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泰米尔人中因子V G1691A和因子II/凝血酶原G20210A基因多态性的患病率。

Prevalence of the Factor V G1691A and the Factor II/prothrombin G20210A gene polymorphisms among Tamilians.

作者信息

Angeline T, Bentley Heather A, Hawk Arnold B, Manners Richard J, Mokashi Harsha A, Jeyaraj Nirmala, Tsongalis Gregory J

机构信息

PG and Research Department of Zoology, Lady Doak College, Madurai, Tamil Nadu, India.

出版信息

Exp Mol Pathol. 2005 Aug;79(1):9-13. doi: 10.1016/j.yexmp.2005.03.003.

Abstract

We have investigated the prevalence of the Factor II G20210A and Factor V G1691A single nucleotide polymorphisms (SNPs) in a South Indian-Tamil Nadu population. The SNP genotyping was performed using a polymerase chain reaction (PCR)/restriction fragment length polymorphism analysis and by a recently FDA-approved LightCycler real-time PCR assay. Of 72 samples that were genotyped, 4 (5.5%) patients were heterozygous for the Factor V SNP and no homozygous mutant patients were identified. None of the patients were shown to be either heterozygous or homozygous mutant for the Factor II SNP. All samples showed 100% concordance between the PCR/RFLP assay and the LightCycler assay. While this study identified the prevalence of the Factor V SNP to be similar to that of other reported populations, the absence of the Factor II allele is consistent with reports in more isolated populations. In addition, the results of this study do not support a role for these SNPs in acute myocardial infarction in the Tamilian population.

摘要

我们调查了印度南部泰米尔纳德邦人群中凝血因子II G20210A和凝血因子V G1691A单核苷酸多态性(SNP)的流行情况。采用聚合酶链反应(PCR)/限制性片段长度多态性分析以及最近获得美国食品药品监督管理局(FDA)批准的LightCycler实时PCR检测法进行SNP基因分型。在72个进行基因分型的样本中,4例(5.5%)患者为凝血因子V SNP杂合子,未发现纯合突变患者。所有患者均未显示为凝血因子II SNP的杂合子或纯合突变。所有样本在PCR/RFLP检测和LightCycler检测之间显示出100%的一致性。虽然本研究确定凝血因子V SNP的流行情况与其他报道人群相似,但凝血因子II等位基因的缺失与更孤立人群中的报道一致。此外,本研究结果不支持这些SNP在泰米尔人群急性心肌梗死中起作用。

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