4.6 Article

Impact of Sirolimus versus Mycophenolate Mofetil on Kidney Function after Calcineurin Inhibitor Dose Reduction in Liver Transplant Recipients

Journal

PHARMACEUTICALS
Volume 16, Issue 8, Pages -

Publisher

MDPI
DOI: 10.3390/ph16081087

Keywords

sirolimus; mycophenolate mofetil; liver transplantation; acute kidney disease; chronic kidney disease

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This study compared adverse kidney outcomes between liver transplant patients treated with a reduced dose of tacrolimus plus sirolimus or mycophenolate mofetil. The results showed that sirolimus use was associated with a higher risk of estimated glomerular filtration rate decline compared to mycophenolate mofetil. Close monitoring of kidney function, dose adjustment, and timely transition to mycophenolate mofetil are necessary for liver transplant patients receiving sirolimus.
Impaired kidney function is associated with increased morbidity and mortality in patients undergoing liver transplantation. Although immunosuppressants are essential in these patients, they impair kidney function. This study aimed to compare adverse kidney outcomes between patients treated with a reduced dose of tacrolimus (calcineurin inhibitor) plus sirolimus or mycophenolate mofetil (MMF) in the liver transplant center at Kaohsiung Chang Gung Memorial Hospital between April 2011 and December 2017. Propensity score matching was used to identify 232 patients. The risk of adverse kidney outcomes was estimated using Cox proportional hazards regression, and changes in kidney function over time were analyzed using linear mixed modeling. Acute kidney disease risks in this study cohort were not significantly different for the two immunosuppressants (aHR 1.04; 95% CI: 0.70-1.55, p = 0.8328). However, sirolimus use was significantly associated with a higher risk of estimated glomerular filtration rate decline > 30% than MMF (aHR, 2.09; 95% CI: 1.33-3.28; p = 0.0014). Our results demonstrate that sirolimus use may have worsened long-term kidney outcomes compared to MMF. Close monitoring of kidney function, dose adjustment, and timely transition to MMF is necessary for LT patients receiving sirolimus.

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