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Updated: Jul 31, 2025

Ultrasonic Assessment of Myocardial Microstructure
Published on: January 14, 2014
A novel echocardiographic risk score for light-chain amyloidosis
Paul Geenty1,2, Shanthosh Sivapathan2, Luke D Stefani1
1Department of Cardiology, Westmead Hospital, Hawkesbury Road, Sydney, Australia.
Insights
Echocardiographic parameters like left atrial volume and left ventricular global longitudinal strain predict survival in light-chain (AL) amyloidosis. A combined score using these measures offers prognostic accuracy comparable to the established Mayo stage for mortality risk.
Area of Science:
- Cardiology
- Hematology
- Medical Diagnostics
Background:
- Light-chain (AL) amyloidosis, a plasma cell disorder, has a prognosis heavily influenced by cardiac involvement.
- Current staging relies on cardiac biomarkers and free light-chain levels (Mayo staging).
Purpose of the Study:
- To assess the prognostic value of echocardiographic parameters in AL amyloidosis.
- To compare the utility of echocardiography with conventional Mayo staging.
Main Methods:
- Retrospective analysis of 75 AL amyloidosis patients with comprehensive echocardiography.
- Evaluation of parameters including LV ejection fraction, mass, diastolic function, GLS, and LA volume.
- Mortality assessment via clinical records, with a median follow-up of 51 months.
Main Results:
- Patients who died had significantly larger LA volume and higher E/e' compared to survivors.
- LA volume and LVGLS were significant independent predictors of mortality.
- A composite echocardiographic score (LA volume + LVGLS) demonstrated prognostic performance similar to Mayo stage (AUC 0.75).
Conclusions:
- Left atrial volume and LVGLS are independent predictors of mortality in AL amyloidosis.
- A composite echocardiographic score shows comparable prognostic power to Mayo stage for all-cause mortality.
Aims:
The prognosis of light-chain (AL) amyloidosis, a plasma cell dyscrasia, is largely determined by the presence of cardiac involvement. Conventional staging is achieved using cardiac biomarkers (high-sensitivity troponin, N-terminal pro-beta natriuretic peptide) and free light-chain difference (Mayo staging). We sought to evaluate the role of echocardiographic parameters as prognostic markers in AL amyloidosis and examine their utility compared with conventional staging.
Methods And Results:
Seventy-five consecutive patients with AL amyloidosis reviewed at a referral amyloid clinic who underwent comprehensive echocardiographic assessment were retrospectively identified. The evaluated echocardiographic parameters included left ventricular (LV) ejection fraction, mass, diastolic function parameters, global longitudinal strain (GLS), and left atrial (LA) volume. Mortality was assessed through a review of clinical records. During a median follow-up of 51 months, 29/75 (39%) patients died. Patients who died had a larger LA volume (47 ± 12 vs. 35 ± 10 mL/m2, P < 0.001) and a higher E/e' (18 ± 10 vs. 14 ± 6, P = 0.026). Univariate clinical and echocardiographic predictors of survival included LA volume, E/e', e', LVGLS, and Mayo stage (at significance of P < 0.1). Left atrial volume and LVGLS were significant determinants of mortality when examined using clinical cut-offs, although E/e' was not. A composite echocardiographic risk score comprising LA volume and LVGLS provided similar prognostic performance to Mayo stage [area under the curve (AUC) 0.75, 95% confidence interval (CI) 0.64-0.85 vs. AUC 0.75, 95% CI 0.65-0.858, P = 0.91].
Conclusion:
Left atrial volume and LVGLS were independent predictors of mortality in AL amyloidosis. A composite echocardiographic score combining LA volume and LVGLS has similar prognostic power to Mayo stage for all-cause mortality.
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