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Influence of mycophenolate mofetil on preservation of kidney function in liver transplant patients
L Barrera-Pulido1, M D Espinosa-Aguilar, D Marín
1Hepatobiliary-pancreatic Unit of Surgery and Liver Transplantation, Virgen del Rocío University Hospital, Seville, Spain. lydiabarrera@hotmail.com
Background:
There are numerous studies on the effect of immunosuppressive therapy with mycophenolate mofetil (MMF) on preservation of kidney function in liver transplant (OLT) patients with chronic kidney damage. However, we have noted few studies that evaluate the role of this drug prescribed from induction on kidney function.
Patients And Methods:
This prospective observational multicenter study included 296 OLT performed from 2005 to 2007. The collected variables were; gender, and age, Child-Pugh stage, Model for End-Stage Liver Disease (MELD) score, transplant indication, induction immunosuppressive therapy, and baseline and 1 year posttransplant values of creatinine and glomerular filtration rate. Patients were classified into 4 groups: group 1 received MMF from induction; group 2 was never treated with MMF; group 3 started MMF in the first month posttransplant, and group 4 started MMF therapy in the third month posttransplant. We used Wilcoxon and Mann-Whitney U statistical tests.
Results:
There was a difference of 0.18 mg/dL in baseline creatinine values between groups 1 and 2 (P < .01). However, although patients who consistently had MMF in their treatment started with worse creatinine values, they were able to maintain them within normal ranges at 12 months. In contrast, patients in group 2 showed a significant worsening of 0.28 mg/dL in the first month that persisted throughout the study. Group 3 displayed worse baseline creatinine values than group 2 (P < .05), and also suffered an increase of 0.29 mg/dL (P < .01) versus baseline at 1 month. When MMF was added to their immunosuppressive therapy, the creatinine values reduced versus 1 month by 0.18 mg/dL (P < .05). Creatinine values remained stable at the other study assessments. Group 4 showed a normal creatinine value at baseline, but were altered at 1 and 3 months (P < .01), with increases versus baseline of 0.46 and 0.35 mg/dL, respectively. However, when MMF was introduced kidney function was restored and maintained over the study.
Conclusion:
Early introduction of MMF improved creatinine values among patients with impaired kidney function, maintaining them at stable levels. Furthermore, patients with altered creatinine values at baseline did not worsen their kidney function if they receive MMF from induction.
Insights
Early use of mycophenolate mofetil (MMF) in liver transplant patients improves kidney function. Starting MMF from induction helps maintain stable kidney function, even in those with pre-existing kidney damage.
Area of Science:
- Nephrology
- Hepatology
- Immunosuppression
Background:
- Limited research exists on the impact of early-initiated mycophenolate mofetil (MMF) on kidney function post-liver transplant.
- Existing studies primarily focus on MMF's effects in patients with pre-existing chronic kidney damage.
Purpose of the Study:
- To evaluate the role of MMF, particularly when initiated at induction, on preserving kidney function in liver transplant recipients.
- To compare kidney function outcomes based on the timing of MMF introduction.
Main Methods:
- A prospective observational multicenter study involving 296 liver transplantations.
- Patients were categorized into four groups based on MMF initiation timing: induction, never treated, 1-month post-transplant, and 3-month post-transplant.
- Kidney function was assessed by serum creatinine and glomerular filtration rate at baseline and 1 year post-transplant.
Main Results:
- Patients receiving MMF from induction (Group 1) maintained normal creatinine levels, despite worse baseline values compared to the never-treated group (Group 2).
- Group 2 showed a significant and persistent decline in kidney function within the first month.
- Early MMF introduction (induction or 1 month) improved or stabilized kidney function, whereas delayed introduction (3 months) initially worsened function before improvement.
Conclusions:
- Early administration of MMF from induction significantly improves and stabilizes kidney function in liver transplant recipients.
- MMF initiation at induction prevents the worsening of kidney function in patients with pre-existing renal impairment.
- The timing of MMF introduction is critical for optimizing renal outcomes after liver transplantation.
Related Concept Videos
Kidney Transplant I: Introduction
Effect of Hepatic Disease on Pharmacokinetics: Pathophysiologic Assessment and Liver Function Test
Effect of Hepatic Disease on Pharmacokinetics: Drug Dosing and Hepatic Blood Flow
Kidney Transplant III: Nursing Management
Kidney Transplant II: Surgical Procedure
Effect of Hepatic Disease on Pharmacokinetics: Active Drug, Metabolite and Fraction of Metabolized Drug
