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重度抑郁症基因研究的荟萃分析。

Meta-analyses of genetic studies on major depressive disorder.

作者信息

López-León S, Janssens A C J W, González-Zuloeta Ladd A M, Del-Favero J, Claes S J, Oostra B A, van Duijn C M

机构信息

Genetic-Epidemiology Unit, Department of Epidemiology and Biostatistics, Erasmus University Medical Center, Rotterdam, The Netherlands.

出版信息

Mol Psychiatry. 2008 Aug;13(8):772-85. doi: 10.1038/sj.mp.4002088. Epub 2007 Oct 16.

Abstract

The genetic basis of major depressive disorder (MDD) has been investigated extensively, but the identification of MDD genes has been hampered by conflicting results from underpowered studies. We review all MDD case-control genetic association studies published before June 2007 and perform meta-analyses for polymorphisms that had been investigated in at least three studies. The study selection and data extraction were performed in duplicate by two independent investigators. The 183 papers that met our criteria studied 393 polymorphisms in 102 genes. Twenty-two polymorphisms (6%) were investigated in at least three studies. Seven polymorphisms had been evaluated in previous meta-analyses, 5 of these had new data available. Hence, we performed meta-analyses for 20 polymorphisms in 18 genes. Pooled odds ratios (ORs) with 95% confidence intervals (CIs) were calculated. Statistically significant associations were found for the APOE varepsilon2 (OR, 0.51), GNB3 825T (OR, 1.38), MTHFR 677T (OR, 1.20), SLC6A4 44 bp Ins/Del S (OR, 1.11) alleles and the SLC6A3 40 bpVNTR 9/10 genotype (OR, 2.06). To date, there is statistically significant evidence for six MDD susceptibility genes (APOE, DRD4, GNB3, MTHFR, SLC6A3 and SLC6A4).

摘要

重度抑郁症(MDD)的遗传基础已得到广泛研究,但由于研究样本量不足导致结果相互矛盾,MDD相关基因的识别工作受到了阻碍。我们回顾了2007年6月之前发表的所有MDD病例对照基因关联研究,并对至少在三项研究中被调查的多态性进行了荟萃分析。研究选择和数据提取由两名独立研究人员重复进行。符合我们标准的183篇论文研究了102个基因中的393个多态性。至少在三项研究中对22个多态性(6%)进行了调查。在之前的荟萃分析中对7个多态性进行了评估,其中5个有新数据可用。因此,我们对18个基因中的20个多态性进行了荟萃分析。计算了合并优势比(OR)及95%置信区间(CI)。发现APOE ε2(OR,0.51)、GNB3 825T(OR,1.38)、MTHFR 677T(OR,1.20)、SLC6A4 44 bp插入/缺失S(OR,1.11)等位基因以及SLC6A3 40 bp可变数目串联重复序列9/10基因型(OR,2.06)存在统计学显著关联。迄今为止,有统计学显著证据表明六个基因(APOE、DRD4、GNB3、MTHFR、SLC6A3和SLC6A4)是MDD的易感基因。

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