Suarez-Kurtz Guilherme, Parra Esteban J
Instituto Nacional de Câncer and Rede Nacional de Farmacogenética, Rio de Janeiro, Brazil.
University of Toronto at Mississauga, Mississauga, ON, Canada.
Adv Pharmacol. 2018;83:133-154. doi: 10.1016/bs.apha.2018.02.001. Epub 2018 Mar 19.
Pharmacogenetics/pharmacogenomics (PGx) relies on human genetic diversity. In this review we initially examine the PGx implications of human demographic history and genetic diversity, and highlight results from recent studies on the worldwide distribution of common and rare variants in pharmacogenes. The abundance of rare variants implies that a substantial effort will be required to identify their putative functional effects and to develop reliable algorithms for PGx-guided prescription. Furthermore, variants in all pharmacogenes relevant to a drug treatment must be considered. This implies a shift of the current paradigm of PGx-informed prescription based on genotyping a few common variants in selected genes toward comprehensive sequencing approaches. The following sections deal with the impact of population admixture on PGx diversity focusing on Latin America, where a kaleidoscopic combination of individual proportions of Native American, European, and sub-Saharan African ancestries prevails. We illustrate this diversity by contrasting Brazil and Mexico, the two most populous countries in Latin America, and show that population average admixture proportions are not predictive of the corresponding proportions at the individual level. As a consequence of admixture, the genetic differentiation of common pharmacogenetic variants in Latin Americans is much attenuated in comparison to their most relevant ancestral populations. Finally, we review data for tacrolimus and warfarin to illustrate the opportunities and challenges presented by Latin American populations for PGx studies and clinical implementation.
药物遗传学/药物基因组学(PGx)依赖于人类遗传多样性。在本综述中,我们首先考察人类人口历史和遗传多样性对PGx的影响,并着重介绍近期关于药物基因中常见和罕见变异全球分布的研究结果。大量罕见变异意味着需要付出巨大努力来确定其假定的功能效应,并开发用于PGx指导处方的可靠算法。此外,必须考虑与药物治疗相关的所有药物基因中的变异。这意味着当前基于对选定基因中的少数常见变异进行基因分型的PGx指导处方范式将转向全面测序方法。以下各节将探讨群体混合对PGx多样性的影响,重点关注拉丁美洲,在那里,美洲原住民、欧洲人和撒哈拉以南非洲人血统的个体比例呈现出千变万化的组合。我们通过对比拉丁美洲人口最多的两个国家巴西和墨西哥来说明这种多样性,并表明群体平均混合比例并不能预测个体层面的相应比例。由于混合,与最相关的祖先群体相比,拉丁美洲人常见药物遗传变异的遗传分化程度大大降低。最后,我们回顾他克莫司和华法林的数据,以说明拉丁美洲人群在PGx研究和临床应用方面所带来的机遇和挑战。