Baker J L, Shriner D, Bentley A R, Rotimi C N
Center for Research on Genomics and Global Health, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA.
Pharmacogenomics J. 2017 Mar;17(2):112-120. doi: 10.1038/tpj.2016.78. Epub 2016 Oct 25.
As the common birthplace of all human populations, modern humans have lived longer on the African continent than in any other geographical region of the world. This long history, along with the evolutionary need to adapt to environmental challenges such as exposure to infectious agents, has led to greater genetic variation in Africans. The vast genetic variation in Africans also extends to genes involved in the absorption, distribution, metabolism and excretion of pharmaceuticals. Ongoing cataloging of these clinically relevant variants reveals huge allele-frequency differences within and between African populations. Here, we examine Africa's large burden of infectious disease, discuss key examples of known genetic variation modulating disease risk, and provide examples of clinically relevant variants critical for establishing dosing guidelines. We propose that a more systematic characterization of the genetic diversity of African ancestry populations is required if the current benefits of precision medicine are to be extended to these populations.
作为所有人类种群的共同发源地,现代人类在非洲大陆生活的时间比在世界上任何其他地理区域都要长。这段悠久的历史,以及适应诸如接触传染病原体等环境挑战的进化需求,导致非洲人有更大的基因变异。非洲人巨大的基因变异还延伸到参与药物吸收、分布、代谢和排泄的基因。对这些临床相关变异的持续编目揭示了非洲人群内部和之间巨大的等位基因频率差异。在这里,我们研究了非洲巨大的传染病负担,讨论了调节疾病风险的已知基因变异的关键例子,并提供了对制定给药指南至关重要的临床相关变异的例子。我们建议,如果要将精准医学目前的益处扩展到这些人群,就需要对非洲裔人群的遗传多样性进行更系统的表征。