Extending Cardiac Functional Assessment with Respiratory-Resolved 3D Cine MRI.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
09 08 2019
Historique:
received: 11 03 2018
accepted: 25 07 2019
entrez: 11 8 2019
pubmed: 11 8 2019
medline: 27 10 2020
Statut: epublish

Résumé

This study aimed to develop a cardiorespiratory-resolved 3D magnetic resonance imaging (5D MRI: x-y-z-cardiac-respiratory) approach based on 3D motion tracking for investigating the influence of respiration on cardiac ventricular function. A highly-accelerated 2.5-minute sparse MR protocol was developed for a continuous acquisition of cardiac images through multiple cardiac and respiratory cycles. The heart displacement along respiration was extracted using a 3D image deformation algorithm, and this information was used to cluster the acquired data into multiple respiratory phases. The proposed approach was tested in 15 healthy volunteers (7 females). Cardiac function parameters, including the end-systolic volume (ESV), end-diastolic volume (EDV), stroke volume (SV), and ejection fraction (EF), were measured for the left and right ventricle in both end-expiration and end-inspiration. Although with the proposed 5D cardiac MRI, there were no significant differences (p > 0.05, t-test) between end-expiration and end-inspiration measurements of the cardiac function in volunteers, incremental respiratory motion parameters that were derived from 3D motion tracking, such as the depth, expiration and inspiration distribution, correlated (p < 0.05, correlation coefficient, Mann-Whitney) with those volume-based parameters of cardiac function and varied between genders. The obtained initial results suggested that this new approach allows evaluation of cardiac function during specific respiratory phases. Thus, it can enable investigation of effects related to respiratory variability and better assessment of cardiac function for studying respiratory and/or cardiac dysfunction.

Identifiants

pubmed: 31399608
doi: 10.1038/s41598-019-47869-z
pii: 10.1038/s41598-019-47869-z
pmc: PMC6689015
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

11563

Subventions

Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States

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Auteurs

Jing Liu (J)

Department of Radiology and Biomedical Imaging, University of California San Francisco, San Francisco, California, United States. jing.liu@ucsf.edu.

Yan Wang (Y)

Department of Radiology and Biomedical Imaging, University of California San Francisco, San Francisco, California, United States.

Zhaoying Wen (Z)

Department of Radiology and Biomedical Imaging, University of California San Francisco, San Francisco, California, United States. zhaoying.wen@ucsf.edu.
Department of Radiology, Anzhen Hospital, Capital Medical University, Beijing, China. zhaoying.wen@ucsf.edu.

Li Feng (L)

Department of Medical Physics, Memorial Sloan Kettering Cancer Center, New York, NY, United States.

Ana Paula Santos Lima (APS)

Department of Radiology and Biomedical Imaging, University of California San Francisco, San Francisco, California, United States.

Vaikom S Mahadevan (VS)

Department of Cardiology, University of California San Francisco, San Francisco, California, United States.

Ann Bolger (A)

Department of Cardiology, University of California San Francisco, San Francisco, California, United States.

David Saloner (D)

Department of Radiology and Biomedical Imaging, University of California San Francisco, San Francisco, California, United States.
Radiology Service, VA Medical Center, San Francisco, California, United States.

Karen Ordovas (K)

Department of Radiology and Biomedical Imaging, University of California San Francisco, San Francisco, California, United States.

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