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Ethnic differences in the linkage disequilibrium and distribution of single-nucleotide polymorphisms in 35 candidate genes for cardiovascular diseases.

机译:心血管疾病的35个候选基因的连锁不平衡和单核苷酸多态性分布的种族差异。

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摘要

Single-nucleotide polymorphisms (SNPs) are commonly used to study genetics for common diseases and predict pharmacological response. The selection of likely informative SNPs in association studies depends on their allele frequencies and on the linkage disequilibrium (LD) between SNPs, both of which may show interethnic differences. Among three populations consisting of 207 Chinese, 858 French, and 395 Spanish, we compared the allele frequency distributions of 64 intragenic SNPs of 35 candidate genes for cardiovascular diseases. Twenty-eight of these SNPs from 12 genes were also examined for intragenic LD. About 20% of SNPs were restricted to Europeans, being monomorphic in Chinese, among them mostly nonsynonymous coding SNPs and noncoding SNPs. Only 1.6% of SNPs were specific in Chinese, commensurate with the detection of these SNPs almost exclusively in Caucasians. Similarly, these SNPs were more often rare (<0.1 minor allele frequency) in Chinese (44.3%) than in Europeans (31.1%). The variant allele frequencies and intermarker LDs in terms of D' and Delta(2) were highly correlated between French and Spanish populations (r = 0.98-0.99, p < 0.001). However, only moderate correlations of allele frequencies and D' were found between the Chinese and the European populations (r = 0.7 and 0.3, respectively) despite a high correlation of Delta(2) values (r = 0.8). These results suggest that ethnic considerations are important in the selection of SNPs for association studies of candidate genes, as this may affect the power of the study as well as the likelihood of asking relevant questions and getting medically meaningful answers.
机译:单核苷酸多态性(SNP)通常用于研究常见疾病的遗传学并预测药理反应。关联研究中可能提供信息丰富的SNP的选择取决于它们的等位基因频率以及SNP之间的连锁不平衡(LD),这两者都可能显示种族差异。在由207个中国人,858个法国人和395个西班牙人组成的三个人群中,我们比较了35个心血管疾病候选基因的64个基因内SNP的等位基因频率分布。还检查了来自12个基因的28个这些SNP的基因内LD。大约20%的SNP限于欧洲人,在中文中是单态的,其中大多数是非同义编码SNP和非编码SNP。中国只有1.6%的SNP是特异性的,这与几乎仅在白种人中发现这些SNP相称。同样,与欧洲人(31.1%)相比,中国人(44.3%)的这些单核苷酸多态性(SNP)更为罕见(<0.1次要等位基因频率)。在法国和西班牙人群之间,以D'和Delta(2)表示的变异等位基因频率和标记间LDs高度相关(r = 0.98-0.99,p <0.001)。然而,尽管Delta(2)值具有高度相关性(r = 0.8),但在中国和欧洲人群之间仅发现了中等等位基因频率与D'的相关性(分别为r = 0.7和0.3)。这些结果表明,族裔因素对于选择候选基因的关联研究的SNP至关重要,因为这可能会影响研究的能力以及提出相关问题和获得医学上有意义的答案的可能性。

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