TCF7L2 Polymorphism Associates with New-Onset Diabetes after Transplantation

Lidia Ghisdal, Christophe Baron, Yannick Le Meur, Arnaud Lionet, Jean-Michel Halimi, Jean-Philippe Rerolle, Francois Glowacki, Yvon Lebranchu, Mireille Drouet, Christian Noel, Hakim El Housni, Pascale Cochaux, Karl Martin Wissing, Daniel Abramowicz, Marc Abramowicz

Research output: Contribution to journalArticlepeer-review

65 Citations (Scopus)

Abstract

New-onset diabetes after transplantation (NODAT) is a serious and frequent complication in transplant recipients. Whether NODAT shares the same susceptibility genes as type 2 diabetes is unknown. In this multicenter study, we genotyped 1076 white patients without diabetes at transplantation for 11 polymorphisms that associate with type 2 diabetes. We defined NODAT as a fasting plasma glucose >= 126 mg/dl on at least two occasions or de novo hypoglycemic therapy. We compared clinical and genetic factors between patients who developed NODAT within 6 mo of transplantation (n = 118; incidence 11 %) and patients without diabetes (n = 958). In multivariate analysis, NODAT significantly associated with the following characteristics: TCF7L2 polymorphism (odds ratio [OR] 1.60 per each T allele; P = 0.002), age (OR 1.03 per year; P <0.001), body mass index at transplantation (OR 1.09 per unit; P <0.001), tacrolimus use (OR 2.26; P <0.001), and the occurrence of a corticoid-treated acute rejection episode (OR 2.78; P <0.001). In summary, our data show that the TCF7L2 rs7903146 polymorphism, a known risk factor for type 2 diabetes in the general population, also associates with NODAT.
Original languageEnglish
Pages (from-to)2459-2467
Number of pages9
JournalJournal of the American Society of Nephrology
Volume20
Issue numberNOV
Publication statusPublished - 2009

Keywords

  • TCF7L2
  • polymorphism
  • new-onset
  • diabetes
  • transplantation

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