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Novel Interleukin-10 Gene Polymorphism Is Linked to Gestational Diabetes in Taiwanese Population

Objective: The association of interleukin-10 (IL-10) polymorphism with diabetes and its complication was recently established, while there were few researches considering the potential role of IL-10 in gestational diabetes (GDM). This study aimed to investigate the association between IL-10 gene rs1...

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Autores principales: Kang, Jessica, Liu, Chia-Hsiung, Lee, Chien-Nan, Li, Hung-Yuan, Yang, Chien-Wen, Huang, Shu-Chien, Lin, Shin-Yu, Jou, Tzuu-Shuh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6401599/
https://www.ncbi.nlm.nih.gov/pubmed/30873205
http://dx.doi.org/10.3389/fgene.2019.00089
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author Kang, Jessica
Liu, Chia-Hsiung
Lee, Chien-Nan
Li, Hung-Yuan
Yang, Chien-Wen
Huang, Shu-Chien
Lin, Shin-Yu
Jou, Tzuu-Shuh
author_facet Kang, Jessica
Liu, Chia-Hsiung
Lee, Chien-Nan
Li, Hung-Yuan
Yang, Chien-Wen
Huang, Shu-Chien
Lin, Shin-Yu
Jou, Tzuu-Shuh
author_sort Kang, Jessica
collection PubMed
description Objective: The association of interleukin-10 (IL-10) polymorphism with diabetes and its complication was recently established, while there were few researches considering the potential role of IL-10 in gestational diabetes (GDM). This study aimed to investigate the association between IL-10 gene rs1800896 (−1082 A/G), rs1800871 (−819 T/C), rs1800872 (−592 A/C), and rs3021094 (3388 A/C) single nucleotide polymorphisms (SNPs) and GDM susceptibility. Methods: This study included 72 GDM patients and 100 healthy pregnant women. Direct sequencing of the products from polymerase chain reactions of the extracted genomic DNA from study subjects were conducted for analyzing IL-10 gene polymorphism and further genotype frequencies were compared. Plasma IL-10 concentration was measured by ELISA method. Results: The results revealed no significant difference in −592 A/C, −819 T/C, and −1082 A/G genotypes. Significantly increased prevalence of A allele (P = 0.028, OR = 1.69, 95% CI = 1.081–2.64) and A/A genotype (P = 0.031, OR = 2.881, 95% CI = 1.145–7.250) at a previously un-characterized rs3021094 SNP were discovered in the GDM group. Increased IL-10 levels and insulin resistance were also related to the genotype of rs3021094. The risk of GDM was increased when IL-10 level was over 6.5 pg/ml. Conclusion: Our study demonstrated that A allele and A/A genotype of rs3021094 SNP in IL-10 gene were linked to increased risk for GDM, IL-10 plasma level and insulin resistance, which could be potential targets for early screening and detection of GDM.
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spelling pubmed-64015992019-03-14 Novel Interleukin-10 Gene Polymorphism Is Linked to Gestational Diabetes in Taiwanese Population Kang, Jessica Liu, Chia-Hsiung Lee, Chien-Nan Li, Hung-Yuan Yang, Chien-Wen Huang, Shu-Chien Lin, Shin-Yu Jou, Tzuu-Shuh Front Genet Genetics Objective: The association of interleukin-10 (IL-10) polymorphism with diabetes and its complication was recently established, while there were few researches considering the potential role of IL-10 in gestational diabetes (GDM). This study aimed to investigate the association between IL-10 gene rs1800896 (−1082 A/G), rs1800871 (−819 T/C), rs1800872 (−592 A/C), and rs3021094 (3388 A/C) single nucleotide polymorphisms (SNPs) and GDM susceptibility. Methods: This study included 72 GDM patients and 100 healthy pregnant women. Direct sequencing of the products from polymerase chain reactions of the extracted genomic DNA from study subjects were conducted for analyzing IL-10 gene polymorphism and further genotype frequencies were compared. Plasma IL-10 concentration was measured by ELISA method. Results: The results revealed no significant difference in −592 A/C, −819 T/C, and −1082 A/G genotypes. Significantly increased prevalence of A allele (P = 0.028, OR = 1.69, 95% CI = 1.081–2.64) and A/A genotype (P = 0.031, OR = 2.881, 95% CI = 1.145–7.250) at a previously un-characterized rs3021094 SNP were discovered in the GDM group. Increased IL-10 levels and insulin resistance were also related to the genotype of rs3021094. The risk of GDM was increased when IL-10 level was over 6.5 pg/ml. Conclusion: Our study demonstrated that A allele and A/A genotype of rs3021094 SNP in IL-10 gene were linked to increased risk for GDM, IL-10 plasma level and insulin resistance, which could be potential targets for early screening and detection of GDM. Frontiers Media S.A. 2019-02-18 /pmc/articles/PMC6401599/ /pubmed/30873205 http://dx.doi.org/10.3389/fgene.2019.00089 Text en Copyright © 2019 Kang, Liu, Lee, Li, Yang, Huang, Lin and Jou. http://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 Genetics
Kang, Jessica
Liu, Chia-Hsiung
Lee, Chien-Nan
Li, Hung-Yuan
Yang, Chien-Wen
Huang, Shu-Chien
Lin, Shin-Yu
Jou, Tzuu-Shuh
Novel Interleukin-10 Gene Polymorphism Is Linked to Gestational Diabetes in Taiwanese Population
title Novel Interleukin-10 Gene Polymorphism Is Linked to Gestational Diabetes in Taiwanese Population
title_full Novel Interleukin-10 Gene Polymorphism Is Linked to Gestational Diabetes in Taiwanese Population
title_fullStr Novel Interleukin-10 Gene Polymorphism Is Linked to Gestational Diabetes in Taiwanese Population
title_full_unstemmed Novel Interleukin-10 Gene Polymorphism Is Linked to Gestational Diabetes in Taiwanese Population
title_short Novel Interleukin-10 Gene Polymorphism Is Linked to Gestational Diabetes in Taiwanese Population
title_sort novel interleukin-10 gene polymorphism is linked to gestational diabetes in taiwanese population
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6401599/
https://www.ncbi.nlm.nih.gov/pubmed/30873205
http://dx.doi.org/10.3389/fgene.2019.00089
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