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Updated: Jun 9, 2025

Lumped-Parameter and Finite Element Modeling of Heart Failure with Preserved Ejection Fraction
Published on: February 13, 2021
Characteristics, Predictors, and Clinical Outcomes in Heart Failure With Reduced Ejection Fraction According to a
Chan Soon Park1,2, Jiesuck Park2,3, Nan Young Bae1,2
1Cardiovascular Center Seoul National University Hospital Seoul Republic of Korea.
Insights
Patients with heart failure with reduced ejection fraction (HFrEF) who improved their left ventricular ejection fraction (LVEF) after ARNI therapy had better outcomes. ARNI treatment showed benefits over RAAS inhibitors for both improved and persistent HFrEF.
Area of Science:
- Cardiology
- Pharmacology
- Clinical Medicine
Background:
- Optimal medical treatment can improve left ventricular ejection fraction (LVEF) in patients with heart failure with reduced ejection fraction (HFrEF).
- Angiotensin receptor-neprilysin inhibitors (ARNI) are a key therapy for HFrEF.
- Understanding outcomes based on LVEF response to ARNI is crucial.
Purpose of the Study:
- To investigate the characteristics, predictors, and outcomes of HFrEF based on 1-year LVEF following ARNI therapy.
- To compare ARNI therapy with renin-angiotensin-aldosterone system (RAAS) inhibitors.
Main Methods:
- Analysis of the STRATS-HF-ARNI registry (N=1074) with baseline and 1-year echocardiography.
- Classification of patients into HF with improved ejection fraction (HFimpEF; LVEF >40%) and persistent HFrEF (perHFrEF; LVEF ≤40%).
- Assessment of all-cause and cardiac mortality as primary and secondary outcomes.
Main Results:
- 46.4% of patients achieved HFimpEF, while 53.6% had perHFrEF.
- Older age, male sex, and larger LV end-diastolic volumes predicted perHFrEF.
- HFimpEF was associated with significantly lower all-cause and cardiac mortality (P<0.001).
- perHFrEF was an independent predictor of poor outcomes (HR 2.402, P=0.008).
- Mortality risk decreased with increasing LVEF up to 40%, with no further reduction beyond that.
- ARNI therapy demonstrated better outcomes than RAAS inhibitors in both HFimpEF and perHFrEF groups.
Conclusions:
- Patients achieving HFimpEF after ARNI therapy have a better prognosis than those with perHFrEF.
- ARNI treatment appears more beneficial than RAAS inhibitors for both HFimpEF and perHFrEF patients.
- LVEF improvement to >40% is associated with improved survival in HFrEF patients on ARNI.
Background:
Optimal medical treatment can lead to improvement in left ventricular ejection fraction (LVEF) in patients with heart failure with reduced EF (HFrEF). We investigated the characteristics, predictors, and outcomes of HFrEF according to the 1-year LVEF following angiotensin receptor-neprilysin inhibitors therapy (ARNI).
Methods And Results:
Using the STRATS-HF-ARNI (Strain for Risk Assessment and Therapeutic Strategies in Patients With Heart Failure Treated With Angiotensin Receptor-Neprilysin Inhibitor) registry, we identified 1074 patients with HFrEF who took ARNI and underwent baseline and 1-year echocardiography. Patients were classified as HF with improved ejection fraction (HFimpEF) and persistent HFrEF (perHFrEF) (1-year LVEF >40% and ≤40%). The primary and secondary outcomes were all-cause and cardiac mortality from the 1-year follow-up. Among 1074 included patients, 498 (46.4%) had HFimpEF, and 576 (53.6%) had perHFrEF. Older age, male sex, and large LV end-diastolic volumes were positive predictors of perHFrEF, whereas atrial fibrillation and high systolic blood pressure were identified as inverse predictors. Patients with HFimpEF showed lower all-cause and cardiac mortality rates (both log-rank P<0.001). In the multivariable analysis, perHFrEF (hazard ratio, 2.402 [95% CI, 1.251-4.610]; P=0.008) was an independent predictor of poor outcomes. The risk of all-cause mortality decreased as the 1-year LVEF increased up to 40%; however, no additional risk reduction was observed beyond 40%. Compared with patients taking renin-angiotensin-aldosterone system inhibitors in the STRATS-AHF (Strain for Risk Assessment and Therapeutic Strategies in Patients With Acute Heart Failure) registry, those in the STRATS-HF-ARNI registry demonstrated better outcomes in both HFimpEF and perHFrEF.
Conclusions:
Patients with HFimpEF had better prognosis than those with perHFrEF, and ARNI treatment in HFrEF could be more beneficial than renin-angiotensin-aldosterone system inhibitors for both HFimpEF and perHFrEF.
Registration:
URL: https://www.who.int/clinical-trials-registry-platform; Unique identifier: KCT0008098.
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