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The effect of GSTT1 GSTM1 and GSTP1 gene polymorphisms on the susceptibility of age-related cataract in Chinese Han population

机译:GSTT1GSTM1和GSTP1基因多态性对中国汉族人群年龄相关性白内障易感性的影响

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摘要

Objective: Age-related cataract (ARC) is one of the most common eye diseases in the elderly worldwide, especially in China. The genetic polymorphisms of many glutathione S-transferases coding genes are likely to be closely related to the development of ARC, especially the GSTT1, the GSTM1 and the GSTP1. This investigation is aimed to determine the possible associations of GSTT1, GSTM1 and GSTP1 polymorphisms with the susceptibility of ARC in Chinese Han Population. Methods: A case-control study including ARC cases (n = 312) and controls (n = 256) in Chinese Han Population was performed. GSTT1 and GSTM1 polymorphisms were detected by duplex polymerase chain reaction (PCR), and two SNPs (rs1695, A/G and rs1138272, C/T) in GSTP1 gene were genotyped by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method, all the results were verified by sequencing method. Results: The GSTT1 null genotype carriers had a much higher risk of ARC compared with non-null genotype (χ2 = 14.091, P<0.001), and the allele G carriers also had a increased risk over the allele A carriers in the SNP (rs1695, A/G) in GSTP1 gene (χ2 = 7.696, P = 0.006), while the GSTM1 polymorphism and the SNP (rs1138272, C/T) in GSTP1 gene seem had no association with the susceptibility of ARC in Chinese Han Population. Conclusions: These preliminary results indicated carriage of null GSTT1 and GSTP1 Val/Val genotypes may contribute to genetic susceptibility to ARC in Chinese Han Population, and these genetic polymorphisms might be used as molecular markers for detecting ARC susceptibility.
机译:目的:年龄相关性白内障(ARC)是全世界老年人中最常见的眼病之一,尤其是在中国。许多谷胱甘肽S-转移酶编码基因的遗传多态性可能与ARC的发展密切相关,尤其是GSTT1,GSTM1和GSTP1。这项调查旨在确定中国汉族人群中GSTT1,GSTM1和GSTP1多态性与ARC易感性的可能关联。方法:进行了一项病例对照研究,包括中国汉族人群的ARC病例(n = 312)和对照(n = 256)。通过双链聚合酶链反应(PCR)检测GSTT1和GSTM1多态性,并通过聚合酶链反应-限制性片段长度多态性(PCR-RFLP)对GSTP1基因中的两个SNP(rs1695,A / G和rs1138272,C / T)进行基因分型。方法,所有结果均通过测序法验证。结果:与非空基因型相比,GSTT1空基因型携带者发生ARC的风险高得多(χ 2 = 14.091,P <0.001),等位基因G携带者的发生风险也高于非空基因型。 GSTP1基因的SNP(rs1695,A / G)中的等位基因A携带者(χ 2 = 7.696,P = 0.006),而GSTP1中的GSTM1多态性和SNP(rs1138272,C / T)该基因似乎与中国汉族人群ARC的易感性无关。结论:这些初步结果表明,空的GSTT1和GSTP1 Val / Val基因型的携带可能有助于中国汉族人群对ARC的遗传易感性,这些遗传多态性可用作检测ARC易感性的分子标记。

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