Replication Study of the Association of GAS6 and PROS1 Polymorphisms with Behçet's Disease in a Japanese Population

Ocul Immunol Inflamm. 2024 May;32(4):447-453. doi: 10.1080/09273948.2023.2173239. Epub 2023 Feb 22.

Abstract

Purpose: To investigate whether polymorphisms of GAS6 and PROS1, which each encode protein ligands for a family of tyrosine kinase receptors, are associated with Behçet's disease (BD) in a Japanese population.

Methods: We recruited 734 Japanese patients with BD and 1789 Japanese healthy controls. In all participants, we genotyped two single-nucleotide polymorphisms (SNPs) reportedly associated with BD: rs9577873 in GAS6 and rs4857037 in PROS1.

Results: We found that GAS6 rs9577873 was not significantly associated with BD. In contrast, PROS1 rs4857037, specifically the A allele, was associated with increased risk for BD. The A allele was also significantly associated with BD under additive and recessive genetic models. Expression analysis revealed that this allele was significantly associated with increased PROS1 expression.

Conclusions: Our findings suggest that increased PROS1 expression related to the A risk allele of rs4857037 affects tyrosine kinase receptor signaling, contributing to the development of BD.

Keywords: Association study; Behçet’s disease; GAS6; PROS1; polymorphisms.

MeSH terms

  • Adult
  • Alleles
  • Asian People / genetics
  • Behcet Syndrome* / genetics
  • East Asian People
  • Female
  • Gene Frequency
  • Genetic Predisposition to Disease*
  • Genotype*
  • Humans
  • Intercellular Signaling Peptides and Proteins* / genetics
  • Japan / epidemiology
  • Male
  • Middle Aged
  • Polymorphism, Single Nucleotide*
  • Protein S* / genetics
  • Protein S* / metabolism

Substances

  • growth arrest-specific protein 6
  • PROS1 protein, human
  • Protein S
  • Intercellular Signaling Peptides and Proteins