Cargando…
Sex Dimorphism in the Myocardial Response to Aortic Stenosis
OBJECTIVES: The goal of this study was to explore sex differences in myocardial remodeling in aortic stenosis (AS) by using echocardiography, cardiac magnetic resonance (CMR), and biomarkers. BACKGROUND: AS is a disease of both valve and left ventricle (LV). Sex differences in LV remodeling are repo...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6278887/ https://www.ncbi.nlm.nih.gov/pubmed/29153564 http://dx.doi.org/10.1016/j.jcmg.2017.08.025 |
_version_ | 1783378447927607296 |
---|---|
author | Treibel, Thomas A. Kozor, Rebecca Fontana, Marianna Torlasco, Camilla Reant, Patricia Badiani, Sveeta Espinoza, Maria Yap, John Diez, Javier Hughes, Alun D. Lloyd, Guy Moon, James C. |
author_facet | Treibel, Thomas A. Kozor, Rebecca Fontana, Marianna Torlasco, Camilla Reant, Patricia Badiani, Sveeta Espinoza, Maria Yap, John Diez, Javier Hughes, Alun D. Lloyd, Guy Moon, James C. |
author_sort | Treibel, Thomas A. |
collection | PubMed |
description | OBJECTIVES: The goal of this study was to explore sex differences in myocardial remodeling in aortic stenosis (AS) by using echocardiography, cardiac magnetic resonance (CMR), and biomarkers. BACKGROUND: AS is a disease of both valve and left ventricle (LV). Sex differences in LV remodeling are reported in AS and may play a role in disease phenotyping. METHODS: This study was a prospective assessment of patients awaiting surgical valve replacement for severe AS using echocardiography, the 6-min walking test, biomarkers (high-sensitivity troponin T and N-terminal pro–brain natriuretic peptide), and CMR with late gadolinium enhancement and extracellular volume fraction, which dichotomizes the myocardium into matrix and cell volumes. LV remodeling was categorized into normal geometry, concentric remodeling, concentric hypertrophy, and eccentric hypertrophy. RESULTS: In 168 patients (age 70 ± 10 years, 55% male, indexed aortic valve area 0.40 ± 0.13 cm(2)/m(2), mean gradient 47 ± 4 mm Hg), no sex or age differences in AS severity or functional capacity (6-min walking test) were found. CMR captured sex dimorphism in LV remodeling not apparent by using 2-dimensional echocardiography. Normal geometry (82% female) and concentric remodeling (60% female) dominated in women; concentric hypertrophy (71% male) and eccentric hypertrophy (76% male) dominated in men. Men also had more evidence of LV decompensation (pleural effusions), lower left ventricular ejection fraction (67 ± 16% vs. 74 ± 13%; p < 0.001), and higher levels of N-terminal pro–brain natriuretic peptide (p = 0.04) and high-sensitivity troponin T (p = 0.01). Myocardial fibrosis was higher in men, with higher focal fibrosis (late gadolinium enhancement 16.5 ± 11.2 g vs. 10.5 ± 8.9 g; p < 0.001) and extracellular expansion (matrix volume 28.5 ± 8.8 ml/m(2) vs. 21.4 ± 6.3 ml/m(2); p < 0.001). CONCLUSIONS: CMR revealed sex differences in associations between AS and myocardial remodeling not evident from echocardiography. Given equal valve severity, the myocardial response to AS seems more maladaptive in men than previously reported. (Regression of Myocardial Fibrosis After Aortic Valve Replacement [RELIEF-AS]; NCT02174471) |
format | Online Article Text |
id | pubmed-6278887 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-62788872018-12-13 Sex Dimorphism in the Myocardial Response to Aortic Stenosis Treibel, Thomas A. Kozor, Rebecca Fontana, Marianna Torlasco, Camilla Reant, Patricia Badiani, Sveeta Espinoza, Maria Yap, John Diez, Javier Hughes, Alun D. Lloyd, Guy Moon, James C. JACC Cardiovasc Imaging Article OBJECTIVES: The goal of this study was to explore sex differences in myocardial remodeling in aortic stenosis (AS) by using echocardiography, cardiac magnetic resonance (CMR), and biomarkers. BACKGROUND: AS is a disease