Serotonergic and BDNF genes and risk of depression after stroke

被引:65
|
作者
Kim, Jae-Min
Stewart, Robert
Bae, Kyung-Yeol
Kim, Sung-Wan
Kang, Hee-Ju
Shin, Il-Seon
Kim, Joon-Tae
Park, Man-Seok
Kim, Myung-Kyu
Park, Sung-Woo
Kim, Young-Hoon
Kim, Jong-Keun
Cho, Ki-Hyun
Yoon, Jin-Sang
机构
[1] Chonnam Natl Univ, Dept Psychiat, Sch Med, Kwangju 501757, South Korea
[2] Chonnam Natl Univ, Dept Neurol, Sch Med, Kwangju 501757, South Korea
[3] Chonnam Natl Univ, Dept Pharmacol, Sch Med, Kwangju 501757, South Korea
[4] Kings Coll London, Inst Psychiat, Epidemiol Sect, London SE5 8AF, England
[5] Inje Univ, Dept Neuropsychiat, Sch Med, Haeundae Paik Hosp,Paik Inst Clin Res, Pusan 612030, South Korea
[6] Inje Univ, Res Grp 1, Pusan 612030, South Korea
基金
新加坡国家研究基金会;
关键词
Stroke; Depression; Brain-derived neurotrophic factor; Serotonin transporter; Serotonin receptor; Genetic association study; 2A RECEPTOR GENE; TRANSPORTER GENE; POSTSTROKE DEPRESSION; NEUROTROPHIC FACTOR; AFFECTIVE-DISORDERS; PROMOTER POLYMORPHISM; VAL66MET POLYMORPHISM; BIPOLAR DISORDER; NO ASSOCIATION; 5-HTTLPR;
D O I
10.1016/j.jad.2011.09.029
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Polymorphisms of serotonin transporter (5-HTT) and brain-derived neurotrophic factor (BDNF) have been investigated as candidate genes for post-stroke depression (PSD). Serotonin 2a receptor (5-HTR2a) genes have not been yet investigated in PSD. This study aimed to investigate whether the 5-HTT, 5-HTR2a, and BDNF genes are associated with PSD independently and/or interactively in a Korean sample with high prevalence of risk alleles. Methods: In 276 stroke cases, depression was diagnosed using DSM-IV at 2 weeks after stroke, further classified to major PSD (N=29), all (major plus minor) PSD (N=77), and control (N=199) groups. Associations between PSD and 5-HTTLPR, STin2 VNTR, 5-HTR2a 1438A/G, 5-HTR2a 102T/C, and BDNF val66met genotypes were estimated using logistic regression models, and gene-gene interactions were investigated using the generalized multifactor dimensionality reduction method. Results: 5-HIR2a 1438 A/A genotype was associated with major PSD, while 5-HTTLPR s/s and BDNF met/met genotypes were associated with all PSD. There was a significant interaction between 5-HTR2a 1438A/G and BDNF val66met polymorphisms for major PSD and a borderline significant interaction between 5-HTTLPR and BDNF val66met polymorphisms for all PSD. Conclusions: In a large cohort, we found evidence for serotonin and BDNF polymorphisms as susceptibility factors and gene-gene interactions between these systems for depression at 2 weeks post-stroke. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:833 / 840
页数:8
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