Fan Ming, Liu Bing, Jiang Tianzi, Jiang Xingpeng, Zhao Huizhi, Zhang Jing
National Laboratory of Pattern Recognition, Institute of Automation, Chinese Academy of Sciences, Beijing, PR China.
Psychiatr Genet. 2010 Feb;20(1):1-7. doi: 10.1097/YPG.0b013e3283351112.
To evaluate the controversial, putative associations between the three common polymorphisms [promoter variable number tandem repeat (uVNTR), T941G, (CA) repeat] of monoamine oxidase A (MAOA) and mood disorders (major depressive or bipolar disorders, BPD) by systematically meta-analyzing published case-control association studies.
We queried PubMed using the keywords 'MAOA', 'association' and 'depression' or 'bipolar'. Nine studies on uVNTR, seven studies on T941G, and eight studies on CA met the inclusion criteria. The meta-analysis was performed by sex and ethnicity.
Our meta-analysis showed a significant association between uVNTR and MDD for the Asian group [odds ratio (OR) = 1.23 (1.02-1.47), P=0.03] and male Asian group [OR = 1.47 (1.06-2.05), P=0.02]. For the CA polymorphism, we found a significant association with BPD in the Caucasian group [OR = 1.28 (1.01-1.62), P=0.04] and female Caucasian group [OR = 1.36 (1.031-1.81), P=0.03]. For the CA polymorphism, we identified significant associations with BPD in all Caucasians for the overall alleles and for the specific alleles in a6 [OR = 1.35 (1.11-1.64), P=0.002] and in female Caucasians for the overall alleles and for the specific alleles in a2 [OR = 0.65 (0.48-0.90), P=0.009], a5 [OR = 1.44 (1.04-1.99), P=0.03], and a6 [OR = 1.41(1.12-1.78), P=0.004].
Our meta-analysis suggests a significant association of the MAOA gene with major depressive disorder and BPD within specific groups, indicating that these three polymorphisms of the MAOA gene may be associated with mood disorders by sex and ethnicity. Moreover, our systematic meta-analysis has revealed that although MAOA may be a common candidate gene for mood disorders, different polymorphisms and alleles appear to play different roles in major depressive disorder and BPD.
通过对已发表的病例对照关联研究进行系统的荟萃分析,评估单胺氧化酶A(MAOA)的三种常见多态性[启动子可变数目串联重复序列(uVNTR)、T941G、(CA)重复序列]与情绪障碍(重度抑郁或双相情感障碍,BPD)之间存在争议的假定关联。
我们在PubMed上使用关键词“MAOA”、“关联”和“抑郁”或“双相情感障碍”进行检索。关于uVNTR的9项研究、关于T941G的7项研究和关于CA的8项研究符合纳入标准。荟萃分析按性别和种族进行。
我们的荟萃分析显示,亚洲组中uVNTR与重度抑郁症之间存在显著关联[比值比(OR)=1.23(1.02 - 1.47),P = 0.03],亚洲男性组中也是如此[OR = 1.47(1.06 - 2.05),P = 0.02]。对于CA多态性,我们发现白种人组中与双相情感障碍存在显著关联[OR = 1.28(1.01 - 1.62),P = 0.04],白种女性组中也是如此[OR = 1.36(1.031 - 1.81),P = 0.03]。对于CA多态性,我们确定在所有白种人中,总体等位基因以及a6中的特定等位基因与双相情感障碍存在显著关联[OR = 1.35(1.11 - 1.64),P = 0.002];在白种女性中,总体等位基因以及a2中的特定等位基因[OR = 0.65(0.48 - 0.90),P = 0.009]、a5中的特定等位基因[OR = 1.44(1.04 - 1.99),P = 0.03]和a6中的特定等位基因[OR = 1.41(1.12 - 1.78),P = 0.004]与双相情感障碍存在显著关联。
我们的荟萃分析表明,MAOA基因在特定组中与重度抑郁症和双相情感障碍存在显著关联,这表明MAOA基因的这三种多态性可能按性别和种族与情绪障碍相关。此外,我们的系统荟萃分析表明,尽管MAOA可能是情绪障碍的一个常见候选基因,但不同的多态性和等位基因在重度抑郁症和双相情感障碍中似乎发挥着不同的作用。