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Changes in hemodynamics associated with metabolic syndrome are more pronounced in women than in men

The increase in cardiovascular risk associated with metabolic syndrome (MS) seems higher in women than in men. We examined hemodynamics during head-up tilt in 252 men and 250 women without atherosclerosis, diabetes, or antihypertensive medication, mean age 48 years, using whole-body impedance cardio...

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Autores principales: Kangas, Pauliina, Tikkakoski, Antti, Kettunen, Jarkko, Eräranta, Arttu, Huhtala, Heini, Kähönen, Mika, Sipilä, Kalle, Mustonen, Jukka, Pörsti, Ilkka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6895092/
https://www.ncbi.nlm.nih.gov/pubmed/31804574
http://dx.doi.org/10.1038/s41598-019-54926-0
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author Kangas, Pauliina
Tikkakoski, Antti
Kettunen, Jarkko
Eräranta, Arttu
Huhtala, Heini
Kähönen, Mika
Sipilä, Kalle
Mustonen, Jukka
Pörsti, Ilkka
author_facet Kangas, Pauliina
Tikkakoski, Antti
Kettunen, Jarkko
Eräranta, Arttu
Huhtala, Heini
Kähönen, Mika
Sipilä, Kalle
Mustonen, Jukka
Pörsti, Ilkka
author_sort Kangas, Pauliina
collection PubMed
description The increase in cardiovascular risk associated with metabolic syndrome (MS) seems higher in women than in men. We examined hemodynamics during head-up tilt in 252 men and 250 women without atherosclerosis, diabetes, or antihypertensive medication, mean age 48 years, using whole-body impedance cardiography and radial pulse wave analysis. MS was defined according to Alberti et al. 2009. Men and women with MS presented with corresponding elevations of systolic and diastolic blood pressure (10-14%, p ≤ 0.001) versus controls. Supine pulse wave velocity (16–17%, p < 0.001) and systemic vascular resistance (7–9%, p ≤ 0.026), and upright cardiac output (6–11%, p ≤ 0.008) were higher in both MS groups than controls. Elevation of supine aortic characteristic impedance was higher in women than in men with MS (16% vs. 8%, p = 0.026), and in contrast to men, no upright impedance reduction was observed in women. When upright, women but not men with MS showed faster return of reflected pressure wave (p = 0.036), and smaller decrease in left cardiac work (p = 0.035) versus controls. The faster upright return of reflected pressure, lower upright decrease in left cardiac work, and higher elevation of aortic characteristic impedance may contribute to the greater increase in MS-related cardiovascular risk in women than in men.
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spelling pubmed-68950922019-12-12 Changes in hemodynamics associated with metabolic syndrome are more pronounced in women than in men Kangas, Pauliina Tikkakoski, Antti Kettunen, Jarkko Eräranta, Arttu Huhtala, Heini Kähönen, Mika Sipilä, Kalle Mustonen, Jukka Pörsti, Ilkka Sci Rep Article The increase in cardiovascular risk associated with metabolic syndrome (MS) seems higher in women than in men. We examined hemodynamics during head-up tilt in 252 men and 250 women without atherosclerosis, diabetes, or antihypertensive medication, mean age 48 years, using whole-body impedance cardiography and radial pulse wave analysis. MS was defined according to Alberti et al. 2009. Men and women with MS presented with corresponding elevations of systolic and diastolic blood pressure (10-14%, p ≤ 0.001) versus controls. Supine pulse wave velocity (16–17%, p < 0.001) and systemic vascular resistance (7–9%, p ≤ 0.026), and upright cardiac output (6–11%, p ≤ 0.008) were higher in both MS groups than controls. Elevation of supine aortic characteristic impedance was higher in women than in men with MS (16% vs. 8%, p = 0.026), and in contrast to men, no upright impedance reduction was observed in women. When upright, women but not men with MS showed faster return of reflected pressure wave (p = 0.036), and smaller decrease in left cardiac work (p = 0.035) versus controls. The faster upright return of reflected pressure, lower upright decrease in left cardiac work, and higher elevation of aortic characteristic impedance may contribute to the greater increase in MS-related cardiovascular risk in women than in men. Nature Publishing Group UK 2019-12-05 /pmc/articles/PMC6895092/ /pubmed/31804574 http://dx.doi.org/10.1038/s41598-019-54926-0 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Kangas, Pauliina
Tikkakoski, Antti
Kettunen, Jarkko
Eräranta, Arttu
Huhtala, Heini
Kähönen, Mika
Sipilä, Kalle
Mustonen, Jukka
Pörsti, Ilkka
Changes in hemodynamics associated with metabolic syndrome are more pronounced in women than in men
title Changes in hemodynamics associated with metabolic syndrome are more pronounced in women than in men
title_full Changes in hemodynamics associated with metabolic syndrome are more pronounced in women than in men
title_fullStr Changes in hemodynamics associated with metabolic syndrome are more pronounced in women than in men
title_full_unstemmed Changes in hemodynamics associated with metabolic syndrome are more pronounced in women than in men
title_short Changes in hemodynamics associated with metabolic syndrome are more pronounced in women than in men
title_sort changes in hemodynamics associated with metabolic syndrome are more pronounced in women than in men
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6895092/
https://www.ncbi.nlm.nih.gov/pubmed/31804574
http://dx.doi.org/10.1038/s41598-019-54926-0
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