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Pharmacokinetics of mycophenolate mofetil in renal transplant recipients on peritoneal dialysis

S Morgera1, H H Neumayer, L Fritsche

  • 1Department of Internal Medicine, Nephrology, Charité, Berlin, Germany.

Insights

Peritoneal dialysis significantly impacts mycophenolic acid (MPA) pharmacokinetics in renal transplant patients. Dialysis reduced MPA and its metabolite mycophenolic acid glucuronide (MPAG) levels in patients with severe kidney impairment.

Area of Science:

  • Nephrology
  • Pharmacology
  • Transplantation Medicine

Background:

  • Pharmacokinetics of mycophenolic acid (MPA) in early post-renal transplant period are not well understood.
  • Impact of renal impairment on MPA pharmacokinetics requires further investigation.

Purpose of the Study:

  • To investigate the effect of peritoneal dialysis on the pharmacokinetics of MPA and its primary metabolite, mycophenolic acid glucuronide (MPAG).
  • To assess MPA and MPAG pharmacokinetics in renal transplant recipients with varying degrees of renal function.

Main Methods:

  • Studied 5 renal transplant patients (3-6 weeks post-transplant) with varying GFRs ( < 10, 32, 58 ml/min).
  • Monitored MPA and MPAG concentrations via HPLC over two consecutive days, with and without peritoneal dialysis (12-hour intervals).
  • MPA dosing was 2 x 1 g/day.

Main Results:

  • Peritoneal dialysis significantly decreased MPA area under the concentration curve (AUC) by 15-59% in patients with GFR < 10 ml/min.
  • MPA clearance increased during peritoneal dialysis in patients with severe renal impairment (14.6 vs 8.1 ml/min/kg).
  • MPAG-AUC decreased up to 26% in patients with severe renal impairment, with significant inverse correlation between GFR and MPAG-AUC (r = 0.91, p < 0.05).
  • MPA-AUC increased and MPA clearance decreased in patients with GFR > 30 ml/min during peritoneal dialysis.
  • MPAG was significantly removed by peritoneal dialysis (up to 2g per 12 hours).

Conclusions:

  • Peritoneal dialysis can alter MPA and MPAG pharmacokinetics, particularly in patients with severe renal impairment.
  • MPAG is effectively removed by peritoneal dialysis, suggesting a role in MPA disposition.
  • Further research is necessary to elucidate the complex pharmacokinetics of mycophenolate mofetil during peritoneal dialysis.

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