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Replication Study Confirms Link between TSPAN18 Mutation and Schizophrenia in Han Chinese
Author(s) -
Jianmin Yuan,
Chunhui Jin,
Hai-De Qin,
JiDong Wang,
Weiwei Sha,
Wang Ming-zhong,
Yunbiao Zhang,
Fuquan Zhang,
Jijiang Li,
Jianfeng Li,
Shui Yu,
Shuguang Qi,
Yin Yao Shugart
Publication year - 2013
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0058785
Subject(s) - single nucleotide polymorphism , allele , genome wide association study , snp , genetics , genotype , genetic association , allele frequency , han chinese , biology , case control study , schizophrenia (object oriented programming) , medicine , gene , psychiatry
Schizophrenia (SCZ) is a severe psychiatric disorder associated with many different risk factors, both genetic and environmental. A recent genome-wide association study (GWAS) of Han Chinese identified three single-nucleotide polymorphisms (SNPs rs11038167, rs11038172, and rs835784) in the tetraspanins gene TSPAN18 as possible susceptibility loci for schizophrenia. Hoping to validate these findings, we conducted a case-control study of Han Chinese with 1093 schizophrenia cases and 1022 healthy controls. Using the LDR-PCR method to genotype polymorphisms in TSPAN18 , we found no significant differences (P>0.05) between patients and controls in either the allele or genotype frequency of the SNPs rs11038167 and rs11038172. We did find, however, that the frequency of the ‘A’ allele of SNP rs835784 is significantly higher in patients than in controls. We further observed a significant association (OR  = 1.197, 95%CI  = 1.047–1.369) between risk for SCZ and this ‘A’ allele. These results confirm the significant association, in Han Chinese populations, of increased SCZ risk and the variant of the TSPAN18 gene containing the ‘A’ allele of SNP rs835784.

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