Myocardial composition in light-chain cardiac amyloidosis more than 1 year after successful therapy Journal Article


Authors: Cuddy, S. A. M.; Jerosch-Herold, M.; Falk, R. H.; Foley Kijewski, M.; Singh, V.; Ruberg, F. L.; Sanchorawala, V.; Landau, H.; Maurer, M. S.; Yee, A. J.; Bianchi, G.; Di Carli, M. F.; Liao, R.; Kwong, R. Y.; Dorbala, S.
Article Title: Myocardial composition in light-chain cardiac amyloidosis more than 1 year after successful therapy
Abstract: Objectives: The goals of this study were to characterize myocardial composition during the active and remission phases of light-chain (AL) cardiac amyloidosis. Background: Cardiac dysfunction in AL amyloidosis is characterized by dual insults to the myocardium from infiltration and toxicity from light chains during the active phase and by infiltration alone in the remission phase. Methods: Prospectively enrolled subjects with cardiac AL amyloidosis (21 remission AL amyloidosis; age: 63.4 ± 7.3 years; 47.6% male; and 48 active AL amyloidosis; age: 62.5 ± 7.4 years; 60.4% male) underwent contrast-enhanced cardiac magnetic resonance with T1 and T2 mapping and measurement of extracellular volume (ECV). By definition, serum free light-chain levels were normal for at least 1 year following successful AL therapy in the remission group and abnormal in the active group. Results: Myocardial ECV was similarly expanded in the remission and active AL amyloidosis groups (0.488 ± 0.082 vs 0.519 ± 0.083, respectively; P = 0.15). However, myocardial T2 relaxation times (47.7 ± 3.2 ms vs 45.5 ± 3.0 ms; P = 0.008) as well as native T1 times (1,368 ms [IQR: 1,290-1,422 ms] vs 1,264 ms [IQR: 1,203-1,380 ms]; P = 0.024) were significantly higher in the remission compared to the active AL amyloidosis group. Conclusions: Myocardial ECV is substantially expanded in the active AL and remission AL cardiac amyloidosis groups, but native T1 values were higher, suggesting a different myocardial composition. There is no evidence of myocardial edema in active AL cardiac amyloidosis. Future phenotyping studies of AL cardiac amyloidosis need to consider complementary myocardial markers that define the interstitial milieu in addition to changes in extracellular volume. (Molecular Imaging of Primary Amyloid Cardiomyopathy; NCT02641145) © 2022 American College of Cardiology Foundation
Keywords: remission; cardiac amyloidosis; light-chain amyloidosis; al; cmr; active al amyloidosis; myocardial composition
Journal Title: JACC: Cardiovascular Imaging
Volume: 15
Issue: 4
ISSN: 1936-878X
Publisher: Elsevier Science, Inc.  
Date Published: 2022-04-01
Start Page: 594
End Page: 603
Language: English
DOI: 10.1016/j.jcmg.2021.09.032
PUBMED: 34922860
PROVIDER: scopus
PMCID: PMC8995332
DOI/URL:
Notes: Article -- Export Date: 25 April 2022 -- Source: Scopus
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  1. Heather Jolie Landau
    419 Landau