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

被引:6
作者
Cha, PC [1 ]
Yamada, R
Sekine, A
Nakamura, Y
Koh, CL
机构
[1] Univ Malaya, Fac Sci, Inst Biol Sci Genet & Mol Biol, Kuala Lumpur 50603, Malaysia
[2] RIKEN, SNP Res Ctr, Lab Rheumat Dis, Yokohama, Kanagawa, Japan
[3] RIKEN, SRC, Lab Genotyping, Yokohama, Kanagawa, Japan
[4] RIKEN, SRC, Res Grp Personalized Med, Yokohama, Kanagawa, Japan
[5] Univ Tokyo, Inst Med Sci, Ctr Human Genome, Mol Med Lab, Tokyo, Japan
关键词
allelic frequency differences; single nucleotide polymorphisms; linkage disequilibrium distributions; drug-related genes; population ancestry;
D O I
10.1007/s10038-004-0190-z
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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.
引用
收藏
页码:558 / 572
页数:15
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