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Association between GLO1 variants and gestational diabetes mellitus susceptibility in a Chinese population: a preliminary study

BACKGROUND: Glyoxalase 1 (GLO1) plays a crucial role in defending against glycation. Single nucleotide polymorphism (SNP) variants in the GLO1 gene may affect gene expression and alter enzyme activity. However, there have been limited studies evaluating the association between GLO1 and diabetes, esp...

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Autores principales: Zeng, Qiaoli, Yang, Taili, Wei, Wenfeng, Zou, Dehua, Wei, Yue, Han, Fengqiong, He, Jieyun, Huang, Jinzhi, Guo, Runmin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10656739/
https://www.ncbi.nlm.nih.gov/pubmed/38027126
http://dx.doi.org/10.3389/fendo.2023.1235581
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author Zeng, Qiaoli
Yang, Taili
Wei, Wenfeng
Zou, Dehua
Wei, Yue
Han, Fengqiong
He, Jieyun
Huang, Jinzhi
Guo, Runmin
author_facet Zeng, Qiaoli
Yang, Taili
Wei, Wenfeng
Zou, Dehua
Wei, Yue
Han, Fengqiong
He, Jieyun
Huang, Jinzhi
Guo, Runmin
author_sort Zeng, Qiaoli
collection PubMed
description BACKGROUND: Glyoxalase 1 (GLO1) plays a crucial role in defending against glycation. Single nucleotide polymorphism (SNP) variants in the GLO1 gene may affect gene expression and alter enzyme activity. However, there have been limited studies evaluating the association between GLO1 and diabetes, especially gestational diabetes mellitus (GDM). Therefore, this study is the first to explore the association of GLO1 SNPs and GDM risk. METHODS: The study included a total of 500 GDM patients and 502 control subjects. The SNPscan™ genotyping assay was used to genotype rs1781735, rs4746 and rs1130534. To assess the disparities in genotype, allele, and haplotype distributions and their correlation with GDM risk, the independent sample t-test, logistic regression, and chi-square test were employed during the data processing phase. Furthermore, one-way ANOVA was conducted to determine the differences in genotype and blood glucose and methylglyoxal(MG) levels. RESULTS: Significant differences were observed in prepregnancy body mass index (pre-BMI), age, systolic blood pressure (SBP), diastolic blood pressure (DBP), and parity between GDM and healthy subjects (P < 0.05). After adjusting for these factors, GLO1 rs1130534 TA remained associated with an increased risk of GDM (TA vs. TT + AA: OR = 1.320; 95% CI: 1.008-1.728; P = 0.044), especially in the pre-BMI ≥ 24 subgroup (TA vs. TT + AA: OR = 2.424; 95% CI: 1.048-5.607; P = 0.039), with fasting glucose levels being significantly elevated in the TA genotype compared to the TT genotype (P < 0.05). Conversely, the GLO1 rs4746 TG was associated with a decreased risk of GDM (TG vs. TT: OR = 0.740; 95% CI: 0.548-0.999; P = 0.049; TG vs. TT + GG: OR = 0.740; 95% CI: 0.548-0.998; P = 0.048). Additionally, the haplotype T-G-T of rs1781735, rs4746 and rs1130534 was associated with a decreased risk of GDM among individuals with a pre-BMI ≥ 24 (OR = 0.423; 95% CI: 0.188-0.955; P = 0.038). Furthermore, the rs1781735 GG genotype was found to be more closely related to maternal MG accumulation and neonatal weight gain (P < 0.05). CONCLUSION: Our findings suggested that GLO1 rs1130534 was associated with an increased susceptibility to GDM and higher blood glucose levels, but GLO1 rs4746 was associated with a decreased risk of GDM. The rs1781735 has been associated with the accumulation of maternal MG and subsequent weight gain in neonates.
