Interleukin-18 Promoter Polymorphisms in Type 1 Diabetes

  1. Adam Kretowski1,
  2. Katarzyna Mironczuk1,
  3. Anna Karpinska1,
  4. Urszula Bojaryn1,
  5. Maciej Kinalski1,
  6. Zbigniew Puchalski2 and
  7. Ida Kinalska1
  1. 1Department of Endocrinology, Diabetology and Internal Medicine, Academy of Bialystok, Bialystok, Poland
  2. 2First Department of General Surgery Medical Academy of Bialystok, Bialystok, Poland

    Abstract

    Type 1 diabetes is believed to be a Th1 lymphocyte–mediated disease, and both environmental and genetic factors play a role in its pathogenesis. It was recently found that interleukin (IL)-18 acts as a proinflammatory cytokine and, in synergy with IL-12, promotes development of Th1 lymphocyte response by induction of γ-interferon production. The aim of our study was to evaluate the frequency of known polymorphisms in the IL-18 promoter in patients with type 1 diabetes in comparison with healthy control subjects, since higher levels of IL-18 were recently reported in the subclinical stage of type 1 diabetes. We studied two recently described single-nucleotide polymorphisms of the promoter of IL-18 gene at the position −137 and −607, which have been suggested to cause differences in transcription factor binding and have an impact on IL-18 gene activity. The genotype distribution differed significantly between patients with type 1 diabetes and control subjects. The difference reflected an increase in the GC genotypes and a decrease in GG genotypes at position −137 in the promoter of IL-18 gene. AA genotype at position −607 was found only in the control group. The results also demonstrated that the contribution of −137GC genotypes to genetic susceptibility to type 1 diabetes differs depending on the combination of IL-18 promotor gene haplotypes. Our study suggests the first evidence of an association between type 1 diabetes and polymorphisms in the promoter of IL-18 gene.

    Footnotes

    • Address correspondence and reprint requests to Dr hab. Adam Kretowski, Department of Endocrinology, Diabetology and Internal Medicine, Medical Academy of Bialystok, M. Sklodowska-Curie 24 a, 15-267 Bialystok, Poland. E-mail: akretows{at}amb.ac.bialystok.pl.

      Received for publication 24 June 2002 and accepted in revised form 8 August 2002.

      IFN-γ, γ-interferon; IL, interleukin.

    « Previous | Next Article »Table of Contents