Ancestral Diversity in Pharmacogenomics Affects Treatment for Hispanic/Latine Populations With Inflammatory Bowel Disease.

IF 11.6 1区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY Clinical Gastroenterology and Hepatology Pub Date : 2024-08-23 DOI:10.1016/j.cgh.2024.07.032
Stephanie Ioannou, Ashley Beecham, Lissette Gomez, Ryan Dauer, Nidah Khakoo, Lauren Pascual, Maria Quintero, Joanna Lopez, James S Leavitt, Norma Solis, Mailenys Ortega, Amar R Deshpande, David H Kerman, Siobhan Proksell, Esther A Torres, Talin Haritunians, Dalin Li, Maria T Abreu, Dermott P B McGovern, Jacob L McCauley, Oriana M Damas
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Abstract

Background and aims: The prevalence of inflammatory bowel disease among Hispanic/Latine communities is increasing. Pharmacogenomic studies reveal genetic markers that influence treatment decisions. The aim of our study was to examine the frequency and impact of genetic polymorphisms on thiopurine-associated leukopenia (NUDT15, TPMT) and anti-tumor necrosis factor (TNF) immunogenicity (HLA-DQA1∗05) in a cohort of Hispanic patients of diverse ancestral backgrounds.

Methods: We performed a multicenter, retrospective cohort study comprising 2225 Hispanic participants. We measured the frequency of variation affecting drug response in NUDT15, TPMT, and HLA-DQA1∗05; their ancestral origin (European, African, or Amerindian); and the rate of development of myelosuppression and immunogenicity to thiopurines and anti-TNFs, in exposed patients.

Results: NUDT15 and TPMT variants were rare, except for rs116855232 in NUDT15, which was common only in alleles of Amerindian origin. All NUDT15 variant alleles were inherited on an Amerindian haplotype, and among the Amerindian allele subset, the variant frequency of NUDT15∗4 (rs147390019) was a remarkable 23% in patients with leukopenia but only 3% in patients without leukopenia. HLA-DQA1∗05 and its European tagging variant rs2097432 were common in alleles from all ancestral origins and demonstrated association with immunogenicity to anti-TNFs. However, rs2097432 was only correlated with HLA-DQA1∗05 in the European allele subset.

Conclusions: These findings indicate that NUDT15 testing should become standard clinical practice before prescribing thiopurines in individuals with Amerindian/Alaska Native ancestry, including Hispanic individuals. Additionally, rs2097432 should not be used as a surrogate for HLA-DQA1∗05 testing for diverse populations. Ultimately, incorporating ancestry in personalized therapeutic approaches is important for treatment of Hispanic patients with inflammatory bowel disease.

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药物基因组学中的祖先多样性会影响西班牙裔/拉丁裔炎症性肠病患者的治疗。
背景和目的:西班牙裔/拉丁裔群体中炎症性肠病(IBD)的发病率正在上升。药物基因组研究揭示了影响治疗决策的遗传标记。我们的研究旨在考察不同祖先背景的西班牙裔患者队列中,硫嘌呤相关性白细胞减少症(NUDT15、TPMT)和抗肿瘤坏死因子免疫原性(HLA-DQA1*05)基因多态性的频率及其影响:我们进行了一项多中心、回顾性队列研究,共有 2225 名西班牙裔参与者参加。我们测量了NUDT15、TPMT和HLA-DQA1*05中影响药物反应的变异频率、其祖先来源(欧洲、非洲或美洲印第安人),以及暴露患者骨髓抑制的发生率和对硫嘌呤类药物和抗肿瘤坏死因子的免疫原性:结果发现:NUDT15和TPMT变异体非常罕见,只有NUDT15中的rs116855232在美洲印第安血统的等位基因中比较常见。所有 NUDT15 变异等位基因都以美洲印第安人单倍型遗传,在美洲印第安人等位基因子集中,NUDT15*4(rs147390019)的变异频率在白细胞减少症患者中高达 23%,而在无白细胞减少症患者中仅为 3%。HLA-DQA1*05 及其欧洲标记变体 rs2097432 在所有祖先来源的等位基因中都很常见,并与抗肿瘤坏死因子的免疫原性有关。然而,rs2097432 仅在欧洲等位基因子集中与 HLA-DQA1*05 相关:这些研究结果表明,在为美洲印第安血统的个体(包括西班牙裔个体)开硫嘌呤类药物处方之前,NUDT15 检测应成为标准临床实践。此外,在不同人群中,rs2097432 不应被用作 HLA-DQA1*05 检测的替代物。最后,将血统纳入个性化治疗方法对于治疗西班牙裔 IBD 患者非常重要。
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来源期刊
CiteScore
16.90
自引率
4.80%
发文量
903
审稿时长
22 days
期刊介绍: Clinical Gastroenterology and Hepatology (CGH) is dedicated to offering readers a comprehensive exploration of themes in clinical gastroenterology and hepatology. Encompassing diagnostic, endoscopic, interventional, and therapeutic advances, the journal covers areas such as cancer, inflammatory diseases, functional gastrointestinal disorders, nutrition, absorption, and secretion. As a peer-reviewed publication, CGH features original articles and scholarly reviews, ensuring immediate relevance to the practice of gastroenterology and hepatology. Beyond peer-reviewed content, the journal includes invited key reviews and articles on endoscopy/practice-based technology, health-care policy, and practice management. Multimedia elements, including images, video abstracts, and podcasts, enhance the reader's experience. CGH remains actively engaged with its audience through updates and commentary shared via platforms such as Facebook and Twitter.
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