Serotonin 1A receptor gene and major depressive disorder: an association study and meta-analysis

被引:56
作者
Kishi, Taro [1 ]
Tsunoka, Tomoko [1 ]
Ikeda, Masashi [1 ,3 ]
Kawashima, Kunihiro [1 ]
Okochi, Tomo [1 ]
Kitajima, Tsuyoshi [1 ]
Kinoshita, Yoko [1 ]
Okumura, Takenori [1 ]
Yamanouchi, Yoshio [1 ]
Inada, Toshiya [4 ]
Ozaki, Norio [2 ]
Iwata, Nakao [1 ]
机构
[1] Fujita Hlth Univ, Sch Med, Dept Psychiat, Aichi 4701192, Japan
[2] Nagoya Univ, Grad Sch Med, Dept Psychiat, Aichi, Japan
[3] Cardiff Univ, Sch Med, Dept Psychol Med, Cardiff, S Glam, Wales
[4] Seiwa Hosp, Neuropsychiat Res Inst, Shinjuku Ku, Tokyo, Japan
关键词
case-control study; functional SNP; major depressive disorder (MDD); meta-analysis; serotonin 1A receptor gene (HTR1A); tagging SNP; MOOD DISORDERS; ANTIDEPRESSANT RESPONSE; BIPOLAR DISORDER; 5-HT1A RECEPTOR; POLYMORPHISM; PROMOTER; SCHIZOPHRENIA; FLUOXETINE; REPRESSION; BINDING;
D O I
10.1038/jhg.2009.84
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Several genetic studies have shown an association between the 5-HT1A receptor gene (HTR1A) and major depressive disorder (MDD); however, results have been rather inconsistent. Moreover, to our knowledge, no association study on HTR1A and MDD in the Japanese population has been reported. Therefore, to evaluate the association between HTR1A and MDD, we conducted a case-control study of Japanese population samples with two single-nucleotide polymorphisms (SNPs), including rs6295 (C-1019G) in HTR1A. In addition, we conducted a meta-analysis of rs6295, which has been examined in other papers. Using one functional SNP (rs6295) and one tagging SNP (rs878567) selected with the HapMap database, we conducted a genetic association analysis of case-control samples (331 patients with MDD and 804 controls) in the Japanese population. Seven population-based association studies, including this study, met our criteria for the meta-analysis of rs6295. We found an association between rs878567 and Japanese MDD patients in the allele-wise analysis, but the significance of this association did not remain after Bonferroni's correction. We also did not detect any association between HTR1A and MDD in the allele/genotype-wise or haplotype-wise analysis. On the other hand, we detected an association between rs6295 and MDD in the meta-analysis (P(Z)=0.0327). In an explorative analysis, rs6295 was associated with Asian MDD patients after correction for multiple testing (P(Z)=0.0176), but not with Caucasian MDD patients (P(Z)=0.138). Our results suggest that HTR1A may not have a role in the pathophysiology of Japanese MDD patients. On the other hand, according to the meta-analysis, HTR1A was associated with MDD patients, especially in the Asian population. Journal of Human Genetics (2009) 54, 629-633; doi:10.1038/jhg.2009.84; published online 4 September 2009
引用
收藏
页码:629 / 633
页数:5
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