Ioannou Stephanie, Beecham Ashley, Gomez Lissette, Dauer Ryan, Khakoo Nidah, Pascual Lauren, Quintero Maria, Lopez Joanna, Leavitt James S, Solis Norma, Ortega Mailenys, Deshpande Amar R, Kerman David H, Proksell Siobhan, Torres Esther A, Haritunians Talin, Li Dalin, Abreu Maria T, McGovern Dermott P B, McCauley Jacob L, Damas Oriana M
Division of Digestive Health and Liver Diseases, University of Miami Miller School of Medicine, Miami, Florida.
John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, Florida.
Clin Gastroenterol Hepatol. 2025 May;23(6):1008-1018.e7. doi: 10.1016/j.cgh.2024.07.032. Epub 2024 Aug 23.
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.
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.
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.
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.
西班牙裔/拉丁裔社区中炎症性肠病的患病率正在上升。药物基因组学研究揭示了影响治疗决策的基因标记。我们研究的目的是在一群具有不同祖先背景的西班牙裔患者中,检查基因多态性对硫嘌呤相关白细胞减少症(NUDT15、TPMT)和抗肿瘤坏死因子(TNF)免疫原性(HLA - DQA1∗05)的频率和影响。
我们进行了一项多中心回顾性队列研究,纳入了2225名西班牙裔参与者。我们测量了影响NUDT15、TPMT和HLA - DQA1∗05中药物反应的变异频率;它们的祖先来源(欧洲、非洲或美洲印第安);以及在暴露患者中硫嘌呤和抗TNF药物骨髓抑制和免疫原性的发生率。
NUDT15和TPMT变异很少见,除了NUDT15中的rs116855232,它仅在美洲印第安人起源的等位基因中常见。所有NUDT15变异等位基因都在美洲印第安单倍型上遗传,在美洲印第安等位基因子集中,白细胞减少症患者中NUDT15∗4(rs147390019)的变异频率高达23%,而无白细胞减少症患者中仅为3%。HLA - DQA1∗05及其欧洲标签变异rs2097432在所有祖先来源的等位基因中都很常见,并显示出与抗TNF免疫原性相关。然而,rs2097432仅在欧洲等位基因子集中与HLA - DQA1∗05相关。
这些发现表明,在为具有美洲印第安/阿拉斯加原住民血统的个体(包括西班牙裔个体)开具硫嘌呤之前,NUDT15检测应成为标准临床实践。此外,对于不同人群,rs2097432不应用作HLA - DQA1∗05检测的替代指标。最终,在个性化治疗方法中纳入祖先信息对于治疗西班牙裔炎症性肠病患者很重要。