3-Dimensional Strain Analysis of Hypertrophic Cardiomyopathy: Insights From the NHLBI International HCM Registry.


Journal

JACC. Cardiovascular imaging
ISSN: 1876-7591
Titre abrégé: JACC Cardiovasc Imaging
Pays: United States
ID NLM: 101467978

Informations de publication

Date de publication:
04 2023
Historique:
received: 22 02 2022
revised: 04 10 2022
accepted: 13 10 2022
medline: 7 4 2023
pubmed: 18 1 2023
entrez: 17 1 2023
Statut: ppublish

Résumé

Abnormal global longitudinal strain (GLS) has been independently associated with adverse cardiac outcomes in both obstructive and nonobstructive hypertrophic cardiomyopathy. The goal of this study was to understand predictors of abnormal GLS from baseline data from the National Heart, Lung, and Blood Institute (NHLBI) Hypertrophic Cardiomyopathy Registry (HCMR). The study evaluated comprehensive 3-dimensional left ventricular myocardial strain from cine cardiac magnetic resonance in 2,311 patients from HCMR using in-house validated feature-tracking software. These data were correlated with other imaging markers, serum biomarkers, and demographic variables. Abnormal median GLS (> -11.0%) was associated with higher left ventricular (LV) mass index (93.8 ± 29.2 g/m Abnormal strain in hypertrophic cardiomyopathy is associated with other imaging and serum biomarkers of increased risk. Further follow-up of the HCMR cohort is needed to understand the independent relationship between LV strain and adverse cardiac outcomes in hypertrophic cardiomyopathy.

Sections du résumé

BACKGROUND
Abnormal global longitudinal strain (GLS) has been independently associated with adverse cardiac outcomes in both obstructive and nonobstructive hypertrophic cardiomyopathy.
OBJECTIVES
The goal of this study was to understand predictors of abnormal GLS from baseline data from the National Heart, Lung, and Blood Institute (NHLBI) Hypertrophic Cardiomyopathy Registry (HCMR).
METHODS
The study evaluated comprehensive 3-dimensional left ventricular myocardial strain from cine cardiac magnetic resonance in 2,311 patients from HCMR using in-house validated feature-tracking software. These data were correlated with other imaging markers, serum biomarkers, and demographic variables.
RESULTS
Abnormal median GLS (> -11.0%) was associated with higher left ventricular (LV) mass index (93.8 ± 29.2 g/m
CONCLUSIONS
Abnormal strain in hypertrophic cardiomyopathy is associated with other imaging and serum biomarkers of increased risk. Further follow-up of the HCMR cohort is needed to understand the independent relationship between LV strain and adverse cardiac outcomes in hypertrophic cardiomyopathy.

Identifiants

pubmed: 36648040
pii: S1936-878X(22)00610-6
doi: 10.1016/j.jcmg.2022.10.005
pii:
doi:

Substances chimiques

Contrast Media 0
Gadolinium AU0V1LM3JT
Biomarkers 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

478-491

Subventions

Organisme : British Heart Foundation
ID : PG/15/71/31731
Pays : United Kingdom
Organisme : NHLBI NIH HHS
ID : U01 HL117006
Pays : United States
Organisme : Department of Health
Pays : United Kingdom

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2023. Published by Elsevier Inc.

Déclaration de conflit d'intérêts

Funding Support and Author Disclosures HCMR was supported by the National Institutes of Health, the National Heart, Lung, and Blood Institute (U01HL117006-01A1), and the NIHR Oxford Biomedical Research Centre. Dr Kramer has received research grants from and been consultant for MyoKardia and Cytokinetics. Dr Antiochos has received research funding from the Swiss National Science Foundation (grant P2LAP3_184037), the Novartis Foundation for Medical-Biological Research, the Bangerter-Rhyner Foundation, and the SICPA Foundation. Dr Kwong has received research support from Siemens Healthineers, Bayer AG, and MyoKardia. Dr Maron has received consulting and research support from iRhythm; and has been a consultant for Celltrion and Cytokinetics. Dr Friedrich has been a board member, shareholder, and consultant of Circle Cardiovascular Imaging Inc. Dr Schulz-Menger has been a consultant for Bayer; has received research grants from Bayer, Siemens Healthineers, and Circle Cardiovascular Imaging. Dr Piechnik holds U.S. patent 9,285,446 B2 (“Systems and methods for shortened look locker inversion recovery [Sh-MOLLI] cardiac gated mapping of T1”). Dr White holds shares in Cohesic and has received a research grant from Siemens Healthineers. Dr Neubauer has received research grants from Boehringer Ingelheim and Cytokinetics. All other authors have reported that they have no relationships relevant to the contents of this paper to disclose.

Auteurs

Bobak Heydari (B)

Stephenson Cardiac Imaging Center, Department of Cardiac Sciences, University of Calgary, Calgary, Canada.

Alessandro Satriano (A)

Stephenson Cardiac Imaging Center, Department of Cardiac Sciences, University of Calgary, Calgary, Canada.

Michael Jerosch-Herold (M)

Department of Radiology, Brigham and Women's Hospital, Boston, Massachusetts, USA.

Paul Kolm (P)

MedStar Heart and Vascular Institute, Washington, DC, USA.

Dong-Yun Kim (DY)

National Heart, Lung, and Blood Institute, Bethesda, Maryland, USA.

Kathleen Cheng (K)

Cardiovascular Division, Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts, USA.

Yuna L Choi (YL)

Cardiovascular Division, Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts, USA.

Panagiotis Antiochos (P)

Department of Cardiology, University of Lausanne, Switzerland.

James A White (JA)

Stephenson Cardiac Imaging Center, Department of Cardiac Sciences, University of Calgary, Calgary, Canada.

Masliza Mahmod (M)

Division of Cardiovascular Medicine, University of Oxford, Oxford, United Kingdom.

Kenneth Chan (K)

Division of Cardiovascular Medicine, University of Oxford, Oxford, United Kingdom.

Betty Raman (B)

Division of Cardiovascular Medicine, University of Oxford, Oxford, United Kingdom.

Milind Y Desai (MY)

Cleveland Clinic, Cleveland, Ohio, USA.

Carolyn Y Ho (CY)

Cardiovascular Division, Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts, USA.

Sarahfaye F Dolman (SF)

MedStar Heart and Vascular Institute, Washington, DC, USA.

Patrice Desvigne-Nickens (P)

National Heart, Lung, and Blood Institute, Bethesda, Maryland, USA.

Martin S Maron (MS)

Lahey Hospital & Medical Center, Boston, Massachusetts, USA.

Matthias G Friedrich (MG)

McGill University, Montreal, Canada.

Jeanette Schulz-Menger (J)

Charité Experimental Clinical Research Center and Helios Clinics Berlin-Buch, Berlin, Germany.

Stefan K Piechnik (SK)

Division of Cardiovascular Medicine, University of Oxford, Oxford, United Kingdom.

Evan Appelbaum (E)

Men's Health, Boston, Massachusetts, USA.

William S Weintraub (WS)

MedStar Heart and Vascular Institute, Washington, DC, USA.

Stefan Neubauer (S)

Division of Cardiovascular Medicine, University of Oxford, Oxford, United Kingdom.

Christopher M Kramer (CM)

Cardiovascular Division, University of Virginia Health System, Charlottesville, Virginia, USA.

Raymond Y Kwong (RY)

Cardiovascular Division, Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts, USA. Electronic address: rykwong@bwh.harvard.edu.

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Classifications MeSH