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Use of Proton Pump Inhibitors Does Not Increase the Risk of Acute Rejection after Renal Transplantation, The

G. van Boekel, C. Kerkhofs, F. van de Logt, L. Hilbrands

Nephrology, Radboud University Nijmegen Medical Centre, Nijmegen, Netherlands

Meeting: 2013 American Transplant Congress

Abstract number: D1586

Background: Mycophenolate mofetil (MMF), is the pro-drug of mycophenolic acid (MPA), which is formed after de-esterification. Adequate exposure to MPA is associated with a decreased rate of acute rejection after renal transplantation. Several studies indicate that concomitant use of proton pump inhibitors (PPI) might impair the exposure to MPA due to incomplete de-esterification of MMF at elevated gastric pH. This could result in an increased risk of acute rejection. In our centre, renal transplant patients are prophylactically treated with a PPI (pantoprazole) or an H2 antagonists (ranitidine) for at least three months after renal transplantation.

Aim: To investigate whether MMF-treated renal transplant patients who concomitantly used pantoprazole, had a higher risk of acute rejection within the first 3 months after transplantation than those who used ranitidine.

Patients and methods: We performed a retrospective study in adult patients, who underwent a kidney transplantation between January 2007 and December 2011. Their immunosuppressive therapy consisted of steroids, tacrolimus and MMF. Exclusion criteria were a history of bowel surgery, the use of a phosphate binder, the switch between PPI and H2 antagonist, and the combined use of PPI and H2 antagonist.

Results: 207 patients were included: 126 with pantoprazole and 81 with ranitidine. Both groups were comparable regarding age, body weight, dose of prednisone and tacrolimus, retransplantations, and donor type. In the first 3 months after transplantation, the cumulative dose of MMF was 142,894±17,718 mg in patients with pantoprazole and 144,289±18,097 mg in patients with ranitidine (NS). The number of patients with a clinical diagnosis of acute rejection within three months after transplantation did not differ between both groups: 26 (19.5%) in the pantoprazole group versus 15 (20,0%) in the ranitidine group. There was also no difference in the number of patients with biopsy-proven acute rejection (13 [10,0%] versus 7 [9,1%]). Logistic regression analysis did not reveal a correlation between the cumulative dose of pantoprazole and the risk of acute rejection. Three months after renal transplantation, the mean estimated glomerular filtration rate did not differ significantly: 49.4±12.5 ml/min/1.73m2 versus 50.7±12.5 ml/min/1.73m2, respectively.

Conclusions: There was no evidence for an increased incidence of acute rejection in patients who concomitantly use MMF and pantoprazole.

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To cite this abstract in AMA style:

Boekel Gvan, Kerkhofs C, Logt Fvande, Hilbrands L. Use of Proton Pump Inhibitors Does Not Increase the Risk of Acute Rejection after Renal Transplantation, The [abstract]. Am J Transplant. 2013; 13 (suppl 5). https://atcmeetingabstracts.com/abstract/use-of-proton-pump-inhibitors-does-not-increase-the-risk-of-acute-rejection-after-renal-transplantation-the/. Accessed May 10, 2025.

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