Literature DB >> 19761733

Aliskiren corrects recurrent hyperreninemia and hyperaldosteronism in autosomal dominant polycystic kidney disease.

P Amico1, S Kalbermatter, D Kiss.   

Abstract

A 47-year-old woman with family history of autosomal-dominant polycystic kidney disease (ADPKD), who underwent living-donor kidney transplantation in 2000, presented with recurrent edema, hyperreninemia, and hyperaldosteronism. Since 2002, her antihypertensive therapy comprised ramipril and spironolactone. The post-transplantation kidney function was stable. Based on the clinical picture and reports of renin secretion by renal cysts in ADPKD, we performed a trial of aliskiren therapy (300 mg/day). The patient showed excellent blood pressure control and reduction of edema, with aldosterone levels normalizing within 2 months. This is a novel report of aliskiren therapy for treatment of edema, hyperreninemia, and hyperaldosteronism in ADPKD.

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Year:  2009        PMID: 19761733     DOI: 10.5414/cnp72237

Source DB:  PubMed          Journal:  Clin Nephrol        ISSN: 0301-0430            Impact factor:   0.975


  3 in total

Review 1.  Novel targets for the treatment of autosomal dominant polycystic kidney disease.

Authors:  Franck A Belibi; Charles L Edelstein
Journal:  Expert Opin Investig Drugs       Date:  2010-03       Impact factor: 6.206

Review 2.  Hypertension in autosomal-dominant polycystic kidney disease (ADPKD).

Authors:  Laia Sans-Atxer; Roser Torra; Patricia Fernández-Llama
Journal:  Clin Kidney J       Date:  2013-04-24

3.  Hypokalemic Hypertension Leading to a Diagnosis of Autosomal Dominant Polycystic Kidney Disease.

Authors:  Wasawat Vutthikraivit; Montira Assanatham; Chutintorn Sriphrapradang
Journal:  Electrolyte Blood Press       Date:  2016-06-30
  3 in total

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