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Updated: Sep 28, 2026

A Rat Model of Pressure Overload Induced Moderate Remodeling and Systolic Dysfunction as Opposed to Overt Systolic Heart Failure
Published on: April 30, 2020
Cardiac Remodeling, Prognostic markers, and Cardiovascular Outcomes Across Heart Failure Phenotypes in Adults with
Amr Moustafa1, Ahmed T Abdelhalim1, Rana Rashwan1
1Department of Cardiovascular Medicine, Mayo Clinic Rochester, MN 55905.
Background:
Data comparing cardiac remodeling, prognostic markers, and cardiovascular outcomes across heart failure (HF) phenotypes in adults with congenital heart disease (CHD) are limited.
Methods:
In this study, adults with CHD and HF were classified based on left ventricular ejection fraction (LVEF): HF with reduced EF (HFrEF; LVEF <40%), HF with mildly reduced EF (HFmrEF; LVEF 41%-49%), and HF with preserved EF (HFpEF; LVEF ≥50% with pulmonary artery wedge pressure ≥15 mmHg). Cardiac function (strain imaging), prognostic markers (NT-proBNP and peak oxygen consumption), and cardiovascular outcomes (HF hospitalization and cardiovascular death/heart transplantation) were compared across groups.
Results:
Among 1,303 patients, 304 (23%) had HFrEF, 551 (42%) had HFmrEF, and 448 (34%) had HFpEF. There was a graded worsening of biatrial and right ventricular function from HFpEF to HFmrEF to HFrEF (all p<0.001). Despite less severe chamber dysfunction, HFpEF was characterized by higher NT-proBNP levels and lower peak oxygen consumption compared with HFmrEF. HFrEF was associated with the highest adjusted risk of HF hospitalization (hazard ratio, 1.52; p=0.005) and cardiovascular death/heart transplantation (hazard ratio, 1.74; p=0.002), compared to HFmrEF and HFpEF. HF therapy was associated with lower event rates overall, with the strongest association in HFrEF, a more modest association in HFmrEF, and no significant association in HFpEF.
Conclusions:
In adults with CHD and HF, LVEF-defined HF phenotypes identified distinct patterns of cardiac remodeling and prognosis, with worse cardiac remodeling and adverse outcomes observed in the HFrEF phenotype. These findings support use of EF phenotype-based approach to HF management in CHD.
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