of both valve and left ventricle (LV). Sex differences in LV remodeling are reported in AS and may play a role in disease phenotyping. METHODS: This study was a prospective assessment of patients awaiting surgical valve replacement for severe AS using echocardiography, the 6-min walking test, biomarkers (high-sensitivity troponin T and N-terminal pro–brain natriuretic peptide), and CMR with late gadolinium enhancement and extracellular volume fraction, which dichotomizes the myocardium into matrix and cell volumes. LV remodeling was categorized into normal geometry, concentric remodeling, concentric hypertrophy, and eccentric hypertrophy. RESULTS: In 168 patients (age 70 ± 10 years, 55% male, indexed aortic valve area 0.40 ± 0.13 cm(2)/m(2), mean gradient 47 ± 4 mm Hg), no sex or age differences in AS severity or functional capacity (6-min walking test) were found. CMR captured sex dimorphism in LV remodeling not apparent by using 2-dimensional echocardiography. Normal geometry (82% female) and concentric remodeling (60% female) dominated in women; concentric hypertrophy (71% male) and eccentric hypertrophy (76% male) dominated in men. Men also had more evidence of LV decompensation (pleural effusions), lower left ventricular ejection fraction (67 ± 16% vs. 74 ± 13%; p < 0.001), and higher levels of N-terminal pro–brain natriuretic peptide (p = 0.04) and high-sensitivity troponin T (p = 0.01). Myocardial fibrosis was higher in men, with higher focal fibrosis (late gadolinium enhancement 16.5 ± 11.2 g vs. 10.5 ± 8.9 g; p < 0.001) and extracellular expansion (matrix volume 28.5 ± 8.8 ml/m(2) vs. 21.4 ± 6.3 ml/m(2); p < 0.001). CONCLUSIONS: CMR revealed sex differences in associations between AS and myocardial remodeling not evident from echocardiography. Given equal valve severity, the myocardial response to AS seems more maladaptive in men than previously reported. (Regression of Myocardial Fibrosis After Aortic Valve Replacement [RELIEF-AS]; NCT02174471) Elsevier 2018-07 /pmc/articles/PMC6278887/ /pubmed/29153564 http://dx.doi.org/10.1016/j.jcmg.2017.08.025 Text en © 2018 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Treibel, Thomas A. Kozor, Rebecca Fontana, Marianna Torlasco, Camilla Reant, Patricia Badiani, Sveeta Espinoza, Maria Yap, John Diez, Javier Hughes, Alun D. Lloyd, Guy Moon, James C. Sex Dimorphism in the Myocardial Response to Aortic Stenosis |
title | Sex Dimorphism in the Myocardial Response to Aortic
Stenosis |
title_full | Sex Dimorphism in the Myocardial Response to Aortic
Stenosis |
title_fullStr | Sex Dimorphism in the Myocardial Response to Aortic
Stenosis |
title_full_unstemmed | Sex Dimorphism in the Myocardial Response to Aortic
Stenosis |
title_short | Sex Dimorphism in the Myocardial Response to Aortic
Stenosis |
title_sort | sex dimorphism in the myocardial response to aortic
stenosis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6278887/ https://www.ncbi.nlm.nih.gov/pubmed/29153564 http://dx.doi.org/10.1016/j.jcmg.2017.08.025 |
work_keys_str_mv | AT treibelthomasa sexdimorphisminthemyocardialresponsetoaorticstenosis AT kozorrebecca sexdimorphisminthemyocardialresponsetoaorticstenosis AT fontanamarianna sexdimorphisminthemyocardialresponsetoaorticstenosis AT torlascocamilla sexdimorphisminthemyocardialresponsetoaorticstenosis AT reantpatricia sexdimorphisminthemyocardialresponsetoaorticstenosis AT badianisveeta sexdimorphisminthemyocardialresponsetoaorticstenosis AT espinozamaria sexdimorphisminthemyocardialresponsetoaorticstenosis AT yapjohn sexdimorphisminthemyocardialresponsetoaorticstenosis AT diezjavier sexdimorphisminthemyocardialresponsetoaorticstenosis AT hughesalund sexdimorphisminthemyocardialresponsetoaorticstenosis AT lloydguy sexdimorphisminthemyocardialresponsetoaorticstenosis AT moonjamesc sexdimorphisminthemyocardialresponsetoaorticstenosis |