Cargando…

Association of solute carrier family 30 A8 zinc transporter gene variations with gestational diabetes mellitus risk in a Chinese population

BACKGROUND: The solute carrier family 30 A8 zinc transporter (SLC30A8) plays a crucial role in insulin secretion. This study aimed to investigate the impact of SLC30A8 gene polymorphisms on gestational diabetes mellitus (GDM). METHODS: The research objective was to select 500 patients with GDM and 5...

Descripción completa

Detalles Bibliográficos
Autores principales: Zeng, Qiaoli, Tan, Bing, Han, Fengqiong, Huang, Xiujuan, Huang, Jinzhi, Wei, Yue, 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/PMC10266221/
https://www.ncbi.nlm.nih.gov/pubmed/37324267
http://dx.doi.org/10.3389/fendo.2023.1159714
_version_ 1785058702120714240
author Zeng, Qiaoli
Tan, Bing
Han, Fengqiong
Huang, Xiujuan
Huang, Jinzhi
Wei, Yue
Guo, Runmin
author_facet Zeng, Qiaoli
Tan, Bing
Han, Fengqiong
Huang, Xiujuan
Huang, Jinzhi
Wei, Yue
Guo, Runmin
author_sort Zeng, Qiaoli
collection PubMed
description BACKGROUND: The solute carrier family 30 A8 zinc transporter (SLC30A8) plays a crucial role in insulin secretion. This study aimed to investigate the impact of SLC30A8 gene polymorphisms on gestational diabetes mellitus (GDM). METHODS: The research objective was to select 500 patients with GDM and 502 control subjects. Rs13266634 and rs2466293 were genotyped using the SNPscan™ genotyping assay. Statistical tests, such as the chi-square test, t-test, logistic regression, ANOVA, and meta-analysis, were conducted to determine the differences in genotypes, alleles, and their associations with GDM risk. RESULTS: Statistically significant differences were observed in age, pregestational BMI, SBP, DBP, and parity between individuals with GDM and healthy subjects (P < 0.05). After adjusting for these factors, rs2466293 remained significantly associated with an increased risk of GDM in overall subjects (GG+AG vs. AA: OR = 1.310; 95% CI: 1.005-1.707; P = 0.046, GG vs. AA: OR = 1.523; 95% CI: 1.010-2.298; P = 0.045 and G vs. A: OR = 1.249; 95% CI: 1.029-1.516; P = 0.024). Rs13266634 was still found to be significantly associated with a decreased risk of GDM in individuals aged ≥ 30 years (TT vs. CT+CC: OR = 0.615; 95% CI: 0.392-0.966; P = 0.035, TT vs. CC: OR = 0.503; 95% CI: 0.294-0.861; P = 0.012 and T vs. C: OR =0.723; 95% CI: 0.557-0.937; P = 0.014). Additionally, the haplotype CG was found to be associated with a higher risk of GDM (P < 0.05). Furthermore, pregnant women with the CC or CT genotype of rs13266634 exhibited significantly higher mean blood glucose levels than those with the TT genotype (P < 0.05). Our findings were further validated by the results of a meta-analysis. CONCLUSION: The SLC30A8 rs2466293 polymorphism was found to be associated with an increased risk of GDM, while rs13266634 was associated with a decreased risk of GDM in individuals aged ≥ 30 years. These findings provide a theoretical basis for GDM testing.
format Online
Article
Text
id pubmed-10266221
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-102662212023-06-15 Association of solute carrier family 30 A8 zinc transporter gene variations with gestational diabetes mellitus risk in a Chinese population Zeng, Qiaoli Tan, Bing Han, Fengqiong Huang, Xiujuan Huang, Jinzhi Wei, Yue Guo, Runmin Front Endocrinol (Lausanne) Endocrinology BACKGROUND: The solute carrier family 30 A8 zinc transporter (SLC30A8) plays a crucial role in insulin secretion. This study aimed to investigate the impact of SLC30A8 gene polymorphisms on gestational diabetes mellitus (GDM). METHODS: The research objective was to select 500 patients with GDM and 502 control subjects. Rs13266634 and rs2466293 were genotyped using the SNPscan™ genotyping assay. Statistical tests, such as the chi-square test, t-test, logistic regression, ANOVA, and meta-analysis, were conducted to