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MTNR1B genetic polymorphisms as risk factors for gestational diabetes mellitus: a case-control study in a single tertiary care center

BACKGROUND: Gestational diabetes mellitus (GDM) is a metabolic disease in pregnancy that causes carbohydrate intolerance and hyper-glycemia. Genome-wide association studies and meta-analyses have found that the single nucleotide polymorphisms (SNPs) rs1387153 and rs10830963 of the melatonin receptor...

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Autores principales: Alharbi, Khalid Khalaf, Al-Sulaiman, Abdulrahman Mohammed, Bin Shedaid, Muath Khalid, Al-Shangiti, Ali M., Marie, Mohammed, Al-Sheikh, Yazeed A., Ali Khan, Imran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: King Faisal Specialist Hospital and Research Centre 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6832319/
https://www.ncbi.nlm.nih.gov/pubmed/31580701
http://dx.doi.org/10.5144/0256-4947.2019.309
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author Alharbi, Khalid Khalaf
Al-Sulaiman, Abdulrahman Mohammed
Bin Shedaid, Muath Khalid
Al-Shangiti, Ali M.
Marie, Mohammed
Al-Sheikh, Yazeed A.
Ali Khan, Imran
author_facet Alharbi, Khalid Khalaf
Al-Sulaiman, Abdulrahman Mohammed
Bin Shedaid, Muath Khalid
Al-Shangiti, Ali M.
Marie, Mohammed
Al-Sheikh, Yazeed A.
Ali Khan, Imran
author_sort Alharbi, Khalid Khalaf
collection PubMed
description BACKGROUND: Gestational diabetes mellitus (GDM) is a metabolic disease in pregnancy that causes carbohydrate intolerance and hyper-glycemia. Genome-wide association studies and meta-analyses have found that the single nucleotide polymorphisms (SNPs) rs1387153 and rs10830963 of the melatonin receptor 1B (MTNR1B) gene are associated with GDM. No studies on the MTNR1B gene effect on GDM have been performed in Saudis, other Arabs, or other Middle Eastern populations. OBJECTIVES: Investigate the association of genotype or allele frequencies of the two SNPs with GDM and with clinical parameters related to GDM. DESIGN: Case-control study. SETTINGS: Tertiary care center, Riyadh. PATIENTS AND METHODS: We recruited 400 pregnant Saudi women ages 18-45 years (200 were diagnosed with GDM, and 200 were healthy controls). Biochemical assays were performed, and rs1387153 and rs10830963 polymorphisms were analyzed by polymerase chain reaction-restriction fragment length polymorphism analysis and real-time polymerase chain reaction with TaqMan genotyping. MAIN OUTCOME MEASURES: The association of MTNR1B gene (rs1387153 and rs10830963 polymorphisms) with GDM and with biochemical parameters related to GDM. SAMPLE SIZE: 200 GDM cases and 200 non-GDM controls. RESULTS: Differences in allele frequencies for GDM vs non-GMD were statistically significant or nearly significant for both SNPs after adjustment for age and body mass index. In a logistic regression analysis, genotype TT was positively associated with post-prandial blood glucose (P=.018), but other associations were not statistically significant. CONCLUSION: The odds ratios for the associations between the rs1387153 and rs10830963 SNPs and GDM exceeded 1.5-fold, which is higher than typically reported for diseases with complex genetic background. These effect sizes for GDM suggest pregnancy-specific factors related to the MTNR1B risk genotypes. LIMITATIONS: Only two SNPs were studied. CONFLICT OF INTEREST: None.
