No association between the rs10503253 polymorphism in the CSMD1 gene and schizophrenia in a Han Chinese population

BMC Psychiatry. 2016 Jul 4:16:206. doi: 10.1186/s12888-016-0923-5.

Abstract

Background: Schizophrenia (SCZ) is a complex, heritable, and devastating psychiatric disorder. Recent genome-wide association studies have identified a single-nucleotide polymorphism (SNP; rs10503253) in the CUB and SUSHI multiple domains 1 (CSMD1) gene as a risk factor for SCZ. In this study, we investigated whether the rs10503253 in CSMD1 contributes to the risk of SCZ in a Han Chinese population.

Methods: We conducted a case-control study in a population from eastern China, involving 1378 SCZ patients and 1091 unrelated healthy controls, using the ligase detection reaction-polymerase chain reaction method to genotype the rs10503253 polymorphism in the CSMD1 gene.

Results: No significant association was found between the SCZ patients and controls for any allele or genotype frequency of the SNP rs10503253 (all P > 0.05).

Conclusions: Our findings do not support an association between CSMD1 rs10503253 and SCZ in a Han Chinese population.

Keywords: CSMD1; Schizophrenia; rs10503253.

MeSH terms

  • Adult
  • Alleles
  • Asian People / genetics*
  • Case-Control Studies
  • China
  • Female
  • Genetic Predisposition to Disease / genetics*
  • Genotype
  • Humans
  • Male
  • Membrane Proteins / genetics*
  • Middle Aged
  • Polymorphism, Single Nucleotide / genetics
  • Risk Factors
  • Schizophrenia / genetics*
  • Tumor Suppressor Proteins

Substances

  • CSMD1 protein, human
  • Membrane Proteins
  • Tumor Suppressor Proteins