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Impact of Valvuloarterial Impedance on Concentric Remodeling in Aortic Stenosis and Its Regression after Valve Replacement

BACKGROUND: Left ventricle (LV) in patients with aortic stenosis (AS) faces a double hemodynamic load incorporating both valvular stenosis and reduced systemic arterial compliance (SAC). This study aimed to evaluate the impact of global LV afterload on LV hypertrophy (LVH) before and after aortic va...

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Autores principales: Jang, Jeong Yoon, Seo, Jeong-Sook, Sun, Byung Joo, Kim, Dae-Hee, Song, Jong-Min, Kang, Duk-Hyun, Song, Jae-Kwan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Echocardiography 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5050308/
https://www.ncbi.nlm.nih.gov/pubmed/27721950
http://dx.doi.org/10.4250/jcu.2016.24.3.201
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author Jang, Jeong Yoon
Seo, Jeong-Sook
Sun, Byung Joo
Kim, Dae-Hee
Song, Jong-Min
Kang, Duk-Hyun
Song, Jae-Kwan
author_facet Jang, Jeong Yoon
Seo, Jeong-Sook
Sun, Byung Joo
Kim, Dae-Hee
Song, Jong-Min
Kang, Duk-Hyun
Song, Jae-Kwan
author_sort Jang, Jeong Yoon
collection PubMed
description BACKGROUND: Left ventricle (LV) in patients with aortic stenosis (AS) faces a double hemodynamic load incorporating both valvular stenosis and reduced systemic arterial compliance (SAC). This study aimed to evaluate the impact of global LV afterload on LV hypertrophy (LVH) before and after aortic valve replacement (AVR). METHODS: The study cohort included 453 patients (247 males; mean age, 64 ± 11 years) who underwent AVR. Pre- and post-AVR echocardiographic examinations were retrospectively analyzed including an index of valvuloarterial impedance (Z(VA)) and LV mass index/LV end-diastolic volume index (LVMI/LVEDVI) as a parameter of LVH. RESULTS: Pre-AVR LVMI/LVEDVI was 2.7 ± 0.9 g/mL with an aortic valve area (AVA) of 0.6 ± 0.2 cm(2). Z(VA) was 5.9 ± 1.9 mm Hg/mL/m(2) and showed a stronger correlation (β = 0.601, p < 0.001) with pre-AVR LVMI/LVEDVI than indexed AVA (β = 0.061, p = 0.19), transvalvular peak velocity (β = 0.211, p < 0.001). During a median follow-up of 3.5 years, patients had a 18.8 ± 10.4% decrease in the LV geometry index with a decrease in SAC from 1.20 ± 0.48 to 1.00 ± 0.38 mL/m(2)/mm Hg (p < 0.001). Pre-AVR LV ejection fraction (r = 0.284, p < 0.001) and Z(VA) (r = 0.523, p < 0.001) were independent factors associated with LVH regression in 322 patients with follow-up duration >1 year after AVR. CONCLUSION: Z(VA) is a major determinant of concentric remodeling in AS before AVR and LVH regression after AVR, which should be incorporated in routine evaluation of AS.
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spelling pubmed-50503082016-10-07 Impact of Valvuloarterial Impedance on Concentric Remodeling in Aortic Stenosis and Its Regression after Valve Replacement Jang, Jeong Yoon Seo, Jeong-Sook Sun, Byung Joo Kim, Dae-Hee Song, Jong-Min Kang, Duk-Hyun Song, Jae-Kwan J Cardiovasc Ultrasound Original Article BACKGROUND: Left ventricle (LV) in patients with aortic stenosis (AS) faces a double hemodynamic load incorporating both valvular stenosis and reduced systemic arterial compliance (SAC). This study aimed to evaluate the impact of global LV afterload on LV hypertrophy (LVH) before and after aortic valve replacement (AVR). METHODS: The study cohort included 453 patients (247 males; mean age, 64 ± 11 years) who underwent AVR. Pre- and post-AVR echocardiographic examinations were retrospectively analyzed including an index of valvuloarterial impedance (Z(VA)) and LV mass index/LV end-diastolic volume index (LVMI/LVEDVI) as a parameter of LVH. RESULTS: Pre-AVR LVMI/LVEDVI was 2.7 ± 0.9 g/mL with an aortic valve area (AVA) of 0.6 ± 0.2 cm(2). Z(VA) was 5.9 ± 1.9 mm Hg/mL/m(2) and showed a stronger correlation (β = 0.601, p < 0.001) with pre-AVR LVMI/LVEDVI than indexed AVA (β = 0.061, p = 0.19), transvalvular peak velocity (β = 0.211, p < 0.001). During a median follow-up of 3.5 years, patients had a 18.8 ± 10.4% decrease in the LV geometry index with a decrease in SAC from 1.20 ± 0.48 to 1.00 ± 0.38 mL/m(2)/mm Hg (p < 0.001). Pre-AVR LV ejection fraction (r = 0.284, p < 0.001) and Z(VA) (r = 0.523, p < 0.001) were independent factors associated with LVH regression in 322 patients with follow-up duration >1 year after AVR. CONCLUSION: Z(VA) is a major determinant of concentric remodeling in AS before AVR and LVH regression after AVR, which should be incorporated in routine evaluation of AS. Korean Society of Echocardiography 2016-09 2016-09-26 /pmc/articles/PMC5050308/ /pubmed/27721950 http://dx.doi.org/10.4250/jcu.2016.24.3.201 Text en Copyright © 2016 Korean Society of Echocardiography http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Jang, Jeong Yoon
Seo, Jeong-Sook
Sun, Byung Joo
Kim, Dae-Hee
Song, Jong-Min
Kang, Duk-Hyun
Song, Jae-Kwan
Impact of Valvuloarterial Impedance on Concentric Remodeling in Aortic Stenosis and Its Regression after Valve Replacement
title Impact of Valvuloarterial Impedance on Concentric Remodeling in Aortic Stenosis and Its Regression after Valve Replacement
title_full Impact of Valvuloarterial Impedance on Concentric Remodeling in Aortic Stenosis and Its Regression after Valve Replacement
title_fullStr Impact of Valvuloarterial Impedance on Concentric Remodeling in Aortic Stenosis and Its Regression after Valve Replacement
title_full_unstemmed Impact of Valvuloarterial Impedance on Concentric Remodeling in Aortic Stenosis and Its Regression after Valve Replacement
title_short Impact of Valvuloarterial Impedance on Concentric Remodeling in Aortic Stenosis and Its Regression after Valve Replacement
title_sort impact of valvuloarterial impedance on concentric remodeling in aortic stenosis and its regression after valve replacement
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5050308/
https://www.ncbi.nlm.nih.gov/pubmed/27721950
http://dx.doi.org/10.4250/jcu.2016.24.3.201
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