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Plasma renin activity, serum aldosterone concentration and selected organ damage indices in essential arterial hypertension

INTRODUCTION: The aim of this study was to assess the relations between plasma renin activity (PRA), serum aldosterone concentration (ALDO) and selected asymptomatic organ damage (AOD) indices in mild primary arterial hypertension (AH). MATERIAL AND METHODS: We measured PRA, ALDO, and selected AOD i...

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Autores principales: Pizoń, Tomasz, Rajzer, Marek, Wojciechowska, Wiktoria, Drożdż, Tomasz, Drożdż, Dorota, Rojek, Marta, Gruszka, Krystian, Czarnecka, Danuta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7811306/
https://www.ncbi.nlm.nih.gov/pubmed/33488850
http://dx.doi.org/10.5114/aoms.2018.73333
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author Pizoń, Tomasz
Rajzer, Marek
Wojciechowska, Wiktoria
Drożdż, Tomasz
Drożdż, Dorota
Rojek, Marta
Gruszka, Krystian
Czarnecka, Danuta
author_facet Pizoń, Tomasz
Rajzer, Marek
Wojciechowska, Wiktoria
Drożdż, Tomasz
Drożdż, Dorota
Rojek, Marta
Gruszka, Krystian
Czarnecka, Danuta
author_sort Pizoń, Tomasz
collection PubMed
description INTRODUCTION: The aim of this study was to assess the relations between plasma renin activity (PRA), serum aldosterone concentration (ALDO) and selected asymptomatic organ damage (AOD) indices in mild primary arterial hypertension (AH). MATERIAL AND METHODS: We measured PRA, ALDO, and selected AOD indices (carotid-femoral pulse wave velocity (cfPWV), central aortic pulse pressure (cPP), estimated glomerular filtration rate (eGFR)) in 122 patients with untreated AH. RESULTS: Patients with high PRA (≥ 0.65 ng/ml/h) were characterized by lower plasma sodium and aldosterone to renin ratio (ARR), higher ALDO, but a similar level of AOD indices compared to patients with low PRA. cfPWV (p = 0.04) and cPP (p = 0.019) increased with ARR, while eGFR decreased with ALDO (p = 0.008). Only eGFR was independently correlated with ALDO. In subjects with simultaneously high PRA and ARR values, we found significantly higher cfPWV (p = 0.02) and cPP (p = 0.04) and lower eGFR (p = 0.02) than in those with high PRA but low ARR values. CONCLUSIONS: Assessment of the influence of the renin-angiotensin-aldosterone system (RAAS) on AOD should include the relationship between renin and aldosterone. The PRA itself has no predictive value for AOD. More advanced arterial stiffness and renal impairment are associated with increased PRA and ARR. The RAAS activity might be useful in AOD prediction and hypertension severity assessment.
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spelling pubmed-78113062021-01-22 Plasma renin activity, serum aldosterone concentration and selected organ damage indices in essential arterial hypertension Pizoń, Tomasz Rajzer, Marek Wojciechowska, Wiktoria Drożdż, Tomasz Drożdż, Dorota Rojek, Marta Gruszka, Krystian Czarnecka, Danuta Arch Med Sci Clinical Research INTRODUCTION: The aim of this study was to assess the relations between plasma renin activity (PRA), serum aldosterone concentration (ALDO) and selected asymptomatic organ damage (AOD) indices in mild primary arterial hypertension (AH). MATERIAL AND METHODS: We measured PRA, ALDO, and selected AOD indices (carotid-femoral pulse wave velocity (cfPWV), central aortic pulse pressure (cPP), estimated glomerular filtration rate (eGFR)) in 122 patients with untreated AH. RESULTS: Patients with high PRA (≥ 0.65 ng/ml/h) were characterized by lower plasma sodium and aldosterone to renin ratio (ARR), higher ALDO, but a similar level of AOD indices compared to patients with low PRA. cfPWV (p = 0.04) and cPP (p = 0.019) increased with ARR, while eGFR decreased with ALDO (p = 0.008). Only eGFR was independently correlated with ALDO. In subjects with simultaneously high PRA and ARR values, we found significantly higher cfPWV (p = 0.02) and cPP (p = 0.04) and lower eGFR (p = 0.02) than in those with high PRA but low ARR values. CONCLUSIONS: Assessment of the influence of the renin-angiotensin-aldosterone system (RAAS) on AOD should include the relationship between renin and aldosterone. The PRA itself has no predictive value for AOD. More advanced arterial stiffness and renal impairment are associated with increased PRA and ARR. The RAAS activity might be useful in AOD prediction and hypertension severity assessment. Termedia Publishing House 2018-02-07 /pmc/articles/PMC7811306/ /pubmed/33488850 http://dx.doi.org/10.5114/aoms.2018.73333 Text en Copyright: © 2018 Termedia & Banach http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
spellingShingle Clinical Research
Pizoń, Tomasz
Rajzer, Marek
Wojciechowska, Wiktoria
Drożdż, Tomasz
Drożdż, Dorota
Rojek, Marta
Gruszka, Krystian
Czarnecka, Danuta
Plasma renin activity, serum aldosterone concentration and selected organ damage indices in essential arterial hypertension
title Plasma renin activity, serum aldosterone concentration and selected organ damage indices in essential arterial hypertension
title_full Plasma renin activity, serum aldosterone concentration and selected organ damage indices in essential arterial hypertension
title_fullStr Plasma renin activity, serum aldosterone concentration and selected organ damage indices in essential arterial hypertension
title_full_unstemmed Plasma renin activity, serum aldosterone concentration and selected organ damage indices in essential arterial hypertension
title_short Plasma renin activity, serum aldosterone concentration and selected organ damage indices in essential arterial hypertension
title_sort plasma renin activity, serum aldosterone concentration and selected organ damage indices in essential arterial hypertension
topic Clinical Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7811306/
https://www.ncbi.nlm.nih.gov/pubmed/33488850
http://dx.doi.org/10.5114/aoms.2018.73333
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