determine the differences in genotypes, alleles, and their associations with GDM risk. RESULTS: Statistically significant differences were observed in age, pregestational BMI, SBP, DBP, and parity between individuals with GDM and healthy subjects (P < 0.05). After adjusting for these factors, rs2466293 remained significantly associated with an increased risk of GDM in overall subjects (GG+AG vs. AA: OR = 1.310; 95% CI: 1.005-1.707; P = 0.046, GG vs. AA: OR = 1.523; 95% CI: 1.010-2.298; P = 0.045 and G vs. A: OR = 1.249; 95% CI: 1.029-1.516; P = 0.024). Rs13266634 was still found to be significantly associated with a decreased risk of GDM in individuals aged ≥ 30 years (TT vs. CT+CC: OR = 0.615; 95% CI: 0.392-0.966; P = 0.035, TT vs. CC: OR = 0.503; 95% CI: 0.294-0.861; P = 0.012 and T vs. C: OR =0.723; 95% CI: 0.557-0.937; P = 0.014). Additionally, the haplotype CG was found to be associated with a higher risk of GDM (P < 0.05). Furthermore, pregnant women with the CC or CT genotype of rs13266634 exhibited significantly higher mean blood glucose levels than those with the TT genotype (P < 0.05). Our findings were further validated by the results of a meta-analysis. CONCLUSION: The SLC30A8 rs2466293 polymorphism was found to be associated with an increased risk of GDM, while rs13266634 was associated with a decreased risk of GDM in individuals aged ≥ 30 years. These findings provide a theoretical basis for GDM testing. Frontiers Media S.A. 2023-05-31 /pmc/articles/PMC10266221/ /pubmed/37324267 http://dx.doi.org/10.3389/fendo.2023.1159714 Text en Copyright © 2023 Zeng, Tan, Han, Huang, Huang, Wei 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
Tan, Bing
Han, Fengqiong
Huang, Xiujuan
Huang, Jinzhi
Wei, Yue
Guo, Runmin
Association of solute carrier family 30 A8 zinc transporter gene variations with gestational diabetes mellitus risk in a Chinese population
title Association of solute carrier family 30 A8 zinc transporter gene variations with gestational diabetes mellitus risk in a Chinese population
title_full Association of solute carrier family 30 A8 zinc transporter gene variations with gestational diabetes mellitus risk in a Chinese population
title_fullStr Association of solute carrier family 30 A8 zinc transporter gene variations with gestational diabetes mellitus risk in a Chinese population
title_full_unstemmed Association of solute carrier family 30 A8 zinc transporter gene variations with gestational diabetes mellitus risk in a Chinese population
title_short Association of solute carrier family 30 A8 zinc transporter gene variations with gestational diabetes mellitus risk in a Chinese population
title_sort association of solute carrier family 30 a8 zinc transporter gene variations with gestational diabetes mellitus risk in a chinese population
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10266221/
https://www.ncbi.nlm.nih.gov/pubmed/37324267
http://dx.doi.org/10.3389/fendo.2023.1159714
work_keys_str_mv AT zengqiaoli associationofsolutecarrierfamily30a8zinctransportergenevariationswithgestationaldiabetesmellitusriskinachinesepopulation
AT tanbing associationofsolutecarrierfamily30a8zinctransportergenevariationswithgestationaldiabetesmellitusriskinachinesepopulation
AT hanfengqiong associationofsolutecarrierfamily30a8zinctransportergenevariationswithgestationaldiabetesmellitusriskinachinesepopulation
AT huangxiujuan associationofsolutecarrierfamily30a8zinctransportergenevariationswithgestationaldiabetesmellitusriskinachinesepopulation
AT huangjinzhi associationofsolutecarrierfamily30a8zinctransportergenevariationswithgestationaldiabetesmellitusriskinachinesepopulation
AT weiyue associationofsolutecarrierfamily30a8zinctransportergenevariationswithgestationaldiabetesmellitusriskinachinesepopulation
AT guorunmin associationofsolutecarrierfamily30a8zinctransportergenevariationswithgestationaldiabetesmellitusriskinachinesepopulation