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Heart failure development in obesity: underlying risk factors and mechanistic pathways

AIMS: People with obesity are at risk for developing heart failure (HF), but little is known about the mechanistic pathways that link obesity with cardiac dysfunction. METHODS AND RESULTS: We included 2030 participants from the Swedish Obese Subjects study who received conventional obesity treatment...

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Autores principales: Jamaly, Shabbar, Carlsson, Lena, Peltonen, Markku, Andersson‐Assarsson, Johanna C., Karason, Kristjan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7835624/
https://www.ncbi.nlm.nih.gov/pubmed/33231382
http://dx.doi.org/10.1002/ehf2.13081
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author Jamaly, Shabbar
Carlsson, Lena
Peltonen, Markku
Andersson‐Assarsson, Johanna C.
Karason, Kristjan
author_facet Jamaly, Shabbar
Carlsson, Lena
Peltonen, Markku
Andersson‐Assarsson, Johanna C.
Karason, Kristjan
author_sort Jamaly, Shabbar
collection PubMed
description AIMS: People with obesity are at risk for developing heart failure (HF), but little is known about the mechanistic pathways that link obesity with cardiac dysfunction. METHODS AND RESULTS: We included 2030 participants from the Swedish Obese Subjects study who received conventional obesity treatment. First‐time detection of HF was obtained by cross‐checking the study population with the Swedish National Patient Register and the Swedish Cause of Death Register. We also examined if atrial fibrillation and myocardial infarction as time‐dependent variables could predict incident HF The mean age of the study cohort was 48.7 years, and 28% were men. The mean body mass index at baseline was 40.1 kg/m(2) and remained stable during a median follow‐up of 20.1 years. First‐time diagnosis of HF occurred in 266 of patients and was related to male sex, increasing age, greater waist–hip ratio, hypertension, higher cholesterol, diabetes mellitus, and elevated free thyroxine in univariable analysis. Estimated glomerular filtration rate was negatively related to HF risk. In multivariable analysis, atrial fibrillation, which is related to HF with preserved ejection fraction (HFpEF), and myocardial infarction, which is linked to HF with reduced ejection fraction (HFrEF), were strongly associated with incident HF with sub‐hazard ratios 3.75 (95% confidence interval: 2.72–5.18, P < 0.001) and 3.68 (95% confidence interval: 2.55–5.30, P < 0.001), respectively. CONCLUSIONS: Both atrial fibrillation and myocardial infarction as time‐dependent variables were independently and strongly related to incident HF in people with excess body fat, suggesting two main obesity‐related mechanistic pathways leading to either HFpEF or HFrEF.
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spelling pubmed-78356242021-02-01 Heart failure development in obesity: underlying risk factors and mechanistic pathways Jamaly, Shabbar Carlsson, Lena Peltonen, Markku Andersson‐Assarsson, Johanna C. Karason, Kristjan ESC Heart Fail Original Research Articles AIMS: People with obesity are at risk for developing heart failure (HF), but little is known about the mechanistic pathways that link obesity with cardiac dysfunction. METHODS AND RESULTS: We included 2030 participants from the Swedish Obese Subjects study who received conventional obesity treatment. First‐time detection of HF was obtained by cross‐checking the study population with the Swedish National Patient Register and the Swedish Cause of Death Register. We also examined if atrial fibrillation and myocardial infarction as time‐dependent variables could predict incident HF The mean age of the study cohort was 48.7 years, and 28% were men. The mean body mass index at baseline was 40.1 kg/m(2) and remained stable during a median follow‐up of 20.1 years. First‐time diagnosis of HF occurred in 266 of patients and was related to male sex, increasing age, greater waist–hip ratio, hypertension, higher cholesterol, diabetes mellitus, and elevated free thyroxine in univariable analysis. Estimated glomerular filtration rate was negatively related to HF risk. In multivariable analysis, atrial fibrillation, which is related to HF with preserved ejection fraction (HFpEF), and myocardial infarction, which is linked to HF with reduced ejection fraction (HFrEF), were strongly associated with incident HF with sub‐hazard ratios 3.75 (95% confidence interval: 2.72–5.18, P < 0.001) and 3.68 (95% confidence interval: 2.55–5.30, P < 0.001), respectively. CONCLUSIONS: Both atrial fibrillation and myocardial infarction as time‐dependent variables were independently and strongly related to incident HF in people with excess body fat, suggesting two main obesity‐related mechanistic pathways leading to either HFpEF or HFrEF. John Wiley and Sons Inc. 2020-11-24 /pmc/articles/PMC7835624/ /pubmed/33231382 http://dx.doi.org/10.1002/ehf2.13081 Text en © 2020 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/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Research Articles
Jamaly, Shabbar
Carlsson, Lena
Peltonen, Markku
Andersson‐Assarsson, Johanna C.
Karason, Kristjan
Heart failure development in obesity: underlying risk factors and mechanistic pathways
title Heart failure development in obesity: underlying risk factors and mechanistic pathways
title_full Heart failure development in obesity: underlying risk factors and mechanistic pathways
title_fullStr Heart failure development in obesity: underlying risk factors and mechanistic pathways
title_full_unstemmed Heart failure development in obesity: underlying risk factors and mechanistic pathways
title_short Heart failure development in obesity: underlying risk factors and mechanistic pathways
title_sort heart failure development in obesity: underlying risk factors and mechanistic pathways
topic Original Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7835624/
https://www.ncbi.nlm.nih.gov/pubmed/33231382
http://dx.doi.org/10.1002/ehf2.13081
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