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spelling pubmed-68323192019-11-21 MTNR1B genetic polymorphisms as risk factors for gestational diabetes mellitus: a case-control study in a single tertiary care center Alharbi, Khalid Khalaf Al-Sulaiman, Abdulrahman Mohammed Bin Shedaid, Muath Khalid Al-Shangiti, Ali M. Marie, Mohammed Al-Sheikh, Yazeed A. Ali Khan, Imran Ann Saudi Med Original Article BACKGROUND: Gestational diabetes mellitus (GDM) is a metabolic disease in pregnancy that causes carbohydrate intolerance and hyper-glycemia. Genome-wide association studies and meta-analyses have found that the single nucleotide polymorphisms (SNPs) rs1387153 and rs10830963 of the melatonin receptor 1B (MTNR1B) gene are associated with GDM. No studies on the MTNR1B gene effect on GDM have been performed in Saudis, other Arabs, or other Middle Eastern populations. OBJECTIVES: Investigate the association of genotype or allele frequencies of the two SNPs with GDM and with clinical parameters related to GDM. DESIGN: Case-control study. SETTINGS: Tertiary care center, Riyadh. PATIENTS AND METHODS: We recruited 400 pregnant Saudi women ages 18-45 years (200 were diagnosed with GDM, and 200 were healthy controls). Biochemical assays were performed, and rs1387153 and rs10830963 polymorphisms were analyzed by polymerase chain reaction-restriction fragment length polymorphism analysis and real-time polymerase chain reaction with TaqMan genotyping. MAIN OUTCOME MEASURES: The association of MTNR1B gene (rs1387153 and rs10830963 polymorphisms) with GDM and with biochemical parameters related to GDM. SAMPLE SIZE: 200 GDM cases and 200 non-GDM controls. RESULTS: Differences in allele frequencies for GDM vs non-GMD were statistically significant or nearly significant for both SNPs after adjustment for age and body mass index. In a logistic regression analysis, genotype TT was positively associated with post-prandial blood glucose (P=.018), but other associations were not statistically significant. CONCLUSION: The odds ratios for the associations between the rs1387153 and rs10830963 SNPs and GDM exceeded 1.5-fold, which is higher than typically reported for diseases with complex genetic background. These effect sizes for GDM suggest pregnancy-specific factors related to the MTNR1B risk genotypes. LIMITATIONS: Only two SNPs were studied. CONFLICT OF INTEREST: None. King Faisal Specialist Hospital and Research Centre 2019-10 2019-10-03 /pmc/articles/PMC6832319/ /pubmed/31580701 http://dx.doi.org/10.5144/0256-4947.2019.309 Text en Copyright © 2019, Annals of Saudi Medicine, Saudi Arabia This is an open access article under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (CC BY-NC-ND). The details of which can be accessed at http://creativecommons.org/licenses/by-nc-nd/4.0/
spellingShingle Original Article
Alharbi, Khalid Khalaf
Al-Sulaiman, Abdulrahman Mohammed
Bin Shedaid, Muath Khalid
Al-Shangiti, Ali M.
Marie, Mohammed
Al-Sheikh, Yazeed A.
Ali Khan, Imran
MTNR1B genetic polymorphisms as risk factors for gestational diabetes mellitus: a case-control study in a single tertiary care center
title MTNR1B genetic polymorphisms as risk factors for gestational diabetes mellitus: a case-control study in a single tertiary care center
title_full MTNR1B genetic polymorphisms as risk factors for gestational diabetes mellitus: a case-control study in a single tertiary care center
title_fullStr MTNR1B genetic polymorphisms as risk factors for gestational diabetes mellitus: a case-control study in a single tertiary care center
title_full_unstemmed MTNR1B genetic polymorphisms as risk factors for gestational diabetes mellitus: a case-control study in a single tertiary care center
title_short MTNR1B genetic polymorphisms as risk factors for gestational diabetes mellitus: a case-control study in a single tertiary care center
title_sort mtnr1b genetic polymorphisms as risk factors for gestational diabetes mellitus: a case-control study in a single tertiary care center
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6832319/
https://www.ncbi.nlm.nih.gov/pubmed/31580701
http://dx.doi.org/10.5144/0256-4947.2019.309
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