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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.
Abstract:
Little is known about the pharmacokinetics of mycophenolatic acid (MPA) in the early posttransplant period after renal transplantation. We studied the impact of peritoneal dialysis on the pharmacokinetics of MPA in 5 patients following renal transplantation (3-6 weeks after transplantation). Three patients had a glomerular filtration rate (GFR) of less than 10 ml/min, 1 patient had a GFR of 32, and 1 of 58 ml/min. Pharmacokinetics of MPA and its main metabolite mycophenolic acid glucuronide (MPAG) were studied on 2 consecutive days (12-hour intervals: with and without peritoneal dialysis). Dosing of MPA was 2 x 1 g/day. MPA and MPAG concentrations were determined by HPLC methods. After initiation of peritoneal dialysis in patients with severe renal impairment (GFR < 10 ml/min) MPA area under the concentration curve (AUC) decreased substantially (15-59%). The calculated clearance of MPA was higher (14.6 vs 8.1 ml/min/kg) on the day of peritoneal dialysis than during the dwell-free day. MPAG-AUC decreased up to 26% in these patients. In both patients with a GFR > 30 ml/min we observed an increase of MPA-AUC on the day of peritoneal dialysis and a decreased MPA clearance. MPAG-AUCs remained stable. Patients with a reduced GFR had much higher MPAG values than patients with a GFR 30 ml/l, however, we did not observe any differences for the MPA levels. We found a significant inverse correlation between GFR and MPAG-AUC (r = 0.91, p < 0.05). While MPA was found only in traces in the peritoneal ultrafiltrate, the cumulative amount of MPAG removed by peritoneal dialysis reached up to 2 g per 12 hours, representing up to 1.2 g of MPA. This is the first report describing a reduction of MPA- and MPAG-AUC during peritoneal dialysis. Further studies are needed to better understand the pharmacokinetics of mycophenolat mofetil during peritoneal dialysis.
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.