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南印度一个基于诊所人群的愤怒基因启动子多态性与糖尿病视网膜病变

Rage gene promoter polymorphisms and diabetic retinopathy in a clinic-based population from South India.

作者信息

Ramprasad S, Radha V, Mathias R A, Majumder P P, Rao M R S, Rema M

机构信息

Madras Diabetes Research Foundation & Dr Mohan's Diabetes Specialities Centre Gopalapuram, Chennai, India.

出版信息

Eye (Lond). 2007 Mar;21(3):395-401. doi: 10.1038/sj.eye.6702239. Epub 2006 Jan 27.

Abstract

PURPOSE

The main objective of this study was to evaluate if the -429T/C, -374T/A and 63 bp deletion polymorphisms in the RAGE gene are associated with diabetic retinopathy (DR) among Type 2 diabetic subjects in a clinic-based population from South India.

METHODS

We screened 149 normal glucose tolerant subjects (NGT), 189 Type 2 diabetes subjects without retinopathy (DM) and 190 subjects with DR for these polymorphisms using the PCR-RFLP method. DR was diagnosed by grading color fundus photography. Logistic regression models were used to evaluate the association of individual polymorphisms with DR. Expectation-maximization algorithms were implemented in haplotype tests of association to examine the combined effects of -429T/C and -374T/A polymorphisms on DR.

RESULTS

The allelic frequencies of -429T are 0.83 in NGT, 0.84 in DM and 0.85 in DR subjects, and that of -374T are 0.93 in NGT, 0.92 in DM and 0.88 in DR subjects. The -374 polymorphism was found to be associated with non-proliferative retinopathy when this subgroup was compared to the DM group (OR=1.814, 95% CI=1.005-3.273). However, this association was not obvious when both the subphenotypes of DR (the nonproliferative and proliferative DR groups) were studied jointly. We found no evidence for associations between the -429T/C polymorphism and the DR phenotype. Finally, extension to a 2-SNP haplotype did not reveal any significant statistical difference between the groups (P=0.668).

CONCLUSION

In this study, we found a modest association with the -374T/A polymorphism in the nonproliferative DR subgroup.

摘要

目的

本研究的主要目的是评估在来自印度南部的临床人群中,晚期糖基化终产物受体(RAGE)基因中的-429T/C、-374T/A和63bp缺失多态性是否与2型糖尿病患者的糖尿病视网膜病变(DR)相关。

方法

我们采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法,对149名糖耐量正常受试者(NGT)、189名无视网膜病变的2型糖尿病受试者(DM)和190名患有DR的受试者进行了这些多态性的筛查。通过对彩色眼底照片进行分级来诊断DR。使用逻辑回归模型评估个体多态性与DR的关联。在单倍型关联测试中采用期望最大化算法,以检验-429T/C和-374T/A多态性对DR的联合作用。

结果

-429T的等位基因频率在NGT组中为0.83,在DM组中为0.84,在DR组中为0.85;-374T的等位基因频率在NGT组中为0.93,在DM组中为0.92,在DR组中为0.88。当将非增殖性视网膜病变亚组与DM组进行比较时,发现-374多态性与非增殖性视网膜病变相关(比值比[OR]=1.814,95%可信区间[CI]=1.005-3.273)。然而,当对DR的两种亚表型(非增殖性DR组和增殖性DR组)进行联合研究时,这种关联并不明显。我们没有发现-429T/C多态性与DR表型之间存在关联的证据。最后,扩展到双单核苷酸多态性单倍型分析未发现各组之间存在任何显著的统计学差异(P=0.668)。

结论

在本研究中,我们发现非增殖性DR亚组与-374T/A多态性存在一定关联。

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