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Variations in subclinical left ventricular dysfunction, functional capacity, and clinical outcomes in different heart failure aetiologies

AIMS: Patients with heart failure (HF) risk factors are described as being in Stage A of this condition (SAHF). Management is directed towards prevention of HF progression, but to date, no evidence has been described to align the intensity of this intervention to HF risk. We sought to what extent SA...

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Autores principales: Wang, Ying, Yang, Hong, Nolan, Mark, Pathan, Faraz, Negishi, Kazuaki, Marwick, Thomas H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5933957/
https://www.ncbi.nlm.nih.gov/pubmed/29405644
http://dx.doi.org/10.1002/ehf2.12257
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author Wang, Ying
Yang, Hong
Nolan, Mark
Pathan, Faraz
Negishi, Kazuaki
Marwick, Thomas H.
author_facet Wang, Ying
Yang, Hong
Nolan, Mark
Pathan, Faraz
Negishi, Kazuaki
Marwick, Thomas H.
author_sort Wang, Ying
collection PubMed
description AIMS: Patients with heart failure (HF) risk factors are described as being in Stage A of this condition (SAHF). Management is directed towards prevention of HF progression, but to date, no evidence has been described to align the intensity of this intervention to HF risk. We sought to what extent SAHF of Type 2 diabetes mellitus (T2DM) and other HF risks showed differences in subclinical left ventricular function, exercise capacity, and prognosis. METHODS AND RESULTS: We recruited 551 elder asymptomatic SAHF patients (age 71 ± 5 years, 49% men, 290 T2DM) with at least one risk factor from a community‐based population with preserved ejection fraction. All underwent a comprehensive echocardiogram including global longitudinal strain (GLS) and a 6 min walk test and were followed for 2 years. The primary endpoints were new‐onset HF and all‐cause mortality. The T2DM group was associated with reduced 6 min walk test distance (451 ± 111 vs. 493 ± 87 m, P < 0.001), worse diastolic function (E/e′ 9.2 ± 2.7 vs. 8.7 ± 2.4, P = 0.028), and impaired GLS (−17.7 ± 2.6% vs. −19.0 ± 2.6%, P < 0.001). Over a median follow‐up of 1.6 years, 49 T2DM‐SAHF and 27 other‐SAHF met the primary endpoint. T2DM‐SAHF had significantly worse outcome than other‐SAHF (P = 0.021). In Cox models, obesity [hazard ratio (HR) = 2.46; P = 0.007], atrial fibrillation (HR = 2.39; P = 0.028), 6 min walk distance (HR = 0.99; P = 0.034), and GLS (HR = 1.14; P = 0.033) were independently associated with the primary endpoint in T2DM‐SAHF, independent of age and glycaemic control. CONCLUSIONS: The T2DM‐SAHF has worse subclinical left ventricular function, exercise capacity, and prognosis than other‐SAHF. Impaired GLS, atrial fibrillation, exercise capacity, and obesity are associated with a worse prognosis in T2DM‐SAHF but not in other‐SAHF.
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spelling pubmed-59339572018-05-10 Variations in subclinical left ventricular dysfunction, functional capacity, and clinical outcomes in different heart failure aetiologies Wang, Ying Yang, Hong Nolan, Mark Pathan, Faraz Negishi, Kazuaki Marwick, Thomas H. ESC Heart Fail Original Research Articles AIMS: Patients with heart failure (HF) risk factors are described as being in Stage A of this condition (SAHF). Management is directed towards prevention of HF progression, but to date, no evidence has been described to align the intensity of this intervention to HF risk. We sought to what extent SAHF of Type 2 diabetes mellitus (T2DM) and other HF risks showed differences in subclinical left ventricular function, exercise capacity, and prognosis. METHODS AND RESULTS: We recruited 551 elder asymptomatic SAHF patients (age 71 ± 5 years, 49% men, 290 T2DM) with at least one risk factor from a community‐based population with preserved ejection fraction. All underwent a comprehensive echocardiogram including global longitudinal strain (GLS) and a 6 min walk test and were followed for 2 years. The primary endpoints were new‐onset HF and all‐cause mortality. The T2DM group was associated with reduced 6 min walk test distance (451 ± 111 vs. 493 ± 87 m, P < 0.001), worse diastolic function (E/e′ 9.2 ± 2.7 vs. 8.7 ± 2.4, P = 0.028), and impaired GLS (−17.7 ± 2.6% vs. −19.0 ± 2.6%, P < 0.001). Over a median follow‐up of 1.6 years, 49 T2DM‐SAHF and 27 other‐SAHF met the primary endpoint. T2DM‐SAHF had significantly worse outcome than other‐SAHF (P = 0.021). In Cox models, obesity [hazard ratio (HR) = 2.46; P = 0.007], atrial fibrillation (HR = 2.39; P = 0.028), 6 min walk distance (HR = 0.99; P = 0.034), and GLS (HR = 1.14; P = 0.033) were independently associated with the primary endpoint in T2DM‐SAHF, independent of age and glycaemic control. CONCLUSIONS: The T2DM‐SAHF has worse subclinical left ventricular function, exercise capacity, and prognosis than other‐SAHF. Impaired GLS, atrial fibrillation, exercise capacity, and obesity are associated with a worse prognosis in T2DM‐SAHF but not in other‐SAHF. John Wiley and Sons Inc. 2018-02-05 /pmc/articles/PMC5933957/ /pubmed/29405644 http://dx.doi.org/10.1002/ehf2.12257 Text en © 2018 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 http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Research Articles
Wang, Ying
Yang, Hong
Nolan, Mark
Pathan, Faraz
Negishi, Kazuaki
Marwick, Thomas H.
Variations in subclinical left ventricular dysfunction, functional capacity, and clinical outcomes in different heart failure aetiologies
title Variations in subclinical left ventricular dysfunction, functional capacity, and clinical outcomes in different heart failure aetiologies
title_full Variations in subclinical left ventricular dysfunction, functional capacity, and clinical outcomes in different heart failure aetiologies
title_fullStr Variations in subclinical left ventricular dysfunction, functional capacity, and clinical outcomes in different heart failure aetiologies
title_full_unstemmed Variations in subclinical left ventricular dysfunction, functional capacity, and clinical outcomes in different heart failure aetiologies
title_short Variations in subclinical left ventricular dysfunction, functional capacity, and clinical outcomes in different heart failure aetiologies
title_sort variations in subclinical left ventricular dysfunction, functional capacity, and clinical outcomes in different heart failure aetiologies
topic Original Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5933957/
https://www.ncbi.nlm.nih.gov/pubmed/29405644
http://dx.doi.org/10.1002/ehf2.12257
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