Key result
Cardiovascular magnetic resonance-derived extracellular volume fraction was a significant independent predictor of HCM-related events (adjusted HR 1.08 per 1% increase; 95% CI 1.02-1.15).
Why the study?
The study investigated the incremental prognostic value of CMR-derived extracellular volume fraction beyond late gadolinium enhancement in hypertrophic cardiomyopathy.
Does CMR-derived extracellular volume fraction (ECV) improve risk stratification for HCM-related events beyond late gadolinium enhancement (LGE) in patients with hypertrophic cardiomyopathy?
Cohort (n=990)
Does CMR-derived extracellular volume fraction (ECV) improve risk stratification for HCM-related events beyond late gadolinium enhancement (LGE) in patients with hypertrophic cardiomyopathy?
CMR-derived extracellular volume fraction (ECV) provides incremental prognostic value beyond late gadolinium enhancement (LGE) for predicting adverse outcomes in patients with hypertrophic cardiomyopathy.
Answers are grounded in this paper and cite their sources.
Hypothesis-generating for ECV in HCM risk stratification; prospective trials needed before clinical adoption.
AIMS: This study investigated the incremental prognostic value of cardiovascular magnetic resonance (CMR)-derived extracellular volume fraction (ECV), a marker of diffuse interstitial fibrosis, beyond late gadolinium enhancement (LGE) in hypertrophic cardiomyopathy (HCM). METHODS AND RESULTS: We analysed 990 consecutive HCM patients (median age 58 years, male 68.3%) who underwent CMR between 2012 and 2024. LGE and global ECV were quantified, and their associations with the primary endpoint of HCM-related events-a composite of sudden cardiac death (SCD) events, heart failure (HF) events, and HCM-related death-were assessed. During a median follow-up of 3.2 years, 64 (6.5%) patients experienced the primary endpoint. While LGE (median 7.1%, IQR 2.3-16.9%) and ECV (median 29.0%, IQR 26.6-32.0%) were moderately correlated (R = 0.604, P < 0.001), both were significantly associated with increased risk of the primary endpoint and individual outcomes of SCD and HF events, and optimal cutoffs were determined as LGE ≥ 27% and ECV ≥ 35%. Patients with ECV ≥ 35% had more symptoms, a more severe phenotype with greater systolic and diastolic dysfunction, and more pathogenic gene variants. Notably, ECV remained a significant predictor of the primary endpoint (adjusted HR 1.08, 95% CI 1.02-1.15, per 1%) after adjustment for key disease variables, including left ventricular ejection fraction and LGE. Elevated ECV effectively identified high-risk individuals even among lower-risk subgroups, including those with low LGE burden. CONCLUSION: Increased ECV is an independent predictor of HCM-related outcomes. ECV may serve as a novel imaging biomarker to refine risk stratification in HCM patients who do not meet traditional LGE-based high-risk criteria.
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Lee et al. (2026) conducted a cohort in hypertrophic cardiomyopathy (n=990). Extracellular volume fraction (ECV) was evaluated on HCM-related events (composite of sudden cardiac death, heart failure events, and HCM-related death) (HR 1.08, 95% CI 1.02-1.15). Cardiovascular magnetic resonance-derived extracellular volume fraction was a significant independent predictor of HCM-related events (adjusted HR 1.08 per 1% increase; 95% CI 1.02-1.15).
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