非洲药物基因组学:基因多样化人群精准医学的潜在催化剂。

IF 7.7 2区 生物学 Q1 GENETICS & HEREDITY
David Twesigomwe, Tinashe A Mazhindu, Mohamed Nagy, Gaye Agesa, Janine Scholefield, Collen Masimirembwa
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引用次数: 0

摘要

遗传变异是人群中药物反应的主要决定因素。由于过去二十年来测序技术的进步,已经在编码介导药物药代动力学或药效学的蛋白质的基因中确定了几种临床可操作的变异或单倍型。因此,药物基因组学作为优化药物治疗、减轻药物不良反应、提高药物疗效的一种有前景的工具,在临床应用中获得了显著的牵引力。然而,药物遗传学检测的实施在非洲和其他资源有限的全球地区一直进展缓慢。此外,有必要解决各种药物基因组学知识库的差距,特别是关于代表性不足人群的遗传多样性。还必须确保新出现的分析方法和技术不会加剧影响非洲人口的现有保健差距。我们介绍了药物基因组学在非洲的现状,强调了其在安全有效使用药物方面影响健康结果的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pharmacogenomics in Africa: A Potential Catalyst for Precision Medicine in Genetically Diverse Populations.

Genetic variation is a major determinant of drug response across populations. Owing to advances in sequencing technologies over the last two decades, several clinically actionable variants or haplotypes have been characterized in genes that encode proteins mediating drug pharmacokinetics or pharmacodynamics. Therefore, clinical application of pharmacogenomics has gained significant traction as a promising tool for enabling drug therapy optimization to mitigate adverse drug reactions while promoting drug efficacy. However, the implementation of pharmacogenetics testing has been slow in African settings and other resource-limited global regions. Moreover, there is a need to address gaps in various pharmacogenomics knowledgebases, especially regarding the genetic diversity in underrepresented populations. It is also important to ensure that emerging assays and technologies do not heighten existing healthcare disparities affecting African populations. We present the status of pharmacogenomics in Africa, highlighting its potential to impact health outcomes in the safe and efficacious use of medicines.

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来源期刊
CiteScore
14.90
自引率
1.10%
发文量
29
期刊介绍: Since its inception in 2000, the Annual Review of Genomics and Human Genetics has been dedicated to showcasing significant developments in genomics as they pertain to human genetics and the human genome. The journal emphasizes genomic technology, genome structure and function, genetic modification, human variation and population genetics, human evolution, and various aspects of human genetic diseases, including individualized medicine.
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