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High body mass index is a predictor of left ventricular reverse remodelling in heart failure with reduced ejection fraction

AIMS: Structural and functional left ventricular alterations can occur in heart failure (HF), referred to as left ventricular reverse remodelling (LVRR). This study aimed to define novel predictors of LVRR besides well‐known effects of medical and device therapy. METHODS AND RESULTS: From echographi...

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Autores principales: Cescau, Arthur, Van Aelst, Lucas N.L., Baudet, Mathilde, Cohen Solal, Alain, Logeart, Damien
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5695192/
https://www.ncbi.nlm.nih.gov/pubmed/28752617
http://dx.doi.org/10.1002/ehf2.12172
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author Cescau, Arthur
Van Aelst, Lucas N.L.
Baudet, Mathilde
Cohen Solal, Alain
Logeart, Damien
author_facet Cescau, Arthur
Van Aelst, Lucas N.L.
Baudet, Mathilde
Cohen Solal, Alain
Logeart, Damien
author_sort Cescau, Arthur
collection PubMed
description AIMS: Structural and functional left ventricular alterations can occur in heart failure (HF), referred to as left ventricular reverse remodelling (LVRR). This study aimed to define novel predictors of LVRR besides well‐known effects of medical and device therapy. METHODS AND RESULTS: From echographic database, we included 295 patients with both left ventricular ejection fraction (LVEF) ≤45% and indexed left ventricular end‐diastolic diameter ≥33 mm/m(2) and who had at least two echocardiographic exams with a delay between 3 and 12 months. LVRR was defined as the combination of (i) normalization of LVEF (LVEF ≥50%) or increase in LVEF ≥10% and (ii) a decrease in indexed left ventricular end‐diastolic diameter ≥10%. Clinical follow‐up was also obtained. LVRR occurred in 53 (18%) patients. Patients in the LVRR group were more likely to present with de novo HF (75% vs. 42%), had lower LVEF and left ventricular end‐diastolic volumes at index examination, yet a higher body mass index (BMI) than non‐LVRR patients. Obesity was observed in 25% of LVRR patients vs. 14% in others. In multivariate analyses, BMI (per each 1 kg/m(2) increase) emerged as a predictor of LVRR: odds ratio 1.10 (95% confidence interval 1.02–1.19) after adjustment to other predictors of LVRR. During a mean follow‐up of 37 months, 32% of patients had a major adverse cardiac event; de novo HF, age, and LVEF were associated with major adverse cardiac event. CONCLUSIONS: We identified significant relationship between high BMI and LVRR. This intriguing novel finding deserves further study.
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spelling pubmed-56951922018-02-14 High body mass index is a predictor of left ventricular reverse remodelling in heart failure with reduced ejection fraction Cescau, Arthur Van Aelst, Lucas N.L. Baudet, Mathilde Cohen Solal, Alain Logeart, Damien ESC Heart Fail Short Communication AIMS: Structural and functional left ventricular alterations can occur in heart failure (HF), referred to as left ventricular reverse remodelling (LVRR). This study aimed to define novel predictors of LVRR besides well‐known effects of medical and device therapy. METHODS AND RESULTS: From echographic database, we included 295 patients with both left ventricular ejection fraction (LVEF) ≤45% and indexed left ventricular end‐diastolic diameter ≥33 mm/m(2) and who had at least two echocardiographic exams with a delay between 3 and 12 months. LVRR was defined as the combination of (i) normalization of LVEF (LVEF ≥50%) or increase in LVEF ≥10% and (ii) a decrease in indexed left ventricular end‐diastolic diameter ≥10%. Clinical follow‐up was also obtained. LVRR occurred in 53 (18%) patients. Patients in the LVRR group were more likely to present with de novo HF (75% vs. 42%), had lower LVEF and left ventricular end‐diastolic volumes at index examination, yet a higher body mass index (BMI) than non‐LVRR patients. Obesity was observed in 25% of LVRR patients vs. 14% in others. In multivariate analyses, BMI (per each 1 kg/m(2) increase) emerged as a predictor of LVRR: odds ratio 1.10 (95% confidence interval 1.02–1.19) after adjustment to other predictors of LVRR. During a mean follow‐up of 37 months, 32% of patients had a major adverse cardiac event; de novo HF, age, and LVEF were associated with major adverse cardiac event. CONCLUSIONS: We identified significant relationship between high BMI and LVRR. This intriguing novel finding deserves further study. John Wiley and Sons Inc. 2017-07-27 /pmc/articles/PMC5695192/ /pubmed/28752617 http://dx.doi.org/10.1002/ehf2.12172 Text en © 2017 The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of the European Society of Cardiology. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Communication
Cescau, Arthur
Van Aelst, Lucas N.L.
Baudet, Mathilde
Cohen Solal, Alain
Logeart, Damien
High body mass index is a predictor of left ventricular reverse remodelling in heart failure with reduced ejection fraction
title High body mass index is a predictor of left ventricular reverse remodelling in heart failure with reduced ejection fraction
title_full High body mass index is a predictor of left ventricular reverse remodelling in heart failure with reduced ejection fraction
title_fullStr High body mass index is a predictor of left ventricular reverse remodelling in heart failure with reduced ejection fraction
title_full_unstemmed High body mass index is a predictor of left ventricular reverse remodelling in heart failure with reduced ejection fraction
title_short High body mass index is a predictor of left ventricular reverse remodelling in heart failure with reduced ejection fraction
title_sort high body mass index is a predictor of left ventricular reverse remodelling in heart failure with reduced ejection fraction
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5695192/
https://www.ncbi.nlm.nih.gov/pubmed/28752617
http://dx.doi.org/10.1002/ehf2.12172
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