Obesity Predisposes Anthracycline-Treated Survivors of Childhood and Adolescent Cancers to Subclinical Cardiac Dysfunction.

Anthracycline Cardiomyopathy Cardiotoxicity Heart failure Pediatric Strain echocardiography

Journal

Pediatric cardiology
ISSN: 1432-1971
Titre abrégé: Pediatr Cardiol
Pays: United States
ID NLM: 8003849

Informations de publication

Date de publication:
08 Mar 2024
Historique:
received: 09 11 2023
accepted: 18 01 2024
medline: 8 3 2024
pubmed: 8 3 2024
entrez: 8 3 2024
Statut: aheadofprint

Résumé

Anthracyclines are effective chemotherapeutics used in approximately 60% of pediatric cancer cases but have a well-documented risk of cardiotoxicity. Existing cardiotoxicity risk calculators do not include cardiovascular risk factors present at the time of diagnosis. The goal of this study is to leverage the advanced sensitivity of strain echocardiography to identify pre-existing risk factors for early subclinical cardiac dysfunction among anthracycline-exposed pediatric patients. We identified 115 pediatric patients with cancer who were treated with an anthracycline between 2013 and 2019. Peak longitudinal left ventricular strain was retroactively calculated on 495 surveillance echocardiograms via the TOMTEC AutoSTRAIN software. Cox proportional hazards models were employed to identify risk factors for abnormal longitudinal strain (> - 16%) following anthracycline treatment. High anthracycline dose (≥ 250 mg/m

Identifiants

pubmed: 38456890
doi: 10.1007/s00246-024-03423-x
pii: 10.1007/s00246-024-03423-x
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NIH HHS
ID : TL1-TR002555
Pays : United States
Organisme : NIH HHS
ID : R38-HL143612
Pays : United States
Organisme : NIH HHS
ID : P30 CA016672
Pays : United States
Organisme : NIH HHS
ID : R01-HL160654
Pays : United States

Informations de copyright

© 2024. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

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Auteurs

Ian A George (IA)

Duke University School of Medicine, Durham, NC, USA.

BriAnna Souder (B)

Duke Department of Pediatrics, Division of Cardiology, Duke University School of Medicine, Durham, NC, USA.

Amy Berkman (A)

Duke Department of Pediatrics, Division of Cardiology, Duke University School of Medicine, Durham, NC, USA.
Department of Oncology, St. Jude Children's Research Hospital, Memphis, TN, USA.

David H Noyd (DH)

Duke Department of Pediatrics, Division of Cardiology, Duke University School of Medicine, Durham, NC, USA.
Seattle Children's Hospital, Seattle, WA, USA.

M Jay Campbell (M)

Duke Department of Pediatrics, Division of Cardiology, Duke University School of Medicine, Durham, NC, USA.

Piers C A Barker (PCA)

Duke Department of Pediatrics, Division of Cardiology, Duke University School of Medicine, Durham, NC, USA.

Michael Roth (M)

Division of Pediatrics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Michelle A T Hildebrandt (MAT)

Department of Lymphoma and Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Kevin C Oeffinger (KC)

Department of Medicine, Duke University and Duke Cancer Institute, Durham, NC, USA.

Andrew W McCrary (AW)

Duke Department of Pediatrics, Division of Cardiology, Duke University School of Medicine, Durham, NC, USA. andrew.mccrary@duke.edu.
Duke University Medical Center, Box 3090, Durham, NC, 27710, USA. andrew.mccrary@duke.edu.

Andrew P Landstrom (AP)

Duke Department of Pediatrics, Division of Cardiology, Duke University School of Medicine, Durham, NC, USA. andrew.landstrom@duke.edu.
Duke University Medical Center, Box 2652, Durham, NC, 27710, USA. andrew.landstrom@duke.edu.

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