Programmed death-1 (PD-1) gene polymorphisms lodged in the genetic predispositions of Kawasaki Disease

Eur J Pediatr. 2010 Feb;169(2):181-5. doi: 10.1007/s00431-009-1002-4. Epub 2009 May 26.

Abstract

The purpose of this study is to investigate the association of programmed death-1 gene (PD-1) polymorphisms with genetic predispositions to Kawasaki disease (KD). A total of 73 patients with KD and 100 healthy controls were enrolled from 2007 to 2008. Two single nucleotide polymorphisms of the PD-1 gene, rs41386349 and rs2227981, were analyzed. Higher T allele frequency of rs41386349 was found in the patient group than the control group (p = 0.007, odds ratio (OR) = 1.9, 95% CI = 1.2-2.9). PD-1 rs2227981 polymorphism was not significant in patients with KD comparing with the control group (p = 0.4, OR = 1.2 (0.8-1.9)). Furthermore, no difference of PD-1 polymorphisms between patients with coronary artery dilatation (CAD) and those without CAD was found. Our data support the possibility that PD-1 gene polymorphism may be related with the genetic susceptibility of KD in Korean population.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Antigens, CD / blood
  • Antigens, CD / genetics*
  • Apoptosis Regulatory Proteins / blood
  • Apoptosis Regulatory Proteins / genetics*
  • Child
  • Child, Preschool
  • DNA / genetics*
  • Female
  • Genetic Predisposition to Disease / genetics*
  • Humans
  • Incidence
  • Lymphocyte Activation
  • Male
  • Mucocutaneous Lymph Node Syndrome / blood
  • Mucocutaneous Lymph Node Syndrome / epidemiology
  • Mucocutaneous Lymph Node Syndrome / genetics*
  • Odds Ratio
  • Polymerase Chain Reaction
  • Polymorphism, Genetic*
  • Programmed Cell Death 1 Receptor
  • Republic of Korea / epidemiology
  • Retrospective Studies
  • Young Adult

Substances

  • Antigens, CD
  • Apoptosis Regulatory Proteins
  • PDCD1 protein, human
  • Programmed Cell Death 1 Receptor
  • DNA