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Lack of Correlation Between MMF Dose and MPA Level in Pediatric and Young Adult Cardiac Transplant Patients: Does the MPA Level Matter? 1
Author(s) -
Gajarski Robert J.,
Crowley Dennis C.,
Zamberlan Mary C.,
Lake Kathleen D.
Publication year - 2004
Publication title -
american journal of transplantation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.89
H-Index - 188
eISSN - 1600-6143
pISSN - 1600-6135
DOI - 10.1111/j.1600-6143.2004.00534.x
Subject(s) - medicine , mycophenolic acid , dosing , calcineurin , mycophenolate , therapeutic drug monitoring , trough level , urology , transplantation , pharmacokinetics , tacrolimus
To determine the correlation between mycophenolate mofetil (MMF) dose and mycophenolic acid (MPA) level as well as its impact on rejection among young cardiac transplant recipients (OHT), trough concentrations of MPA and its metabolite, mycophenolic acid glucuronide (MPAG), were measured following MMF doses of 1200 mg/m 2 /d (max 3000 mg/d). Corresponding endomyocardial biopsy (EMB) grades and calcineurin inhibitor levels were recorded with simultaneous MPA/MPAG levels. Correlation coefficients were derived between MMF dose and MPA/MPAG levels. Contingency analysis evaluated the relation between MPA level and EMB score.Twenty‐six patients (median age 15.4 years) had 120 MPA/MPAG levels measured. Average MMF dose was 1208.8 mg/m 2 /d with median MPA and MPAG concentrations: 2.1 (therapeutic: 1.0–3.5 μg/mL) and 48 μg/mL (reference range: 35–100 μg/mL), respectively. Only 50% of patients consistently achieved therapeutic levels with standard dosing. No correlation was found between MMF dose and MPA/MPAG levels. In the presence of therapeutic calcineurin inhibition, EMB grade ≥ 2 occurred more with MPA concentrations <2.5 μg/mL (p = 0.01).In young OHT patients, MMF dose does not correlate with MPA/MPAG levels, and standard MMF dosing fails to consistently achieve ‘therapeutic’ MPA concentrations. An MPA trough level <2.5 μg/mL was more frequently associated with EMB grade ≥ 2. Concentration rather than dose‐driven management is a more prudent strategy when using MMF.