Longitudinal evaluation of mycophenolic acid pharmacokinetics in pediatric kidney transplant recipients. The role of post-transplant clinical and therapeutic variables |
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Authors: | Luciana Ghio Mariano Ferraresso Graziella Zacchello Luisa Murer Fabrizio Ginevri Mirco Belingheri Licia Peruzzi Franco Zanon Francesco Perfumo Luisa Berardinelli Silvia Tirelli Luca Dello Strologo Iris Fontana Umberto Valente Massimo Cardillo Alberto Edefonti |
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Affiliation: | Pediatric Nephrology Unit, Maggiore Policlinico Hospital, Mangiagalli and Regina Elena Foundation, IRCCS, Milan;, Division of General Surgery and Kidney Transplantation, Maggiore Policlinico Hospital, Mangiagalli and Regina Elena Foundation, IRCCS, Milan;, Department of Pediatrics, University of Padua Medical School, Padua;, Pediatric Nephrology Unit, G. Gaslini Institute, Genova;, Nephrology, Dialysis and Transplantation Unit, University of Turin Medical School, Turin;, Division of Pediatric Surgery University of Padua Medical School, Padua;, Laboratory of Clinical Pathology, Maggiore Policlinico Hospital, Mangiagalli and Regina Elena Foundation, IRCCS, Milan;, Nephrology and Dialysis Unit, Bambin GesùChildren's Hospital and Research Institute, Milan;, Department of Transplantation, San Martino University Hospital, Genova;, Transplant Immunology and Blood Bank, Maggiore Policlinico Hospital, Mangiagalli and Regina Elena Foundation, IRCCS, Milan, Italy |
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Abstract: | Abstract: This longitudinal study assessed the influence of post-transplant clinical and therapeutic variables in 50 kidney transplant recipients aged 2–19 yr receiving a triple immunosuppressive regimen consisting of cyclosporine microemulsion (CsA), steroids and MMF (300–400 mg/m2 body surface area twice daily), the full pharmacokinetic profile (10 points) of which was investigated on post-transplant days 6, 30, 180 and 360. Total plasma MPA was measured by Enzyme Multiplied Immunoassay Technique. CsA therapeutic drug monitoring (TDM) was performed via C2 blood monitoring, while MPA TDM via C0. MPA Cmax, tmax, AUC0-12 and AUC0-4 pharmacokinetic profile changed significantly during the first post-transplant year. C0 was a poor predictor of the total MPA exposure [as measured by the area under the concentration-time curve AUC)], while a truncated AUC was a good surrogate of the 12-h profile (r = 0.91; p < 0.001) Graft function and cyclosporine therapy influenced MPA pharmacokinetics, as shown by the univariate and multivariate analyses. We conclude that because after transplantation MPA exposure varied over time, a strict TDM is advisable in the pediatric population. |
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Keywords: | mycophenolate mofetil mycophenolic acid pediatric kidney transplantation pharmacokinetics therapeutic drug monitoring |
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