Genetic variants on 17q21 are associated with ankylosing spondylitis susceptibility and severity in a Chinese Han population

Scand J Rheumatol. 2013;42(6):469-72. doi: 10.3109/03009742.2013.786755.

Abstract

Objectives: The aim of this study was to test whether orosomucoid like 3 (ORMDL3) and 17q21 variants are associated with susceptibility to ankylosing spondylitis (AS) in a Chinese population.

Method: A total of 753 unrelated AS patients and 1120 ethnically matched healthy controls were recruited. Seven single nucleotide polymorphisms (SNPs: rs7216389, rs12603332, rs12936231, rs9303277, rs11557467, rs1007654, and rs17608925), which were selected from chromosome 17q21 containing the genes ORMDL3, GSDMB, ZPBP2, and IKZF3, were genotyped by the Taqman SNP genotyping assay.

Results: Five of the SNPs (rs7216389, rs12603332, rs12936231, rs9303277, and rs11557467) were associated with AS (all p ≤ 0.01), especially in males (all p < 0.001). Of these, rs7216389, rs12603332, rs12936231, and rs11557467 were strongly associated with severity of the disease based on radiographic findings (p < 0.05).

Conclusions: Our study confirmed that variants in chromosome 17q21 are significantly associated with AS in a Chinese Han population.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Asian People / genetics*
  • Case-Control Studies
  • China / epidemiology
  • Chromosomes, Human, Pair 17 / genetics*
  • Female
  • Gene Frequency / genetics
  • Genetic Predisposition to Disease / epidemiology
  • Genetic Predisposition to Disease / ethnology
  • Genetic Predisposition to Disease / genetics*
  • Genotype
  • Haplotypes / genetics
  • Humans
  • Male
  • Membrane Proteins / genetics*
  • Polymorphism, Single Nucleotide / genetics*
  • Severity of Illness Index*
  • Sex Factors
  • Spondylitis, Ankylosing / epidemiology
  • Spondylitis, Ankylosing / ethnology
  • Spondylitis, Ankylosing / genetics*

Substances

  • Membrane Proteins
  • ORMDL3 protein, human