Imatinib and type 2 diabetes

Endocr Pract. 2007 Mar-Apr;13(2):126-30. doi: 10.4158/EP.13.2.126.

Abstract

Objective: To characterize the effect, if any, of imatinib mesylate, an inhibitor of abl tyrosine kinase used in the treatment of chronic myeloid leukemia, on type 2 diabetes.

Methods: The centralized pharmacy database was used to identify all patients who had received imatinib at the Mayo Clinic in Rochester, Minnesota, during a 5-year period. The electronic medical records were subsequently reviewed to identify which of these patients had type 2 diabetes. In addition, relevant biochemical data, prior to, during, and after imatinib treatment, were abstracted from the electronic laboratory database and medical records.

Results: At the Mayo Clinic in Rochester, Minnesota, a total of 164 patients received imatinib during the period of study (1999 to 2004). Of these 164 patients, 7 had preexisting type 2 diabetes, and diabetes developed in 2 patients during treatment with imatinib. Despite 2 previous reports of improvement in glycemic control with use of imatinib in patients with type 2 diabetes, no net effect on glycemic control or diabetes therapy was noted in our study cohort.

Conclusion: On the basis of our current study, it seems unlikely that imatinib substantially affects glycemic control in patients with type 2 diabetes.

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Animals
  • Benzamides
  • Blood Glucose / metabolism
  • Body Mass Index
  • Body Weight / drug effects
  • Diabetes Mellitus, Type 2 / blood
  • Diabetes Mellitus, Type 2 / drug therapy*
  • Humans
  • Imatinib Mesylate
  • Male
  • Medical Records Systems, Computerized / statistics & numerical data
  • Middle Aged
  • Piperazines / administration & dosage
  • Piperazines / therapeutic use*
  • Protein Kinase Inhibitors / administration & dosage
  • Protein Kinase Inhibitors / therapeutic use
  • Pyrimidines / administration & dosage
  • Pyrimidines / therapeutic use*
  • Time Factors
  • Treatment Outcome

Substances

  • Benzamides
  • Blood Glucose
  • Piperazines
  • Protein Kinase Inhibitors
  • Pyrimidines
  • Imatinib Mesylate