Cited by 157Bipolar Disorder and TreatmentGenetic Associations and EpidemiologySchizophrenia research and treatment

Genome-wide association study of bipolar I disorder in the Han Chinese population

Lee, M T M, Chen, C H, Lee, C S, Chen, C C, Chong, M Y, Ouyang, W C, Chiu, N Y, Chuo, L J +29 more·2011·Molecular Psychiatry

Abstract

We report the first genome-wide association study in 1000 bipolar I patients and 1000 controls, with a replication of the top hits in another 409 cases and 1000 controls in the Han Chinese population. Four regions with most strongly associated single-nucleotide polymorphisms (SNPs) were detected, of which three were not found in previous GWA studies in the Caucasian populations. Among them, SNPs close to specificity protein 8 (SP8) and ST8 α-N-acetyl- neuraminide α-2,8-sialyltransferase (ST8SIA2) are associated with Bipolar I, with P-values of 4.87 × 10(-7) (rs2709736) and 6.05 × 10(-6) (rs8040009), respectively. We have also identified SNPs in potassium channel tetramerization domain containing 12 gene (KCTD12) (rs2073831, P=9.74 × 10(-6)) and in CACNB2 (Calcium channel, voltage-dependent, β-2 subunit) gene (rs11013860, P=5.15 × 10(-5)), One SNP nearby the rs1938526 SNP of ANK3 gene and another SNP nearby the SNP rs11720452 in chromosome 3 reported in previous GWA studies also showed suggestive association in this study (P=6.55 × 10(-5) and P=1.48 × 10(-5), respectively). This may suggest that there are common and population-specific susceptibility genes for bipolar I disorder.

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Crossref · 10.1038/mp.2010.43

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Authors
Lee, M. T. M., Chen, C. H., Lee, C. S., Chen, C. C., Chong, M. Y., Ouyang, W. C., Chiu, N. Y., Chuo, L. J., Chen, C. Y., Tan, H. K. L., Lane, H. Y., Chang, T. J., Lin, C. H., Jou, S. H., Hou, Y. M., Feng, J., Lai, T. J., Tung, C. L., Chen, T. J., Chang, C. J., Lung, F. W., Chen, C. K., Shiah, I. S., Liu, C. Y., Teng, P. R., Chen, K. H., Shen, L. J., Cheng, C. S., Chang, T. P., Li, C. F., Chou, C. H., Chen, C. Y., Wang, K. H. T., Fann, C. S. J., Wu, J. Y., Chen, Y. T., & Cheng, A. T. A.
Affiliations
  • China Medical University (TW)
  • Chang Gung University (TW)
  • Jianan Mental Hospital (TW)
  • Changhua Christian Hospital (TW)
  • Taichung Veterans General Hospital (TW)
  • Tao Yuan General Hospital (TW)
  • China Medical University Hospital (TW)
  • Kaohsiung Municipal Kai-Syuan Psychiatric Hospital (TW)
  • Chia-Yi Christian Hospital (TW)
  • Far Eastern Memorial Hospital (TW)
  • Chung Shan Medical University Hospital (TW)
  • E-Da Hospital (TW)
  • Cathay General Hospital (TW)
  • Zuoying Armed Forces General Hospital (TW)
  • Tri-Service General Hospital (TW)
  • Chang Bing Show Chwan Memorial Hospital (TW)
  • Taipei City Hospital (TW)
  • Kaohsiung Medical University Chung-Ho Memorial Hospital (TW)
  • Institute of Biomedical Sciences, Academia Sinica (TW)
Corresponding author
Cheng, A T A
Venue
Molecular Psychiatry
Published
2010-04-13
Volume
16
Issue
5
Pages
548-556
ISSN
  • 1359-4184 (ISSN-L)
  • 1476-5578
OpenAlex
W2040863019
Cited by
157
References
35
Citations by year
2026: 2 · 2025: 8 · 2024: 4 · 2023: 3 · 2022: 7 · 2021: 7 · 2020: 9 · 2019: 15 · 2018: 5 · 2017: 9 · 2016: 17 · 2015: 10 · 2014: 13 · 2013: 15 · 2012: 15
FWCI
10.47
Type
journal article
Language
en
Open access
closed
Locations
  • Molecular Psychiatry (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Psychiatry and Mental health › Bipolar Disorder and Treatment
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
  • Health Sciences › Medicine › Psychiatry and Mental health › Schizophrenia research and treatment
Keywords
bipolar I disorder, Han Chinese, single nucleotide polymorphisms, genetic susceptibility, Sp8, ST8SIA2, KCTD12, CACNB2, ANK3, replication
MeSH terms
Bipolar Disorder, DNA-Binding Proteins, Female, Genotype, Humans, Male, Phenotype, Proteins, Sialyltransferases, Transcription Factors, Reproducibility of Results, Odds Ratio, Ankyrins, Genetic Predisposition to Disease, Polymorphism, Single Nucleotide, Calcium Channels, L-Type, Asian People, Genome-Wide Association Study

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