Key result
NYHA class >II (HR 1.65; 95% CI 1.09-2.50) and NT-proBNP (HR 1.57; 95% CI 1.17-2.11) were independent predictors of mortality in patients with biopsy-proven cardiac AL amyloidosis.
Why the study?
Cardiac involvement is a main determinant of mortality in light chain amyloidosis, but data on survival in patients with endomyocardial biopsy-proven cardiac involvement are sparse.
Cohort (n=174)
No
Hazard Ratio: 1.65 (95% CI 1.09–2.5)
p-value: p=0.019
In patients with biopsy-proven cardiac AL amyloidosis, clinical, echocardiographic (including global longitudinal strain), and biomarker parameters are independent predictors of mortality, highlighting the need for multimodality risk stratification.
May aid risk stratification in cardiac AL amyloidosis; leaves open prospective validation before guiding therapy.
BACKGROUND: Cardiac involvement is a main determinant of mortality in light chain (AL) amyloidosis but data on survival of patients with cardiac AL amyloidosis proven by endomyocardial biopsy (EMB) are sparse. METHODS: This study analysed clinical, laboratory, electrocardiography and echocardiographic parameters for their prognostic value in the assessment of patients with AL amyloidosis and cardiac involvement. Patients with AL amyloidosis who had their first visit to the amyloidosis centre at the University Hospital Heidelberg between 2006 and 2017 (n=1628) were filtered for cardiac involvement proven by EMB. In the final cohort, mortality-associated markers were analysed by univariate and multivariable Cox regression. Cut-off values for each parameter were calculated using the survival time. RESULTS: One-hundred and seventy-four patients could be identified. Median overall survival time was 1.5 years and median follow-up time was 5.2 years. At the end of the investigation period, 115 patients had died. In multivariable analysis, New York Heart Association-functional class >II (HR 1.65; 95% CI 1.09 to 2.50; p=0.019), left ventricular global longitudinal strain (HR 1.12; 95% CI 1.03 to 1.22; p=0.007), left ventricular end-systolic volume (HR 1.02; 95% CI 1.01 to 1.03; p=0.001), systolic pulmonary artery pressure (HR 0.98; 95% CI 0.96 to 0.99; p=0.027), N-terminal pro-B-type natriuretic peptide (HR 1.57; 95% CI 1.17 to 2.11; p=0.003) and difference in free light chains (HR 1.30; 95% CI 1.05 to 1.62; p=0.017) were independently predictive. CONCLUSION: Among all patients with AL amyloidosis those with cardiac involvement represent a high-risk population with limited therapy options. Therefore, accurate risk stratification is necessary to identify cardiac amyloidosis patients with favourable prognosis. Incorporation of modern imaging techniques into existing or newly developed scoring systems is a promising option that might enable the implementation of risk-adapted therapeutic strategies.
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Aurich et al. (2023) conducted a cohort in Light chain (AL) amyloidosis with cardiac involvement (n=174). Prognostic markers (e.g., NYHA class >II, NT-proBNP) was evaluated on Mortality (HR 1.65, 95% CI 1.09-2.50, p=0.019). NYHA class >II (HR 1.65; 95% CI 1.09-2.50) and NT-proBNP (HR 1.57; 95% CI 1.17-2.11) were independent predictors of mortality in patients with biopsy-proven cardiac AL amyloidosis.
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