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Cardiovascular risk in primary aldosteronism: A systematic review and meta-analysis

AIM: This study aimed to evaluate whether the increased cardiovascular risk and the incidence of cerebrovascular (CCV) events in hypertensive patients were related to primary aldosteronism (PA). METHODS: The PubMed, EmBase, and the Cochrane Central Register of Controlled Trials were searched to eval...

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Autores principales: Wu, Xueyi, Yu, Jie, Tian, Haoming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6617487/
https://www.ncbi.nlm.nih.gov/pubmed/31261504
http://dx.doi.org/10.1097/MD.0000000000015985
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author Wu, Xueyi
Yu, Jie
Tian, Haoming
author_facet Wu, Xueyi
Yu, Jie
Tian, Haoming
author_sort Wu, Xueyi
collection PubMed
description AIM: This study aimed to evaluate whether the increased cardiovascular risk and the incidence of cerebrovascular (CCV) events in hypertensive patients were related to primary aldosteronism (PA). METHODS: The PubMed, EmBase, and the Cochrane Central Register of Controlled Trials were searched to evaluate the risk of CCV in PA patients and compared to essential hypertension (EH) patients. The mean differences (MD) and the risk ratios (RR) were calculated to assess the risk of main outcomes, such as stroke, coronary artery disease, left ventricular hypertrophy (LVH), levels of systolic blood pressure (SBP), diastolic blood pressure (DBP), blood glucose, and urinary potassium. RESULTS: We identified 31 individual studies including 4546 patients in PA group and 52,284 patients in EH group. Our results revealed that PA was significantly associated with increased risk of stroke (RR=2.03, 95% CI = 1.71–2.39, P(heterogeneity) = .331, I(2) = 12.7%), coronary artery disease (RR = 1.67, 95% CI = 1.23–2.25, P(heterogeneity) = .043, I(2) = 48.3%), and LVH (RR = 1.54, 95% CI = 1.29–1.83, P(heterogeneity) = .004, I(2) = 62.6%) when compared with those in the EH group. Moreover, PA group had significantly increased levels of SBP (WMD = 4.14, 95% CI = 2.60–5.68, P(heterogeneity) < .001, I(2) = 84.3%), DBP (WMD = 2.65, 95% CI = 1.83–3.47, P(heterogeneity) < .001, I(2) = 77.7%), and urinary potassium (SMD = 0.04, 95% CI = -0.03–0.11, P(heterogeneity) = .827, I(2) = 0%) when compared to EH group. However, no significant difference was observed in the levels of blood glucose between the groups. CONCLUSIONS: These findings suggested that PA significantly increased the risk of cardiac and cerebrovascular complications. In addition, patients with PA might benefit from a periodic assessment of CCV risk.
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spelling pubmed-66174872019-07-22 Cardiovascular risk in primary aldosteronism: A systematic review and meta-analysis Wu, Xueyi Yu, Jie Tian, Haoming Medicine (Baltimore) Research Article AIM: This study aimed to evaluate whether the increased cardiovascular risk and the incidence of cerebrovascular (CCV) events in hypertensive patients were related to primary aldosteronism (PA). METHODS: The PubMed, EmBase, and the Cochrane Central Register of Controlled Trials were searched to evaluate the risk of CCV in PA patients and compared to essential hypertension (EH) patients. The mean differences (MD) and the risk ratios (RR) were calculated to assess the risk of main outcomes, such as stroke, coronary artery disease, left ventricular hypertrophy (LVH), levels of systolic blood pressure (SBP), diastolic blood pressure (DBP), blood glucose, and urinary potassium. RESULTS: We identified 31 individual studies including 4546 patients in PA group and 52,284 patients in EH group. Our results revealed that PA was significantly associated with increased risk of stroke (RR=2.03, 95% CI = 1.71–2.39, P(heterogeneity) = .331, I(2) = 12.7%), coronary artery disease (RR = 1.67, 95% CI = 1.23–2.25, P(heterogeneity) = .043, I(2) = 48.3%), and LVH (RR = 1.54, 95% CI = 1.29–1.83, P(heterogeneity) = .004, I(2) = 62.6%) when compared with those in the EH group. Moreover, PA group had significantly increased levels of SBP (WMD = 4.14, 95% CI = 2.60–5.68, P(heterogeneity) < .001, I(2) = 84.3%), DBP (WMD = 2.65, 95% CI = 1.83–3.47, P(heterogeneity) < .001, I(2) = 77.7%), and urinary potassium (SMD = 0.04, 95% CI = -0.03–0.11, P(heterogeneity) = .827, I(2) = 0%) when compared to EH group. However, no significant difference was observed in the levels of blood glucose between the groups. CONCLUSIONS: These findings suggested that PA significantly increased the risk of cardiac and cerebrovascular complications. In addition, patients with PA might benefit from a periodic assessment of CCV risk. Wolters Kluwer Health 2019-06-28 /pmc/articles/PMC6617487/ /pubmed/31261504 http://dx.doi.org/10.1097/MD.0000000000015985 Text en Copyright © 2019 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0
spellingShingle Research Article
Wu, Xueyi
Yu, Jie
Tian, Haoming
Cardiovascular risk in primary aldosteronism: A systematic review and meta-analysis
title Cardiovascular risk in primary aldosteronism: A systematic review and meta-analysis
title_full Cardiovascular risk in primary aldosteronism: A systematic review and meta-analysis
title_fullStr Cardiovascular risk in primary aldosteronism: A systematic review and meta-analysis
title_full_unstemmed Cardiovascular risk in primary aldosteronism: A systematic review and meta-analysis
title_short Cardiovascular risk in primary aldosteronism: A systematic review and meta-analysis
title_sort cardiovascular risk in primary aldosteronism: a systematic review and meta-analysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6617487/
https://www.ncbi.nlm.nih.gov/pubmed/31261504
http://dx.doi.org/10.1097/MD.0000000000015985
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