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Erschienen in: International Urology and Nephrology 2/2016

01.02.2016 | Nephrology - Review

Direct inhibition of plasmatic renin activity with aliskiren: a promising but under-investigated therapeutic option for non-diabetic glomerulonephritis

verfasst von: Mariadelina Simeoni, Ramona Nicotera, Maria Colao, Maria Lucia Citraro, Elena Pelagi, Annamaria Cerantonio, Nicola Comi, Giuseppe Coppolino, Giorgio Fuiano

Erschienen in: International Urology and Nephrology | Ausgabe 2/2016

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Abstract

Non-diabetic glomerulonephritis is a frequent cause of end-stage renal disease. The use of renin–angiotensin–aldosterone system blockers is a fundamental therapeutic approach. However, converting enzyme inhibitors (ACE-is) and angiotensin receptor blockers do not always achieve the desired target of proteinuria. The induction of the prorenin and renin up-regulation is a possible explanation. Aliskiren is the first drug acting as direct inhibitor of plasmatic renin activity, also able to interfere with the prorenin and renin profibrotic escape. We aimed at reviewing the literature for the assessment of potential efficacy and safety of aliskiren in the treatment of non-diabetic glomerulonephritis. The data on this topic are limited; however, we concluded for a possible usefulness of aliskiren. The renal safety profile appears potentially acceptable in non-diabetic patients although extreme carefulness, particularly with respect to long-term renal and cardiovascular tolerability, is recommended.
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Metadaten
Titel
Direct inhibition of plasmatic renin activity with aliskiren: a promising but under-investigated therapeutic option for non-diabetic glomerulonephritis
verfasst von
Mariadelina Simeoni
Ramona Nicotera
Maria Colao
Maria Lucia Citraro
Elena Pelagi
Annamaria Cerantonio
Nicola Comi
Giuseppe Coppolino
Giorgio Fuiano
Publikationsdatum
01.02.2016
Verlag
Springer Netherlands
Erschienen in
International Urology and Nephrology / Ausgabe 2/2016
Print ISSN: 0301-1623
Elektronische ISSN: 1573-2584
DOI
https://doi.org/10.1007/s11255-015-1128-4

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