Fast Tac metabolizers at risk – It is time for a C/D ratio calculation

Thölking, G; Schütte-Nütgen, K; Steinke, J; Pavenstädt, H; Schmidt, R; Suwelack, B; Reuter, S

Forschungsartikel (Zeitschrift) | Peer reviewed

Zusammenfassung

Tacrolimus (Tac) is a part of the standard immunosuppressive regimen after renal transplantation (RTx). However, its metabolism rate is highly variable. A fast Tac metabolism rate, defined by the Tac blood trough concentration (C) divided by the daily dose (D), is associated with inferior renal function after RTx. Therefore, we hypothesize that the Tac metabolism rate impacts patient and graft survival after RTx. We analyzed all patients who received a RTx between January 2007 and December 2012 and were initially treated with an immunosuppressive regimen containing Tac (Prograf®), mycophenolate mofetil, prednisolone and induction therapy. Patients with a Tac C/D ratio <1.05 ng/mL × 1/mg at three months after RTx were characterized as fast metabolizers and those with a C/D ratio ≥1.05 ng/mL×1/mg as slow metabolizers. Five-year patient and overall graft survival were noticeably reduced in fast metabolizers. Further, fast metabolizers showed a faster decline of eGFR (estimated glomerular filtration rate) within five years after RTx and a higher rejection rate compared to slow metabolizers. Calculation of the Tac C/D ratio three months after RTx may assist physicians in their daily clinical routine to identify Tac-treated patients at risk for the development of inferior graft function, acute rejections, or even higher mortality.

Details zur Publikation

FachzeitschriftJournal of Clinical Medicine (J Clin Med)
Jahrgang / Bandnr. / Volume8
Ausgabe / Heftnr. / Issue5
StatusVeröffentlicht
Veröffentlichungsjahr2019
Sprache, in der die Publikation verfasst istEnglisch
DOI10.3390/jcm8050587
StichwörterC/D-ratio; kidney transplantation; pharmacokinetics; tacrolimus

Autor*innen der Universität Münster

Reuter, Stefan Johannes
Medizinische Klinik D (Med D)
Schmidt, Rene
Institut für Biometrie und Klinische Forschung (IBKF)
Schütte-Nütgen, Katharina
Medizinische Klinik D (Med D)
Suwelack, Barbara Maria
Medizinische Klinik D (Med D)
Thölking, Gerold
Medizinische Klinik D (Med D)