Lack of association of CCR4 single nucleotide polymorphism with atopic dermatitis in Japanese patients

Acta Derm Venereol. 2004;84(3):187-90. doi: 10.1080/00015550410025859.

Abstract

CCR4, a member of the CC chemokine receptor family, is believed to play an important role in the pathogenesis of atopic dermatitis. To examine whether CCR4 single nucleotide polymorphism (SNP) is associated with susceptibility to atopic dermatitis, we investigated the allele and genotype frequencies of C1014T SNP of CCR4 in 198 Japanese patients with atopic dermatitis and controls by a PCR-restriction fragment length polymorphism method. There was no significant difference in allele or genotype frequencies between patients with atopic dermatitis and controls. Serum IgE levels and peripheral blood eosinophil counts were not significantly different among genotypes. There was also no significant difference in allele or genotype frequencies between the patient subgroup with and without asthma, with mild or moderate disease, with and without family history of atopic dermatitis, or with and without family history of atopic disorders. C1014T SNP of CCR4 does not appear to be associated with susceptibility to atopic dermatitis in Japanese patients.

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Aged, 80 and over
  • Asian People / genetics*
  • Case-Control Studies
  • Child
  • Dermatitis, Atopic / ethnology
  • Dermatitis, Atopic / genetics*
  • Eosinophils / physiology
  • Female
  • Gene Frequency
  • Genetic Predisposition to Disease
  • Genotype
  • Humans
  • Immunoglobulin E / blood
  • Japan
  • Leukocyte Count
  • Male
  • Middle Aged
  • Polymerase Chain Reaction
  • Polymorphism, Single Nucleotide*
  • Receptors, CCR4
  • Receptors, Chemokine / genetics*

Substances

  • CCR4 protein, human
  • Receptors, CCR4
  • Receptors, Chemokine
  • Immunoglobulin E