A comparison of tacrolimus and cyclosporine in liver transplantation: effects on renal function and cardiovascular risk status.

Published

Journal Article

A retrospective chart review of 1065 consecutive liver allograft recipients in 11 centers from January 1997 to September 1998 was performed. Patients were followed for 3 years or until graft loss. Patients received either tacrolimus (n = 594), cyclosporine (n = 450) or no calcineurin inhibitor (n = 21). Model for end-stage liver disease (MELD) scores at time of transplant were similar between the two groups. During follow-up, more patients switched from cyclosporine to tacrolimus (26.7%) than from tacrolimus to cyclosporine (12.8%; p < 0.0001). Patient and graft survival were equivalent. Corticosteroid use was more common in cyclosporine-treated patients (p < 0.00001). Patients receiving tacrolimus experienced lower serum creatinine levels at months 3 through 36 (p < 0.0001). Systolic blood pressure was lower in patients receiving tacrolimus (p < 0.001) despite a reduced requirement for anti-hypertensive agents (p < 0.0001). In addition, tacrolimus was associated with lower total cholesterol and triglyceride levels for months 3 through 24 and 3 through 12, respectively (p < 0.01), despite a reduced requirement for anti-hyperlipidemic agents. The incidence of new-onset diabetes mellitus was similar in both groups. While both calcineurin inhibitors were associated with excellent patient and graft survival, renal function, blood pressure and serum lipid levels were significantly better with tacrolimus treatment.

Full Text

Duke Authors

Cited Authors

  • Lucey, MR; Abdelmalek, MF; Gagliardi, R; Granger, D; Holt, C; Kam, I; Klintmalm, G; Langnas, A; Shetty, K; Tzakis, A; Woodle, ES

Published Date

  • May 2005

Published In

Volume / Issue

  • 5 / 5

Start / End Page

  • 1111 - 1119

PubMed ID

  • 15816894

Pubmed Central ID

  • 15816894

International Standard Serial Number (ISSN)

  • 1600-6135

Digital Object Identifier (DOI)

  • 10.1111/j.1600-6143.2005.00808.x

Language

  • eng

Conference Location

  • United States