Institution where the work was performed: Sungkyunkwan University School of Medicine, Samsung Medical Center, Seoul, Korea.
Linkage and association of schizophrenia with genetic variations in the locus of neuregulin 1 in Korean population†
Article first published online: 8 MAR 2006
Copyright © 2006 Wiley-Liss, Inc.
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
Volume 141B, Issue 3, pages 281–286, 5 April 2006
How to Cite
Kim, J. W., Lee, Y.-S., Cho, E.-Y., Jang, Y. L., Park, D. Y., Choi, K.-S., Jeun, H. O., Cho, S.-H., Jang, S.-Y. and Hong, K. S. (2006), Linkage and association of schizophrenia with genetic variations in the locus of neuregulin 1 in Korean population. Am. J. Med. Genet., 141B: 281–286. doi: 10.1002/ajmg.b.30209
- Issue published online: 27 MAR 2006
- Article first published online: 8 MAR 2006
- Manuscript Accepted: 17 MAY 2005
- Manuscript Received: 23 JAN 2005
- Basic Research Program of the Korea Science & Engineering Foundation. Grant Number: 01-2002-000-20002-0
- Korea Health 21 R&D Project, Ministry of Health & Welfare, Republic of Korea. Grant Number: 0405-NS01-0704-0001
- Samsung. Grant Number: SBRI C-A2-229-1
- chromosome 8p12;
- neuregulin 1;
Chromosome 8p21-12 has been reported to be a susceptibility locus for schizophrenia based on genome-wide linkage scans. After neuregulin 1 (NRG1) was identified as a positional candidate gene for schizophrenia in this locus, several independent association studies have reported controversial results. To determine whether genetic variations in this locus are associated with schizophrenia in the Korean population, we investigated multiplex families and unrelated patients using linkage and association analyses. Seven microsatellite markers in 8p21-12 were genotyped for 40 families with schizophrenia, and a non-parametric linkage analysis was applied. The association study was performed with 242 unrelated schizophrenia patients and the same number of normal controls for three single nucleotide polymorphisms (SNPs), two microsatellite markers and their haplotypes. A significant linkage signal was observed on D8S1769, which is located 352 kb upstream of the 5′ end of the first exon of NRG1 for two (“narrow” and “narrow with auditory hallucination (AH)”) of the three adopted phenotype classes. In the association study, the G allele of SNP8NRG241930 was significantly in excess in the subgroup of patients with AHs. We also found haplotypes which were associated with schizophrenia with a protective effect. This study provides additional suggestive evidence for both the linkage and association of genetic variations on 8p12, a locus of NRG1, with schizophrenia. NRG1 might either play a role in the predisposition to schizophrenia or be in linkage disequilibrium (LD) with a causal locus of this illness. © 2006 Wiley-Liss, Inc.