Multi-Echo-Based Echo-Planar Spectroscopic Imaging Using a 3T MRI Scanner.
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ABSTRACT:
SUBMITTER: Furuyama JK
PROVIDER: S-EPMC5448876 | biostudies-other | 2011 Oct
REPOSITORIES: biostudies-other
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Project description:To detect regional metabolic differences in amyotrophic lateral sclerosis (ALS) with whole-brain echo-planar spectroscopic imaging.Sixteen patients with ALS (nine men, seven women; mean age, 56.6 years), five persons suspected of having ALS (four men, one woman; mean age, 62.6 years), and 10 healthy control subjects (five men, five women; mean age, 56.1 years) underwent echo-planar spectroscopic imaging after providing informed consent. The study was approved by the institutional review board and complied with HIPAA. Data were analyzed with the Metabolic Imaging and Data Analysis System software, and processed metabolite maps were coregistered and normalized to a standard brain template. Metabolite maps of creatine (Cr), choline (Cho), and N-acetylaspartate (NAA) were segmented into 81 regions with Automated Anatomical Labeling software to measure metabolic changes throughout the brains of patients with ALS. Statistical analysis involved an unpaired, uncorrected, two-sided Student t test.The NAA/Cho ratio across six regions was significantly lower by a mean of 23% (P ≤ .01) in patients with ALS than in control subjects. These regions included the caudate, lingual gyrus, supramarginal gyrus, and right and left superior and right inferior occipital lobes. The NAA/Cr ratio was significantly lower (P ≤ .01) in eight regions in the patient group, by a mean of 16%. These included the caudate, cuneus, frontal inferior operculum, Heschl gyrus, precentral gyrus, rolandic operculum, and superior and inferior occipital lobes. The Cho/Cr ratio did not significantly differ in any region between patient and control groups.Whole-brain echo-planar spectroscopic imaging permits detection of regional metabolic abnormalities in ALS, including not only the motor cortex but also several other regions implicated in ALS pathophysiologic findings.
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Project description:PURPOSE:To measure temperature over a large brain volume with fine spatiotemporal resolution. METHODS:A three-dimensional stack-of-stars echo-planar imaging sequence combining echo-planar imaging and radial sampling with golden angle spacing was implemented at 3T for proton resonance frequency-shift temperature imaging. The sequence acquires a 188x188x43 image matrix with 1.5x1.5x2.75 mm3 spatial resolution. Temperature maps were reconstructed using sensitivity encoding (SENSE) image reconstruction followed by the image domain hybrid method, and using the k-space hybrid method. In vivo temperature maps were acquired without heating to measure temperature precision in the brain, and in a phantom during high-intensity focused ultrasound sonication. RESULTS:In vivo temperature standard deviation was less than 1°C at dynamic scan times down to 0.75 s. For a given frame rate, scanning at a minimum repetition time (TR) with minimum acceleration yielded the lowest standard deviation. With frame rates around 3 s, the scan was tolerant to a small number of receive coils, and temperature standard deviation was 48% higher than a standard two-dimensional Fourier transform temperature mapping scan, but provided whole-brain coverage. Phantom temperature maps with no visible aliasing were produced for dynamic scan times as short as 0.38 s. k-Space hybrid reconstructions were more tolerant to acceleration. CONCLUSION:Three-dimensional stack-of-stars echo-planar imaging temperature mapping provides volumetric brain coverage and fine spatiotemporal resolution. Magn Reson Med 79:2003-2013, 2018. © 2017 International Society for Magnetic Resonance in Medicine.
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