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Exact hr scanner

Manufactured by Siemens
Sourced in Germany

The EXACT HR+ scanner is a high-resolution computed tomography (CT) system designed for medical imaging. It is capable of producing detailed images of the human body to assist healthcare professionals in diagnosis and treatment. The EXACT HR+ scanner utilizes advanced imaging technology to capture precise anatomical information.

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Lab products found in correlation

7 protocols using exact hr scanner

1

Quantifying Brain Amyloid Deposition via PiB-PET

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Details on the acquisition and post-processing of the PiB-PET examinations have been previously described (Johnson et al., 2014 (link); Okonkwo et al., 2014 (link)). Briefly, 3-dimensional PiB-PET data were acquired on a Siemens EXACT HR+ scanner (Siemens AG, Erlangen, Germany). Imaging consisted of a 6-minute transmission scan and a 70-minute dynamic scan upon bolus injection. Post-processing was based on an in-house automated pipeline (Floberg et al., 2012 (link)). We derived distribution volume ratio (DVR) maps from the PiB images using the Logan method, with a cerebellar gray matter reference (Price et al., 2005 (link)).
An anatomical atlas (Tzourio-Mazoyer et al., 2002 (link)) was used to extract quantitative DVR data from eight bilateral regions of interest (ROIs) that are sensitive to Aβ accumulation (Rosario et al., 2011 (link)). These ROIs were the precuneus, posterior cingulate, orbitofrontal cortex, anterior cingulate, angular gyrus, supramarginal gyrus, middle temporal gyrus, and superior temporal gyrus. The DVR data from the ROIs were combined to form a composite measure of global Aβ load. The time interval between the PET scan and the GXT was 3.10 ± .47 years. GXT was subsequent to the PiB-PET scan for all 69 participants.
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2

PiB-PET Neuroimaging Protocol for Alzheimer's Disease

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For the second research question, participants were selected who underwent a 70-minute dynamic [11C]Pittsburgh compound B (PiB) scan on a Siemens EXACT HR+ scanner (and prior to 2015, a T1-weighted magnetic resonance imaging (MRI) scan on a GE 3.0 T MR750 using an 8-channel head coil). Neuroimaging was completed, on average, 1.4 years (SD = 1.4) after the first visit at which story recall was administered (median visit 2). [11C]PiB radiosynthesis, acquisition and reconstruction parameters, image processing and quantification have been described previously (Johnson et al., 2014 (link)). Briefly, the PET time series was motion corrected, de-noised, and co-registered to T1-w MRI. Time-activity curves were extracted from the co-registered PET data in subject MRI space from gray matter restricted Anatomic Labeling atlas (AAL, Tzourio-Mazoyer, Landeau, et al., 2002) regions of interest (ROIs) warped to MRI space and used to estimate ROI-level distribution volume ratios (DVRs; Logan Graphical Analysis, cerebellum GM reference region, ®k2 =0.149 min−1; (Logan et al., 1996 (link); Lopresti et al., 2005 (link)). PiB positivity was ascertained by applying a threshold to the mean DVR (global PiB) across eight bilateral ROIs (global DVR ≥ 1.19) (Racine et al., 2016 ).
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3

Quantifying Hypoxia with 18F-FMISO PET

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In all cases, patients were injected intravenously with 3.7 MBq/kg of 18F-FMISO. A 20-minute static 18F-FMISO PET emission image was acquired at about 120 minutes after injection of 18F-FMISO. PET scans were performed on two devices, both of which were calibrated. On a CTI EXACT HR+ scanner and a Siemens Biograph40 mCT scanner as previously described (8 (link)). The tumor ROIs on the 18F-FMISO PET images included all regions where there was FMISO uptake, and two 2 cm diameter ROIs on both sides of the cerebellar cortex were used as the image derived blood surrogate to determine the surrogate of tissue to blood ratio (TB ratio). HV was determined by the number of pixels with TB ratio above 1.2.
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4

Brain Imaging Scanners Comparison

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The dedicated brain scanner GEMS PC2048-15B (General Electric Medical Systems, Milwaukee, WI, USA), which was used for Cohort I, had an axial field of view of 15 cm and 15 image planes spaced 6.5 mm apart. The whole body ECAT EXACT HR+ scanner (Siemens CTI), which was used for Cohorts II and III, had an axial field of view of 15.5 cm and 63 slices spaced 2.46 mm apart. The in-plane resolution, after application of a 6 mm post-reconstruction filter, was 8.1 mm for both scanners.
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5

PET Imaging of Serotonin Transporter

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The 5-HTT selective, carbon-11-labeled radiotracer was applied as previously described.7 (link), 46 (link) After 10 min transmission scan from three 68Ga sources for attenuation correction and intravenous bolus injection (90 s) of 484±10 MBq [11C]DASB a dynamic PET scan was performed to collect emission data by using an ECAT EXACT HR+ scanner (Siemens; intrinsic resolution at the center 4.3 mm (full width at half maximum, FWHM), axial resolution: 5–6 mm, field of view: 15.5 cm, 3–4 mm FWHM) in a 3D mode over 90 min (23 frames: 4 × 0.25, 4 × 1, 5 × 2, 5 × 5, 5 × 10 min). Data were iteratively reconstructed (10 iterations, 16 subsets) in transverse image series (63 slices, 128 × 128 matrix, voxel size 2.6 × 2.6 × 2.4 mm) with a Hann filter (cutoff 4.9 mm).
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6

PiB PET Amyloid Imaging Protocol

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All participants in the Aim 2 analyses underwent a [11C] Pittsburgh compound B (PiB) PET scan on a Siemens EXACT HR+ scanner; PiB processing and quantification methods are described in detail elsewhere (Johnson et al., 2014 (link)). A 70-min dynamic acquisition using reference Logan graphical analysis (cerebellum gray matter reference region) was used to estimate the PiB distribution volume ratio (DVR). A previously defined global DVR threshold of >1.19 (Sprecher et al., 2015 (link)) was used to dichotomize individuals as amyloid positive or negative (Aβ+/−).
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7

FDG-PET Imaging of Posterior Cingulate Cortex

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Participants underwent 18F-fluorodeoxyglucose (FDG) positron emission tomography (FDG-PET) imaging after a four-hour fast from food, nicotine, caffeine, and alcohol. Details of the FDG-PET scan have been published previously [31– 33 (link)]. Images were acquired on a Siemens EXACT HR+ scanner (Siemens AG, Erlangen, Germany) using the Alzheimer’s Disease Neuroimaging Initiative (ADNI) protocol [34 (link)] which involves a 5 mCi FDG injection. Imaging began after a 30-minute uptake period, and the scan was a 30-minute transaxial acquisition. Post-processing was done using an automated pipeline [35 (link)]. Each FDG-PET image was proportionally scaled to the mean FDG signal from the cerebellar vermis and pons. We focused on the posterior cingulate cortex (PCC), a well-established inception site for AD-related neurometabolic alterations [36 (link)], and sampled FDG uptake values from it using the PCC mask within the ADNI FDG Meta-ROI suite [37 (link)]. The mean FDG uptake in the entire PCC was calculated for each group for statistical analysis.
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