Abstract

BackgroundThe differentiated assessment of functional parameters besides morphological changes is essential for the evaluation of prognosis in systemic immunoglobulin light chain (AL) amyloidosis.MethodsSeventy-four subjects with AL amyloidosis and presence of late gadolinium enhancement (LGE) pattern typical for cardiac amyloidosis were analyzed. Long axis strain (LAS) and myocardial contraction fraction (MCF), as well as morphological and functional markers, were measured. The primary endpoint was death, while death and heart transplantation served as a composite secondary endpoint.ResultsAfter a median follow-up of 41 months, 29 out of 74 patients died and 10 received a heart transplant. Left ventricular (LV) functional parameters were reduced in patients, who met the composite endpoint (LV ejection fraction 51% vs. 61%, LAS − 6.9% vs − 10%, GLS − 12% vs − 15% and MCF 42% vs. 69%; p < 0.001 for all). In unadjusted univariate analysis, LAS (HR = 1.05, p < 0.001) and MCF (HR = 0.96, p < 0.001) were associated with reduced transplant-free survival. Kaplan-Meier analyses showed a significantly lower event-free survival in patients with reduced MCF. MCF and LAS performed best to identify high risk patients for secondary endpoint (Log-rank test p < 0.001) in a combined model. Using sequential Cox regression analysis, the addition of LAS and MCF to LV ejection fraction led to a significant increase in the predictive power of the model (χ2 (df = 1) = 28.2, p < 0.001).ConclusionsLAS and MCF as routinely available and robust CMR-derived parameters predict outcome in LGE positive AL amyloidosis. Patients with impaired LV function in combination with reduced LAS and MCF are at the highest risk for death and heart transplantation.

Highlights

  • Immunoglobulin light chain (AL) amyloidosis is the most common type of systemic amyloidois

  • Baseline characteristics Initially 94 patients with systemic AL amyloidosis were included in the study

  • After the follow-up period, 35 patients were alive without Heart Transplantation (HTX) (47.3%), leaving 39 patients (52.7%), who reached the combined endpoint of death or HTX

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Summary

Introduction

Immunoglobulin light chain (AL) amyloidosis is the most common type of systemic amyloidois. Especially the two biomarkers, N-terminale natriuretic peptide (NT-proBNP) and cardiac Troponin-T (cTNT) are established [11,12,13]. Based on these biomarkers the widely used Mayo Clinic staging was developed for risk stratification of AL patients [11, 14]. The differentiated assessment of functional parameters besides morphological changes is essential for the evaluation of prognosis in systemic immunoglobulin light chain (AL) amyloidosis

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