The Frequencies distribution of CYP3A5 rs776746 and ABCB1 rs1045642 polymorphisms in the west Algerian population and relationships with pharmacogenetics.

Amina Ammour, Meriem Aberkane, Abdallah Boudjema, Wefa Boughrara, Sounnia Mediene Benchekor
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Abstract

Introduction: 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.

Methods: 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).

Results: 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.

Conclusion: 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.

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阿尔及利亚西部人群中 CYP3A5 rs776746 和 ABCB1 rs1045642 多态性的频率分布及其与药物遗传学的关系。
简介:药物基因标记物,如 ATP 结合盒(ABCB1)和细胞色素 P450(CYP)3A5 酶,根据个体或人群的基因变异影响药物的疗效和毒性,在个性化医疗中发挥着重要作用。本研究旨在调查阿尔及利亚西部人群中 CYP3A5(rs776746)和 ABCB1(rs1045642)的基因多态性,并将其基因型和等位基因分布与不同种族人群的基因型和等位基因分布进行比较:研究涉及阿尔及利亚西部人口中的 472 名无血缘关系的健康受试者。DNA 基因分型采用 TaqMan 等位基因鉴别测定法进行。我们人群中的变异与 "1000 基因组计划 "中其他种族人群中的变异进行了比较。基因型和等位基因频率采用卡方检验(chi-square test)和哈代-温伯格平衡(HWE)进行计算:结果发现,CYP3A5 6986A 和 ABCB1 3435T 的小等位基因频率分别为 0.21 和 0.34。这些频率与在北非人群中观察到的频率相似,而与某些白种人和非洲人群相比则存在明显差异:结论:这些多态性的等位基因和基因型分布差异突出表明,需要对经 CYP3A5 代谢和 ABCB1 转运的药物进行剂量调整,以优化治疗效果。
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