Identifying High-risk Fontan Phenotypes Using K-means Clustering of CMR-based Dyssynchrony Metrics.

Fontan, cardiovascular magnetic, resonance imaging, dyssynchrony pediatrics unsuperivsed machine learning

Journal

Journal of cardiovascular magnetic resonance : official journal of the Society for Cardiovascular Magnetic Resonance
ISSN: 1532-429X
Titre abrégé: J Cardiovasc Magn Reson
Pays: England
ID NLM: 9815616

Informations de publication

Date de publication:
12 Jul 2024
Historique:
received: 30 03 2024
revised: 20 06 2024
accepted: 08 07 2024
medline: 15 7 2024
pubmed: 15 7 2024
entrez: 14 7 2024
Statut: aheadofprint

Résumé

Individuals with a Fontan circulation encompass a heterogenous group with adverse outcomes linked to ventricular dilation, dysfunction, and dyssynchrony. The purpose of this study was to assess if unsupervised machine learning cluster analysis of cardiac magnetic resonance (CMR)-derived dyssynchrony metrics can separate ventricles in the Fontan circulation from normal control left ventricles and identify prognostically distinct subgroups within the Fontan cohort. This single-center, retrospective study used 503 CMR studies from Fontan patients (median age 15y) and 42 from age-matched controls from January 2005 to May 2011. Feature tracking on short-axis cine stacks assessed radial and circumferential strain, strain rate, and displacement. Unsupervised K-means clustering was applied to 24 mechanical dyssynchrony metrics derived from these deformation measurements. Clusters were compared for demographic, anatomical, and composite outcome of death, or heart transplantation. Four distinct phenotypic clusters were identified. Over a median follow-up of 4.2y (IQR 1.7-8.8y), 58 (11.5%) patients met the composite outcome. The highest risk cluster (largely comprised of right or mixed ventricular morphology and dilated, dyssynchronous ventricles) exhibited a higher hazard for the composite outcome compared to the lowest-risk cluster while controlling for ventricular morphology (HR 6.4; 95% CI 2.1-19.3; P value 0.001) and higher indexed end-diastolic volume (HR 3.2; 95% CI 1.04-10.0; P value 0.043) per 10ml/m Unsupervised machine learning using CMR-derived dyssynchrony metrics identified four distinct clusters of patients with Fontan circulation and healthy controls with varying clinical characteristics and risk profiles. This technique can be used to guide future studies and identify more homogeneous subsets of patients from an overall heterogeneous population.

Sections du résumé

BACKGROUND BACKGROUND
Individuals with a Fontan circulation encompass a heterogenous group with adverse outcomes linked to ventricular dilation, dysfunction, and dyssynchrony. The purpose of this study was to assess if unsupervised machine learning cluster analysis of cardiac magnetic resonance (CMR)-derived dyssynchrony metrics can separate ventricles in the Fontan circulation from normal control left ventricles and identify prognostically distinct subgroups within the Fontan cohort.
MATERIALS AND METHODS METHODS
This single-center, retrospective study used 503 CMR studies from Fontan patients (median age 15y) and 42 from age-matched controls from January 2005 to May 2011. Feature tracking on short-axis cine stacks assessed radial and circumferential strain, strain rate, and displacement. Unsupervised K-means clustering was applied to 24 mechanical dyssynchrony metrics derived from these deformation measurements. Clusters were compared for demographic, anatomical, and composite outcome of death, or heart transplantation.
RESULTS RESULTS
Four distinct phenotypic clusters were identified. Over a median follow-up of 4.2y (IQR 1.7-8.8y), 58 (11.5%) patients met the composite outcome. The highest risk cluster (largely comprised of right or mixed ventricular morphology and dilated, dyssynchronous ventricles) exhibited a higher hazard for the composite outcome compared to the lowest-risk cluster while controlling for ventricular morphology (HR 6.4; 95% CI 2.1-19.3; P value 0.001) and higher indexed end-diastolic volume (HR 3.2; 95% CI 1.04-10.0; P value 0.043) per 10ml/m
CONCLUSIONS CONCLUSIONS
Unsupervised machine learning using CMR-derived dyssynchrony metrics identified four distinct clusters of patients with Fontan circulation and healthy controls with varying clinical characteristics and risk profiles. This technique can be used to guide future studies and identify more homogeneous subsets of patients from an overall heterogeneous population.

Identifiants

pubmed: 39004418
pii: S1097-6647(24)01087-1
doi: 10.1016/j.jocmr.2024.101060
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

101060

Informations de copyright

Published by Elsevier Inc.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Addison Gearhart (A)

Department of Cardiology, Boston Children's Hospital, Boston, MA, USA; Department of Pediatrics, Harvard Medical School, Boston, MA, USA. Electronic address: Addison.gearhart@cardio.chboston.org.

Sunakshi Bassi (S)

Department of Pediatrics, Harvard Medical School, Boston, MA, USA.

Rahul H Rathod (RH)

Department of Cardiology, Boston Children's Hospital, Boston, MA, USA; Department of Pediatrics, Harvard Medical School, Boston, MA, USA.

Rebecca S Beroukhim (RS)

Department of Cardiology, Boston Children's Hospital, Boston, MA, USA; Department of Pediatrics, Harvard Medical School, Boston, MA, USA.

Stuart Lipsitz (S)

Department of Cardiology, Boston Children's Hospital, Boston, MA, USA; Division of General Internal Medicine, Brigham and Women's Hospital, Boston, MA.

Maxwell P Gold (MP)

Massachusetts Institute of Technology, Boston, MA.

David M Harrild (DM)

Department of Cardiology, Boston Children's Hospital, Boston, MA, USA; Department of Pediatrics, Harvard Medical School, Boston, MA, USA.

Audrey Dionne (A)

Department of Cardiology, Boston Children's Hospital, Boston, MA, USA; Department of Pediatrics, Harvard Medical School, Boston, MA, USA.

Sunil J Ghelani (SJ)

Department of Cardiology, Boston Children's Hospital, Boston, MA, USA; Department of Pediatrics, Harvard Medical School, Boston, MA, USA.

Classifications MeSH