Effects of Dipeptidyl Peptidase-4 Inhibitors on Hyperglycemia and Blood Cyclosporine Levels in Renal Transplant Patients with Diabetes: A Pilot Study

被引:25
作者
Bae, Jaehyun [1 ]
Lee, Min Jung [2 ]
Choe, Eun Yeong [3 ]
Jung, Chang Hee [2 ]
Wang, Hye Jin [4 ]
Kim, Myoung Soo [5 ]
Kim, Yu Seun [5 ]
Park, Joong-Yeol [2 ]
Kang, Eun Seok [1 ,6 ]
机构
[1] Yonsei Univ, Coll Med, Dept Internal Med, Div Endocrinol & Metab, 50-1 Yonsei Ro, Seoul 03722, South Korea
[2] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Internal Med, 88 Olympic Ro 43 Gil, Seoul 05505, South Korea
[3] Catholic Kwandong Univ, Coll Med, Int St Marys Hosp, Div Endocrinol,Dept Internal Med, Incheon, South Korea
[4] Yonsei Univ, Coll Med, Brain Korea PLUS Project Med Sci 21, Seoul, South Korea
[5] Yonsei Univ Hlth Syst, Dept Transplantat Surg, Seoul, South Korea
[6] Yonsei Univ, Coll Med, Inst Endocrine Res, Seoul, South Korea
基金
新加坡国家研究基金会;
关键词
Dipeptidyl-peptidase IV inhibitors; Sitagliptin phosphate; Vildagliptin; Linagliptin; Cyclosporine; Kidney transplantation; Diabetes mellitus;
D O I
10.3803/EnM.2016.31.1.161
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: 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. Methods: 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 Alc (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. Results: HbAlc 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. ConclusIon: 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.
引用
收藏
页码:161 / 167
页数:7
相关论文
共 28 条
  • [1] Role of P-glycoprotein in cyclosporine cytotoxicity in the cyclosporine-sirolimus interaction
    Anglicheau, D.
    Pallet, N.
    Rabant, M.
    Marquet, P.
    Cassinat, B.
    Meria, P.
    Beaune, P.
    Legendre, C.
    Thervet, E.
    [J]. KIDNEY INTERNATIONAL, 2006, 70 (06) : 1019 - 1025
  • [2] The Metabolism and Disposition of the Oral Dipeptidyl Peptidase-4 Inhibitor, Linagliptin, in Humans
    Blech, Stefan
    Ludwig-Schwellinger, Eva
    Graefe-Mody, Eva Ulrike
    Withopf, Barbara
    Wagner, Klaus
    [J]. DRUG METABOLISM AND DISPOSITION, 2010, 38 (04) : 667 - 678
  • [3] ALTERNATIVE CYCLOSPORINE METABOLIC PATHWAYS AND TOXICITY
    CHRISTIANS, U
    SEWING, KF
    [J]. CLINICAL BIOCHEMISTRY, 1995, 28 (06) : 547 - 559
  • [4] Transport of the dipeptidyl peptidase-4 inhibitor sitagliptin by human organic anion transporter 3, organic anion transporting polypeptide 4C1, and multidrug resistance P-glycoprotein
    Chu, Xiao-Yan
    Bleasby, Kelly
    Yabut, Jocelyn
    Cai, Xiaoxin
    Chan, Grace Hoyee
    Hafey, Michael J.
    Xu, Shiyao
    Bergman, Arthur J.
    Braun, Matthew P.
    Dean, Dennis C.
    Evers, Raymond
    [J]. JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2007, 321 (02) : 673 - 683
  • [5] CYCLOSPORINE - A NEW IMMUNOSUPPRESSIVE AGENT FOR ORGAN-TRANSPLANTATION
    COHEN, DJ
    LOERTSCHER, R
    RUBIN, MF
    TILNEY, NL
    CARPENTER, CB
    STROM, TB
    [J]. ANNALS OF INTERNAL MEDICINE, 1984, 101 (05) : 667 - 682
  • [6] Davidson Jaime A, 2009, Cleve Clin J Med, V76 Suppl 5, pS28, DOI 10.3949/ccjm.76.s5.05
  • [7] DPP-4 Inhibitors Impact on glycemic control and cardiovascular risk factors
    Dicker, Dror
    [J]. DIABETES CARE, 2011, 34 : S276 - S278
  • [8] Excretion of the dipeptidyl peptidase-4 inhibitor linagliptin in rats is primarily by biliary excretion and P-gp-mediated efflux
    Fuchs, Holger
    Runge, Frank
    Held, Heinz-Dieter
    [J]. EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2012, 45 (05) : 533 - 538
  • [9] 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 diabetes
    Hamamoto, S.
    Kanda, Y.
    Shimoda, M.
    Tatsumi, F.
    Kohara, K.
    Tawaramoto, K.
    Hashiramoto, M.
    Kaku, K.
    [J]. DIABETES OBESITY & METABOLISM, 2013, 15 (02) : 153 - 163
  • [10] Evaluation of pharmacokinetic interactions between vildagliptin and digoxin in healthy volunteers
    He, Yon-Ling
    Sabo, Ron
    Sunkara, Gongadhar
    Bizot, Marie-Noelle
    Riviere, Gilles-Jacques
    Leon, Selene
    Ligueros-Saylan, Monica
    Dole, William R.
    Howard, Dan
    [J]. JOURNAL OF CLINICAL PHARMACOLOGY, 2007, 47 (08) : 998 - 1004