dc.contributor.author
Faragli, Alessandro
dc.contributor.author
Tanacli, Radu
dc.contributor.author
Kolp, Carolin
dc.contributor.author
Abawi, Dawud
dc.contributor.author
Lapinskas, Tomas
dc.contributor.author
Stehning, Christian
dc.contributor.author
Schnackenburg, Bernhard
dc.contributor.author
Lo Muzio, Francesco P.
dc.contributor.author
Fassina, L.
dc.contributor.author
Pieske, Burkert
dc.contributor.author
Nagel, Eike
dc.contributor.author
Post, Heiner
dc.contributor.author
Kelle, Sebastian
dc.contributor.author
Alogna, Alessio
dc.date.accessioned
2022-06-21T11:11:13Z
dc.date.available
2022-06-21T11:11:13Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/35356
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-35072
dc.description.abstract
Background: Cardiovascular magnetic resonance (CMR) strain imaging is an established technique to quantify myocardial deformation. However, to what extent left ventricular (LV) systolic strain, and therefore LV mechanics, reflects classical hemodynamic parameters under various inotropic states is still not completely clear. Therefore, the aim of this study was to investigate the correlation of LV global strain parameters measured via CMR feature tracking (CMR-FT, based on conventional cine balanced steady state free precession (bSSFP) images) with hemodynamic parameters such as cardiac index (CI), cardiac power output (CPO) and end-systolic elastance (Ees) under various inotropic states.
Methods: Ten anaesthetized, healthy Landrace swine were acutely instrumented closed-chest and transported to the CMR facility for measurements. After baseline measurements, two steps were performed: (1) dobutamine-stress (Dobutamine) and (2) verapamil-induced cardiovascular depression (Verapamil). During each protocol, CMR images were acquired in the short axisand apical 2Ch, 3Ch and 4Ch views. MEDIS software was utilized to analyze global longitudinal (GLS), global circumferential (GCS), and global radial strain (GRS).
Results: Dobutamine significantly increased heart rate, CI, CPO and Ees, while Verapamil decreased them. Absolute values of GLS, GCS and GRS accordingly increased during Dobutamine infusion, while GLS and GCS decreased during Verapamil. Linear regression analysis showed a moderate correlation between GLS, GCS and LV hemodynamic parameters, while GRS correlated poorly. Indexing global strain parameters for indirect measures of afterload, such as mean aortic pressure or wall stress, significantly improved these correlations, with GLS indexed for wall stress reflecting LV contractility as the clinically widespread LV ejection fraction.
Conclusion: GLS and GCS correlate accordingly with LV hemodynamics under various inotropic states in swine. Indexing strain parameters for indirect measures of afterload substantially improves this correlation, with GLS being as good as LV ejection fraction in reflecting LV contractility. CMR-FT-strain imaging may be a quick and promising tool to characterize LV hemodynamics in patients with varying degrees of LV dysfunction.
en
dc.rights.uri
https://creativecommons.org/licenses/by/4.0/
dc.subject
Cardiovascular magnetic resonance
en
dc.subject
Feature tracking
en
dc.subject
Left ventricular strain
en
dc.subject
Contractile function
en
dc.subject
Porcine model
en
dc.subject
Translational studies
en
dc.subject
Hemodynamics
en
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::610 Medizin und Gesundheit
dc.title
Cardiovascular magnetic resonance-derived left ventricular mechanics—strain, cardiac power and end-systolic elastance under various inotropic states in swine
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.articlenumber
79
dcterms.bibliographicCitation.doi
10.1186/s12968-020-00679-z
dcterms.bibliographicCitation.journaltitle
Journal of Cardiovascular Magnetic Resonance
dcterms.bibliographicCitation.originalpublishername
Springer Nature
dcterms.bibliographicCitation.volume
22
refubium.affiliation
Charité - Universitätsmedizin Berlin
refubium.funding
Springer Nature DEAL
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.bibliographicCitation.pmid
33256761
dcterms.isPartOf.eissn
1532-429X