Related Experiment Video
Updated: Jul 11, 2026

Quantification of the Immunosuppressant Tacrolimus on Dried Blood Spots Using LC-MS/MS
Published on: November 8, 2015
Variability of mycophenolate mofetil trough levels in stable kidney transplant patients
A Fernández1, J Martins, J J Villlafruela
1Nephrology, Hospital Ramón y Cajal, Madrid, Spain. Afernandezr.hrc@salud.madrid.org
Abstract:
Great interindividual variability in the pharmacokinetics of mycophenolate mofetil (MMF) exists among kidney transplanted patients. The within-patient variability in stable transplanted patients is not well established. We performed 258 determinations of trough MMF levels in 86 stable transplant patients without hematological or gastrointestinal toxicity after at least year of a functioning kidney and a fixed dose of MMF. We examined the within-patient variability of levels related with clinical factors (age, gender, underlying cause of kidney failure, time since transplant, associated immunosuppression, and MMF dose) and analytical factors (serum creatinine, proteinuria, hemoglobin). Trough MMF levels were 3.6 mg/L, percentile (Pc) 25 1.6 mg/L, Pc 75 4.4 mg/L with intraindividual variability median of 65% (Pc 25 14%, Pc 75 79%). For the data analysis a variation of 14% was chosen, which corresponded to the 25th percentile. We did not observed differences between patients with variation below or above the Pc 25 in age, gender, underling cause of kidney failure, basal MMF levels, and MMF dose. Patients with greater variations showed significantly higher serum creatinine and proteinuria values than the others (1.84 +/- 0.54 vs 1.46 +/- 0.44 mg/dL and 0.45 +/- 0.42 vs 0.19 +/- 0.14 g/L; P < .05). Therefore, great within-patient variability in trough MMF levels was associated with poor kidney function and proteinuria.
Insights
Significant within-patient variability in mycophenolate mofetil (MMF) levels occurs in stable kidney transplant recipients. Higher MMF variability is linked to poorer kidney function and increased proteinuria, impacting treatment efficacy.
Area of Science:
- Nephrology
- Pharmacology
- Immunosuppression
Background:
- Interindividual variability in mycophenolate mofetil (MMF) pharmacokinetics is known in kidney transplant patients.
- Within-patient variability of MMF levels in stable transplant recipients requires further investigation.
Purpose of the Study:
- To assess the within-patient variability of trough MMF levels in stable kidney transplant patients.
- To identify clinical and analytical factors associated with MMF level variability.
Main Methods:
- 258 trough MMF level determinations were performed in 86 stable kidney transplant patients.
- Patients had functioning kidneys for at least one year and a fixed MMF dose.
- Variability was analyzed in relation to clinical factors and serum creatinine, proteinuria, and hemoglobin.
Main Results:
- The median intraindividual variability in trough MMF levels was 65%.
- Greater MMF level variability correlated with significantly higher serum creatinine and proteinuria.
- No significant differences in variability were observed based on age, gender, kidney failure cause, MMF dose, or time since transplant.
Conclusions:
- Substantial within-patient variability in trough MMF levels is present in stable kidney transplant recipients.
- Elevated MMF variability is associated with impaired kidney function and proteinuria.
- Monitoring MMF levels and kidney function is crucial for optimizing immunosuppression in transplant patients.
Related Concept Videos
Pharmacogenetics of Phase II Enzymes: N-acetyltransferase, Thiopurine S-methyltransferase, UDP-glucuronosyltransferase
Pharmacogenetic Phenotypes: Alterations in Pharmacokinetics, Drug Targets and Biologic Milieu
Effect of Hepatic Disease on Pharmacokinetics: Pathophysiologic Assessment and Liver Function Test
Drug Dosing in Renal Diseases: Dose Adjustments Based on Drug Clearance and Elimination Rate Constant
Kidney Transplant I: Introduction
Renal Failure: Dose Adjustments
Reduced renal clearance and elimination rate are common outcomes of renal impairment. These alterations lead to a prolonged elimination half-life and an altered apparent volume of distribution for drugs. As a result, dosage adjustments are typically necessary to maintain optimal drug levels in the body.
However, dosage adjustments...
