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去甲肾上腺素转运体 T-182C 多态性与重度抑郁症的关联:荟萃分析。

Association between norepinephrine transporter T-182C polymorphism and major depressive disorder: a meta-analysis.

机构信息

Epidemiology and Biostatistics School of Public Health, Anhui Medical University, Hefei, China.

Epidemiology and Biostatistics School of Public Health, Anhui Medical University, Hefei, China.

出版信息

Neurosci Lett. 2014 Feb 21;561:64-8. doi: 10.1016/j.neulet.2013.12.035. Epub 2013 Dec 25.

Abstract

The human norepinephrine transporter (NET) gene is one of the key candidates for genetic studies in major depressive disorder (MDD). The association between NET T-182C gene polymorphisms and MDD risk has been widely reported, but results were controversial and underpowered. The purpose of this study was to derive a more precise estimation of the relationship between NET T-182C polymorphisms and MDD risk through a meta-analysis. Relevant studies were identified from PubMed, Web of Science, Chinese Biomedical Database (CBM), Chinese National Knowledge Infrastructure (CNKI), Ovid and Wan Fang (Chinese) up to March 2013. Finally, seven studies containing 1779 cases and 1584 controls were included. The pooled odds ratio (OR) and 95% confidence interval (CI) were performed. The combined results showed that there was no significant difference between MDD group and control group in all comparison models (T vs. C: OR=1.00, 95% CI=0.83-1.22; TC+TT vs. CC: OR=0.87, 95% CI=0.55-1.36; TT vs. TC+CC: OR=0.96, 95% CI=0.76-1.20; TT vs. CC: OR=1.09, 95% CI=0.66-1.80). When stratifying for the race, there was still no significant difference in genotype distribution between MDD and controls. No publication bias was observed. Conclusively, the present meta-analysis did not suggest a confirmed association between the T-182C polymorphism of the NET gene and MDD.

摘要

人类去甲肾上腺素转运体(NET)基因是重度抑郁症(MDD)遗传研究的关键候选基因之一。NET T-182C 基因多态性与 MDD 风险之间的关联已被广泛报道,但结果存在争议且效力不足。本研究的目的是通过荟萃分析得出更精确的 NET T-182C 多态性与 MDD 风险之间关系的估计。从 PubMed、Web of Science、中国生物医学文献数据库(CBM)、中国知网(CNKI)、Ovid 和万方(中文)中检索截至 2013 年 3 月的相关研究。最终纳入了 7 项研究,共包含 1779 例病例和 1584 例对照。采用合并优势比(OR)及其 95%置信区间(CI)进行分析。合并结果显示,在所有比较模型中,MDD 组与对照组之间无显著差异(T 等位基因与 C 等位基因:OR=1.00,95%CI=0.83-1.22;TC+TT 基因型与 CC 基因型:OR=0.87,95%CI=0.55-1.36;TT 基因型与 TC+CC 基因型:OR=0.96,95%CI=0.76-1.20;TT 基因型与 CC 基因型:OR=1.09,95%CI=0.66-1.80)。按种族分层时,MDD 与对照组之间基因型分布仍无显著差异。未观察到发表偏倚。综上,本荟萃分析未证实 NET 基因 T-182C 多态性与 MDD 之间存在明确关联。

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