Metabolic effects of a corticosteroid-free immunosuppressive regimen in recipients of pancreatic transplant

Livio Luzi, Lucia Piceni Sereni, Alberto Battezzati, Attilio Elli, Jean Paul Soulillou, Diego Cantarovich

Research output: Contribution to journalArticlepeer-review

Abstract

Background. A corticosteroid (CS)-free immunosuppressive regimen may be considered less diabetogenic than treatments including CSs principally after pancreas transplantation. Methods. To test whether a CS-free immunosuppressive treatment is metabolically superior to a regimen including CSs, we prospectively studied 19 CS-free simultaneous pancreas and kidney (SPK) transplant recipients (body mass index=22±1 kg/m2; cyclosporine dose=400±19 mg/kg/day; azathioprine dose= 77±8 mg/day; basal plasma C-peptide=1.3±0.12 ng/mL) and 12 matched CS-treated SPK transplant recipients (prednisone dose=9±1 mg/day; basal C-peptide=2.2±0.2 ng/mL) by means of the 6,6-2H2-glucose infusion and the euglycemic insulin clamp (1 mU/kg/min, insulin infusion rate). In addition, six renal transplant recipients receiving a CS-free regimen were also studied as a control group. Results. In the postabsorptive state, CS-treated SPK transplant recipients demonstrated comparable plasma glucose levels but higher plasma insulin levels than CS-free SPK transplant recipients. Plasma triglyceride levels were significantly higher in CS-treated SPK patients than in CS-free SPK patients (1.16±0.16 mg/dL vs. 0.88±0.08; P1 levels were similar in both groups. No difference was observed in pyruvate, lactate, β-OH-butyrate, and basal endogenous glucose production in all three groups of patients studied. During euglycemic hyperinsulinemia, the inhibition of endogenous glucose production and the stimulation of tissue glucose disposal were not statistically different among the three groups. Conclusions. SPK recipients receiving chronic low-dose CS maintenance therapy do not present a lower glucose disposal than CS-free recipients. Nonetheless, this is obtained at the expense of a higher endogenous insulin secretion, which can cause an alteration of the triglyceride profile.

Original languageEnglish
Pages (from-to)2018-2023
Number of pages6
JournalTransplantation
Volume75
Issue number12
DOIs
Publication statusPublished - Jun 27 2003

ASJC Scopus subject areas

  • Transplantation
  • Immunology

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