Laboratoire de Génétique Moléculaire et Cellulaire (LGMC), Université des Sciences et de la Technologie d'Oran Mohamed BOUDIAF (USTO-MB), BP 1505, El M'naouer, 31000 Oran, Algeria.
Department of Pharmacy, Faculty of Medicine, University of Oran 1 Ahmed Ben Bella, 31000 Oran, Algeria.
Afr Health Sci. 2024 Mar;24(1):307-312. doi: 10.4314/ahs.v24i1.36.
Pharmacogenetic markers, such as the ATP Binding Cassette (ABCB1) and cytochrome P450 (CYP) 3A5 enzymes, play a crucial role in personalized medicine by influencing drug efficacy and toxicity based on individuals' or populations' genetic variations.This study aims to investigate the genetic polymorphisms of CYP3A5 (rs776746) and ABCB1 (rs1045642) in the West Algerian population and compare the genotypes and allelic distributions with those of various ethnic groups.
The study involved 472 unrelated healthy subjects from the Western Algerian population. DNA genotyping was performed using TaqMan allelic discrimination assay. The variants in our population were compared to those in other ethnic groups available in the 1000 Genomes Project. Genotype and allele frequencies were calculated using the chi-square test and the Hardy-Weinberg equilibrium (HWE).
The minor allele frequencies were found to be 0.21 for CYP3A5 6986A and 0.34 for ABCB1 3435T. These frequencies were similar to those observed in North African populations, while notable differences were observed in comparison to certain Caucasian and African populations.
The difference in the allelic and genotypic distribution of these polymorphisms emphasize the need for dose adjustments in drugs metabolized by CYP3A5 and transported by ABCB1 to optimize treatments outcomes.
药物遗传学标记物,如 ATP 结合盒(ABCB1)和细胞色素 P450(CYP)3A5 酶,通过根据个体或人群的遗传变异影响药物疗效和毒性,在个性化医疗中发挥着关键作用。本研究旨在研究西阿尔及利亚人群中 CYP3A5(rs776746)和 ABCB1(rs1045642)的遗传多态性,并将基因型和等位基因分布与其他种族进行比较。
该研究涉及来自西阿尔及利亚人群的 472 名无关健康个体。使用 TaqMan 等位基因鉴别分析进行 DNA 基因分型。将我们人群中的变体与 1000 基因组计划中其他种族的变体进行比较。使用卡方检验和 Hardy-Weinberg 平衡(HWE)计算基因型和等位基因频率。
发现 CYP3A5 6986A 的次要等位基因频率为 0.21,ABCB1 3435T 的频率为 0.34。这些频率与北非人群观察到的频率相似,而与某些白人和非洲人群观察到的频率存在显著差异。
这些多态性的等位基因和基因型分布的差异强调了需要调整 CYP3A5 代谢和 ABCB1 转运的药物剂量,以优化治疗效果。