首页> 外文期刊>European journal of ophthalmology >Glutathione S-transferase M1, T1, and P1 gene polymorphism in exudative age-related macular degeneration: a preliminary report.
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Glutathione S-transferase M1, T1, and P1 gene polymorphism in exudative age-related macular degeneration: a preliminary report.

机译:渗出的年龄相关性黄斑变性中谷胱甘肽S-转移酶M1,T1和P1基因多态性:初步报告。

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PURPOSE: To elucidate whether the gene polymorphisms of glutathione S-transferase (GST) M1, T1, and P1 are associated with the development of exudative age-related macular degeneration. METHODS: The authors genotyped 35 white patients with exudative age-related macular degeneration and 159 healthy controls. Genomic DNA from peripheral blood was examined using polymerase chain reaction and defined for the genetic polymorphisms of GST. RESULTS: No association was observed between GSTM1, GSTT1, and GSTP1 polymorphisms and age-related macular degeneration risk (p>0.05). The frequencies of the combination of the GSTM1 (null) and GSTP1 (mutant), GSTM1 (null), and GSTT1 (null) genotype polymorphisms in patients with exudative age-related macular degeneration differed greatly from those of the control group (p=0.001 OR [95% CI]: 7.70 [2.28-25.98] and p=0.007 OR [95% CI]: 3.88 [1.51-10.02], respectively). CONCLUSIONS: The present study suggests that the GSTM1 (null) and GSTT1 (null), GSTM1 (null), and GSTP1 (mutant) combinations may be a genetic risk factor for the development of exudative age-related macular degeneration. However, the potential role of GST polymorphisms as a marker of susceptibility to age-related macular degeneration needs further studies in a larger number of patients.
机译:目的:阐明谷胱甘肽S-转移酶(GST)M1,T1和P1的基因多态性是否与渗出性年龄相关性黄斑变性的发生有关。方法:作者对35名白人患者进行了基因分型,这些患者是与年龄相关的渗出性黄斑变性和159名健康对照者。使用聚合酶链反应检查了来自外周血的基因组DNA,并确定了GST的遗传多态性。结果:GSTM1,GSTT1和GSTP1多态性与年龄相关性黄斑变性风险之间没有相关性(p> 0.05)。渗出性年龄相关性黄斑变性患者中GSTM1(null)和GSTP1(突变),GSTM1(null)和GSTT1(null)基因型多态性组合的频率与对照组有很大差异(p = 0.001 OR [95%CI]:7.70 [2.28-25.98]和p = 0.007 OR [95%CI]:3.88 [1.51-10.02]。结论:本研究表明,GSTM1(无效)和GSTT1(无效),GSTM1(无效)和GSTP1(突变)组合可能是与年龄相关的渗出性黄斑变性发展的遗传危险因素。然而,GST多态性作为年龄相关性黄斑变性易感性标志物的潜在作用需要在大量患者中进行进一步研究。

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