Key result
High CMR-derived extracellular volume linked to ~145% increased mortality in ATTR amyloidosis beyond biomarker staging.
Why the study?
Does incorporating CMR parameters into NAC staging improve prognostic accuracy for mortality in patients with ATTR-CA?
Cohort (n=266)
Yes
Does incorporating CMR parameters into NAC staging improve prognostic accuracy for mortality in patients with ATTR-CA?
Answers are grounded in this paper and cite their sources.
CMR-derived extracellular volume and indexed left atrial volume provide incremental prognostic value beyond standard biomarker staging in ATTR-CA, improving risk stratification.
AIMS: While cardiac magnetic resonance (CMR) provides prognostic value in transthyretin cardiac amyloidosis (ATTR-CA), current ATTR-CA staging relies on serum biomarkers. We evaluated the incremental value of incorporating CMR parameters into the National Amyloidosis Center (NAC) staging and assessed their utility in guiding evaluation for advanced heart failure (HF) therapies and emerging disease-modifying treatments. METHODS AND RESULTS: We retrospectively analyzed a multicenter cohort of 266 ATTR-CA patients who underwent CMR between 2007-2023. Cox regressions were used to assess time to death. A baseline model was constructed using the NAC stage. CMR predictor variables were selected a priori based on clinical relevance and non-collinearity, then refined using stepwise backward elimination regression with NAC stage control; variables retained in ≥60% of 1,000 bootstrapped samples were included. Internal validation was performed via bootstrapping, with performance reported as Harrell's C-statistic and calibration slope. Decision curve analysis evaluated clinical utility.85 patients (32%) died over a median follow up of 20 months (IQR 8-35). Extracellular volume (ECV ≥59%, HR 2.45, 95% CI 1.2-5.2, p = 0.020) and indexed left atrial volume (LAVi ≥54 ml/m2, HR 2.00, 95% CI 1.1-3.7, p = 0.026) were independently associated with mortality after NAC adjustment and improved prognostic accuracy across all biomarker stages. When risk prediction was framed around initiation of advanced HF or emerging disease-modifying therapies, incorporating CMR alongside NAC staging facilitated identification of 28 additional high-risk patients per 1,000. CONCLUSION: CMR-derived ECV and LAVi were associated with incremental prognostic value in ATTR-CA beyond biomarker staging and may inform clinical risk stratification.
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Chiou et al. (2026) conducted a cohort in Transthyretin cardiac amyloidosis (ATTR-CA) (n=266). Cardiac magnetic resonance (CMR) parameters (ECV ≥59% and LAVi ≥54 ml/m2) vs. Lower ECV and LAVi (or NAC staging alone) was evaluated on Mortality (time to death) (HR 2.45, 95% CI 1.2-5.2, p=0.020). CMR-derived extracellular volume ≥59% (HR 2.45; 95% CI 1.2-5.2) and indexed left atrial volume ≥54 ml/m2 (HR 2.00) were independently associated with mortality in ATTR-CA beyond biomarker staging.
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