Back to Search Start Over

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

Authors :
Philippe Saas
Jamal Bamoulid
Christophe Ferrand
Cécile Courivaud
Pierre Tiberghien
Marina Deschamps
Alfred Penfornis
Patricia Mercier
Didier Ducloux
Jean-Marc Chalopin
Interactions hôte-greffon-tumeur, ingénierie cellulaire et génique - UFC (UMR INSERM 1098) (RIGHT)
Institut National de la Santé et de la Recherche Médicale (INSERM)-Etablissement français du sang [Bourgogne-Franche-Comté] (EFS [Bourgogne-Franche-Comté])-Université de Franche-Comté (UFC)
Université Bourgogne Franche-Comté [COMUE] (UBFC)-Université Bourgogne Franche-Comté [COMUE] (UBFC)
Service d'urologie, andrologie et transplantation rénale
Centre Hospitalier Régional Universitaire de Besançon (CHRU Besançon)-Hôpital Saint-Jacques
Plateforme de Biomonitoring
Etablissement français du sang [Bourgogne-Franche-Comté] (EFS [Bourgogne-Franche-Comté])
Service de Diabétologie - Endocrinologie [CHRU Besançon]
Centre Hospitalier Régional Universitaire de Besançon (CHRU Besançon)
Centre d'Investigation Clinique de Besançon (Inserm CIC 1431)
Université de Franche-Comté (UFC)
Université Bourgogne Franche-Comté [COMUE] (UBFC)-Université Bourgogne Franche-Comté [COMUE] (UBFC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre Hospitalier Régional Universitaire de Besançon (CHRU Besançon)-Etablissement français du sang [Bourgogne-Franche-Comté] (EFS [Bourgogne-Franche-Comté])
Saas, Philippe
Hôpital Saint-Jacques-Centre Hospitalier Régional Universitaire de Besançon (CHRU Besançon)
Source :
Journal of the American Society of Nephrology, Journal of the American Society of Nephrology, American Society of Nephrology, 2006, 17 (8), pp.2333-40. ⟨10.1681/ASN.2006010066⟩
Publication Year :
2006
Publisher :
HAL CCSD, 2006.

Abstract

International audience; 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.

Details

Language :
English
ISSN :
10466673 and 15333450
Database :
OpenAIRE
Journal :
Journal of the American Society of Nephrology, Journal of the American Society of Nephrology, American Society of Nephrology, 2006, 17 (8), pp.2333-40. ⟨10.1681/ASN.2006010066⟩
Accession number :
edsair.doi.dedup.....ca46ee36f0e24cd8878878bb11f24fb8