FAS Gene Copy Numbers are Associated with Susceptibility to Behçet Disease and VKH Syndrome in Han Chinese

Hum Mutat. 2015 Nov;36(11):1064-9. doi: 10.1002/humu.22829. Epub 2015 Aug 3.

Abstract

Previous studies have identified that disturbed apoptosis was involved in the pathogenesis of Behçet disease (BD) and Vogt-Koyanagi-Harada (VKH) syndrome. This study aims to investigate whether copy number variations of apoptosis-related genes, including FAS, CASPASE8, CASPASE3, and BCL2, are associated with BD and VKH syndrome in Han Chinese. A two-stage association study was performed in 1,014 BD patients, 1,051 VKH syndrome patients, and 2,076 healthy controls. TaqMan(®) Copy Number Assays and real-time PCR were performed. The first-stage study showed that increased frequency of high FAS copy number (>2) was found in BD (P = 1.05 × 10(-3) ) and VKH syndrome (P = 2.56 × 10(-3) ). Replication and combined study confirmed the association of high copy number (>2) of FAS with BD (P = 3.35 × 10(-8) ) and VKH syndrome (P = 9.77 × 10(-8) ). A significant upregulated mRNA expression of FAS was observed in anti-CD3/CD28 antibodies-stimulated CD4(+) T cells from individuals carrying a high gene copy number (>2) as compared to normal diploid 2 copy number carriers (P = 0.004). Moreover, the mRNA expression of FAS both in active patients with BD and VKH syndrome was significantly higher than that in controls (P = 0.001 and P = 0.007, respectively). Our findings suggest that a high copy number of FAS gene confers risk for BD and VKH syndrome.

Keywords: BD; Behcet disease; FAS; VKH syndrome; copy number variation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Apoptosis / genetics
  • Asian People / genetics*
  • Behcet Syndrome / diagnosis
  • Behcet Syndrome / genetics*
  • Case-Control Studies
  • Caspase 3 / genetics
  • Caspase 8 / genetics
  • Female
  • Gene Dosage*
  • Gene Expression
  • Genetic Association Studies*
  • Genetic Predisposition to Disease*
  • Humans
  • Male
  • Odds Ratio
  • Phenotype
  • Proto-Oncogene Proteins c-bcl-2 / genetics
  • Uveomeningoencephalitic Syndrome / diagnosis
  • Uveomeningoencephalitic Syndrome / genetics*
  • Young Adult
  • fas Receptor / genetics*
  • fas Receptor / metabolism

Substances

  • Proto-Oncogene Proteins c-bcl-2
  • fas Receptor
  • Caspase 3
  • Caspase 8