Feng Wen-Ping, Zhang Bo, Li Wen, Liu Juan
Department of Neurology, the affiliated Hospital of Shangluo Vocational and Technical College, Shangluo, China.
Department of Neurology, Central Hospital of Shangluo, Shangluo, China.
PLoS One. 2014 Feb 12;9(2):e88575. doi: 10.1371/journal.pone.0088575. eCollection 2014.
To assess the association of P2RX7 gene rs2230912 polymorphism with mood disorders using a meta-analysis.
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.
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).
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.
采用荟萃分析评估P2RX7基因rs2230912多态性与心境障碍的相关性。
从以下电子数据库收集数据:PubMed、医学文摘数据库、爱思唯尔科学Direct数据库、考克兰图书馆和中国生物医学文献数据库,最后一份报告截至2013年4月1日。采用比值比(OR)及95%置信区间(CI)评估相关性强度。根据各研究间异质性检验结果,选择固定效应模型(Mantel-Haenszel)或随机效应模型(DerSimonian-Laird)汇总合并后的OR。
通过检索确定了13项独立研究(6962例病例和9262例对照)。我们检测到研究间存在显著异质性。未发现该多态性与心境障碍有显著相关性(P>0.05)。我们还对单相抑郁和双相情感障碍进行了疾病特异性荟萃分析。未发现该多态性与单相抑郁或双相情感障碍有显著相关性(P>0.05)。此外,我们按不同类型病例进行了亚组分析。在临床队列或基于人群的队列中,未发现该多态性与心境障碍有显著相关性(P>0.05)。在基于家系的队列中,发现该多态性与心境障碍的等位基因对比有显著相关性(OR = 1.26,95%CI = 1.05 - 1.50,P = 0.01)。
总体而言,我们的荟萃分析表明,采用病例对照设计时,P2RX7基因rs2230912多态性可能与心境障碍的发病风险无关。鉴于不同类型病例亚组分析结果不一致,仍需要基于更大样本量的进一步研究。