J Korean Med Sci.  2009 Jun;24(3):438-442. 10.3346/jkms.2009.24.3.438.

Association of Interleukin-10 A-592C Polymorphism in Taiwanese Children with Kawasaki Disease

Affiliations
  • 1Department of Pediatrics, China Medical University Hospital, Taichung, Taiwan.
  • 2Department of Medical Research, China Medical University Hospital, Taichung, Taiwan. d0704@mail.cmuh.org.tw
  • 3Graduate Institute of Acupuncture Science, China Medical University, Taichung, Taiwan.
  • 4Graduate Institute of Chinese Medical Science, China Medical University, Taichung, Taiwan.
  • 5Department of Biotechnology and Bioinformatics, Asia University, Taichung, Taiwan.
  • 6Department of Obstetrics and Gynecology, Mackay Memorial Hospital, Taipei, Taiwan.

Abstract

Elevated serum levels of interleukin-10 (IL-10) have been reported in patients with Kawasaki disease (KD). IL-10 reduces the inflammatory actions of macrophages and T cells and it may play a significant role in the regulation of inflammatory vascular damage associated with systemic vasculitis. The aim of this study was to examine whether -592 IL-10 promoter polymorphism is a susceptibility or severity marker of KD in Chinese patients in Taiwan. The study included 105 KD patients and 100 normal controls. Genotype and allelic frequencies for the IL-10 gene polymorphism in both groups were compared. There were no significant between-group differences in the genotype distribution of IL-10 A-592C gene polymorphism (P=0.08). However, the frequency of the -592*A allele was significantly increased in the patients with KD compared with controls (71.9% vs. 61.0%, P=0.019). The odds ratio for developing KD in individuals with IL-10-592*A allele was 1.64 (95% confidence interval, 1.06-2.52) compared to individuals with the IL-10-592*C allele. No significant difference was observed in the genotype and allelic frequencies for the IL-10 A-592C polymorphism between patients with and without coronary artery lesions. The IL-10-592*A allele may be involved in the development of KD in Taiwanese children.

Keyword

Mucocutaneous Lymph Node Syndrome; Polymorphism; Interleukin-10

MeSH Terms

Alleles
Asian Continental Ancestry Group/*genetics
Child
Child, Preschool
Female
Gene Frequency
Genotype
Humans
Infant
Interleukin-10/blood/*genetics
Male
Mucocutaneous Lymph Node Syndrome/diagnosis/*genetics
Polymorphism, Genetic
Promoter Regions, Genetic
Taiwan

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