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Impact of the Noninvasive Diagnostic Algorithm on Clinical Presentation and Prognosis in Cardiac Amyloidosis

Tini, Giacomo
•
Cristiano, Ernesto
•
Zampieri, Mattia
altro
Musumeci, Beatrice
2024
  • journal article

Periodico
JACC. ADVANCES
Abstract
Background: The introduction of a noninvasive diagnostic algorithm in 2016 led to increased awareness and recognition of cardiac amyloidosis (CA). Objectives: The purpose of this study was to analyze the impact of the introduction of the noninvasive diagnostic algorithm on diagnosis and prognosis in a multicenter Italian CA cohort. Methods: This was a retrospective analysis of 887 CA patients from 5 Italian Cardiomyopathies Referral Centers: 311 light-chain CA, 87 variant transthyretin (TTR)-related CA, 489 wild-type TTR-related CA. Clinical characteristics and outcomes (all-cause mortality and heart failure [HF] hospitalizations) were compared overall and for each CA subtype between patients diagnosed before versus after 2016. Outcomes were further compared by propensity score weighted Kaplan-Meier analysis and Cox regression analysis. Results: CA diagnoses increased after 2016, in particular for wild-type TTR-related CA. Patients diagnosed after versus before 2016 were older, had less frequently a history of HF prior to diagnosis, and NYHA functional class III-IV at diagnosis. Over a median follow-up of 18 months, 172 (86%) patients diagnosed before 2016 died or had an HF hospitalization, versus 300 (44%) diagnosed after 2016. Propensity score weighted Kaplan-Meier analysis showed worse outcomes (P < 0.001) for patients diagnosed before 2016. At Cox regression analysis, CA diagnosis after 2016 was an independent protective factor for the composite outcome (HR: 0.69; P = 0.001), with interaction by CA subtype (significant in TTR-related CA and null in light-chain). Conclusions: CA patients diagnosed after 2016 showed a less severe phenotype and a better prognosis. The impact of the noninvasive diagnostic algorithm on outcomes was particularly relevant in TTR-related CA.
DOI
10.1016/j.jacadv.2024.101232
WOS
WOS:001492722000007
Archivio
https://hdl.handle.net/11368/3091080
info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85202941597
https://www.sciencedirect.com/science/article/pii/S2772963X24004630?via=ihub
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11405895/
Diritti
open access
license:creative commons
license:digital rights management non definito
license uri:http://creativecommons.org/licenses/by-nc-nd/4.0/
license uri:iris.pri00
Soggetti
  • AL cardiac amyloidosi...

  • cardiac amyloidosi

  • heart failure

  • noninvasive diagnosi

  • transthyretin cardiac...

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