Haplotype Analysis of RAGE Gene Polymorphisms and Association with Increased Risk of Diabetic Nephropathy

Publish Year: 1401
نوع سند: مقاله ژورنالی
زبان: English
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JR_JKMU-29-1_006

تاریخ نمایه سازی: 19 دی 1401

Abstract:

Background: The present study aimed at evaluating the association between the -۴۲۹T/C and -۳۷۴T/A polymorphisms of RAGE (Receptor for Advanced Glycation End Products) gene promoter and diabetic nephropathy as well as examining its possible application as candidate markers of diabetic nephropathy among the population of Qazvin, Iran.Methods: In this study, the diabetic patients were divided into the two groups of with or without nephropathy. The frequency of genotype and allele were determined using TETRA-Primer ARMS-PCR. Hardy-Weinberg equilibrium test and correlation of polymorphisms, odds ratio (OR), and FAMHAP software were used for haplotype analysis.Results: Based on our data, the CC genotype of -۴۲۹T/C polymorphism may play a protective role against the development of nephropathy (OR=۰.۵۸۶, ۹۵%; CI: ۰.۱۵۸-۲.۱۶۷) while, the AA genotype may be associated with increased risk of the disease (OR=۱.۸۸۹, ۹۵%; CI: ۰.۴۵۴-۷.۸۵۴). Allele’s analysis revealed that the C allele of -۴۲۹T/C polymorphism maybe protective against the appearance of nephropathy (OR=۰.۷۹۴, ۹۵%; CI: ۰.۴۸-۱.۳۱۴) whereas, the A allele may be related to increased risk for nephropathy (OR=۱.۴۵۲, ۹۵%; CI: ۰.۷۸۳-۲.۶۹۵). Haplotype analysis demonstrated that there was no significant correlation between the two -۴۲۹T/C and -۳۷۴T/A SNPs (χ۲=۵.۱۲۵, p value=۰.۱۳۵). However, it was found that the CA haplotype may have a protective effect against the development of nephropathy (OR=۰.۴۸, ۹۵%; CI: ۰.۱۴-۱.۶۴) while, the TA haplotype may increase the risk of the disease (OR=۲.۰۶, ۹۵%; CI:۱.۰۱-۴.۲۳).Conclusion: Overall, no correlation between the -۳۷۴T/A and -۴۲۹T/C polymorphisms and the haplotypes in RAGE gene and the occurrence of diabetic nephropathy, was established.

Keywords:

Nephropathy , Type ۲ diabetes , Haplotype , Receptor for Advanced Glycation End Products , SNP , Iran

Authors

Abbas Tavakoli

Student Research Committee, School of Medicine, Qazvin University of Medical Sciences, Qazvin, Iran

Iman Salahshourifar

Department of Biology, Science and Research Branch, Islamic Azad University, Tehran, Iran

Elham Hajialilo

Medical Microbiology Research Center, Qazvin University of Medical Sciences, Qazvin, Iran

Hashem Haghdoost-Yazdi

Cellular and Molecular Research Center, Research Institute for prevention of Non-Communicable Disease, Qazvin University of Medical Sciences, Qazvin, Iran

Dariush Ilghari

Midland Memorial Hospital ۴۰۰ Rosalind Redfern Grover Pkwy, Midland, TX ۷۹۷۰۱, USA

Hossein Piri

Cellular and Molecular Research Center, Research Institute for prevention of Non-Communicable Disease, Qazvin University of Medical Sciences, Qazvin, Iran & Department of Biochemistry and Genetics, School of Medicine, Qazvin University of

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