Serotonin Transporter Gene 5-HTTLPR Polymorphism as a Protective Factor Against the Progression of Post-Stroke Depression

被引:29
作者
Zhao, Qiang [1 ,2 ,3 ]
Guo, Yi [4 ]
Yang, Dong [5 ]
Yang, Tiansong [6 ]
Meng, Xianghui [1 ,2 ]
机构
[1] Chinese Peoples Liberat Army Gen Hosp, Dept Neurosurg, Beijing 100853, Peoples R China
[2] PLA Med Sch, Beijing 100853, Peoples R China
[3] Baoding 1 Hosp, Dept Neurosurg, Baoding 071000, Peoples R China
[4] Hebei Univ, Dept Neurosurg, Affiliated Hosp, Baoding 071000, Peoples R China
[5] China Japan Friendship Hosp, Dept Neurosurg, Beijing 100029, Peoples R China
[6] Hebei Med Univ, Grad Sch, Shijiazhuang 050017, Peoples R China
关键词
Post-stroke depression; 5-HTT; BDNF; Polymorphisms; BDNF VAL66MET POLYMORPHISM; METAANALYSIS; ASSOCIATION;
D O I
10.1007/s12035-015-9120-7
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Polymorphisms in the 5-HTT and BDNF genes are shown to affect their function at the molecular and serum level. Prior work has tried to correlate the polymorphisms with post-stroke depression (PSD), the results nevertheless remain indefinitive. A plausible reason accounting for the uncertainty relates to the small sample of each published trial. In this study, we have performed a comprehensive meta-analysis in order to evaluate the effects of 5-HTT and BDNF polymorphisms (5-HTTLPR, STin2 VNTR, 5-HTR2a 102 T/C, Val66Met) on genetic risk of PSD. Human case-control trials were identified by computer-assisted and manual searches. The article search was performed until October 2014. Odds ratios (ORs) and 95 % confidence intervals (CIs) were calculated using the fixed effects meta-analysis to measure the effects 5-HTT and BDNF polymorphisms exerted on PSD. We also performed test of heterogeneity, test of publication bias, and sensitivity analysis to examine the reliability and stability of combined effects. 5-HTTLPR was clearly associated with genetic risk of PSD. The association seemed to be more pronounced in the homozygous model (OR = 0.34, 95 % CI = 0.23-0.51, P (Q-test) = 0.63). Both the heterozygous model and the recessive model showed 50 % decreased risk of PSD (OR = 0.50, 95 % CI = 0.37-0.67, P (Q-test) = 0.91; OR = 0.50, 95 % CI = 0.36-0.70, P (Q-test) = 0.43, respectively). Such significant association was also detected for Caucasian and Asian. These results were reliable and stable based on related analyses. Taken together, 5-HTTLPR polymorphism of the 5-HTT gene seems to protect against the occurrence of PSD. Small sample size for the polymorphisms within 5-HTT and BDNF genes may have caused underestimated associations, and a larger study is required to further assess the relations.
引用
收藏
页码:1699 / 1705
页数:7
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