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Right Ventricular Morphology and the Onset of Dyspnea: The MESA-Right Ventricle Study

BACKGROUND: The association of right ventricular (RV) structure and function with symptoms in individuals without cardiopulmonary disease is unknown. We hypothesized that greater RV mass and RV end-diastolic volume (RVEDV), smaller RV stroke volume (RVSV), and lower RV ejection fraction (RVEF) measu...

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Autores principales: Kaufmann, Michael R., Barr, R. Graham, Lima, João A. C., Praestgaard, Amy, Jain, Aditya, Tandri, Harikrishna, Bluemke, David A., Kawut, Steven M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3574101/
https://www.ncbi.nlm.nih.gov/pubmed/23457622
http://dx.doi.org/10.1371/journal.pone.0056826
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author Kaufmann, Michael R.
Barr, R. Graham
Lima, João A. C.
Praestgaard, Amy
Jain, Aditya
Tandri, Harikrishna
Bluemke, David A.
Kawut, Steven M.
author_facet Kaufmann, Michael R.
Barr, R. Graham
Lima, João A. C.
Praestgaard, Amy
Jain, Aditya
Tandri, Harikrishna
Bluemke, David A.
Kawut, Steven M.
author_sort Kaufmann, Michael R.
collection PubMed
description BACKGROUND: The association of right ventricular (RV) structure and function with symptoms in individuals without cardiopulmonary disease is unknown. We hypothesized that greater RV mass and RV end-diastolic volume (RVEDV), smaller RV stroke volume (RVSV), and lower RV ejection fraction (RVEF) measured by cardiac magnetic resonance imaging (MRI) in participants free of clinical cardiovascular disease at baseline would be associated with a greater risk of self-reported dyspnea. METHODS: The Multi-Ethnic Study of Atherosclerosis (MESA) performed cardiac MRIs on participants without clinical cardiovascular disease between 2000 and 2002. We excluded subjects who reported “prevalent” dyspnea at the first assessment (24 months). The presence of dyspnea was assessed at 24 months, 42 months, and 60 months from baseline. Cox proportional hazards models were used to examine the relationship between RV measures and incident dyspnea. RESULTS: In the final study sample (N = 2763), there were significant interactions between RV measures and sex in terms of the risk of dyspnea (p<0.05). Among men (N = 1453), lower RV mass (p = 0.003), smaller RVEDV (p<0.001), smaller RV end-systolic volume (RVESV) (p = 0.03) and decreased RVSV (p<0.001) were associated with an increased risk of developing dyspnea after adjusting for covariates. Associations remained after adjusting for left ventricular function and lung function. However, there were no significant associations between RV measures and the risk of dyspnea in women. CONCLUSIONS: Lower RV mass and smaller RV volumes were associated with an increased risk of dyspnea in men, but not in women.
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spelling pubmed-35741012013-03-01 Right Ventricular Morphology and the Onset of Dyspnea: The MESA-Right Ventricle Study Kaufmann, Michael R. Barr, R. Graham Lima, João A. C. Praestgaard, Amy Jain, Aditya Tandri, Harikrishna Bluemke, David A. Kawut, Steven M. PLoS One Research Article BACKGROUND: The association of right ventricular (RV) structure and function with symptoms in individuals without cardiopulmonary disease is unknown. We hypothesized that greater RV mass and RV end-diastolic volume (RVEDV), smaller RV stroke volume (RVSV), and lower RV ejection fraction (RVEF) measured by cardiac magnetic resonance imaging (MRI) in participants free of clinical cardiovascular disease at baseline would be associated with a greater risk of self-reported dyspnea. METHODS: The Multi-Ethnic Study of Atherosclerosis (MESA) performed cardiac MRIs on participants without clinical cardiovascular disease between 2000 and 2002. We excluded subjects who reported “prevalent” dyspnea at the first assessment (24 months). The presence of dyspnea was assessed at 24 months, 42 months, and 60 months from baseline. Cox proportional hazards models were used to examine the relationship between RV measures and incident dyspnea. RESULTS: In the final study sample (N = 2763), there were significant interactions between RV measures and sex in terms of the risk of dyspnea (p<0.05). Among men (N = 1453), lower RV mass (p = 0.003), smaller RVEDV (p<0.001), smaller RV end-systolic volume (RVESV) (p = 0.03) and decreased RVSV (p<0.001) were associated with an increased risk of developing dyspnea after adjusting for covariates. Associations remained after adjusting for left ventricular function and lung function. However, there were no significant associations between RV measures and the risk of dyspnea in women. CONCLUSIONS: Lower RV mass and smaller RV volumes were associated with an increased risk of dyspnea in men, but not in women. Public Library of Science 2013-02-15 /pmc/articles/PMC3574101/ /pubmed/23457622 http://dx.doi.org/10.1371/journal.pone.0056826 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose.
spellingShingle Research Article
Kaufmann, Michael R.
Barr, R. Graham
Lima, João A. C.
Praestgaard, Amy
Jain, Aditya
Tandri, Harikrishna
Bluemke, David A.
Kawut, Steven M.
Right Ventricular Morphology and the Onset of Dyspnea: The MESA-Right Ventricle Study
title Right Ventricular Morphology and the Onset of Dyspnea: The MESA-Right Ventricle Study
title_full Right Ventricular Morphology and the Onset of Dyspnea: The MESA-Right Ventricle Study
title_fullStr Right Ventricular Morphology and the Onset of Dyspnea: The MESA-Right Ventricle Study
title_full_unstemmed Right Ventricular Morphology and the Onset of Dyspnea: The MESA-Right Ventricle Study
title_short Right Ventricular Morphology and the Onset of Dyspnea: The MESA-Right Ventricle Study
title_sort right ventricular morphology and the onset of dyspnea: the mesa-right ventricle study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3574101/
https://www.ncbi.nlm.nih.gov/pubmed/23457622
http://dx.doi.org/10.1371/journal.pone.0056826
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