Literature DB >> 3307061

The impact of cyclosporine and combination immunosuppression on the incidence of posttransplant diabetes in renal allograft recipients.

J P Boudreaux, L McHugh, D M Canafax, N Ascher, D E Sutherland, W Payne, R L Simmons, J S Najarian, D S Fryd.   

Abstract

The incidence of posttransplant diabetes mellitus (PTDM) was compared in three groups of renal transplant recipients: nondiabetic patients who had been randomized between 1980 and 1983 to receive antilymphoblast globulin (ALG), azathioprine (AZA), and prednisone (P) (group 1) or cyclosporine (CsA) plus prednisone (group 2). Group 3 consisted of a more recent (1984-85) cohort who were given a combination of azathioprine, cyclosporine, and prednisone (+/- ALG). PTDM developed in 20 of 173 previously nondiabetic 18-55-year-old patients. Three of 47 patients (6.4%) in group 1, 4 of 58 patients (6.9%) in group 2, and 13 of 68 patients in group 3 (19.1%) developed PTDM. Thus in the two groups composing the concurrent prospective randomized trial (groups 1 and 2) the incidence of PTDM did not differ. The subsequent patients who were given a combination of ALG, azathioprine, cyclosporine, and prednisone developed a significantly greater incidence of PTDM even though the total dose of cyclosporine and prednisone were lower than in groups 1 and 2. PTDM usually occurred within two months of transplantation, and 11 of 17 patients who initially required insulin are still dependent upon exogenous insulin. The incidence of PTDM was not significantly affected by sex of the recipient, HLA-type, primary renal disease, rejection episodes, primary vs. secondary transplant, or prior splenectomy. The incidence of PTDM is greater in patients older than 45 (34.2% vs. 5.2%), and heavier than 70 kg (21.1% vs. 5.1%); in recipients of cadaveric allografts (15.7% vs. 4.6%); and in patients who were hospitalized for infections (22.4% vs. 4.7%). CsA levels tended to be higher in the group 2 and 3 patients who developed PTDM than in those who remained nondiabetic. One-year actuarial patient survival in those with PTDM was 83.3% vs. 98% (P less than .01) in the nondiabetic and graft survival was 77.1% vs. 87.1% (NS). The combination of Minnesota ALG, azathioprine, cyclosporine, and prednisone appears to predispose older, heavier recipients of cadaver allografts to the development of PTDM. The risk of PTDM must be weighed against the more usual results of improved patient and graft survival using this combination of immunosuppression.

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Year:  1987        PMID: 3307061     DOI: 10.1097/00007890-198709000-00010

Source DB:  PubMed          Journal:  Transplantation        ISSN: 0041-1337            Impact factor:   4.939


  39 in total

1.  Single-centre study of 628 adult, primary kidney transplant recipients showing no unfavourable effect of new-onset diabetes after transplant.

Authors:  Jeffrey J Gaynor; Gaetano Ciancio; Giselle Guerra; Junichiro Sageshima; Lois Hanson; David Roth; Michael J Goldstein; Linda Chen; Warren Kupin; Adela Mattiazzi; Lissett Tueros; Sandra Flores; Luis J Barba; Adrian Lopez; Jose Rivas; Phillip Ruiz; Rodrigo Vianna; George W Burke
Journal:  Diabetologia       Date:  2014-11-01       Impact factor: 10.122

2.  Effect of FK 506 on human pancreatic islets following renal subcapsular transplantation in diabetic nude mice.

Authors:  C Ricordi; Y Zeng; R Alejandro; A Tzakis; P Carroll; H L Rilo; R Venkataramanan; J J Fung; D Bereiter; T E Starzl
Journal:  Transplant Proc       Date:  1992-06       Impact factor: 1.066

Review 3.  Dysglycemia after renal transplantation: Definition, pathogenesis, outcomes and implications for management.

Authors:  David Langsford; Karen Dwyer
Journal:  World J Diabetes       Date:  2015-08-25

4.  Liver transplantation of American veterans under FK 506 immunosuppression: a preliminary report.

Authors:  L A Mieles; J J Fung; I Yokoyama; J McCauley; N Singh; S Todo; R D Gordon; T E Starzl
Journal:  Transplant Proc       Date:  1991-12       Impact factor: 1.066

5.  FK 506 in clinical kidney transplantation.

Authors:  R Shapiro; M Jordan; V Scantlebury; J Fung; C Jensen; A Tzakis; J McCauley; P Carroll; C Ricordi; A J Demetris
Journal:  Transplant Proc       Date:  1991-12       Impact factor: 1.066

6.  Kidney transplantation under FK 506 immunosuppression.

Authors:  R Shapiro; M Jordan; J Fung; J McCauley; J Johnston; Y Iwaki; A Tzakis; T Hakala; S Todo; T E Starzl
Journal:  Transplant Proc       Date:  1991-02       Impact factor: 1.066

7.  Glycemia and insulin need following FK 506 rescue therapy in liver transplant recipients.

Authors:  L Mieles; R D Gordon; D Mintz; R M Toussaint; O Imventarza; T E Starzl
Journal:  Transplant Proc       Date:  1991-02       Impact factor: 1.066

8.  Pilot study: association of traditional and genetic risk factors and new-onset diabetes mellitus following kidney transplantation.

Authors:  H A Chakkera; R L Hanson; S M Raza; J K DiStefano; M P Millis; R L Heilman; D C Mulligan; K S Reddy; M J Mazur; K Hamawi; A A Moss; K L Mekeel; J R Cerhan
Journal:  Transplant Proc       Date:  2009-12       Impact factor: 1.066

9.  Renal transplantation at the University of Pittsburgh: the impact of FK506.

Authors:  R Shapiro; M Jordan; V P Scantlebury; C Vivas; H A Gritsch; A S Rao; M Trucco; A Zeevi; A J Demetris; P Randhawa
Journal:  Clin Transpl       Date:  1994

10.  Sirolimus is associated with new-onset diabetes in kidney transplant recipients.

Authors:  Olwyn Johnston; Caren L Rose; Angela C Webster; John S Gill
Journal:  J Am Soc Nephrol       Date:  2008-04-02       Impact factor: 10.121

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