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Aldosterone breakthrough does not alter central hemodynamics

INTRODUCTION: Angiotensin-converting enzyme inhibitors and angiotensin receptor blockers are widely used in congestive heart failure and chronic kidney disease, but up to 40% of patients will experience aldosterone breakthrough, with aldosterone levels rising above pre-treatment levels after 6–12 mo...

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Autores principales: Beenken, Andrew, Bomback, Andrew S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5843861/
https://www.ncbi.nlm.nih.gov/pubmed/28992758
http://dx.doi.org/10.1177/1470320317735002
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author Beenken, Andrew
Bomback, Andrew S.
author_facet Beenken, Andrew
Bomback, Andrew S.
author_sort Beenken, Andrew
collection PubMed
description INTRODUCTION: Angiotensin-converting enzyme inhibitors and angiotensin receptor blockers are widely used in congestive heart failure and chronic kidney disease, but up to 40% of patients will experience aldosterone breakthrough, with aldosterone levels rising above pre-treatment levels after 6–12 months of renin-angiotensin-aldosterone system blockade. Aldosterone breakthrough has been associated with worsening congestive heart failure and chronic kidney disease, yet the pathophysiology remains unclear. Breakthrough has not been associated with elevated peripheral blood pressure, but no studies have assessed its effect on central blood pressure. METHODS: Nineteen subjects with well-controlled peripheral blood pressure on stable doses of angiotensin-converting enzyme inhibitor/angiotensin receptor blocker had aldosterone levels checked and central blood pressure parameters measured using the SphygmoCor system. The central blood pressure parameters of subjects with or without breakthrough, defined as serum aldosterone >15 ng/dl, were compared. RESULTS: Of the 19 subjects, six had breakthrough with a mean aldosterone level of 33.8 ng/dl, and 13 were without breakthrough with a mean level of 7.1 ng/dl. There was no significant difference between the two groups in any central blood pressure parameter. CONCLUSIONS: We found no correlation between aldosterone breakthrough and central blood pressure. The clinical impact of aldosterone breakthrough likely depends on its non-genomic, pro-fibrotic, pro-inflammatory effects rather than its regulation of extracellular volume.
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spelling pubmed-58438612018-03-20 Aldosterone breakthrough does not alter central hemodynamics Beenken, Andrew Bomback, Andrew S. J Renin Angiotensin Aldosterone Syst Original Article INTRODUCTION: Angiotensin-converting enzyme inhibitors and angiotensin receptor blockers are widely used in congestive heart failure and chronic kidney disease, but up to 40% of patients will experience aldosterone breakthrough, with aldosterone levels rising above pre-treatment levels after 6–12 months of renin-angiotensin-aldosterone system blockade. Aldosterone breakthrough has been associated with worsening congestive heart failure and chronic kidney disease, yet the pathophysiology remains unclear. Breakthrough has not been associated with elevated peripheral blood pressure, but no studies have assessed its effect on central blood pressure. METHODS: Nineteen subjects with well-controlled peripheral blood pressure on stable doses of angiotensin-converting enzyme inhibitor/angiotensin receptor blocker had aldosterone levels checked and central blood pressure parameters measured using the SphygmoCor system. The central blood pressure parameters of subjects with or without breakthrough, defined as serum aldosterone >15 ng/dl, were compared. RESULTS: Of the 19 subjects, six had breakthrough with a mean aldosterone level of 33.8 ng/dl, and 13 were without breakthrough with a mean level of 7.1 ng/dl. There was no significant difference between the two groups in any central blood pressure parameter. CONCLUSIONS: We found no correlation between aldosterone breakthrough and central blood pressure. The clinical impact of aldosterone breakthrough likely depends on its non-genomic, pro-fibrotic, pro-inflammatory effects rather than its regulation of extracellular volume. SAGE Publications 2017-10-09 /pmc/articles/PMC5843861/ /pubmed/28992758 http://dx.doi.org/10.1177/1470320317735002 Text en © The Author(s) 2017 http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page(https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Article
Beenken, Andrew
Bomback, Andrew S.
Aldosterone breakthrough does not alter central hemodynamics
title Aldosterone breakthrough does not alter central hemodynamics
title_full Aldosterone breakthrough does not alter central hemodynamics
title_fullStr Aldosterone breakthrough does not alter central hemodynamics
title_full_unstemmed Aldosterone breakthrough does not alter central hemodynamics
title_short Aldosterone breakthrough does not alter central hemodynamics
title_sort aldosterone breakthrough does not alter central hemodynamics
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5843861/
https://www.ncbi.nlm.nih.gov/pubmed/28992758
http://dx.doi.org/10.1177/1470320317735002
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