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In Vivo Quantitative Assessment of Myocardial Structure, Function, Perfusion and Viability Using Cardiac Micro-computed Tomography
Published on: February 16, 2016
Assessment of Myocardial Microstructural Dynamics by In Vivo Diffusion Tensor Cardiac Magnetic Resonance
Sonia Nielles-Vallespin1, Zohya Khalique2, Pedro F Ferreira2
1National Heart, Lung, and Blood Institute, National Institutes of Health, Department of Health and Human Services, Bethesda, Maryland; Cardiovascular Magnetic Resonance Unit, Royal Brompton and Harefield National Health Service Foundation Trust, London, United Kingdom; National Heart and Lung Institute, Imperial College London, London, United Kingdom.
Diffusion tensor cardiac magnetic resonance (DT-CMR) reveals abnormal cardiomyocyte sheetlet function in dilated cardiomyopathy (DCM) and hypertrophic cardiomyopathy (HCM). This noninvasive technique uncovers unique microstructural dynamics in these heart conditions.
Area of Science:
- Cardiovascular Imaging
- Cardiac MRI
- Biomedical Engineering
Background:
- Cardiomyocytes form microstructures called sheetlets, which change orientation during left ventricular thickening.
- Dilated cardiomyopathy (DCM) involves abnormal heart muscle with poorly understood sheetlet function.
- Diffusion tensor cardiac magnetic resonance (DT-CMR) offers a potential noninvasive method to study cardiac microstructure dynamics in vivo.
Purpose of the Study:
- Validate in vivo DT-CMR measures of cardiac microstructure against histological data.
- Characterize microstructural dynamics during left ventricular wall thickening.
- Apply DT-CMR to study hypertrophic cardiomyopathy (HCM) and DCM patients.
Main Methods:
- Acquired in vivo DT-CMR throughout the cardiac cycle in healthy swine.
- Validated DT-CMR measures against in situ and ex vivo DT-CMR and histology.
- Performed in vivo DT-CMR in human subjects: 19 controls, 19 DCM patients, and 13 HCM patients.
Main Results:
- In swine, sheetlet reorientation (E2A) correlated strongly with wall thickening (r²=0.75-0.89) and aligned with histology.
- Healthy humans showed significant E2A increase from diastole (18°) to systole (65°).
- HCM patients exhibited reduced E2A mobility (23°) and altered diastolic conformation; DCM patients showed reduced systolic E2A (40°) and impaired mobility (20°).
Conclusions:
- In vivo DT-CMR can characterize myocardial microstructure dynamics.
- DCM shows abnormal sheetlet function with altered systolic conformation and reduced mobility.
- HCM demonstrates reduced mobility with altered diastolic conformation, offering new insights into contractile dysfunction.
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