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.

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.

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