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Genetic Studies of Metabolic Syndrome in Arab Populations: A Systematic Review and Meta-Analysis

Background: The metabolic syndrome (MetS) is prevalent in Arabian populations. Several small-scale studies have been performed to investigate the genetic basis of MetS. This systematic review and meta-analysis aimed to examine whether candidate gene polymorphisms are associated with MetS susceptibil...

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Autores principales: Al-Homedi, Zahrah, Afify, Nariman, Memon, Mashal, Alsafar, Habiba, Tay, Guan, Jelinek, Herbert F., Mousa, Mira, Abu-Samra, Nadia, Osman, Wael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8637276/
https://www.ncbi.nlm.nih.gov/pubmed/34868209
http://dx.doi.org/10.3389/fgene.2021.733746
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author Al-Homedi, Zahrah
Afify, Nariman
Memon, Mashal
Alsafar, Habiba
Tay, Guan
Jelinek, Herbert F.
Mousa, Mira
Abu-Samra, Nadia
Osman, Wael
author_facet Al-Homedi, Zahrah
Afify, Nariman
Memon, Mashal
Alsafar, Habiba
Tay, Guan
Jelinek, Herbert F.
Mousa, Mira
Abu-Samra, Nadia
Osman, Wael
author_sort Al-Homedi, Zahrah
collection PubMed
description Background: The metabolic syndrome (MetS) is prevalent in Arabian populations. Several small-scale studies have been performed to investigate the genetic basis of MetS. This systematic review and meta-analysis aimed to examine whether candidate gene polymorphisms are associated with MetS susceptibility among ethnic groups of the Arabian world and to suggest possible directions for future research regarding genetic markers and MetS. Methods: A search was conducted for peer-reviewed articles that examined the genetic association of MetS in Arabian populations in the following databases: Medline, Embase, Scopus, Direct Science, Web of Science, ProQuest, and Google Scholar until March 31, 2021. Articles were eligible if they were case-control studies, which investigated MetS as a dichotomous outcome (MetS vs no MetS). To assess the quality of the studies, the Q-Genie tool (Quality of Genetic Association Studies) was used. A non-central chi2 (random-effect) distribution was used to determine the heterogeneity (H) of Q and I (Galassi et al., The American journal of medicine, 2006, 119, 812–819) statistics. Results: Our search strategy identified 36 studies that met our inclusion criteria. In most cases, studies were excluded due to a lack of statistical information such as odds ratios, confidence intervals, and p-values. According to the Q-Genie tool, 12 studies scored poorly (a score of≤35), 13 studies scored moderately ( >35 and≤45), and 12 studies had good quality ( >45 or higher). The most frequently studied genes were FTO and VDR (both included in four studies). Three SNPs indicated increased risk for MetS after calculating the pooled odds ratios: FTO-rs9939609 (odds ratio 1.49, 95% CI: 0.96–2.32); LEP-rs7799039 (odds ratio 1.85, 95% CI: 1.37–2.5); and SERPINA12-rs2236242 (odds ratio 1.65, 95% CI: 1.21–2.24). Meta-analysis studies showed no significant heterogeneity. Conclusion: There were many sources of heterogeneity in the study settings. Most of the studies had low to moderate quality because of sample size and power issues, not considering all potential sources of bias, and not providing details about genotyping methods and results. As most studies were small-scale, aimed to replicate findings from other populations, we did not find any unique genetic association between MetS and Arabian populations.
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spelling pubmed-86372762021-12-03 Genetic Studies of Metabolic Syndrome in Arab Populations: A Systematic Review and Meta-Analysis Al-Homedi, Zahrah Afify, Nariman Memon, Mashal Alsafar, Habiba Tay, Guan Jelinek, Herbert F. Mousa, Mira Abu-Samra, Nadia Osman, Wael Front Genet Genetics Background: The metabolic syndrome (MetS) is prevalent in Arabian populations. Several small-scale studies have been performed to investigate the genetic basis of MetS. This systematic review and meta-analysis aimed to examine whether candidate gene polymorphisms are associated with MetS susceptibility among ethnic groups of the Arabian world and to suggest possible directions for future research regarding genetic markers and MetS. Methods: A search was conducted for peer-reviewed articles that examined the genetic association of MetS in Arabian populations in the following databases: Medline, Embase, Scopus, Direct Science, Web of Science, ProQuest, and Google Scholar until March 31, 2021. Articles were eligible if they were case-control studies, which investigated MetS as a dichotomous outcome (MetS vs no MetS). To assess the quality of the studies, the Q-Genie tool (Quality of Genetic Association Studies) was used. A non-central chi2 (random-effect) distribution was used to determine the heterogeneity (H) of Q and I (Galassi et al., The American journal of medicine, 2006, 119, 812–819) statistics. Results: Our search strategy identified 36 studies that met our inclusion criteria. In most cases, studies were excluded due to a lack of statistical information such as odds ratios, confidence intervals, and p-values. According to the Q-Genie tool, 12 studies scored poorly (a score of≤35), 13 studies scored moderately ( >35 and≤45), and 12 studies had good quality ( >45 or higher). The most frequently studied genes were FTO and VDR (both included in four studies). Three SNPs indicated increased risk for MetS after calculating the pooled odds ratios: FTO-rs9939609 (odds ratio 1.49, 95% CI: 0.96–2.32); LEP-rs7799039 (odds ratio 1.85, 95% CI: 1.37–2.5); and SERPINA12-rs2236242 (odds ratio 1.65, 95% CI: 1.21–2.24). Meta-analysis studies showed no significant heterogeneity. Conclusion: There were many sources of heterogeneity in the study settings. Most of the studies had low to moderate quality because of sample size and power issues, not considering all potential sources of bias, and not providing details about genotyping methods and results. As most studies were small-scale, aimed to replicate findings from other populations, we did not find any unique genetic association between MetS and Arabian populations. Frontiers Media S.A. 2021-11-18 /pmc/articles/PMC8637276/ /pubmed/34868209 http://dx.doi.org/10.3389/fgene.2021.733746 Text en Copyright © 2021 Al-Homedi, Afify, Memon, Alsafar, Tay, Jelinek, Mousa, Abu-Samra and Osman. 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 Genetics
Al-Homedi, Zahrah
Afify, Nariman
Memon, Mashal
Alsafar, Habiba
Tay, Guan
Jelinek, Herbert F.
Mousa, Mira
Abu-Samra, Nadia
Osman, Wael
Genetic Studies of Metabolic Syndrome in Arab Populations: A Systematic Review and Meta-Analysis
title Genetic Studies of Metabolic Syndrome in Arab Populations: A Systematic Review and Meta-Analysis
title_full Genetic Studies of Metabolic Syndrome in Arab Populations: A Systematic Review and Meta-Analysis
title_fullStr Genetic Studies of Metabolic Syndrome in Arab Populations: A Systematic Review and Meta-Analysis
title_full_unstemmed Genetic Studies of Metabolic Syndrome in Arab Populations: A Systematic Review and Meta-Analysis
title_short Genetic Studies of Metabolic Syndrome in Arab Populations: A Systematic Review and Meta-Analysis
title_sort genetic studies of metabolic syndrome in arab populations: a systematic review and meta-analysis
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8637276/
https://www.ncbi.nlm.nih.gov/pubmed/34868209
http://dx.doi.org/10.3389/fgene.2021.733746
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