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四个亚洲人群中109个药物相关基因的240个候选单核苷酸多态性(SNP)的连锁不平衡与等位基因频率分布之间关系的推断。

Inference from the relationships between linkage disequilibrium and allele frequency distributions of 240 candidate SNPs in 109 drug-related genes in four Asian populations.

作者信息

Cha Pei-Chieng, Yamada Ryo, Sekine Akihiro, Nakamura Yusuke, Koh Chong-Lek

机构信息

Institute of Biological Sciences (Genetics and Molecular Biology), Faculty of Science, University of Malaya, 50603, Lembah Pantai, Kuala Lumpur, Malaysia.

Laboratory for Rheumatic Diseases, SNP Research Center (SRC), Institute of Physical and Chemical Research (RIKEN), Yokohama, Japan.

出版信息

J Hum Genet. 2004;49(10):558-572. doi: 10.1007/s10038-004-0190-z. Epub 2004 Sep 11.

Abstract

The extensive nucleotide diversity in drug-related genes predisposes individuals to different drug responses and is a major problem in current clinical practice and drug development. Striking allelic frequency differences exist in these genes between populations. In this study, we genotyped 240 sites known to be polymorphic in the Japanese population in each of 270 unrelated healthy individuals comprising 90 each of Malaysian Malays, Indians, and Chinese. These sites are distributed in 109 genes that are drug related, such as genes encoding drug-metabolizing enzymes and drug transporters. Allele frequency and linkage disequilibrium distributions of these sites were determined and compared. They were also compared with similar data of 752 Japanese. Extensive similarities in allele frequency and linkage disequilibrium distributions were observed among Japanese, Malaysian Chinese, and Malays. However, significant differences were observed between Japanese and Malaysian Chinese with Malaysian Indians. These four populations were grouped into two genetic clusters of different ancestries. However, a higher correlation was found between Malaysian Malays and Indians, indicating the existence of extensive admixture between them. The results also imply the possible and rational use of existing single nucleotide polymorphism databases as references to assist future pharmacogenetic studies involving populations of similar ancestry.

摘要

药物相关基因中广泛的核苷酸多样性使个体易产生不同的药物反应,这是当前临床实践和药物研发中的一个主要问题。这些基因在不同人群之间存在显著的等位基因频率差异。在本研究中,我们对270名无亲缘关系的健康个体(其中马来西亚马来人、印度人和中国人各90名)中的每一个个体,对已知在日本人群中具有多态性的240个位点进行了基因分型。这些位点分布在109个与药物相关的基因中,如编码药物代谢酶和药物转运蛋白的基因。确定并比较了这些位点的等位基因频率和连锁不平衡分布。还将它们与752名日本人的类似数据进行了比较。在日本人、马来西亚华人及马来人之间观察到等位基因频率和连锁不平衡分布存在广泛的相似性。然而,在日本人和马来西亚华人与马来西亚印度人之间观察到显著差异。这四个人群被分为两个不同祖先的遗传簇。然而,发现马来西亚马来人和印度人之间的相关性更高,表明他们之间存在广泛的混合。研究结果还意味着,现有单核苷酸多态性数据库有可能被合理用作参考,以协助未来涉及相似祖先人群的药物遗传学研究。

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