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The Effect of Antihypertensive Medications on Testing for Primary Aldosteronism

Primary aldosteronism (PA) is a potentially curable form of secondary hypertension caused by excessive renin-independent aldosterone secretion, leading to increased target organ damage and cardiovascular morbidity and mortality. The diagnosis of PA requires measuring renin and aldosterone to calcula...

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Autores principales: Jędrusik, Piotr, Symonides, Bartosz, Lewandowski, Jacek, Gaciong, Zbigniew
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8155700/
https://www.ncbi.nlm.nih.gov/pubmed/34054559
http://dx.doi.org/10.3389/fphar.2021.684111
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author Jędrusik, Piotr
Symonides, Bartosz
Lewandowski, Jacek
Gaciong, Zbigniew
author_facet Jędrusik, Piotr
Symonides, Bartosz
Lewandowski, Jacek
Gaciong, Zbigniew
author_sort Jędrusik, Piotr
collection PubMed
description Primary aldosteronism (PA) is a potentially curable form of secondary hypertension caused by excessive renin-independent aldosterone secretion, leading to increased target organ damage and cardiovascular morbidity and mortality. The diagnosis of PA requires measuring renin and aldosterone to calculate the aldosterone-to-renin ratio, followed by confirmatory tests to demonstrate renin-independent aldosterone secretion and/or PA subtype differentiation. Various antihypertensive drug classes interfere with the renin-angiotensin-aldosterone axis and hence evaluation for PA should ideally be performed off-drugs. This is, however, often precluded by the risks related to suboptimal control of blood pressure and serum potassium level in the evaluation period. In the present review, we summarized the evidence regarding the effect of various antihypertensive drug classes on biochemical testing for PA, and critically appraised the issue whether and which antihypertensive medications should be withdrawn or, conversely, might be continued in patients evaluated for PA. The least interfering drugs are calcium antagonists, alpha-blockers, hydralazine, and possibly moxonidine. If necessary, the testing may also be attempted during treatment with beta-blockers, angiotensin-converting enzyme inhibitors, and angiotensin receptor blockers but renin and aldosterone measurements must be interpreted in the context of known effects of these drugs on these parameters. Views are evolving on the feasibility of testing during treatment with mineralocorticoid receptor antagonists, as these drugs are now increasingly considered acceptable in specific patient subsets, particularly in those with severe hypokalemia and/or poor blood pressure control on alternative treatment.
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spelling pubmed-81557002021-05-28 The Effect of Antihypertensive Medications on Testing for Primary Aldosteronism Jędrusik, Piotr Symonides, Bartosz Lewandowski, Jacek Gaciong, Zbigniew Front Pharmacol Pharmacology Primary aldosteronism (PA) is a potentially curable form of secondary hypertension caused by excessive renin-independent aldosterone secretion, leading to increased target organ damage and cardiovascular morbidity and mortality. The diagnosis of PA requires measuring renin and aldosterone to calculate the aldosterone-to-renin ratio, followed by confirmatory tests to demonstrate renin-independent aldosterone secretion and/or PA subtype differentiation. Various antihypertensive drug classes interfere with the renin-angiotensin-aldosterone axis and hence evaluation for PA should ideally be performed off-drugs. This is, however, often precluded by the risks related to suboptimal control of blood pressure and serum potassium level in the evaluation period. In the present review, we summarized the evidence regarding the effect of various antihypertensive drug classes on biochemical testing for PA, and critically appraised the issue whether and which antihypertensive medications should be withdrawn or, conversely, might be continued in patients evaluated for PA. The least interfering drugs are calcium antagonists, alpha-blockers, hydralazine, and possibly moxonidine. If necessary, the testing may also be attempted during treatment with beta-blockers, angiotensin-converting enzyme inhibitors, and angiotensin receptor blockers but renin and aldosterone measurements must be interpreted in the context of known effects of these drugs on these parameters. Views are evolving on the feasibility of testing during treatment with mineralocorticoid receptor antagonists, as these drugs are now increasingly considered acceptable in specific patient subsets, particularly in those with severe hypokalemia and/or poor blood pressure control on alternative treatment. Frontiers Media S.A. 2021-05-13 /pmc/articles/PMC8155700/ /pubmed/34054559 http://dx.doi.org/10.3389/fphar.2021.684111 Text en Copyright © 2021 Jędrusik, Symonides, Lewandowski and Gaciong. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Jędrusik, Piotr
Symonides, Bartosz
Lewandowski, Jacek
Gaciong, Zbigniew
The Effect of Antihypertensive Medications on Testing for Primary Aldosteronism
title The Effect of Antihypertensive Medications on Testing for Primary Aldosteronism
title_full The Effect of Antihypertensive Medications on Testing for Primary Aldosteronism
title_fullStr The Effect of Antihypertensive Medications on Testing for Primary Aldosteronism
title_full_unstemmed The Effect of Antihypertensive Medications on Testing for Primary Aldosteronism
title_short The Effect of Antihypertensive Medications on Testing for Primary Aldosteronism
title_sort effect of antihypertensive medications on testing for primary aldosteronism
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8155700/
https://www.ncbi.nlm.nih.gov/pubmed/34054559
http://dx.doi.org/10.3389/fphar.2021.684111
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