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Updated: Feb 1, 2026

Author Spotlight: Exploring the Relationship Between Lipotoxicity and HFpEF
Published on: March 29, 2024
Predictors of reverse cardiac remodeling after sacubitril/valsartan in heart failure with reduced ejection fraction
Minjae Yoon1, Soo Young Lee1, Jin Joo Park1
1Division of Cardiology, Department of Internal medicine, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam, Republic of Korea.
Insights
Early initiation of sacubitril/valsartan (Sac/Val) and higher doses are linked to reverse cardiac remodeling in heart failure with reduced ejection fraction (HFrEF). This finding highlights key factors for improving patient outcomes.
Area of Science:
- Cardiology
- Pharmacology
Background:
- Sacubitril/valsartan (Sac/Val) promotes reverse cardiac remodeling in heart failure with reduced ejection fraction (HFrEF).
- Predictors for this remodeling effect remain incompletely understood.
Purpose of the Study:
- To identify predictors of reverse cardiac remodeling in HFrEF patients treated with Sac/Val.
- Specifically investigate the impact of heart failure (HF) duration and Sac/Val dosage.
Main Methods:
- Retrospective, multicenter cohort study of 294 HFrEF patients with 12-month follow-up echocardiography.
- Reverse cardiac remodeling defined by significant improvements in LVEF and LV end-diastolic volume index.
- Analysis of HF duration at Sac/Val initiation and average daily Sac/Val dose.
Main Results:
- 107 out of 294 patients (36.4%) showed reverse cardiac remodeling.
- Shorter HF duration (<12 months) and higher Sac/Val dose (≥200 mg/day) were associated with significantly higher rates of remodeling.
- Low baseline LVEF, short HF duration, and higher Sac/Val dose independently predicted reverse cardiac remodeling.
Conclusions:
- Early initiation of Sac/Val after HF diagnosis is associated with greater reverse cardiac remodeling.
- Higher Sac/Val doses are also linked to improved reverse cardiac remodeling in HFrEF.
- These findings suggest optimizing treatment timing and dosage can enhance therapeutic benefits.
Abstract:
Sacubitril/valsartan (Sac/Val) is associated with reverse cardiac remodeling in heart failure with reduced ejection fraction (HFrEF). However, the predictors of reverse cardiac remodeling after Sac/Val have not yet been fully established. We aimed to evaluate the predictors of reverse cardiac remodeling in patients with HFrEF, with a focus on HF duration and the dose of Sac/Val. In this retrospective, multicenter cohort study, 600 patients with HFrEF who received a Sac/Val prescription were enrolled at six tertiary hospitals in Korea between February 2017 and April 2019. After excluding patients without baseline or 12-month follow-up echocardiographic data, 294 patients were enrolled. Reverse cardiac remodeling was defined by comparing the baseline and follow-up echocardiographic data: an absolute increase in left ventricular ejection fraction (LVEF) ≥ 10% and a relative decrease in left ventricular end-diastolic volume index ≥ 10%. The average daily Sac/Val dose was calculated during the first 6 and 12 months after initiation. Among the 294 patients, 107 presented with reverse cardiac remodeling at 12 months. Patients with HF duration < 12 months at the time of Sac/Val initiation showed a higher proportion of reverse cardiac remodeling than patients with HF duration ≥ 12 months (46.1% vs. 25.7%; P < 0.001). Patients with an average daily Sac/Val dose ≥ 200 mg/day over 6 months also had a higher proportion of reverse cardiac remodeling than patients with Sac/Val < 200 mg/day (44.0% vs. 31.9%; P < 0.001). Multivariable logistic regression revealed low baseline LVEF, HF duration < 12 months, and higher Sac/Val dose as independent predictors of reverse cardiac remodeling. In conclusion, early initiation of Sac/Val following HF diagnosis and higher Sac/Val doses were associated with a higher likelihood of reverse cardiac remodeling in HFrEF.
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