Lack of evidence for genetic association to RUNX1 binding site at PSORS2 in different German psoriasis cohorts

J Invest Dermatol. 2005 Jan;124(1):107-10. doi: 10.1111/j.0022-202X.2004.23571.x.

Abstract

A DNA variant, rs734232, altering a RUNX1 binding site was recently reported as susceptibility allele at PSORS2 (17q25) in cohorts of psoriasis patients from the US. A testing of this variant in psoriasis patients from Germany did not confirm this association in 300 trios nor in two case-control studies with 281 patients with psoriasis vulgaris and 375 patients with psoriatic arthritis, respectively. These results fail to support rs734232 as a psoriasis susceptibility factor in German psoriasis patients.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Arthritis, Psoriatic / epidemiology
  • Arthritis, Psoriatic / genetics*
  • Binding Sites / genetics
  • Case-Control Studies
  • Chromosomes, Human, Pair 17*
  • Chromosomes, Human, Pair 6
  • Cohort Studies
  • Core Binding Factor Alpha 2 Subunit
  • DNA-Binding Proteins / genetics*
  • Gene Frequency
  • Germany / epidemiology
  • Haplotypes
  • Humans
  • Middle Aged
  • Proto-Oncogene Proteins / genetics*
  • Psoriasis / epidemiology
  • Psoriasis / genetics*
  • Risk Factors
  • Transcription Factors / genetics*

Substances

  • Core Binding Factor Alpha 2 Subunit
  • DNA-Binding Proteins
  • Proto-Oncogene Proteins
  • RUNX1 protein, human
  • Transcription Factors