Author:
Tylicki Leszek,Debska-Slizien Alicja M.,Lizakowski Slawomir,Przybylska Milena,Heleniak Zbigniew,Renke Marcin,Chamienia Andrzej L.,Biedunkiewicz Bogdan,Rutkowski Przemyslaw,Małgorzewicz Sylwia,Rutkowski Boleslaw
Abstract
Background: The renoprotective effects of agents inhibiting the renin-angiotensin system in renal transplant recipients have been supposed but not finally proven. We performed a double-blind, placebo and losartan controlled, cross-over study to evaluate the influence of aliskiren, direct renin inhibitor on albuminuria and other surrogate markers of kidney injury in patients after renal transplantation. The safety of this therapy was also evaluated. Method: 16 of 18 patients (12M, 4F), 48.3 ± 9.0 years, 57.7 ± 9.1 months after kidney transplantation, with hypertension and stable serum creatinine 1.4±0.08 without proteinuria, completed the protocol. Each patient underwent two 8-week treatment periods (one with aliskiren 150 mg and one with losartan 50 mg) in random order, allowing an 8-week placebo washout between them. Results: Aliskiren decreased 24h systolic and 24h diastolic blood pressure as compared to placebo (post hoc: p=0.009 and p=0.003). Aliskiren decreased albuminuria more effectively than placebo as well (post hoc: p=0.032). There were no differences between aliskiren and losartan in these regards. The influence of aliskiren on N-acetyl-β-D-glucosaminidase, transforming growth factor β-1 and 15-F2t-isoprostanes urine excretions was not significant. Serum potassium, creatinine, eGFR and trough blood cyclosporine or tacrolimus level were unaffected. A significant but not clinically relevant decrease in haemoglobin level after aliskiren was observed. Conclusion: Aliskiren decreases albuminuria in renal transplant recipients with clinically minimal side effects.
Publisher
Polskie Towarzystwo Biochemiczne (Polish Biochemical Society)
Subject
General Biochemistry, Genetics and Molecular Biology
Cited by
5 articles.
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