Role of FOXP3 gene polymorphisms (SNPs rs3761547, rs3761549, and rs2232365) in the development of Type 2 diabetes mellitus
Type 2 diabetes mellitus (T2DM) is a multifactorial disease induced by an intricated interaction of several genetic variants and multiples environmental factors. A total of 281 patients diagnosed with T2DM and 281 non-diabetic control were enrolled in this study. Three SNPs (rs3761547, rs3761549, an...
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my.utm.973832022-10-10T04:24:10Z http://eprints.utm.my/id/eprint/97383/ Role of FOXP3 gene polymorphisms (SNPs rs3761547, rs3761549, and rs2232365) in the development of Type 2 diabetes mellitus Chua, Lee Suan Dawood, Dawood Ali Salim Tan, Tian Swee Ahmed Fadhil, Alshemary TP Chemical technology Type 2 diabetes mellitus (T2DM) is a multifactorial disease induced by an intricated interaction of several genetic variants and multiples environmental factors. A total of 281 patients diagnosed with T2DM and 281 non-diabetic control were enrolled in this study. Three SNPs (rs3761547, rs3761549, and rs2232365) in the FOXP3 gene were selected to study their role in the development of T2DM and T2DM-associated hypertension in an Iraqi population. The DNA extraction and genotyping were performed using allele-specific PCR. Our results showed that 212 patients were positive for a family history of T2DM, and 69 patients were negative (P < 0.001). The distribution of the rs3761547 genotypes among the diabetic patients with a positive family history was statistically significant (P < 0.001). Moreover, 205 patients were positive for hypertension, and 76 patients were negative (P < 0.001). The distribution of the rs3761547 genotypes among the diabetic patients with hypertension was statistically significant (P < 0.001). Furthermore, there was a statistical association for the rs3761549 genotype distribution among the diabetic patients without hypertension (P = 0.038). The correlation of the rs3761547 genotypes between the patients and controls was strongly significant for AA, GG, and AG (P < 0.001, P < 0.001, and P < 0.001, respectively). In contrast, there was no statistical significance for the rs3761549 genotypes (CC, TT, and CT; P = 0.362, P = 0.584, and P = 0.140, respectively). The rs2232365 (GG) genotype revealed a significant relationship (P < 0.001), while no statistical significance was displayed for the AA genotype (P = 0.130) and the AG genotype (P = 0.081). We concluded the FOXP3 gene polymorphisms rs3761547 and rs2232365 are linked with T2DM, while rs3761549 is not. Elsevier Inc. 2021 Article PeerReviewed Chua, Lee Suan and Dawood, Dawood Ali Salim and Tan, Tian Swee and Ahmed Fadhil, Alshemary (2021) Role of FOXP3 gene polymorphisms (SNPs rs3761547, rs3761549, and rs2232365) in the development of Type 2 diabetes mellitus. Gene Reports, 24 (NA). pp. 1-5. ISSN 2452-0144 http://dx.doi.org/10.1016/j.genrep.2021.101253 DOI : 10.1016/j.genrep.2021.101253 |
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TP Chemical technology Chua, Lee Suan Dawood, Dawood Ali Salim Tan, Tian Swee Ahmed Fadhil, Alshemary Role of FOXP3 gene polymorphisms (SNPs rs3761547, rs3761549, and rs2232365) in the development of Type 2 diabetes mellitus |
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Type 2 diabetes mellitus (T2DM) is a multifactorial disease induced by an intricated interaction of several genetic variants and multiples environmental factors. A total of 281 patients diagnosed with T2DM and 281 non-diabetic control were enrolled in this study. Three SNPs (rs3761547, rs3761549, and rs2232365) in the FOXP3 gene were selected to study their role in the development of T2DM and T2DM-associated hypertension in an Iraqi population. The DNA extraction and genotyping were performed using allele-specific PCR. Our results showed that 212 patients were positive for a family history of T2DM, and 69 patients were negative (P < 0.001). The distribution of the rs3761547 genotypes among the diabetic patients with a positive family history was statistically significant (P < 0.001). Moreover, 205 patients were positive for hypertension, and 76 patients were negative (P < 0.001). The distribution of the rs3761547 genotypes among the diabetic patients with hypertension was statistically significant (P < 0.001). Furthermore, there was a statistical association for the rs3761549 genotype distribution among the diabetic patients without hypertension (P = 0.038). The correlation of the rs3761547 genotypes between the patients and controls was strongly significant for AA, GG, and AG (P < 0.001, P < 0.001, and P < 0.001, respectively). In contrast, there was no statistical significance for the rs3761549 genotypes (CC, TT, and CT; P = 0.362, P = 0.584, and P = 0.140, respectively). The rs2232365 (GG) genotype revealed a significant relationship (P < 0.001), while no statistical significance was displayed for the AA genotype (P = 0.130) and the AG genotype (P = 0.081). We concluded the FOXP3 gene polymorphisms rs3761547 and rs2232365 are linked with T2DM, while rs3761549 is not. |
format |
Article |
author |
Chua, Lee Suan Dawood, Dawood Ali Salim Tan, Tian Swee Ahmed Fadhil, Alshemary |
author_facet |
Chua, Lee Suan Dawood, Dawood Ali Salim Tan, Tian Swee Ahmed Fadhil, Alshemary |
author_sort |
Chua, Lee Suan |
title |
Role of FOXP3 gene polymorphisms (SNPs rs3761547, rs3761549, and rs2232365) in the development of Type 2 diabetes mellitus |
title_short |
Role of FOXP3 gene polymorphisms (SNPs rs3761547, rs3761549, and rs2232365) in the development of Type 2 diabetes mellitus |
title_full |
Role of FOXP3 gene polymorphisms (SNPs rs3761547, rs3761549, and rs2232365) in the development of Type 2 diabetes mellitus |
title_fullStr |
Role of FOXP3 gene polymorphisms (SNPs rs3761547, rs3761549, and rs2232365) in the development of Type 2 diabetes mellitus |
title_full_unstemmed |
Role of FOXP3 gene polymorphisms (SNPs rs3761547, rs3761549, and rs2232365) in the development of Type 2 diabetes mellitus |
title_sort |
role of foxp3 gene polymorphisms (snps rs3761547, rs3761549, and rs2232365) in the development of type 2 diabetes mellitus |
publisher |
Elsevier Inc. |
publishDate |
2021 |
url |
http://eprints.utm.my/id/eprint/97383/ http://dx.doi.org/10.1016/j.genrep.2021.101253 |
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