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Reverse Myocardial Remodeling Following Valve Replacement in Patients With Aortic Stenosis

BACKGROUND: Left ventricular (LV) hypertrophy, a key process in human cardiac disease, results from cellular (hypertrophy) and extracellular matrix expansion (interstitial fibrosis). OBJECTIVES: This study sought to investigate whether human myocardial interstitial fibrosis in aortic stenosis (AS) i...

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Autores principales: Treibel, Thomas A., Kozor, Rebecca, Schofield, Rebecca, Benedetti, Giulia, Fontana, Marianna, Bhuva, Anish N., Sheikh, Amir, López, Begoña, González, Arantxa, Manisty, Charlotte, Lloyd, Guy, Kellman, Peter, Díez, Javier, Moon, James C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Biomedical 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5821681/
https://www.ncbi.nlm.nih.gov/pubmed/29471937
http://dx.doi.org/10.1016/j.jacc.2017.12.035
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author Treibel, Thomas A.
Kozor, Rebecca
Schofield, Rebecca
Benedetti, Giulia
Fontana, Marianna
Bhuva, Anish N.
Sheikh, Amir
López, Begoña
González, Arantxa
Manisty, Charlotte
Lloyd, Guy
Kellman, Peter
Díez, Javier
Moon, James C.
author_facet Treibel, Thomas A.
Kozor, Rebecca
Schofield, Rebecca
Benedetti, Giulia
Fontana, Marianna
Bhuva, Anish N.
Sheikh, Amir
López, Begoña
González, Arantxa
Manisty, Charlotte
Lloyd, Guy
Kellman, Peter
Díez, Javier
Moon, James C.
author_sort Treibel, Thomas A.
collection PubMed
description BACKGROUND: Left ventricular (LV) hypertrophy, a key process in human cardiac disease, results from cellular (hypertrophy) and extracellular matrix expansion (interstitial fibrosis). OBJECTIVES: This study sought to investigate whether human myocardial interstitial fibrosis in aortic stenosis (AS) is plastic and can regress. METHODS: Patients with symptomatic, severe AS (n = 181; aortic valve area index 0.4 ± 0.1 cm(2)/m(2)) were assessed pre–aortic valve replacement (AVR) by echocardiography (AS severity, diastology), cardiovascular magnetic resonance (CMR) (for volumes, function, and focal or diffuse fibrosis), biomarkers (N-terminal pro–B-type natriuretic peptide and high-sensitivity troponin T), and the 6-min walk test. CMR was used to measure the extracellular volume fraction (ECV), thereby deriving matrix volume (LV mass × ECV) and cell volume (LV mass × [1 − ECV]). Biopsy excluded occult bystander disease. Assessment was repeated at 1 year post-AVR. RESULTS: At 1 year post-AVR in 116 pacemaker-free survivors (age 70 ± 10 years; 54% male), mean valve gradient had improved (48 ± 16 mm Hg to 12 ± 6 mm Hg; p < 0.001), and indexed LV mass had regressed by 19% (88 ± 26 g/m(2) to 71 ± 19 g/m(2); p < 0.001). Focal fibrosis by CMR late gadolinium enhancement did not change, but ECV increased (28.2 ± 2.9% to 29.9 ± 4.0%; p < 0.001): this was the result of a 16% reduction in matrix volume (25 ± 9 ml/m(2) to 21 ± 7 ml/m(2); p < 0.001) but a proportionally greater 22% reduction in cell volume (64 ± 18 ml/m(2) to 50 ± 13 ml/m(2); p < 0.001). These changes were accompanied by improvement in diastolic function, N-terminal pro–B-type natriuretic peptide, 6-min walk test results, and New York Heart Association functional class. CONCLUSIONS: Post-AVR, focal fibrosis does not resolve, but diffuse fibrosis and myocardial cellular hypertrophy regress. Regression is accompanied by structural and functional improvements suggesting that human diffuse fibrosis is plastic, measurable by CMR and a potential therapeutic target. (Regression of Myocardial Fibrosis After Aortic Valve Replacement; NCT02174471)
