IL-6 promoter polymorphism -174 is associated with new-onset diabetes after transplantation

J Am Soc Nephrol. 2006 Aug;17(8):2333-40. doi: 10.1681/ASN.2006010066. Epub 2006 Jul 12.

Abstract

New-onset diabetes after transplantation (NODAT) is a serious complication of transplantation. This study tested whether IL-6 production capacity may influence the development of NODAT in two different groups of patients. The occurrence of NODAT was analyzed with respect to IL-6 gene promoter polymorphism at position -174 (G-->C) and other relevant risk factors retrospectively in 217 renal transplant recipients and prospectively in 132. A linear increase in both circulating IL-6 (P = 0.09) and C-reactive protein (an indicator of basal IL-6 secretion; P = 0.03) concentrations from the CC genotype to the GG genotype was observed. In the multivariate model, the CC genotype was associated with a decreased risk for NODAT compared with the GG genotype in the two cohorts. Homeostasis Model Assessment for Insulin Resistance also revealed lesser insulin sensitivity in the GG carriers than in the CC carriers (2.15 +/- 2 versus 1.32 +/- 1.03; P = 0.03). Subgroup analysis showed that the influence of IL-6 gene promoter polymorphism on the development of NODAT was restricted mostly to overweight patients. These results highly suggest that IL-6 production capacity influences the development of NODAT and that diabetes-inducing drug administration should be limited in overweight patients who carry the GG genotype.

Publication types

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

MeSH terms

  • Adult
  • C-Reactive Protein / analysis
  • Cohort Studies
  • Diabetes Mellitus / blood*
  • Fasting
  • Female
  • Humans
  • Insulin / blood
  • Insulin Resistance / genetics
  • Insulin Resistance / immunology
  • Interleukin-6 / blood
  • Interleukin-6 / genetics*
  • Kidney Transplantation / adverse effects*
  • Male
  • Middle Aged
  • Multivariate Analysis
  • Polymorphism, Genetic*
  • Postoperative Complications / blood
  • Promoter Regions, Genetic*
  • Prospective Studies
  • Retrospective Studies
  • Risk Factors

Substances

  • Insulin
  • Interleukin-6
  • C-Reactive Protein