Related Experiment Video
Updated: Mar 3, 2026

Quantification of the Immunosuppressant Tacrolimus on Dried Blood Spots Using LC-MS/MS
Published on: November 8, 2015
A Retrospective Study on Mycophenolic Acid Drug Interactions: Effect of Prednisone, Sirolimus, and Tacrolimus With
Ana C Alvarez-Elías1, Elisa C Yoo, Ekaterina K Todorova
1*Department of Pediatrics, Schulich School of Medicine and Dentistry, London, Ontario, Canada; †Postgraduate Unit, Universidad Nacional Autónoma de México; ‡Laboratorio de Investigación en Nefrología, Hospital Infantil de México Federico Gómez, Mexico City, Mexico; and Departments of §Pathology and Laboratory Medicine and ¶Medicine, Schulich School of Medicine and Dentistry, University of Western Ontario, London, Ontario, Canada.
Abstract:
Mycophenolic acid (MPA), the active compound of mycophenolate mofetil (MMF), is widely used as an antirejection drug after renal transplantation. There is growing evidence supporting the notion that there is substantial variability in the intra- and interpatient exposure to MPA. Drug interactions involving MPA with tacrolimus, steroids, and sirolimus have been understudied. The objective of this study was to determine the relationship between MPA, steroids, tacrolimus, and sirolimus. MPA trough concentrations from 37 pediatric renal transplant recipients (mean age 7.6 years at transplant) followed for a median follow-up of 7.8 years were analyzed retrospectively and 2131 dose-normalized MPA trough concentrations were evaluated against all known covariates including all concomitant immunosuppressant drug doses and exposure, age, albumin, hematocrit, and estimated glomerular filtration rate (eGFR). Age, hematocrit, and estimated glomerular filtration rate affected the dose-normalized MPA trough concentrations. The authors used appropriate linear regression univariate models and created 5 different multivariate models to examine individual drug-drug interactions (DDIs). Although the authors' findings support the notion that there is a DDI between MMF and both sirolimus and steroids, the sample size was small, and these findings should be confirmed in future studies. The authors found no DDIs between tacrolimus and MMF, the prodrug of MPA. These findings are important because there is a tendency to under-dose MMF early and to overdose late after transplantation. The DDI between sirolimus and MMF has not been described. Although therapeutic drug monitoring of MMF therapy is often not performed, the data presented here indicate a necessity for therapeutic drug monitoring. This is especially true when converting from tacrolimus to sirolimus, as a way to avoid MPA underexposure and organ rejection.
Insights
Mycophenolate mofetil (MMF) drug interactions with sirolimus and steroids were studied in pediatric renal transplant patients. Findings suggest MMF drug-drug interactions necessitate therapeutic drug monitoring, especially during tacrolimus to sirolimus conversion, to prevent organ rejection.
Area of Science:
- Pharmacology
- Nephrology
- Immunosuppression
Background:
- Mycophenolic acid (MPA), the active metabolite of mycophenolate mofetil (MMF), is a key immunosuppressant post-renal transplant.
- Significant inter- and intrapatient variability in MPA exposure is observed.
- Drug interactions involving MPA, particularly with tacrolimus, steroids, and sirolimus, require further investigation.
Purpose of the Study:
- To investigate the drug-drug interactions (DDIs) between mycophenolate mofetil (MMF) and concomitant immunosuppressants: tacrolimus, steroids, and sirolimus.
- To identify factors influencing MMF exposure in pediatric renal transplant recipients.
Main Methods:
- Retrospective analysis of MPA trough concentrations from 37 pediatric renal transplant recipients.
- Evaluation of 2131 dose-normalized MPA trough concentrations against covariates including concomitant drug doses, age, albumin, hematocrit, and eGFR.
- Utilized linear regression univariate and multivariate models to assess DDIs.
Main Results:
- Age, hematocrit, and estimated glomerular filtration rate (eGFR) significantly impacted dose-normalized MPA trough concentrations.
- A drug-drug interaction (DDI) was suggested between MMF and sirolimus, and between MMF and steroids.
- No DDIs were identified between MMF and tacrolimus.
Conclusions:
- The study suggests a potential DDI between MMF and sirolimus, and MMF and steroids, though further validation is needed due to sample size.
- No MMF-tacrolimus DDI was found.
- Therapeutic drug monitoring of MMF is recommended, particularly when switching from tacrolimus to sirolimus, to optimize MPA exposure and prevent rejection.
More Related Videos
10:31Surgical Angiogenesis in Porcine Tibial Allotransplantation: A New Large Animal Bone Vascularized Composite Allotransplantation Model
Published on: August 13, 2017
05:28A Semi-Quantitative Drug Affinity Responsive Target Stability DARTS assay for studying Rapamycin/mTOR interaction
Published on: August 27, 2019
Related Concept Videos
Pharmacogenetics of Phase II Enzymes: N-acetyltransferase, Thiopurine S-methyltransferase, UDP-glucuronosyltransferase
Effect of Hepatic Disease on Pharmacokinetics: Dose Adjustments Due to Hepatic Impairment
Pharmacokinetics in Geriatric Patients: Effect of Age on Drug Metabolism
Therapeutic Drug Monitoring: Affecting Factors
Impact of Pharmacokinetic–Pharmacodynamic Models: Regulatory Decisions
Drugs for Treatment of Crohn's Disease in IBD Using Immunomodulatory Agents