韩国队列CYP2D6基因分型:与亚洲、高加索和非洲人群的比较分析

IF 1.9 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Tak Don Kim, Jung-Sook Kwak, Jae-Gook Shin, Ho-Sook Kim, Young-Ran Yoon, Mi-Ri Gwon, Min-Gul Kim, Seol Ju Moon, SeungHwan Lee, Chan Song Park, Ji Hye Song, Jang Hee Hong, Jung Sunwoo
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引用次数: 0

摘要

背景:细胞色素P450 2D6 (CYP2D6)是一种高度多态性酶,负责代谢约20%的常用处方药。其遗传变异性有助于个体间和种族间药物反应的差异。然而,关于CYP2D6等位基因在韩国人群中的分布的大规模研究仍然有限。方法:我们对从五所大学医院招募的3874名无血缘关系的韩国人进行了CYP2D6基因分型,包括拷贝数变异分析。利用CPIC活性评分系统分配基因型和表型。结果:最常见的等位基因是功能降低*10(44.9%),其次是功能正常*1(32.8%)和2(11.0%)。基因缺失5占5.7%。在表型中,广泛代谢型占62.2%,中间代谢型占36.1%,超快速代谢型占0.9%,差代谢型占0.4%。我们还鉴定了CYP2D6 × 65,这是以前未在韩国报道过的,以及一种新的重复变异CYP2D6 × 49x2。结论:这是迄今为止韩国人群中最大规模的CYP2D6多态性研究。它为韩国药物基因组学提供了全面的参考,并突出了重要的种族间差异。研究结果支持基于人群特异性药物遗传数据的个性化医疗策略的发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
CYP2D6 genotyping in a Korean cohort: comparative analysis with Asian, Caucasian, and African populations.

Background: Cytochrome P450 2D6 (CYP2D6) is a highly polymorphic enzyme responsible for metabolizing approximately 20% of commonly prescribed drugs. Its genetic variability contributes to interindividual and interethnic differences in drug response. However, large-scale studies on CYP2D6 allele distributions in the Korean population remain limited.

Methods: We conducted CYP2D6 genotyping, including copy number variation analysis, in 3,874 unrelated Korean individuals recruited from five university hospitals. Genotypes were assigned diplotypes and phenotypes using the CPIC activity score system.

Results: The most frequent allele was the decreased-function *10 (44.9%), followed by normal-function *1 (32.8%) and 2 (11.0%). The gene deletion five accounted for 5.7%. Among phenotypes, 62.2% were extensive metabolizers, 36.1% intermediate metabolizers, 0.9% ultrarapid metabolizers, and 0.4% poor metabolizers. We also identified CYP2D6 × 65, previously unreported in Koreans, and a novel duplication variant, CYP2D6 × 49x2.

Conclusion: This is the largest study of CYP2D6 polymorphisms in a Korean population to date. It provides a comprehensive reference for Korean pharmacogenomics and highlights important interethnic differences. The findings support the development of personalized medicine strategies based on population-specific pharmacogenetic data.

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来源期刊
Pharmacogenomics
Pharmacogenomics 医学-药学
CiteScore
3.40
自引率
9.50%
发文量
88
审稿时长
4-8 weeks
期刊介绍: Pharmacogenomics (ISSN 1462-2416) is a peer-reviewed journal presenting reviews and reports by the researchers and decision-makers closely involved in this rapidly developing area. Key objectives are to provide the community with an essential resource for keeping abreast of the latest developments in all areas of this exciting field. Pharmacogenomics is the leading source of commentary and analysis, bringing you the highest quality expert analyses from corporate and academic opinion leaders in the field.
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