Changing the paradigm in heart failure: shifting from treatment to prevention
- PMID: 39441333
- DOI: 10.1007/s10741-024-10454-2
Changing the paradigm in heart failure: shifting from treatment to prevention
Abstract
Heart failure (HF) poses a major global health challenge with rising prevalence, significant morbidity and mortality, and substantial associated healthcare costs. With aging of the population and an increasing burden of comorbidities, the complex interplay between cardiovascular, kidney, and metabolic risk factors have been thrust into the spotlight and have broadened the traditional focus from HF treatment to an increased emphasis on prevention. In recognition of the evolving HF landscape, the American Heart Association released the PREVENT models which are comprehensive risk assessment tools that estimate 10- and 30-year risk of incident cardiovascular disease and its subtypes, including atherosclerotic cardiovascular disease (ASCVD) and, for the first time, HF. While it is an accurate risk estimation tool and represents a step forward in improving risk stratification for primary prevention of HF, there remain several limitations and unknowns like model performance across disaggregated racial and ethnic groups, the role of traditional ASCVD vs. HF-specific risk factors, HF prediction among those with known ASCVD, and the use of traditional regression techniques in lieu of potentially more powerful machine learning-based modeling approaches. Furthermore, it remains unclear how to optimize risk estimation in clinical care. The emergence of multiple novel pharmacological therapies that prevent incident HF, including sodium-glucose co-transporter 2 (SGLT2) inhibitors, glucagon-like peptide 1 (GLP1) receptor agonists, and nonsteroidal mineralocorticoid receptor antagonists (MRAs), highlights the importance of accurate HF risk prediction. To provide HF prevention with these effective but costly therapies, we must understand the optimal strategy in sequencing and combining these therapies and prioritize patients at highest risk. Such implementation requires both accurate risk stratification and a better understanding of how to communicate risk to patients and providers. This state-of-the-art review aims to provide a comprehensive overview of recent trends in HF prevention, including risk assessment, care management strategies, and emerging and novel treatments.
Keywords: Cardiovascular-Kidney-Metabolic; Heart Failure; Lifestyle; Pharmacotherapies; Prevention; Risk stratification.
© 2024. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.
Conflict of interest statement
Declarations. Competing interest: Dr. Greene has received research support from the Duke University Department of Medicine Chair’s Research Award, American Heart Association , Amgen, AstraZeneca, Boehinger Ingelheim, Bristol Myers Squibb, Cytokinetics, Merck, Novartis, Pfizer, and Sanofi; has served on advisory boards or as consultant for Amgen, AstraZeneca, Bayer, Boehringer Ingelheim, Bristol Myers Squibb, Corcept Therapeutics, Corteria Pharmaceuticals, CSL Vifor, Cytokinetics, Eli Lilly, Lexicon, Merck, Otsuka, Roche Diagnostics, Sanofi, scPharmaceuticals, Tricog Health, and Urovant Pharmaceuticals; and has received speaker fees from AstraZeneca, Bayer, Boehringer Ingelheim, Cytokinetics, Lexicon, and Roche Diagnostics. Dr. Sandhu has received research support from National Institutes of Health, American Heart Association , Novartis Pharmaceuticals, and Repreive Cardiovascular and has served as a consultant for Lexicon Pharmaceuticals. Dr. Go has received research support from the National Heart, Lung and Blood Institute and the National Institute of Diabetes, Digestive and Kidney Diseases. Dr. Ambrosy has received relevant research support through grants to his institution from the National Heart, Lung, and Blood Institute (K23HL150159), the American Heart Association (2nd Century Early Faculty Independence Award), The Permanente Medical Group, Northern California Community Benefits Programs, Garfield Memorial Fund, Abbott Laboratories, Amarin Pharma, Inc., Bayer, Cordio Medical, Edwards Lifesciences LLC, Esperion Therapeutics, Inc., Merck, and Novartis. Dr. Stephen J. Greene, Dr. Josephine Harrington, and Dr. Andrew P. Ambrosy are Editorial Board members of Heart Failure Reviews. All other authors report no relevant disclosures.
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References
-
- Martin SS, Aday AW, Almarzooq ZI et al (2024) 2024 heart disease and stroke statistics: a report of US and global data from the American Heart Association. Circulation 149(8):e347–e913. https://doi.org/10.1161/CIR.0000000000001209 - DOI - PubMed
-
- Bleumink GS, Knetsch AM, Sturkenboom MC et al (2004) Quantifying the heart failure epidemic: prevalence, incidence rate, lifetime risk and prognosis of heart failure The Rotterdam Study. Eur Heart J 25(18):1614–1619. https://doi.org/10.1016/j.ehj.2004.06.038 - DOI - PubMed
-
- Ho KK, Pinsky JL, Kannel WB, Levy D (1993) The epidemiology of heart failure: the Framingham Study. J Am Coll Cardiol 22(4 Suppl A):6A-13A. https://doi.org/10.1016/0735-1097(93)90455-a - DOI - PubMed
-
- Nichols GA, Qiao Q, Déruaz-Luyet A, Kraus BJ (2023) The clinical burden of newly diagnosed Heart failure among patients with Reduced, mildly Reduced, and preserved ejection fraction. Int J Cardiol Heart Vasc 47:101182. Published 2023 Feb 14. https://doi.org/10.1016/0735-1097(93)90455-a
-
- Steinberg BA, Zhao X, Heidenreich PA et al (2012) Trends in patients hospitalized with heart failure and preserved left ventricular ejection fraction: prevalence, therapies, and outcomes. Circulation 126(1):65–75. https://doi.org/10.1161/CIRCULATIONAHA.111.080770 - DOI - PubMed
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