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Gene–disease association study of tumor necrosis factor‐α G‐308A gene polymorphism with risk of major depressive disorder: A systematic review and meta‐analysis

INTRODUCTION: The single nucleotide polymorphism (SNP) of the tumor necrosis factor‐α (TNF‐α) G‐308A gene is the most studied regarding susceptibility to major depressive disorder (MDD). However, results have been controversial perhaps due to the heterogeneous genetic backgrounds influenced by race...

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Autores principales: Wang, Xin, Zhang, Hongxiu, Cao, Xianling, Shi, Wei, Zhou, Xiaoyu, Chen, Qian, Ma, Ke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7303370/
https://www.ncbi.nlm.nih.gov/pubmed/32307924
http://dx.doi.org/10.1002/brb3.1628
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author Wang, Xin
Zhang, Hongxiu
Cao, Xianling
Shi, Wei
Zhou, Xiaoyu
Chen, Qian
Ma, Ke
author_facet Wang, Xin
Zhang, Hongxiu
Cao, Xianling
Shi, Wei
Zhou, Xiaoyu
Chen, Qian
Ma, Ke
author_sort Wang, Xin
collection PubMed
description INTRODUCTION: The single nucleotide polymorphism (SNP) of the tumor necrosis factor‐α (TNF‐α) G‐308A gene is the most studied regarding susceptibility to major depressive disorder (MDD). However, results have been controversial perhaps due to the heterogeneous genetic backgrounds influenced by race as well as subtypes of depression. METHODS AND MATERIALS: A systematic MEDLINE search was performed to retrieve all published studies that identified the connection between the TNF‐α G‐308A gene polymorphism and the risk of MDD. RESULTS: There was no statistical difference between the allele frequencies or genotypes of TNF‐α G‐308A gene and the depressive patients or healthy subjects in the five models tested. Further, subgroup analyses showed that the TNF‐α G‐308A gene polymorphism also did not confer susceptibility to poststroke, late‐life, maternal, or major depression. Publication bias analysis showed p values were more than .05, suggesting that the 9 articles included in the current analysis had no publication bias. CONCLUSION: Neither the allele frequencies nor genotypes of TNF‐α G‐308A gene could be served as an independent risk factor of depression.
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spelling pubmed-73033702020-06-19 Gene–disease association study of tumor necrosis factor‐α G‐308A gene polymorphism with risk of major depressive disorder: A systematic review and meta‐analysis Wang, Xin Zhang, Hongxiu Cao, Xianling Shi, Wei Zhou, Xiaoyu Chen, Qian Ma, Ke Brain Behav Review Article INTRODUCTION: The single nucleotide polymorphism (SNP) of the tumor necrosis factor‐α (TNF‐α) G‐308A gene is the most studied regarding susceptibility to major depressive disorder (MDD). However, results have been controversial perhaps due to the heterogeneous genetic backgrounds influenced by race as well as subtypes of depression. METHODS AND MATERIALS: A systematic MEDLINE search was performed to retrieve all published studies that identified the connection between the TNF‐α G‐308A gene polymorphism and the risk of MDD. RESULTS: There was no statistical difference between the allele frequencies or genotypes of TNF‐α G‐308A gene and the depressive patients or healthy subjects in the five models tested. Further, subgroup analyses showed that the TNF‐α G‐308A gene polymorphism also did not confer susceptibility to poststroke, late‐life, maternal, or major depression. Publication bias analysis showed p values were more than .05, suggesting that the 9 articles included in the current analysis had no publication bias. CONCLUSION: Neither the allele frequencies nor genotypes of TNF‐α G‐308A gene could be served as an independent risk factor of depression. John Wiley and Sons Inc. 2020-04-19 /pmc/articles/PMC7303370/ /pubmed/32307924 http://dx.doi.org/10.1002/brb3.1628 Text en © 2020 The Authors. Brain and Behavior published by Wiley Periodicals LLC. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Wang, Xin
Zhang, Hongxiu
Cao, Xianling
Shi, Wei
Zhou, Xiaoyu
Chen, Qian
Ma, Ke
Gene–disease association study of tumor necrosis factor‐α G‐308A gene polymorphism with risk of major depressive disorder: A systematic review and meta‐analysis
title Gene–disease association study of tumor necrosis factor‐α G‐308A gene polymorphism with risk of major depressive disorder: A systematic review and meta‐analysis
title_full Gene–disease association study of tumor necrosis factor‐α G‐308A gene polymorphism with risk of major depressive disorder: A systematic review and meta‐analysis
title_fullStr Gene–disease association study of tumor necrosis factor‐α G‐308A gene polymorphism with risk of major depressive disorder: A systematic review and meta‐analysis
title_full_unstemmed Gene–disease association study of tumor necrosis factor‐α G‐308A gene polymorphism with risk of major depressive disorder: A systematic review and meta‐analysis
title_short Gene–disease association study of tumor necrosis factor‐α G‐308A gene polymorphism with risk of major depressive disorder: A systematic review and meta‐analysis
title_sort gene–disease association study of tumor necrosis factor‐α g‐308a gene polymorphism with risk of major depressive disorder: a systematic review and meta‐analysis
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7303370/
https://www.ncbi.nlm.nih.gov/pubmed/32307924
http://dx.doi.org/10.1002/brb3.1628
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