Genetic studies of ankylosing spondylitis in Koreans confirm associations with ERAP1 and 2p15 reported in white patients

J Rheumatol. 2011 Feb;38(2):322-4. doi: 10.3899/jrheum.100652. Epub 2010 Nov 1.

Abstract

Objective: Investigators from the Australo-Anglo-American Spondyloarthritis Consortium have reported additional genes associated with ankylosing spondylitis (AS) susceptibility including IL1R2, ANTXR2, and gene deserts at 2p15 and 21q22. We evaluated these new candidate genes in a large cohort of Korean patients with AS.

Methods: A group of 1164 patients with AS and 752 healthy controls were enrolled for our study. Eight single-nucleotide polymorphisms (SNP) were analyzed to define genetic association with AS by MassARRAY system.

Results: Significant positive associations of AS with endoplasmic reticulum aminopeptidase 1 SNP, rs27037 (p = 1.31 × 10(-4)), and rs27434 (p = 4.59 × 10(-6)), were observed. The rs10865331 of gene desert at 2p15 also showed a significant association with AS (p = 4.63 × 10(-5)).

Conclusion: This is the first confirmation in a nonwhite population that genetic polymorphisms of rs27037, rs27434, and rs10865331 are associated with AS, implicating common pathogenetic mechanisms in Korean and white patients with AS.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Alleles
  • Aminopeptidases / genetics*
  • Asian People / genetics
  • Chromosomes, Human, Pair 2*
  • Female
  • Gene Frequency
  • Genetic Association Studies
  • Genetic Loci*
  • Genetic Predisposition to Disease
  • Genotype
  • Humans
  • Male
  • Minor Histocompatibility Antigens
  • Odds Ratio
  • Polymorphism, Single Nucleotide
  • Spondylitis, Ankylosing / genetics*
  • Surveys and Questionnaires

Substances

  • Minor Histocompatibility Antigens
  • Aminopeptidases
  • ERAP1 protein, human