GLP1R rs3765467 Polymorphism Is Associated with the Risk of Early Onset Type 2 Diabetes

Objective. To investigate the relationship between glucagon-like peptide-1 receptor gene polymorphisms and susceptibility to early onset type 2 diabetes. Methods. Samples from 316 type 2 diabetes patients with early onset type 2 diabetes (n = 137) and late-onset type 2 diabetes (n = 179) and 145 non...

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Main Authors: Yunyun Fang, Jingjing Zhang, Linlin Ji, Chaoyu Zhu, Yuanyuan Xiao, Qingge Gao, Wenjing Song, Li Wei
Format: Article
Language:English
Published: Wiley 2023-01-01
Series:International Journal of Endocrinology
Online Access:http://dx.doi.org/10.1155/2023/8729242
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author Yunyun Fang
Jingjing Zhang
Linlin Ji
Chaoyu Zhu
Yuanyuan Xiao
Qingge Gao
Wenjing Song
Li Wei
author_facet Yunyun Fang
Jingjing Zhang
Linlin Ji
Chaoyu Zhu
Yuanyuan Xiao
Qingge Gao
Wenjing Song
Li Wei
author_sort Yunyun Fang
collection DOAJ
description Objective. To investigate the relationship between glucagon-like peptide-1 receptor gene polymorphisms and susceptibility to early onset type 2 diabetes. Methods. Samples from 316 type 2 diabetes patients with early onset type 2 diabetes (n = 137) and late-onset type 2 diabetes (n = 179) and 145 nondiabetic individuals were analyzed. Multiplex PCR combined with resequencing Hi-Reseq technology was used to detect single nucleotide polymorphisms of the glucagon-like peptide-1 receptor gene, and the allele frequency, genotype distribution, and clinical parameters were analyzed between each diabetes subgroup and the control group. Results. Sixteen single nucleotide polymorphisms were identified in the exonic region of the glucagon-like peptide-1 receptor gene according to the minor allele frequency (MAF > 0.05) in the participants. Among these, the glucagon-like peptide-1 receptor rs3765467 (G⟶A) mutation was statistically associated with early onset type 2 diabetes. Compared with that of the GG carriers, carriers of genotype AA at rs3765467 had a decreased risk of early onset type 2 diabetes after adjusting for sex and body mass index. In the dominant model, the frequencies of the rs3765467 AA + GA genotype were significantly decreased in the early onset type 2 diabetes group, and carriers of genotype AA + GA at rs3765467 had a decreased risk of early onset type 2 diabetes after adjusting for sex and body mass index. Moreover, fasting C peptide levels were significantly higher in GA + AA genotype carriers than those in GG genotype carriers. Conclusion. The glucagon-like peptide 1 receptor rs3765467 polymorphism was significantly associated with age at type 2 diabetes diagnosis and thus may be used as a marker to screen and detect individuals at risk of developing early onset type 2 diabetes.
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spelling doaj-art-2a27c3d057cb46dda34c01db8fe99edf2025-08-20T03:17:43ZengWileyInternational Journal of Endocrinology1687-83452023-01-01202310.1155/2023/8729242GLP1R rs3765467 Polymorphism Is Associated with the Risk of Early Onset Type 2 DiabetesYunyun Fang0Jingjing Zhang1Linlin Ji2Chaoyu Zhu3Yuanyuan Xiao4Qingge Gao5Wenjing Song6Li Wei7Department of Endocrinology and MetabolismNational Demonstration Center for Experimental Fisheries Science EducationDepartment of Endocrinology and MetabolismDepartment of Endocrinology and MetabolismDepartment of Endocrinology and MetabolismDepartment of Endocrinology and MetabolismDepartment of Endocrinology and MetabolismDepartment of Endocrinology and MetabolismObjective. To investigate the relationship between glucagon-like peptide-1 receptor gene polymorphisms and susceptibility to early onset type 2 diabetes. Methods. Samples from 316 type 2 diabetes patients with early onset type 2 diabetes (n = 137) and late-onset type 2 diabetes (n = 179) and 145 nondiabetic individuals were analyzed. Multiplex PCR combined with resequencing Hi-Reseq technology was used to detect single nucleotide polymorphisms of the glucagon-like peptide-1 receptor gene, and the allele frequency, genotype distribution, and clinical parameters were analyzed between each diabetes subgroup and the control group. Results. Sixteen single nucleotide polymorphisms were identified in the exonic region of the glucagon-like peptide-1 receptor gene according to the minor allele frequency (MAF > 0.05) in the participants. Among these, the glucagon-like peptide-1 receptor rs3765467 (G⟶A) mutation was statistically associated with early onset type 2 diabetes. Compared with that of the GG carriers, carriers of genotype AA at rs3765467 had a decreased risk of early onset type 2 diabetes after adjusting for sex and body mass index. In the dominant model, the frequencies of the rs3765467 AA + GA genotype were significantly decreased in the early onset type 2 diabetes group, and carriers of genotype AA + GA at rs3765467 had a decreased risk of early onset type 2 diabetes after adjusting for sex and body mass index. Moreover, fasting C peptide levels were significantly higher in GA + AA genotype carriers than those in GG genotype carriers. Conclusion. The glucagon-like peptide 1 receptor rs3765467 polymorphism was significantly associated with age at type 2 diabetes diagnosis and thus may be used as a marker to screen and detect individuals at risk of developing early onset type 2 diabetes.http://dx.doi.org/10.1155/2023/8729242
spellingShingle Yunyun Fang
Jingjing Zhang
Linlin Ji
Chaoyu Zhu
Yuanyuan Xiao
Qingge Gao
Wenjing Song
Li Wei
GLP1R rs3765467 Polymorphism Is Associated with the Risk of Early Onset Type 2 Diabetes
International Journal of Endocrinology
title GLP1R rs3765467 Polymorphism Is Associated with the Risk of Early Onset Type 2 Diabetes
title_full GLP1R rs3765467 Polymorphism Is Associated with the Risk of Early Onset Type 2 Diabetes
title_fullStr GLP1R rs3765467 Polymorphism Is Associated with the Risk of Early Onset Type 2 Diabetes
title_full_unstemmed GLP1R rs3765467 Polymorphism Is Associated with the Risk of Early Onset Type 2 Diabetes
title_short GLP1R rs3765467 Polymorphism Is Associated with the Risk of Early Onset Type 2 Diabetes
title_sort glp1r rs3765467 polymorphism is associated with the risk of early onset type 2 diabetes
url http://dx.doi.org/10.1155/2023/8729242
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