Assessment of Myocardial Microstructural Dynamics by In Vivo Diffusion Tensor Cardiac Magnetic Resonance

Autor: Philip J. Kilner, Robert S. Balaban, Peter D. Gatehouse, Dumitru Mazilu, Pedro F. Ferreira, Eric Aliotta, Archontis Giannakidis, Daniel B. Ennis, Andrew E. Arai, Ranil de Silva, Laura Ann McGill, Peter Kellman, Andrew D Scott, Dudley J. Pennell, Zohya Khalique, Majid Al-Khalil, Sonia Nielles-Vallespin, David N. Firmin
Přispěvatelé: Heart Research UK, British Heart Foundation, Royal Brompton & Harefield NHS Foundation Trust
Jazyk: angličtina
Rok vydání: 2017
Předmět:
Male
Pathology
Cardiac & Cardiovascular Systems
Magnetic Resonance Spectroscopy
Swine
030204 cardiovascular system & hematology
030218 nuclear medicine & medical imaging
0302 clinical medicine
sheetlet structure
laminar structure
1102 Cardiorespiratory Medicine and Haematology
Cardiac cycle
medicine.diagnostic_test
Ventricular Remodeling
Hypertrophic cardiomyopathy
Myocardial Perfusion Imaging
Dilated cardiomyopathy
WALL
Heart
Middle Aged
WATER DIFFUSION
EUROPEAN-SOCIETY
Diffusion Tensor Imaging
FIBER ORIENTATION
helical structure
Cardiology
cardiovascular system
Female
Cardiology and Cardiovascular Medicine
Life Sciences & Biomedicine
MRI
Adult
Cardiomyopathy
Dilated

medicine.medical_specialty
LEFT-VENTRICLE
STRAIN
left ventricle
Diastole
Magnetic Resonance Imaging
Cine

Article
1117 Public Health and Health Services
03 medical and health sciences
Myocardial perfusion imaging
LAMINAR ARCHITECTURE
Internal medicine
medicine
Animals
Humans
cardiovascular diseases
Systole
Ventricular remodeling
Aged
Science & Technology
business.industry
Myocardium
Cardiomyopathy
Hypertrophic

medicine.disease
hypertrophic cardiomyopathy
dilated cardiomyopathy
Disease Models
Animal

Cardiovascular System & Hematology
Case-Control Studies
Cardiovascular System & Cardiology
business
Diffusion MRI
TASK-FORCE
Zdroj: Journal of the American College of Cardiology
ISSN: 1558-3597
0735-1097
Popis: BACKGROUND Cardiomyocytes are organized in microstructures termed sheetlets that reorientate during left ventricular thickening. Diffusion tensor cardiac magnetic resonance (DT-CMR) may enable noninvasive interrogation of in vivo cardiac microstructural dynamics. Dilated cardiomyopathy (DCM) is a condition of abnormal myocardium with unknown sheetlet function. OBJECTIVES This study sought to validate in vivo DT-CMR measures of cardiac microstructure against histology, characterize microstructural dynamics during left ventricular wall thickening, and apply the technique in hypertrophic cardiomyopathy (HCM) and DCM. METHODS In vivo DT-CMR was acquired throughout the cardiac cycle in healthy swine, followed by in situ and ex vivo DT-CMR, then validated against histology. In vivo DT-CMR was performed in 19 control subjects, 19 DCM, and 13 HCM patients. RESULTS In swine, a DT-CMR index of sheetlet reorientation (E2A) changed substantially (E2A mobility ~46°). E2A changes correlated with wall thickness changes (in vivo r2 = 0.75; in situ r2 = 0.89), were consistently observed under all experimental conditions, and accorded closely with histological analyses in both relaxed and contracted states. The potential contribution of cyclical strain effects to in vivo E2A was ~17%. In healthy human control subjects, E2A increased from diastole (18°) to systole (65°; p < 0.001; E2A mobility = 45°). HCM patients showed significantly greater E2A in diastole than control subjects did (48 ; p < 0.001) with impaired E2A mobility (23°; p < 0.001). In DCM, E2A was similar to control subjects in diastole, but systolic values were markedly lower (40° ; p < 0.001) with impaired E2A mobility (20°; p < 0.001). CONCLUSIONS Myocardial microstructure dynamics can be characterized by in vivo DT-CMR. Sheetlet function was abnormal in DCM with altered systolic conformation and reduced mobility, contrasting with HCM, which showed reduced mobility with altered diastolic conformation. These novel insights significantly improve understanding of contractile dysfunction at a level of noninvasive interrogation not previously available in humans. (J Am Coll Cardiol 2017;69:661–76) Published by Elsevier on behalf of the American College of Cardiology Foundation.
Databáze: OpenAIRE