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Updated: Sep 29, 2025

Lumped-Parameter and Finite Element Modeling of Heart Failure with Preserved Ejection Fraction
Published on: February 13, 2021
Heart Failure and Drug Therapies: A Metabolic Review
Frank Yu1,2, Bianca McLean3, Mitesh Badiwala1,2,4
1Peter Munk Cardiac Centre, Toronto General Hospital, Toronto, ON M5G 2C4, Canada.
Insights
Heart failure (HF) impacts millions globally. Investigating cardiac metabolism, especially with -omic technologies and drugs like SGLT2 inhibitors, offers new insights into HF progression and treatment.
Area of Science:
- Cardiovascular Research
- Metabolomics
- Pharmacology
Background:
- Cardiovascular disease is a leading global cause of death, with heart failure (HF) affecting millions.
- The heart's high ATP turnover makes cardiac metabolism crucial for maintaining homeostasis.
- Understanding HF pathophysiology is vital for developing effective treatments.
Purpose of the Study:
- To review cardiac metabolism in healthy and failing hearts.
- To explore the role of metabolomics and lipidomics in characterizing HF.
- To discuss the metabolic mechanisms of HF drugs, particularly SGLT2 inhibitors.
Main Methods:
- Review of existing literature on cardiac metabolism and HF.
- Analysis of findings from metabolomics and lipidomics studies in HF.
- Examination of clinical evidence for the metabolic effects of HF therapies.
Main Results:
- -Omic technologies have enhanced the understanding of HF pathologies and identified novel pathways.
- Metabolic alterations are central to the progression of heart failure.
- Sodium-glucose transport protein 2 inhibitors show significant promise, potentially via metabolic actions.
Conclusions:
- Cardiac metabolism is a key area for understanding and treating heart failure.
- Metabolomics and lipidomics provide powerful tools for HF research.
- Targeting metabolic pathways represents a promising therapeutic strategy for HF.
Abstract:
Cardiovascular disease is the leading cause of mortality globally with at least 26 million people worldwide living with heart failure (HF). Metabolism has been an active area of investigation in the setting of HF since the heart demands a high rate of ATP turnover to maintain homeostasis. With the advent of -omic technologies, specifically metabolomics and lipidomics, HF pathologies have been better characterized with unbiased and holistic approaches. These techniques have identified novel pathways in our understanding of progression of HF and potential points of intervention. Furthermore, sodium-glucose transport protein 2 inhibitors, a drug that has changed the dogma of HF treatment, has one of the strongest types of evidence for a potential metabolic mechanism of action. This review will highlight cardiac metabolism in both the healthy and failing heart and then discuss the metabolic effects of heart failure drugs.
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Heart Failure Drugs: Inhibitors of Renin-Angiotensin System
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