scholarly journals Reproducibility of in-vivo diffusion tensor cardiovascular magnetic resonance in hypertrophic cardiomyopathy

2012 ◽  
Vol 14 (1) ◽  
pp. 86 ◽  
Author(s):  
Laura-Ann McGill ◽  
Tevfik F Ismail ◽  
Sonia Nielles-Vallespin ◽  
Pedro Ferreira ◽  
Andrew D Scott ◽  
...  
2013 ◽  
Vol 15 (1) ◽  
pp. 22 ◽  
Author(s):  
Laura-Ann McGill ◽  
Tevfik Ismail ◽  
Sonia Nielles-Vallespin ◽  
Pedro Ferreira ◽  
Andrew D Scott ◽  
...  

2018 ◽  
Vol 81 (4) ◽  
pp. 2759-2773 ◽  
Author(s):  
Jan N. Rose ◽  
Sonia Nielles‐Vallespin ◽  
Pedro F. Ferreira ◽  
David N. Firmin ◽  
Andrew D. Scott ◽  
...  

2017 ◽  
Vol 80 (2) ◽  
pp. 648-654 ◽  
Author(s):  
Margarita Gorodezky ◽  
Andrew D. Scott ◽  
Pedro F. Ferreira ◽  
Sonia Nielles-Vallespin ◽  
Dudley J. Pennell ◽  
...  

2019 ◽  
Vol 33 (3) ◽  
pp. 331-342
Author(s):  
Zohya Khalique ◽  
Andrew D. Scott ◽  
Pedro F. Ferreira ◽  
Sonia Nielles-Vallespin ◽  
David N. Firmin ◽  
...  

Abstract Objectives Diffusion tensor cardiovascular magnetic resonance (DT-CMR) interrogates myocardial microstructure. Two frequently used in vivo DT-CMR techniques are motion-compensated spin echo (M2-SE) and stimulated echo acquisition mode (STEAM). Whilst M2-SE is strain-insensitive and signal to noise ratio efficient, STEAM has a longer diffusion time and motion compensation is unnecessary. Here we compare STEAM and M2-SE DT-CMR in patients. Materials and methods Biphasic DT-CMR using STEAM and M2-SE, late gadolinium imaging and pre/post gadolinium T1-mapping were performed in a mid-ventricular short-axis slice, in ten hypertrophic cardiomyopathy (HCM) patients at 3 T. Results Adequate quality data were obtained from all STEAM, but only 7/10 (systole) and 4/10 (diastole) M2-SE acquisitions. Compared with STEAM, M2-SE yielded higher systolic mean diffusivity (MD) (p = 0.02) and lower fractional anisotropy (FA) (p = 0.02, systole). Compared with segments with neither hypertrophy nor late gadolinium, segments with both had lower systolic FA using M2-SE (p = 0.02) and trend toward higher MD (p = 0.1). The negative correlation between FA and extracellular volume fraction was stronger with STEAM than M2-SE (r2 = 0.29, p < 0.001 STEAM vs. r2 = 0.10, p = 0.003 M2-SE). Discussion In HCM, only STEAM reliably assesses biphasic myocardial microstructure. Higher MD and lower FA from M2-SE reflect the shorter diffusion times. Further work will relate DT-CMR parameters and microstructural changes in disease.


2019 ◽  
Vol 95 (1126) ◽  
pp. 433-438
Author(s):  
Zohya Khalique ◽  
Dudley Pennell

Cardiac structure and function are complex and inter-related. Current in vivo techniques assess the heart on a macroscopic scale, but a novel technique called diffusion tensor cardiovascular magnetic resonance (DT-CMR) can now assess the cardiac microstructure non-invasively. It provides information on the helical arrangement of cardiomyocytes that drives torsion and offers dynamic assessment of the sheetlets (aggregated cardiomyocytes) that rotate through the cardiac cycle to facilitate wall thickening. Through diffusion biomarkers, the expansion and organisation of the underlying myocardium can be described. DT-CMR has already identified novel microstructural abnormalities in cardiomyopathy, and ischaemic and congenital heart disease. This new knowledge supports the potential of DT-CMR to improve diagnostics and prognostication in various cardiac diseases.


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