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spelling pubmed-106567392023-01-01 Association between GLO1 variants and gestational diabetes mellitus susceptibility in a Chinese population: a preliminary study Zeng, Qiaoli Yang, Taili Wei, Wenfeng Zou, Dehua Wei, Yue Han, Fengqiong He, Jieyun Huang, Jinzhi Guo, Runmin Front Endocrinol (Lausanne) Endocrinology BACKGROUND: Glyoxalase 1 (GLO1) plays a crucial role in defending against glycation. Single nucleotide polymorphism (SNP) variants in the GLO1 gene may affect gene expression and alter enzyme activity. However, there have been limited studies evaluating the association between GLO1 and diabetes, especially gestational diabetes mellitus (GDM). Therefore, this study is the first to explore the association of GLO1 SNPs and GDM risk. METHODS: The study included a total of 500 GDM patients and 502 control subjects. The SNPscan™ genotyping assay was used to genotype rs1781735, rs4746 and rs1130534. To assess the disparities in genotype, allele, and haplotype distributions and their correlation with GDM risk, the independent sample t-test, logistic regression, and chi-square test were employed during the data processing phase. Furthermore, one-way ANOVA was conducted to determine the differences in genotype and blood glucose and methylglyoxal(MG) levels. RESULTS: Significant differences were observed in prepregnancy body mass index (pre-BMI), age, systolic blood pressure (SBP), diastolic blood pressure (DBP), and parity between GDM and healthy subjects (P < 0.05). After adjusting for these factors, GLO1 rs1130534 TA remained associated with an increased risk of GDM (TA vs. TT + AA: OR = 1.320; 95% CI: 1.008-1.728; P = 0.044), especially in the pre-BMI ≥ 24 subgroup (TA vs. TT + AA: OR = 2.424; 95% CI: 1.048-5.607; P = 0.039), with fasting glucose levels being significantly elevated in the TA genotype compared to the TT genotype (P < 0.05). Conversely, the GLO1 rs4746 TG was associated with a decreased risk of GDM (TG vs. TT: OR = 0.740; 95% CI: 0.548-0.999; P = 0.049; TG vs. TT + GG: OR = 0.740; 95% CI: 0.548-0.998; P = 0.048). Additionally, the haplotype T-G-T of rs1781735, rs4746 and rs1130534 was associated with a decreased risk of GDM among individuals with a pre-BMI ≥ 24 (OR = 0.423; 95% CI: 0.188-0.955; P = 0.038). Furthermore, the rs1781735 GG genotype was found to be more closely related to maternal MG accumulation and neonatal weight gain (P < 0.05). CONCLUSION: Our findings suggested that GLO1 rs1130534 was associated with an increased susceptibility to GDM and higher blood glucose levels, but GLO1 rs4746 was associated with a decreased risk of GDM. The rs1781735 has been associated with the accumulation of maternal MG and subsequent weight gain in neonates. Frontiers Media S.A. 2023-11-03 /pmc/articles/PMC10656739/ /pubmed/38027126 http://dx.doi.org/10.3389/fendo.2023.1235581 Text en Copyright © 2023 Zeng, Yang, Wei, Zou, Wei, Han, He, Huang and Guo https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Endocrinology
Zeng, Qiaoli
Yang, Taili
Wei, Wenfeng
Zou, Dehua
Wei, Yue
Han, Fengqiong
He, Jieyun
Huang, Jinzhi
Guo, Runmin
Association between GLO1 variants and gestational diabetes mellitus susceptibility in a Chinese population: a preliminary study
title Association between GLO1 variants and gestational diabetes mellitus susceptibility in a Chinese population: a preliminary study
title_full Association between GLO1 variants and gestational diabetes mellitus susceptibility in a Chinese population: a preliminary study
title_fullStr Association between GLO1 variants and gestational diabetes mellitus susceptibility in a Chinese population: a preliminary study
title_full_unstemmed Association between GLO1 variants and gestational diabetes mellitus susceptibility in a Chinese population: a preliminary study
title_short Association between GLO1 variants and gestational diabetes mellitus susceptibility in a Chinese population: a preliminary study
title_sort association between glo1 variants and gestational diabetes mellitus susceptibility in a chinese population: a preliminary study
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10656739/
https://www.ncbi.nlm.nih.gov/pubmed/38027126
http://dx.doi.org/10.3389/fendo.2023.1235581
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