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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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 |
work_keys_str_mv |
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