Suarez-Kurtz Guilherme, Araújo Gilderlanio Santana de, de Sousa Sandro José
Coordenação de Pesquisa, Instituto Nacional do Câncer.
Rede Nacional de Farmacogenética, Rio de Janeiro.
Pharmacogenet Genomics. 2020 Jan;30(1):1-4. doi: 10.1097/FPC.0000000000000388.
TPMT and NUDT15 polymorphisms are major determinants of tolerance to thiopurine drugs used in leukemias and nonmalignant immunologic disorders. We adopted an extreme discordant phenotype approach to explore the impact of Native American versus European ancestry on the distribution of TPMT and NUDT15 polymorphisms, and inferred metabolic phenotypes in the 1000 Genomes Ad Mixed American superpopulation. Significant differences were observed in the distribution of TPMT and NUDT15 haplotypes (star alleles) between individuals with predominant (>70%) European versus Native ancestry. The largest difference is related to NUDT15 rs116855232. Based on the combined TPMT/NUDT15 metabolic phenotypes, the Clinical Pharmacogenetics Implementation Consortium recommendations for thiopurine dose adjustment applies to 40.1% of individuals with major Native American ancestry, compared to 12.8% of individuals with predominantly European ancestry. These findings may be relevant to the adoption and interpretation of pharmacogenetic tests for thiopurine drugs across Latin America peoples with different European and Native-American ancestries.
硫嘌呤甲基转移酶(TPMT)和NUDT15基因多态性是白血病和非恶性免疫性疾病中使用的硫嘌呤类药物耐受性的主要决定因素。我们采用极端不一致表型方法,探讨美洲原住民与欧洲人血统对TPMT和NUDT15基因多态性分布的影响,并在千人基因组计划的 admixed American超级人群中推断代谢表型。在主要为欧洲血统(>70%)与美洲原住民血统的个体之间,观察到TPMT和NUDT15单倍型(星号等位基因)分布存在显著差异。最大的差异与NUDT15 rs116855232有关。基于联合的TPMT/NUDT15代谢表型,临床药物基因组学实施联盟关于硫嘌呤剂量调整的建议适用于40.1%主要为美洲原住民血统的个体,而主要为欧洲血统的个体中这一比例为12.8%。这些发现可能与针对不同欧洲和美洲原住民血统的拉丁美洲人群进行硫嘌呤类药物药物基因组学检测的应用和解读相关。