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3.0t biograph mmr

Manufactured by Siemens
Sourced in United States, Germany

The 3.0T Biograph mMR is a magnetic resonance imaging (MRI) system developed by Siemens. It provides high-field magnetic resonance imaging capabilities for medical and research applications. The system integrates magnetic resonance and positron emission tomography (PET) imaging technologies within a single platform.

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2 protocols using 3.0t biograph mmr

1

Assessing Amyloid-Beta Deposition via PET-MRI

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Participants underwent simultaneous three-dimensional (3D) PiB-PET and 3D T1-weighted MRI using a 3.0T Biograph mMR (PET-MR) scanner (Siemens, Washington, DC, United States) according to the manufacturer’s protocols. Details of PiB-PET imaging acquisition and preprocessing are described elsewhere (Supplementary Material).
The automatic anatomic labeling algorithm and a region combining method (Reiman et al., 2009 (link)) were conducted to determine regions of interest (ROIs) and to characterize the PiB retention level in the frontal, lateral parietal, posterior cingulate-precuneus, and lateral temporal regions. The standardized uptake value ratios (SUVRs) were calculated by dividing the mean value for all voxels within each ROI by the mean cerebellar uptake value in the same image. Each participant was classified as cerebral Aβ positive if the SUVR value was >1.4. A global cortical ROI consisting of the four ROIs was defined, and a global Aβ deposition value was generated by dividing the mean value for all voxels of the global cortical ROI by the mean cerebellar uptake value in the same image (Choe et al., 2014 (link)).
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2

FDG-PET and MRI Multimodal Imaging Protocol

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FDG-PET scans were performed using a 3.0T Biograph mMR (PET-MR) scanner (Siemens, Germany) and 3D T1-weighted magnetic resonance imaging was simultaneously performed with PET. Details of the acquisition were described previously (Byun et al., 2017 (link)).
The FDG-PET data were preprocessed using Statistical Parametric Mapping 12 (SPM12; Institute of Neurology, University College of London, United Kingdom) implemented in Matlab 2015ba (Mathworks, Natick, MA, USA). In the first step, static FDG-PET images were co-registered to individual T1 structural images. Next, transformation parameters were calculated from the individual T1 images that were coregistered to the MNI template image. The forward parameters were used to spatially normalize individual T1 and FDG-PET images to the MNI template. The spatially normalized FDG-PET images were smoothed with a 12-mm Gaussian filter and pons were used as the reference region for intensity normalized (Minoshima et al., 1995 (link)).
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