Association of promoter genetic variants in interleukin-10 and Kawasaki disease with coronary artery aneurysms

J Clin Lab Anal. 2014 Nov;28(6):461-4. doi: 10.1002/jcla.21710. Epub 2014 Mar 22.

Abstract

Background: Kawasaki disease (KD) is an acute, self-limited vasculitis in infants and young children. Interleukin-10 (IL-10) is a potent cytokine that exerts pleiotropic effects on immunoregulation and inflammation. Elevated IL-10 serum levels have been reported in the KD patients.

Methods: In this study, we investigated whether IL-10 genetic polymorphisms contribute to coronary artery aneurysm (CAA) development among KD patients in Taiwan. A total of 58 KD patients with CAA and 277 unrelated healthy children matched for sex and age were enrolled for this study.

Results: Higher G allele frequencies of IL-10 at -1082 position were observed in KD patients with CAA compared to the controls (P = 0.016, OR: 2.86, 95% CI, 1.17-6.98). In addition, higher IL-10 GCC haplotype frequencies were also observed in KD patients with CAA (P = 0.016, OR: 2.85, 95% CI, 1.17-6.98).

Conclusion: Our data support the possibility that IL-10 gene polymorphisms may be related with CAA development of KD in Taiwanese population.

Keywords: Kawasaki disease; coronary artery aneurysms; genetic polymorphism; interleukin-10.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Case-Control Studies
  • Child
  • Child, Preschool
  • Coronary Aneurysm / complications
  • Coronary Aneurysm / genetics*
  • Female
  • Gene Frequency
  • Haplotypes
  • Humans
  • Infant
  • Interleukin-10 / genetics*
  • Male
  • Mucocutaneous Lymph Node Syndrome / complications*
  • Mucocutaneous Lymph Node Syndrome / genetics
  • Polymorphism, Genetic
  • Promoter Regions, Genetic / genetics*
  • Taiwan

Substances

  • Interleukin-10