Population genetic polymorphisms of pharmacogenes in Zimbabwe, a potential guide for the safe and efficacious use of medicines in people of African ancestry.

IF 1.7 3区 医学 Q4 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Bianza T Mbavha, Comfort R Kanji, Nadina Stadler, Julia Stingl, Andrea Stanglmair, Catharina Scholl, William Wekwete, Collen Masimirembwa
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引用次数: 4

Abstract

Objective: Pharmacogenomics (PGx) is a clinically significant factor in the safe and efficacious use of medicines. While PGx knowledge is abundant for other populations, there are scarce PGx data on African populations and is little knowledge on drug-gene interactions for medicines used to treat diseases common in Africa. The aim of this study was to use a custom-designed open array to genotype clinically actionable variants in a Zimbabwean population. This study also identified some of the commonly used drugs in Zimbabwe and the associated genes involved in their metabolism.

Methods: A custom-designed open array that covers 120 genetic variants was used to genotype 522 black Zimbabwean healthy volunteers using TaqMan-based single nucleotide polymorphism genotyping. Data were also accessed from Essential Drugs' List in Zimbabwe (EDLIZ), and the medicines were grouped into the associated biomarker groups based on their metabolism. We also estimated the national drug procurement levels for medicines that could benefit from PGx-guided use based on the data obtained from the national authorities in Zimbabwe.

Results: The results demonstrate the applicability of an open-array chip in simultaneously determining multiple genetic variants in an individual, thus significantly reducing cost and time to generate PGx data. There were significantly high frequencies of African-specific variants, such as the CYP2D6*17 and *29 variants and the CYP2B6*18 variant. The data obtained showed that the Zimbabwean population exhibits PGx variations in genes important for the safe and efficacious use of drugs approved by the EDLIZ and are procured at significantly large amounts annually. The study has established a cohort of genotyped healthy volunteers that can be accessed and used in the conduct of clinical pharmacogenetic studies for drugs entering a market of people of predominantly African ancestry.

Conclusion: Our study demonstrated the potential benefit of integrating PGx in Zimbabwe for the safe and efficacious use of drugs that are commonly used.

津巴布韦药物基因的群体遗传多态性,为非洲血统人群安全有效地使用药物提供潜在指导。
目的:药物基因组学(PGx)是影响药物安全有效使用的重要因素。虽然对其他人群的PGx知识丰富,但对非洲人群的PGx数据很少,而且对用于治疗非洲常见疾病的药物的药物-基因相互作用知之甚少。本研究的目的是使用定制设计的开放阵列对津巴布韦人群中临床可操作的变异进行基因分型。这项研究还确定了津巴布韦一些常用药物及其代谢相关基因。方法:采用基于taqman的单核苷酸多态性基因分型方法,对522名津巴布韦黑人健康志愿者进行基因分型。还从津巴布韦基本药物清单(EDLIZ)中获取了数据,并根据药物的代谢将这些药物分组为相关的生物标志物组。我们还根据从津巴布韦国家当局获得的数据,估计了可能受益于pgx指导使用的药品的国家药品采购水平。结果:结果证明了开放阵列芯片在同时确定个体多个遗传变异方面的适用性,从而显著降低了生成PGx数据的成本和时间。非洲特异性变异的频率显著较高,如CYP2D6*17和*29变异以及CYP2B6*18变异。获得的数据表明,津巴布韦人口在基因中显示出PGx变异,这对安全有效地使用经EDLIZ批准的药物至关重要,并且每年的采购量非常大。该研究建立了一个基因分型的健康志愿者队列,可用于进入以非洲血统为主的市场的药物的临床药物遗传学研究。结论:我们的研究证明了在津巴布韦整合PGx对于安全有效地使用常用药物的潜在益处。
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来源期刊
Pharmacogenetics and genomics
Pharmacogenetics and genomics 医学-生物工程与应用微生物
CiteScore
3.20
自引率
3.80%
发文量
47
审稿时长
3 months
期刊介绍: ​​​​Pharmacogenetics and Genomics is devoted to the rapid publication of research papers, brief review articles and short communications on genetic determinants in response to drugs and other chemicals in humans and animals. The Journal brings together papers from the entire spectrum of biomedical research and science, including biochemistry, bioinformatics, clinical pharmacology, clinical pharmacy, epidemiology, genetics, genomics, molecular biology, pharmacology, pharmaceutical sciences, and toxicology. Under a single cover, the Journal provides a forum for all aspects of the genetics and genomics of host response to exogenous chemicals: from the gene to the clinic.
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