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3.0t biograph mmr pet mr scanner

Manufactured by Siemens
Sourced in United States

The 3.0T Biograph mMR (PET-MR) scanner is a medical imaging device that combines positron emission tomography (PET) and magnetic resonance imaging (MRI) technologies in a single system. It is designed to acquire simultaneous PET and MRI data, allowing for the integration of functional and anatomical information.

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10 protocols using 3.0t biograph mmr pet mr scanner

1

Multimodal Imaging of Brain in Participants

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Participants underwent two-sessions of PET-MR scanning to obtain multi-modal imaging including [11C]PiB-PET, [18F]FDG-PET, MRI, and MRA using a 3.0T Biograph mMR (PET-MR) scanner (Siemens, Washington, DC, USA) according to the manufacturer's approved guidelines. Detailed information on image preprocessing procedures will be described in more specialized papers.
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2

PiB-PET and MRI Imaging of Amyloid-Beta

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All participants underwent simultaneous three-dimensional [11C] Pittsburg compound B (PiB)-positron emission tomography (PET) and T1-weighted MRI scans using a 3.0 T Biograph mMR (PET-MR) scanner (Siemens; Washington DC, WC, USA) according to the manufacturer’s guidelines. The details of PiB-PET acquisition and preprocessing were described in our previous report30 (link). An AAL algorithm and a region-combining method31 (link) were applied to determine the regions of interest (ROIs) for characterization of PiB retention levels in the frontal, lateral parietal, posterior cingulate-precuneus, and lateral temporal regions. The standardized uptake value ratio (SUVR) values for each ROI were calculated by dividing the mean value for all voxels within each ROI by the mean cerebellar uptake value on the same image. Each participant was classified as Aβ positive (Aβ+) if the SUVR value was >1.4 in at least one of the four ROIs31 (link),32 (link). Considering the bimodal distribution of our PiB data, only Aβ positivity was used as an outcome variable33 (link),34 (link).
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3

Amyloid PET Imaging and Brain Regions

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All the participants underwent simultaneous three-dimensional (3D) [11C] Pittsburgh compound B-positron emission tomography (PiB-PET), and 3D T1-weighted MRI, using the 3.0 T Biograph mMR (PET-MR) scanner (Siemens, Washington, DC, USA). Details of PiB-PET imaging acquisition and preprocessing were previously described [27 (link)].
The automated anatomical labeling algorithm [28 (link)] and a region-combining method [29 (link)] were applied to determine the regions of interest (ROIs) to measure global amyloid retention level in the frontal, lateral parietal, precuneus/posterior cingulate precuneus (PC/PCC), and lateral temporal regions. The standardized uptake value ratios (SUVR) were generated by the mean value for all voxels within the ROIs by the mean cerebellar uptake value in the same image [28 (link), 29 (link)]. Participants were classified as Aβ positive if the SUVR value was > 1.4.
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4

Multimodal Neuroimaging of Amyloid Deposition

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All subjects underwent simultaneous three-dimensional (3D) [11C] Pittsburgh compound B (PiB)-PET and 3D T1-weighted magnetization-prepared rapid acquisition with gradient echo (MPRAGE) sequence MRI scans using a 3.0T Biograph mMR (PET-MR) scanner (Siemens, Washington DC, USA) according to the manufacturer’s approved guidelines. 3D T1-weighted images were acquired in the sagittal orientation, and the acquisition parameters were as follows: repetition time = 1670 ms, echo time = 1.89 ms, field of view = 250 mm, and a 256 × 256 matrix with a 1.0-mm slice thickness. For PiB-PET, a 30-minute emission scan was obtained 40 minutes after intravenous administration of 555 MBq of [11C]PiB (range, 450–610 MBq). The PiB-PET data collected in list mode were processed for routine corrections such as uniformity, UTE-based attenuation, and decay corrections and were reconstructed into a 344 × 344 image matrix using iterative methods (5 iterations with 21 subsets).
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5

Multimodal Neuroimaging of Amyloid Deposition

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All subjects underwent simultaneous three-dimensional (3D) [11C] Pittsburgh compound B (PiB)-positron emission tomography (PET), 3D T1-weighted MRI, fluid-attenuated inversion (FLAIR) images, and 3D time-of-flight (TOF)-MR angiography using the 3.0-T Biograph mMR (PET-MR) scanner (Siemens, Washington DC, USA). Acquisition parameters for MRI and MR angiography are described in Methods S1 (Additional file 1).
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6

