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Serotonin 1A receptor gene,schizophrenia and bipolar disorder: An association study and meta-analysis
Authors:Taro Kishi  Tomo Okochi  Tomoko Tsunoka  Takenori Okumura  Tsuyoshi Kitajima  Kunihiro Kawashima  Yoshio Yamanouchi  Yoko Kinoshita  Hiroshi Naitoh  Toshiya Inada  Hiroshi Kunugi  Tadafumi Kato  Takeo Yoshikawa  Hiroshi Ujike  Norio Ozaki  Nakao Iwata
Affiliation:1. Research Institute for Advanced Industrial Technology, Korea University, Sejong, Republic of Korea;2. Neuroscience Research Institute, Gachon University, Incheon, Republic of Korea;3. Department of Psychiatry, Gachon University Gil Medical Center, Gachon University School of Medicine, Incheon, Republic of Korea;4. Department of Biomedical Engineering, College of Health Science, Gachon University, Incheon, Republic of Korea;5. Department of Radiological Science, College of Health Science, Gachon University, Incheon, Republic of Korea;6. Department of Electrical and Computer Engineering, Seoul National University, Seoul, Republic of Korea;7. Center for Magnetic Resonance Research, University of Minnesota Medical School, Minneapolis, USA
Abstract:Several investigations have reported associations between serotonin 1A (5-HT1A) receptor and major psychiatric disorders, such as schizophrenia and bipolar disorder (BP), making the 5-HT1A receptor gene (HTR1A) a good candidate gene for the pathophysiology of schizophrenia and BP. To evaluate the association between HTR1A and schizophrenia and BP, 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 studies. Using one functional single- nucleotide polymorphism (SNP; rs6295) and one tagging SNP (rs878567), we conducted a genetic association analysis of case-control samples (857 schizophrenic patients, 1028 BP patients and 1810 controls) in the Japanese population. Two association studies for schizophrenia and three association studies for BP, including this study, met our criteria for the meta-analysis of rs6295. We found an association between HTR1A and Japanese BP in a haplotype-wise analysis, the significance of which remained after Bonferroni correction. In addition, we detected an association between rs6295 and BP in the meta-analysis (fixed model: P(Z) = 0.000400). However, we did not detect an association between HTR1A and schizophrenia in the allele/genotype-wise, haplotype-wise or meta-analysis. HTR1A may play an important role in the pathophysiology of BP, but not schizophrenia in the Japanese population. In the meta-analysis, rs6295 in HTR1A was associated with BP patients.
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