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spelling pubmed-58216812018-02-27 Reverse Myocardial Remodeling Following Valve Replacement in Patients With Aortic Stenosis Treibel, Thomas A. Kozor, Rebecca Schofield, Rebecca Benedetti, Giulia Fontana, Marianna Bhuva, Anish N. Sheikh, Amir López, Begoña González, Arantxa Manisty, Charlotte Lloyd, Guy Kellman, Peter Díez, Javier Moon, James C. J Am Coll Cardiol Article BACKGROUND: Left ventricular (LV) hypertrophy, a key process in human cardiac disease, results from cellular (hypertrophy) and extracellular matrix expansion (interstitial fibrosis). OBJECTIVES: This study sought to investigate whether human myocardial interstitial fibrosis in aortic stenosis (AS) is plastic and can regress. METHODS: Patients with symptomatic, severe AS (n = 181; aortic valve area index 0.4 ± 0.1 cm(2)/m(2)) were assessed pre–aortic valve replacement (AVR) by echocardiography (AS severity, diastology), cardiovascular magnetic resonance (CMR) (for volumes, function, and focal or diffuse fibrosis), biomarkers (N-terminal pro–B-type natriuretic peptide and high-sensitivity troponin T), and the 6-min walk test. CMR was used to measure the extracellular volume fraction (ECV), thereby deriving matrix volume (LV mass × ECV) and cell volume (LV mass × [1 − ECV]). Biopsy excluded occult bystander disease. Assessment was repeated at 1 year post-AVR. RESULTS: At 1 year post-AVR in 116 pacemaker-free survivors (age 70 ± 10 years; 54% male), mean valve gradient had improved (48 ± 16 mm Hg to 12 ± 6 mm Hg; p < 0.001), and indexed LV mass had regressed by 19% (88 ± 26 g/m(2) to 71 ± 19 g/m(2); p < 0.001). Focal fibrosis by CMR late gadolinium enhancement did not change, but ECV increased (28.2 ± 2.9% to 29.9 ± 4.0%; p < 0.001): this was the result of a 16% reduction in matrix volume (25 ± 9 ml/m(2) to 21 ± 7 ml/m(2); p < 0.001) but a proportionally greater 22% reduction in cell volume (64 ± 18 ml/m(2) to 50 ± 13 ml/m(2); p < 0.001). These changes were accompanied by improvement in diastolic function, N-terminal pro–B-type natriuretic peptide, 6-min walk test results, and New York Heart Association functional class. CONCLUSIONS: Post-AVR, focal fibrosis does not resolve, but diffuse fibrosis and myocardial cellular hypertrophy regress. Regression is accompanied by structural and functional improvements suggesting that human diffuse fibrosis is plastic, measurable by CMR and a potential therapeutic target. (Regression of Myocardial Fibrosis After Aortic Valve Replacement; NCT02174471) Elsevier Biomedical 2018-02-27 /pmc/articles/PMC5821681/ /pubmed/29471937 http://dx.doi.org/10.1016/j.jacc.2017.12.035 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
Schofield, Rebecca
Benedetti, Giulia
Fontana, Marianna
Bhuva, Anish N.
Sheikh, Amir
López, Begoña
González, Arantxa
Manisty, Charlotte
Lloyd, Guy
Kellman, Peter
Díez, Javier
Moon, James C.
Reverse Myocardial Remodeling Following Valve Replacement in Patients With Aortic Stenosis
title Reverse Myocardial Remodeling Following Valve Replacement in Patients With Aortic Stenosis
title_full Reverse Myocardial Remodeling Following Valve Replacement in Patients With Aortic Stenosis
title_fullStr Reverse Myocardial Remodeling Following Valve Replacement in Patients With Aortic Stenosis
title_full_unstemmed Reverse Myocardial Remodeling Following Valve Replacement in Patients With Aortic Stenosis
title_short Reverse Myocardial Remodeling Following Valve Replacement in Patients With Aortic Stenosis
title_sort reverse myocardial remodeling following valve replacement in patients with aortic stenosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5821681/
https://www.ncbi.nlm.nih.gov/pubmed/29471937
http://dx.doi.org/10.1016/j.jacc.2017.12.035
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