (OSBPL10 rs1376606, DERL3 rs5030613, RGS6 rs9323567) showed suggestive significance, and a variant in UNC5C was linked to increased HTPR risk. These findings highlight the unique genetic landscape of Caribbean Hispanics and challenge the significance of CYP2C19*2 in predicting clopidogrel response in patients with high non-European ancestry. Further studies are needed to replicate these results in other diverse cohorts.

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来源期刊
NPJ Genomic Medicine
NPJ Genomic Medicine Biochemistry, Genetics and Molecular Biology-Molecular Biology
CiteScore
9.40
自引率
1.90%
发文量
67
审稿时长
17 weeks
期刊介绍: npj Genomic Medicine is an international, peer-reviewed journal dedicated to publishing the most important scientific advances in all aspects of genomics and its application in the practice of medicine. The journal defines genomic medicine as "diagnosis, prognosis, prevention and/or treatment of disease and disorders of the mind and body, using approaches informed or enabled by knowledge of the genome and the molecules it encodes." Relevant and high-impact papers that encompass studies of individuals, families, or populations are considered for publication. An emphasis will include coupling detailed phenotype and genome sequencing information, both enabled by new technologies and informatics, to delineate the underlying aetiology of disease. Clinical recommendations and/or guidelines of how that data should be used in the clinical management of those patients in the study, and others, are also encouraged.
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