A genetic coding variant rs72474224 in GJB2 is associated with clinical features of psoriasis vulgaris in a Chinese Han population

Tissue Antigens. 2015 Aug;86(2):134-8. doi: 10.1111/tan.12595. Epub 2015 Jun 24.

Abstract

Our recent targeted sequencing study identified a missense single-nucleotide polymorphism rs72474224 (c.324C>T) in GJB2. To investigate the correlation between rs72474224 (c.324C>T) and subphenotypes of psoriasis, genotype data for rs72474224 (c.324C>T, p.Val37Ile) was analyzed in 9946 cases and 9906 controls. The additive model provided the best fit for rs72474224 (P = 7.34 × 10(-9)). The genotypic and allelic frequency distributions were associated with plaque psoriasis in case-only (Pgenotype = 2.67 × 10(-3), Pallele = 6.22 × 10(-4)) and subphenotype-control (Pgenotype = 1.58 × 10(-11), Pallele = 8.16 × 10(-12)) analyses. No other significant difference was found in case-only analyses. Rs72474224 in GJB2 is preferentially associated with plaque psoriasis in Chinese population and might contribute to the complexity of psoriasis clinical features.

Keywords: GJB2; genotype-phenotype correlation; psoriasis vulgaris; single-nucleotide polymorphism; susceptibility gene.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Aged, 80 and over
  • Alleles
  • Asian People
  • Case-Control Studies
  • Child
  • Child, Preschool
  • Connexin 26
  • Connexins / genetics*
  • Connexins / immunology
  • Exons*
  • Female
  • Gene Expression
  • Gene Frequency
  • Genetic Association Studies
  • Genetic Predisposition to Disease
  • Genotype
  • Humans
  • Infant
  • Male
  • Middle Aged
  • Models, Genetic
  • Polymorphism, Single Nucleotide*
  • Psoriasis / ethnology
  • Psoriasis / genetics*
  • Psoriasis / immunology
  • Psoriasis / pathology

Substances

  • Connexins
  • GJB2 protein, human
  • Connexin 26