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Extracellular volume fraction mapping at 3T with non-rigid image co-registration
Journal of Cardiovascular Magnetic Resonance volume 18, Article number: P32 (2016)
MOLLI-based T1-mapping is a robust method for myocardial tissue characterization. Extracellular volume fraction (ECV), a marker of diffuse fibrosis, requires pre- and post-contrast T1 values. However, ECV mapping is not widely available because of complexities in motion correction and image co-registration. Here, we demonstrated ECV mapping using a novel approach for motion compensation at 3T.
All patients underwent cardiovascular magnetic resonance (CMR) on a 3T system (Philips Ingenia). T1 maps were acquired in the basal and mid-cavity short-axis level, pre- and 20-min post-contrast (Gadovist 0.1 mmol/kg) with a 5s(3s)3s and 4s(1s)3s(1s)2s MOLLI acquisition scheme, respectively. A modified non-rigid, non-parametric registration method consisting of elastic registration steps was applied to generate motion-corrected T1 maps and subsequent ECV maps . T1 error maps and overlay images were used as an indication for quality control. Global ECV values were expressed as mean+/-standard deviation (SD).
A total of 33 ECV maps were obtained in 18 patients (mean age 47+/-19 years, 12 males): 10 with chronic myocardial infarction and 8 with dilated and hypertrophic cardiomyopathies. 28 cases (85%) demonstrated clear improvement in image quality after motion correction and co-registration. Two examples are shown in Figures 1 and 2. Global ECV values in the patients with myocardial infarction and cardiomyopathies were 34.9+/-4.9% and 36.4+/-6.0%, respectively.
Automated motion correction and co-registration improved the quality of T1 and ECV maps at 3T, making ECV mapping feasible for clinical application.
Kabus : WBIR. 2010
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Le, T.T., Zhang, S., Kabus, S. et al. Extracellular volume fraction mapping at 3T with non-rigid image co-registration. J Cardiovasc Magn Reson 18, P32 (2016). https://doi.org/10.1186/1532-429X-18-S1-P32
- Cardiovascular Magnetic Resonance
- Hypertrophic Cardiomyopathy
- Motion Correction
- Diffuse Fibrosis
- Chronic Myocardial Infarction