Effects of Dipeptidyl Peptidase-4 Inhibitors on Hyperglycemia and Blood Cyclosporine Levels in Renal Transplant Patients with Diabetes: A Pilot Study
Open Access
- 1 January 2016
- journal article
- Published by Korean Endocrine Society in Endocrinology and Metabolism
- Vol. 31 (1) , 161-167
Abstract
The use of dipeptidyl peptidase-4 (DPP-4) inhibitors is increasing among renal transplant patients with diabetes. However, the glucose-lowering efficacies of various DPP-4 inhibitors and their effects on blood cyclosporine levels have not been fully investigated. We compared the glucose-lowering efficacies of DPP 4 inhibitors and evaluate their effects on the blood levels of cyclosporine in renal transplant recipients with diabetes. Sixty-five renal allograft recipients who received treatment with DPP-4 inhibitors (vildagliptin, sitagliptin, or linagliptin) following kidney transplant were enrolled. The glucose-lowering efficacies of the DPP-4 inhibitors were compared according to the changes in the hemoglobin A1c (HbA1c) levels after 3 months of treatment. Changes in the trough levels of the cyclosporine were also assessed 2 months after treatment with each DPP-4 inhibitor. HbA1c significantly decreased in the linagliptin group in comparison with other DPP-4 inhibitors (vildagliptin -0.38%±1.03%, sitagliptin -0.53%±0.95%, and linagliptin -1.40±1.34; P=0.016). Cyclosporine trough levels were significantly increased in the sitagliptin group compared with vildagliptin group (30.62±81.70 ng/mL vs. -24.22±53.54 ng/mL, P=0.036). Cyclosporine trough levels were minimally changed in patients with linagliptin. Linagliptin demonstrates superior glucose-lowering efficacy and minimal effect on cyclosporine trough levels in comparison with other DPP-4 inhibitors in kidney transplant patients with diabetes.Keywords
Funding Information
- Yonsei University College of Medicine (6-2012-0148)
- National Research Foundation of Korea (NRF-2010-013-E0008, NRF-2012000891)
This publication has 28 references indexed in Scilit:
- Vildagliptin preserves the mass and function of pancreatic β cells via the developmental regulation and suppression of oxidative and endoplasmic reticulum stress in a mouse model of diabetesDiabetes, Obesity and Metabolism, 2012
- Excretion of the dipeptidyl peptidase-4 inhibitor linagliptin in rats is primarily by biliary excretion and P-gp-mediated effluxEuropean Journal of Pharmaceutical Sciences, 2012
- DPP-4 InhibitorsDiabetes Care, 2011
- The association of early post-transplant glucose levels with long-term mortalityDiabetologia, 2011
- Dipeptidylpeptitase-4 Inhibitors (Gliptins)Clinical Pharmacokinetics, 2010
- Glucose Control is Associated With Patient Survival in Diabetic Patients After Renal TransplantationTransplantation, 2010
- Transport of the Dipeptidyl Peptidase-4 Inhibitor Sitagliptin by Human Organic Anion Transporter 3, Organic Anion Transporting Polypeptide 4C1, and Multidrug Resistance P-glycoproteinThe Journal of Pharmacology and Experimental Therapeutics, 2007
- Therapeutic Monitoring of Calcineurin Inhibitors for the NephrologistClinical Journal of the American Society of Nephrology, 2007
- Role of P-glycoprotein in cyclosporine cytotoxicity in the cyclosporine–sirolimus interactionKidney International, 2006
- Glycaemic control and graft loss following renal transplantationNephrology Dialysis Transplantation, 2001