Literature DB >> 15848604

Prospective, multicenter, randomized trial to compare incidence of new-onset diabetes mellitus and glucose metabolism in patients receiving cyclosporine microemulsion versus tacrolimus after de novo kidney transplantation.

F Vincenti1, M Tuncer, M Castagneto, M Klinger, S Friman, E-H Scheuermann, A Wiecek, G R Russ, A Martinek, B Nonnast-Daniel.   

Abstract

New-onset diabetes mellitus (NODM) is associated with increased risk of graft failure and death in renal transplant recipients. Some clinical studies have indicated that NODM risk is higher with tacrolimus than cyclosporine, but no comparative trial has used American Diabetic Association (ADA)/World Health Organization (WHO) criteria for diagnosis of diabetes mellitus. The Diabetes Incidence After Renal Transplantation, Neoral C2 Monitoring Versus Tacrolimus (DIRECT) study is a 6-month open-label, multicenter trial comparing the impact of tacrolimus and Neoral (cyclosporine microemulsion) on glucose metabolism in 700 de novo kidney transplant recipients, based on ADA/WHO criteria. Patients are randomized to tacrolimus (C0 monitoring) or Neoral (C2 monitoring), stratified by baseline diabetic status and ethnicity. All patients receive basiliximab, corticosteroids, and mycophenolate mofetil or enteric-coated mycophenolate acid (myfortic). Pooled interim 3-month results from a subset of 115 patients receiving either tacrolimus or Neoral showed that the primary efficacy end-point (biopsy-proven acute rejection [BPAR], graft loss or death) occurred in 11 patients (10%). There were four graft losses and only one death, which occurred after graft loss. Eight patients experienced BPAR (7.3%). Among 99 patients who were nondiabetic at baseline, 14 developed NODM by month 3, 17 developed impaired fasting glucose or impaired glucose tolerance, and another 5 patients received hypoglycemic treatment for at least 14 consecutive days or at the month 3 visit, resulting in a 36% incidence of impaired glucose metabolism. At 3 months, median GFR (Nankivell) was 63.7 mL/min; median serum creatinine was 137 micromol/L. Full complete results are expected in December 2005.

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Year:  2005        PMID: 15848604     DOI: 10.1016/j.transproceed.2004.12.017

Source DB:  PubMed          Journal:  Transplant Proc        ISSN: 0041-1345            Impact factor:   1.066


  4 in total

1.  Cardiovascular outcomes in the outpatient kidney transplant clinic: the Framingham risk score revisited.

Authors:  Bryce Kiberd; Romuald Panek
Journal:  Clin J Am Soc Nephrol       Date:  2008-03-05       Impact factor: 8.237

2.  Early Conversion from Tacrolimus to Belatacept in a Highly Sensitized Renal Allograft Recipient with Calcineurin Inhibitor-Induced de novo Post-Transplant Hemolytic Uremic Syndrome.

Authors:  Vasishta S Tatapudi; Bonnie E Lonze; Ming Wu; Robert A Montgomery
Journal:  Case Rep Nephrol Dial       Date:  2018-01-19

3.  HNF4alpha and HNF1alpha dysfunction as a molecular rational for cyclosporine induced posttransplantation diabetes mellitus.

Authors:  Jürgen Borlak; Monika Niehof
Journal:  PLoS One       Date:  2009-03-02       Impact factor: 3.240

4.  Nuclear Factor of Activated T Cell-regulated Cytokine Gene Expression for Adjustment of Tacrolimus in Kidney Transplant Recipients: A Randomized Controlled Pilot Trial.

Authors:  Allison B Webber; Vasishta Tatapudi; Thin T Maw; Carmen Peralta; Joey C Y Leung; Flavio Vincenti
Journal:  Transplant Direct       Date:  2018-06-27
  4 in total

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