Outcome of cystic fibrosis-related diabetes two years after lung transplantation

Respiration. 2013;86(1):32-8. doi: 10.1159/000339928. Epub 2012 Aug 25.

Abstract

Background: Although transplantation is known to impair glucose tolerance, evolution of pre-existing diabetes after lung transplantation (LT) in cystic fibrosis (CF) has never been described.

Objectives: We aimed to assess the outcome of CF-related diabetes (CFRD) after LT, with the hypothesis that suppressing chronic inflammatory foci may improve glucose tolerance in some patients.

Methods: In a retrospective study of 29 CF diabetic patients treated with insulin and undergoing LT, CFRD control was assessed 3 months before LT and 1 (n = 27) and 2 (n = 18) years after LT by measuring insulin dosage, fasting blood glucose and glycosylated hemoglobin (HbA1c) levels. Patients with HbA1c ≤7% and an insulin dose ≤1 UI/kg/day were defined as having controlled CFRD (group A). Other patients were assigned to group B.

Results: Before LT, 19 (65.5%) patients were in group A. At 2 years, 6 of 10 (60%) patients who were in group B prior to LT had moved into group A, which then comprised 77.8% of all patients. Insulin could have been stopped in 5 patients. Uncontrolled CFRD before LT (OR = 16) and a long delay between the diagnosis of CFRD and LT (OR = 1.3) were significant predictors of uncontrolled CFRD at 1 year.

Conclusions: LT does not seem to worsen CFRD in some patients, suggesting that in some cases, glucose tolerance may be improved by the suppression of chronic pulmonary infection.

Publication types

  • Observational Study

MeSH terms

  • Adrenal Cortex Hormones / adverse effects
  • Adult
  • Blood Glucose
  • Cystic Fibrosis / complications
  • Cystic Fibrosis / surgery*
  • Diabetes Mellitus / blood
  • Diabetes Mellitus / etiology
  • Diabetes Mellitus / physiopathology*
  • Disease Progression
  • Exocrine Pancreatic Insufficiency / etiology
  • Female
  • Glycated Hemoglobin
  • Humans
  • Immunosuppressive Agents / adverse effects
  • Insulin / metabolism
  • Insulin Resistance / physiology*
  • Insulin Secretion
  • Logistic Models
  • Lung Transplantation*
  • Male
  • Retrospective Studies
  • Treatment Outcome
  • Young Adult

Substances

  • Adrenal Cortex Hormones
  • Blood Glucose
  • Glycated Hemoglobin A
  • Immunosuppressive Agents
  • Insulin
  • hemoglobin A1c protein, human