Analysis of the type 2 diabetes-associated single nucleotide polymorphisms in the genes IRS1, KCNJ11, and PPARG2 in type 1 diabetes.

نویسندگان

  • Christina Eftychi
  • Joanna M M Howson
  • Bryan J Barratt
  • Adrian Vella
  • Felicity Payne
  • Deborah J Smyth
  • Rebecca C J Twells
  • Neil M Walker
  • Helen E Rance
  • Eva Tuomilehto-Wolf
  • Jaakko Tuomilehto
  • Dag E Undlien
  • Kjersti S Rønningen
  • Cristian Guja
  • Constantin Ionescu-Tîirgovişte
  • David A Savage
  • John A Todd
چکیده

It has been proposed that type 1 and 2 diabetes might share common pathophysiological pathways and, to some extent, genetic background. However, to date there has been no convincing data to establish a molecular genetic link between them. We have genotyped three single nucleotide polymorphisms associated with type 2 diabetes in a large type 1 diabetic family collection of European descent: Gly972Arg in the insulin receptor substrate 1 (IRS1) gene, Glu23Lys in the potassium inwardly-rectifying channel gene (KCNJ11), and Pro12Ala in the peroxisome proliferative-activated receptor gamma2 gene (PPARG2). We were unable to confirm a recently published association of the IRS1 Gly972Arg variant with type 1 diabetes. Moreover, KCNJ11 Glu23Lys showed no association with type 1 diabetes (P > 0.05). However, the PPARG2 Pro12Ala variant showed evidence of association (RR 1.15, 95% CI 1.04-1.28, P = 0.008). Additional studies need to be conducted to confirm this result.

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عنوان ژورنال:
  • Diabetes

دوره 53 3  شماره 

صفحات  -

تاریخ انتشار 2004