Lack of association of P2RX7 gene rs2230912 polymorphism with mood disorders: a meta-analysis.

BACKGROUND: To assess the association of P2RX7 gene rs2230912 polymorphism with mood disorders using a meta-analysis. METHODS: Data were collected from the following electronic databases: PubMed, Excerpta Medica Database, Elsevier Science Direct, Cochrane Library, and Chinese Biomedical Literature D...

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Main Authors: Wen-Ping Feng, Bo Zhang, Wen Li, Juan Liu
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3922924?pdf=render
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spelling doaj-fe8b10dba7a74deea685394f86bfa4d52020-11-25T01:34:36ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-0192e8857510.1371/journal.pone.0088575Lack of association of P2RX7 gene rs2230912 polymorphism with mood disorders: a meta-analysis.Wen-Ping FengBo ZhangWen LiJuan LiuBACKGROUND: To assess the association of P2RX7 gene rs2230912 polymorphism with mood disorders using a meta-analysis. METHODS: Data were collected from the following electronic databases: PubMed, Excerpta Medica Database, Elsevier Science Direct, Cochrane Library, and Chinese Biomedical Literature Database, with the last report up to April 1, 2013. Odds ratio (OR) with 95% confidence interval (CI) was used to assess the strength of the association. Dependent on the results of heterogeneity test among individual studies, the fixed effect model (Mantel-Haenszel) or random effect model (DerSimonian-Laird) was selected to summarize the pooled OR. RESULTS: We identified 13 separate studies using search (6,962 cases and 9,262 controls). We detected significant between-study heterogeneity. No significant association of this polymorphism with mood disorders was found (P>0.05). We also performed disease-specific meta-analysis in unipolar depression and bipolar disorder. No significant association of this polymorphism with unipolar depression or bipolar disorder was found (P>0.05). Additionally, we performed subgroup analysis by different types of cases. No significant association of this polymorphism with mood disorders in clinical cohorts or population-based cohorts (P>0.05). A significant association of this polymorphism with mood disorders was found for the allele contrast in family-based cohorts (OR = 1.26, 95%CI = 1.05-1.50, P = 0.01). CONCLUSIONS: Overall, our meta-analysis suggests that P2RX7 gene rs2230912 polymorphism may not contribute to the risk of developing mood disorders using a case-control design. Given the discordance in the subgroup analysis by different types of cases, further studies based on larger sample size are still needed.http://europepmc.org/articles/PMC3922924?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Wen-Ping Feng
Bo Zhang
Wen Li
Juan Liu
spellingShingle Wen-Ping Feng
Bo Zhang
Wen Li
Juan Liu
Lack of association of P2RX7 gene rs2230912 polymorphism with mood disorders: a meta-analysis.
PLoS ONE
author_facet Wen-Ping Feng
Bo Zhang
Wen Li
Juan Liu
author_sort Wen-Ping Feng
title Lack of association of P2RX7 gene rs2230912 polymorphism with mood disorders: a meta-analysis.
title_short Lack of association of P2RX7 gene rs2230912 polymorphism with mood disorders: a meta-analysis.
title_full Lack of association of P2RX7 gene rs2230912 polymorphism with mood disorders: a meta-analysis.
title_fullStr Lack of association of P2RX7 gene rs2230912 polymorphism with mood disorders: a meta-analysis.
title_full_unstemmed Lack of association of P2RX7 gene rs2230912 polymorphism with mood disorders: a meta-analysis.
title_sort lack of association of p2rx7 gene rs2230912 polymorphism with mood disorders: a meta-analysis.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2014-01-01
description BACKGROUND: To assess the association of P2RX7 gene rs2230912 polymorphism with mood disorders using a meta-analysis. METHODS: Data were collected from the following electronic databases: PubMed, Excerpta Medica Database, Elsevier Science Direct, Cochrane Library, and Chinese Biomedical Literature Database, with the last report up to April 1, 2013. Odds ratio (OR) with 95% confidence interval (CI) was used to assess the strength of the association. Dependent on the results of heterogeneity test among individual studies, the fixed effect model (Mantel-Haenszel) or random effect model (DerSimonian-Laird) was selected to summarize the pooled OR. RESULTS: We identified 13 separate studies using search (6,962 cases and 9,262 controls). We detected significant between-study heterogeneity. No significant association of this polymorphism with mood disorders was found (P>0.05). We also performed disease-specific meta-analysis in unipolar depression and bipolar disorder. No significant association of this polymorphism with unipolar depression or bipolar disorder was found (P>0.05). Additionally, we performed subgroup analysis by different types of cases. No significant association of this polymorphism with mood disorders in clinical cohorts or population-based cohorts (P>0.05). A significant association of this polymorphism with mood disorders was found for the allele contrast in family-based cohorts (OR = 1.26, 95%CI = 1.05-1.50, P = 0.01). CONCLUSIONS: Overall, our meta-analysis suggests that P2RX7 gene rs2230912 polymorphism may not contribute to the risk of developing mood disorders using a case-control design. Given the discordance in the subgroup analysis by different types of cases, further studies based on larger sample size are still needed.
url http://europepmc.org/articles/PMC3922924?pdf=render
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