Quantifying Cerebral Amyloid-Beta Burden

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Participants underwent simultaneous three-dimensional (3D) [11C] Pittsburgh compound B (PiB) positron emission tomography (PET) and 3D T1-weighted MRI using a 3.0T Biograph mMR (PET-MR) scanner (Siemens, Washington, DC, USA) according to the manufacturer’s guidelines. Details of PiB-PET image acquisition and preprocessing are described in the Supplementary material.
The automatic anatomic labeling algorithm and a region-combining method40 were applied to determine regions of interest (ROIs) to characterize the PiB retention level in the frontal, lateral parietal, posterior cingulate-precuneus, and lateral temporal regions. The standardized uptake value ratio (SUVR) for each ROI was calculated by dividing the mean value for all voxels within the ROI by the mean cerebellar uptake value in the same image. Each participant was classified as Aβ positive (Aβ+) if the SUVR value was >1.4 in at least one of the four ROIs or as Aβ negative (Aβ−) if the SUVR values was ≤1.4 for all four ROIs.40 ,41 A global cortical ROI comprising the four ROIs was also defined, and a global cerebral Aβ retention 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.
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7

Quantifying Brain Amyloid Deposition via PET-MRI

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All participants underwent simultaneous three-dimensional (3D) [11C] Pittsburg compound B (PiB)-positron emission tomography (PET) and 3D T1-weighted MRI using a 3.0T Biograph mMR (PET-MR) scanner (Siemens, Washington DC, USA) according to the manufacturer’s protocols. We have described the details of PiB-PET image acquisition and preprocessing previously [24 (link)]. The automatic anatomic labeling algorithm and the region combination method [25 (link)] were used to determine regions of interest (ROIs) and to characterize PiB retention in the frontal, lateral parietal, posterior cingulate-precuneus, and lateral temporal regions. A global cortical ROI (consisting of the four smaller ROIs) was also defined. A global Aβ retention value, the standardized uptake value ratio (SUVR) for the global cortical ROI, was calculated by dividing the mean values for all voxels of the global cortical ROI by the mean cerebellar uptake value evident in the same images [26 (link)]. A participant was classified as Aβ positive if the SUVR of the global ROI was >1.21 [27 (link)].
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8

Multimodal Imaging of Cerebral Amyloid and Tau

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All participants underwent simultaneous three-dimensional (3D) [11C] Pittsburg compound B (PiB)-PET and 3D T1-weighted MRI using the 3.0T Biograph mMR (PET-MR) scanner (Siemens, Washington DC, USA) at both the initial assessment and 2-year follow-up (Fig. 1). The image processing was conducted utilizing SPM8. An automatic anatomic labeling algorithm and a region combining method were applied to identify specific regions of interests (ROIs) [29 , 30 (link)]. To quantify the extent of cerebral Aβ deposition, the uptake value of [11C] PiB was extracted from ROIs encompassing the frontal, lateral parietal, posterior cingulate-precuneus, and lateral temporal regions. The calculation of the voxel-weighted mean standardized uptake value ratio (SUVR) for these ROIs was achieved by dividing the mean [11C] PiB uptake value of these ROIs by the corresponding mean uptake values of cerebrum white matter, cerebellar white matter, pons and inferior cerebellar gray matter regions [31 (link)–33 (link)]. More detailed information about the methodology used for measuring cerebral Aβ deposition can be found in a prior publication [21 (link)].

Datasets for analysis. Dataset for analysis of association between Aβ or Tau deposition and WMH volume. Aβ = Beta-amyloid, WMH = White matter hyperintensity. A = Aβ-PET, M = MRI scan, T = Tau-PET

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9

PiB-PET and MRI Brain Imaging Protocol

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All participants underwent simultaneous three-dimensional (3D) [11C] Pittsburgh compound B (PiB) PET and 3D T1-weighted MRI scans using a 3.0-T Biograph mMR (PET-MR) scanner (Siemens; Washington DC, USA); the details of the PiB-PET and MRI acquisition and preprocessing have been described in a previous report from our research group [22 (link)]. The automated anatomical labeling algorithm [23 (link)] and a region-combining method [24 (link)] were applied to determine the region of interests (ROIs) to characterize 11C-PiB retention levels in the frontal, lateral parietal, posterior cingulate-precuneus, and lateral temporal regions of the brain. The standardized uptake value ratio (SUVR) for each ROI was calculated by dividing the mean value for all voxels within each ROI by the mean cerebellar uptake value [25 (link)]. Participants were classified as Aβ positive if the SUVR was > 1.4 in at least one of the four ROIs or as Aβ negative if the SUVR each of the four ROIs was ≤ 1.4 [24 (link), 26 (link)]. A global Aβ retention 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 [24 (link), 25 (link), 27 (link)].
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10

3D PiB-PET and MRI Vascular Protocol

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All subjects underwent simultaneous three-dimensional (3D) [ 11 C] Pittsburgh compound B (PiB)-positron emission tomography (PET) and 3D T1-weighted MRI using the 3.0T Biograph mMR (PET-MR) scanner (Siemens, Washington DC, USA). The vascular protocol including 3D time-of-ight (TOF)-MR angiography was also administered by trained MRI technologists. Acquisition parameters for 3D TOF-MR angiography, 3D T1-weighted images, uid attenuated inversion images are described in elsewhere (See Additional le 1).
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