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Metabolic Syndrome-Related Features in Controlled and Resistant Hypertensive Subjects
BACKGROUND: Metabolic syndrome (MetS) is widespread among hypertensive patients. Clinical features and potential biomarkers of MetS in the presence of hypertension and resistant hypertension (RHTN) represent a great area of interest for investigation. OBJECTIVE: The purpose of this study was to eval...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedade Brasileira de Cardiologia - SBC
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6023630/ https://www.ncbi.nlm.nih.gov/pubmed/30226908 http://dx.doi.org/10.5935/abc.20180076 |
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author | Catharina, Arthur Santa Modolo, Rodrigo Ritter, Alessandra Mileni Versuti Sabbatini, Andréa Rodrigues Lopes, Heno Ferreira Moreno Junior, Heitor de Faria, Ana Paula |
author_facet | Catharina, Arthur Santa Modolo, Rodrigo Ritter, Alessandra Mileni Versuti Sabbatini, Andréa Rodrigues Lopes, Heno Ferreira Moreno Junior, Heitor de Faria, Ana Paula |
author_sort | Catharina, Arthur Santa |
collection | PubMed |
description | BACKGROUND: Metabolic syndrome (MetS) is widespread among hypertensive patients. Clinical features and potential biomarkers of MetS in the presence of hypertension and resistant hypertension (RHTN) represent a great area of interest for investigation. OBJECTIVE: The purpose of this study was to evaluate the prevalence of MetS and the clinical features associated with it in resistant and mild to moderate hypertensives. METHODS: This cross-sectional study included 236 patients, (i) 129 mild to moderate hypertensive patients and (ii) 107 patients with RHTN. We measured blood pressure (BP) and adipokines levels, and performed bioelectrical impedance analysis. Microalbuminuria (MA), cardiac hypertrophy and arterial stiffness were also assessed. The significance level of alpha = 0.05 was adopted. RESULTS: We found a MetS prevalence of 73% in resistant and 60% in mild-to-moderate hypertensive patients. In a multiple regression analysis, MA (odds ratio = 8.51; p = 0.01), leptin/adiponectin ratio (LAR) (odds ratio = 4.13; p = 0.01) and RHTN (odds ratio = 3.75; p = 0.03) were independently associated with the presence of MetS apart from potential confounders. CONCLUSIONS: Our findings suggest that both resistant and controlled hypertensive subjects have a high prevalence of MetS. In addition, MetS-related metabolic derangements may cause early renal and hormonal changes. Finally, LAR may be useful as a reliable biomarker for identifying those hypertensive subjects who are at risk for developing MetS. |
format | Online Article Text |
id | pubmed-6023630 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Sociedade Brasileira de Cardiologia - SBC |
record_format | MEDLINE/PubMed |
spelling | pubmed-60236302018-07-06 Metabolic Syndrome-Related Features in Controlled and Resistant Hypertensive Subjects Catharina, Arthur Santa Modolo, Rodrigo Ritter, Alessandra Mileni Versuti Sabbatini, Andréa Rodrigues Lopes, Heno Ferreira Moreno Junior, Heitor de Faria, Ana Paula Arq Bras Cardiol Original Article BACKGROUND: Metabolic syndrome (MetS) is widespread among hypertensive patients. Clinical features and potential biomarkers of MetS in the presence of hypertension and resistant hypertension (RHTN) represent a great area of interest for investigation. OBJECTIVE: The purpose of this study was to evaluate the prevalence of MetS and the clinical features associated with it in resistant and mild to moderate hypertensives. METHODS: This cross-sectional study included 236 patients, (i) 129 mild to moderate hypertensive patients and (ii) 107 patients with RHTN. We measured blood pressure (BP) and adipokines levels, and performed bioelectrical impedance analysis. Microalbuminuria (MA), cardiac hypertrophy and arterial stiffness were also assessed. The significance level of alpha = 0.05 was adopted. RESULTS: We found a MetS prevalence of 73% in resistant and 60% in mild-to-moderate hypertensive patients. In a multiple regression analysis, MA (odds ratio = 8.51; p = 0.01), leptin/adiponectin ratio (LAR) (odds ratio = 4.13; p = 0.01) and RHTN (odds ratio = 3.75; p = 0.03) were independently associated with the presence of MetS apart from potential confounders. CONCLUSIONS: Our findings suggest that both resistant and controlled hypertensive subjects have a high prevalence of MetS. In addition, MetS-related metabolic derangements may cause early renal and hormonal changes. Finally, LAR may be useful as a reliable biomarker for identifying those hypertensive subjects who are at risk for developing MetS. Sociedade Brasileira de Cardiologia - SBC 2018-07 /pmc/articles/PMC6023630/ /pubmed/30226908 http://dx.doi.org/10.5935/abc.20180076 Text en http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Catharina, Arthur Santa Modolo, Rodrigo Ritter, Alessandra Mileni Versuti Sabbatini, Andréa Rodrigues Lopes, Heno Ferreira Moreno Junior, Heitor de Faria, Ana Paula Metabolic Syndrome-Related Features in Controlled and Resistant Hypertensive Subjects |
title | Metabolic Syndrome-Related Features in Controlled and Resistant
Hypertensive Subjects |
title_full | Metabolic Syndrome-Related Features in Controlled and Resistant
Hypertensive Subjects |
title_fullStr | Metabolic Syndrome-Related Features in Controlled and Resistant
Hypertensive Subjects |
title_full_unstemmed | Metabolic Syndrome-Related Features in Controlled and Resistant
Hypertensive Subjects |
title_short | Metabolic Syndrome-Related Features in Controlled and Resistant
Hypertensive Subjects |
title_sort | metabolic syndrome-related features in controlled and resistant
hypertensive subjects |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6023630/ https://www.ncbi.nlm.nih.gov/pubmed/30226908 http://dx.doi.org/10.5935/abc.20180076 |
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