Right Ventricular Free Wall Strain Predicts ATTR Prognosis as Well as Biomarker- Based Staging Systems.

prognosis right ventricle strain wild-type transthyretin amyloidosis

Journal

European heart journal. Cardiovascular Imaging
ISSN: 2047-2412
Titre abrégé: Eur Heart J Cardiovasc Imaging
Pays: England
ID NLM: 101573788

Informations de publication

Date de publication:
18 Sep 2024
Historique:
received: 02 05 2024
revised: 21 07 2024
accepted: 17 09 2024
medline: 18 9 2024
pubmed: 18 9 2024
entrez: 18 9 2024
Statut: aheadofprint

Résumé

The diagnosis of transthyretin amyloidosis (ATTR) significantly impacts the management and prognosis of patients initially presenting with heart failure (HF). Despite recent advances in treatment, prognosticating ATTR remains challenging. We aimed to assess echocardiographic parameters associated with mid-term prognosis in patients with wild-type ATTR using a biomarker staging system as a reference point. We studied 182 consecutive patients with wild-type ATTR (91% male, median age 82 years) who were referred to our center between 2016 and 2022. Using NT- proBNP and eGFR cutoffs, we divided patients into stage I (101 patients, 55.5%), stage II (53, 29.0%), and stage III disease (28, 15.5%). We then compared traditional echocardiographic indices and markers of subclinical ventricular dysfunction (LV global longitudinal strain, RV free wall strain, and LA strain) among groups. Over a fixed follow-up of 18 months, which included treatment with tafamidis 61 mg daily, 48 patients (26.4%) experienced the composite outcome of death or HF hospitalization. When compared with stage I ATTR, the hazard ratio for death or hospitalization was 1.55 (95% CI 0.62-3.86) for stage II ATTR and 4.53 (95% CI 1.66-12.4, p = 0.0116) for stage III ATTR. Among echocardiographic parameters, reduced RV FWS was independently associated with all-cause mortality or HF hospitalization after adjustment for the staging system (HR 2.03, 95% CI 1.07-3.85, p < 0.05). RV FWS should be routinely assessed for all patients with ATTR. It is an independent predictor of poor prognosis and provides additional value beyond biomarker staging systems.

Identifiants

pubmed: 39292174
pii: 7760098
doi: 10.1093/ehjci/jeae242
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press on behalf of the European Society of Cardiology. All rights reserved. For commercial re-use, please contact reprints@oup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact journals.permissions@oup.com.

Auteurs

Sabina Istratoaie (S)

University of Rennes, CHU Rennes, Inserm, LTSI - UMR 1099, 2 Rue Henri le Guilloux, 35000 Rennes, France.
Department of Pharmacology, Toxicology, and Clinical Pharmacology, Iuliu Haţieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.

Corentin Bourg (C)

University of Rennes, CHU Rennes, Inserm, LTSI - UMR 1099, 2 Rue Henri le Guilloux, 35000 Rennes, France.

K Charlotte Lee (KC)

Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.

Benjamin Marut (B)

University of Rennes, CHU Rennes, Inserm, LTSI - UMR 1099, 2 Rue Henri le Guilloux, 35000 Rennes, France.

Jerome Antonelli (J)

University of Rennes, CHU Rennes, Inserm, LTSI - UMR 1099, 2 Rue Henri le Guilloux, 35000 Rennes, France.

Guillaume L'official (G)

University of Rennes, CHU Rennes, Inserm, LTSI - UMR 1099, 2 Rue Henri le Guilloux, 35000 Rennes, France.

Adrien Al Wazzan (A)

University of Rennes, CHU Rennes, Inserm, LTSI - UMR 1099, 2 Rue Henri le Guilloux, 35000 Rennes, France.

Erwan Donal (E)

University of Rennes, CHU Rennes, Inserm, LTSI - UMR 1099, 2 Rue Henri le Guilloux, 35000 Rennes, France.

Classifications MeSH