Exenatide and sitagliptin are not associated with increased risk of acute renal failure: a retrospective claims analysis

Diabetes Obes Metab. 2012 Jul;14(7):596-600. doi: 10.1111/j.1463-1326.2012.01567.x. Epub 2012 Feb 20.

Abstract

Aim: This study evaluated whether the risk of acute renal failure (ARF) increases with exenatide and sitagliptin use.

Methods: A retrospective cohort study of a large medical and pharmacy claims database was performed. Data for 4 91 539 patients were analysed. Cox proportional hazard models were used to compare the risk of ARF between diabetic and non-diabetic subjects and between diabetic patients treated with exenatide, sitagliptin and control medications.

Results: Adjusted Cox analyses showed diabetic subjects had a higher risk of ARF [HR 1.51, confidence interval (CI) 1.26-1.81, p < 0.001] than non-diabetic controls. Compared with diabetic controls, neither exenatide (HR 0.77, CI 0.42-1.41, p = 0.40) nor sitagliptin (HR 1.17, CI 0.82-1.65, p = 0.39) increased the risk of ARF.

Conclusion: Our study revealed an increased incidence of ARF in diabetic versus non-diabetic patients but no association between use of exenatide or sitagliptin and ARF. Because of the limitations of this observational analysis, we cannot exclude the possibility of a very small increased risk.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Kidney Injury / chemically induced*
  • Acute Kidney Injury / etiology
  • Acute Kidney Injury / physiopathology
  • Adolescent
  • Adult
  • Cohort Studies
  • Diabetes Mellitus, Type 2 / complications
  • Diabetes Mellitus, Type 2 / drug therapy*
  • Diabetes Mellitus, Type 2 / physiopathology
  • Dipeptidyl-Peptidase IV Inhibitors / administration & dosage
  • Dipeptidyl-Peptidase IV Inhibitors / adverse effects
  • Dipeptidyl-Peptidase IV Inhibitors / pharmacology*
  • Drug Labeling
  • Exenatide
  • Female
  • Humans
  • Incidence
  • Male
  • Middle Aged
  • Peptides / administration & dosage
  • Peptides / adverse effects
  • Peptides / pharmacology*
  • Proportional Hazards Models
  • Pyrazines / administration & dosage
  • Pyrazines / adverse effects
  • Pyrazines / pharmacology*
  • Retrospective Studies
  • Risk Assessment
  • Sitagliptin Phosphate
  • Triazoles / administration & dosage
  • Triazoles / adverse effects
  • Triazoles / pharmacology*
  • Venoms / administration & dosage
  • Venoms / adverse effects
  • Venoms / pharmacology*
  • Young Adult

Substances

  • Dipeptidyl-Peptidase IV Inhibitors
  • Peptides
  • Pyrazines
  • Triazoles
  • Venoms
  • Exenatide
  • Sitagliptin Phosphate