HTGC was quantified by proton magnetic resonance spectroscopy (1H-MRS) of the liver (35 (link)). An 8-mL voxel was positioned in the right lobe of the liver, avoiding gross vascular structures and adipose tissue depots. Sixty-four averages were collected with water suppression. Spectra were obtained with an echo time of 26 ms and a repetition time of 3000 ms. Data points (1024) were collected with use of a 1000-Hz spectral line. Without changing any parameters, spectra without water suppression, with a repetition time of 10 s and 4 averages were obtained as an internal reference. 1H-MRS data were fitted with use of Java-based magnetic resonance user interface software (jMRUI version 2.2), as described previously (36 (link)). HTGC relative to water was calculated as the sum of the signal amplitudes of methyl and methylene divided by the signal amplitude of water ×100.
1.5 tesla mr system
The 1.5 Tesla MR system is a magnetic resonance imaging (MRI) device manufactured by Philips. It generates a static magnetic field of 1.5 Tesla, which is used to produce detailed images of the body's internal structures. The system's core function is to provide high-quality diagnostic imaging capabilities for healthcare professionals.
Lab products found in correlation
7 protocols using 1.5 tesla mr system
Quantifying Visceral Fat and Hepatic Triglycerides
HTGC was quantified by proton magnetic resonance spectroscopy (1H-MRS) of the liver (35 (link)). An 8-mL voxel was positioned in the right lobe of the liver, avoiding gross vascular structures and adipose tissue depots. Sixty-four averages were collected with water suppression. Spectra were obtained with an echo time of 26 ms and a repetition time of 3000 ms. Data points (1024) were collected with use of a 1000-Hz spectral line. Without changing any parameters, spectra without water suppression, with a repetition time of 10 s and 4 averages were obtained as an internal reference. 1H-MRS data were fitted with use of Java-based magnetic resonance user interface software (jMRUI version 2.2), as described previously (36 (link)). HTGC relative to water was calculated as the sum of the signal amplitudes of methyl and methylene divided by the signal amplitude of water ×100.
Hippocampal Volume Quantification from MRI
Hepatic Triglyceride and CETP Assessment
MRI-Guided Radiosurgery Planning Workflow
Abdominal Fat and Liver Triglyceride Quantification
Hepatic triglyceride content was quantified by 1H-MRS of the liver as described previously (Hammer et al. 2008 (link)). Briefly, an 8-mL voxel was positioned in the right lobe of the liver. Spectra were obtained with and without water suppression with free breathing and fitted using Java based MR user interface software (jMRUI version 3.0, Leuven, Belgium) (Naressi et al. 2001 (link)). Mean line widths were calculated. The resonances of methylene and methyl were fitted and used for calculation of triglycerides. HTGC relative to water was calculated as (signal amplitude of triglyceride)/(signal amplitude of water) × 100.
Quantifying Liver Fat Content via 1H-MRS
Quantifying Abdominal Fat Composition
Imaging was performed on a 1.5 Tesla MR system (Philips Medical Systems, Best, the Netherlands). At the level of the fifth lumbar vertebra, three transverse images each with a slice thickness of 10 mm were obtained during a breathhold. Abdominal subcutaneous and visceral fat areas were quantified by converting the number of pixels to square cm for all three slides, and the mean of SAT and VAT areas of the three slides was used in the analyses. Earlier studies have shown that such cross-sectional images are highly correlated to total volumes (correlation coefficients around 0.8) and can therefore validly represent abdominal SAT and VAT. 20
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