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962 hr ecat pet scanner

Manufactured by Siemens

The 962 HR+ ECAT PET scanner is a medical imaging device designed to perform Positron Emission Tomography (PET) scans. The core function of the 962 HR+ ECAT PET scanner is to detect and measure the distribution of positron-emitting radiopharmaceuticals within the human body, providing information about the body's physiological processes.

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2 protocols using 962 hr ecat pet scanner

1

PiB PET Imaging Protocol for Amyloid Assessment

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The PiB PET assessment has been previously described in detail (Su et al., 2013 (link), 2014 ). Imaging was conducted on a Siemens 962 HR+ ECAT PET scanner or a Siemens Biograph 40 scanner. PET data were analyzed using previously developed methods (Su et al., 2013 (link), 2015 (link)). FreeSurfer segmentation (Fischl et al., 2002 (link)) (http://freesurfer.net/) was used as the basis for quantitative analysis to obtain regional SUVR with cerebellar gray matter serving as the reference region. Partial volume correction was also performed using a regional spread function technique (Rousset et al., 1998 (link); Su et al., 2015 (link)).
PiB positivity was defined using the MC SUVR across the precuneus, prefrontal, gyrus rectus, and temporal FreeSurfer regions of interest (ROIs) (Morris et al., 2010 (link)). A cutoff value of 1.42 was used which is comparable to an MC binding potential of 0.18 that was previously defined (Mintun et al., 2006 (link); Su et al., 2013 (link)). Characteristic SUVR images are presented in Fig. 1. The equivalence for an MC SUVR of 1.42 and MC-BP of 0.18 was previously determined using regression in an independent sample (unpublished data). Because of the criticality of this cutoff for subsequent analyses, primary results are also replicated using an alternative cutoff determined from this sample (Supplementary Material).
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2

Multimodal Neuroimaging for Amyloid Evaluation

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High resolution T1-weighted structural MRI was performed at 1.5 Tesla (n=63, Siemens Vision, Erlangen, Germany) or 3T (n=111, Siemens TIM Trio) using a magnetization-prepared rapid gradient echo (MPRAGE) sequence as previously described19 (link), 20 (link). Pittsburgh compound B (PIB) PET21 (link) was used as the imaging biomarker for β-amyloid. Participants underwent a 60-minute dynamic PET scan following injection of ~10 mCi PIB22 (link). The PIB PET imaging has been described in detail17 (link), 22 (link) and was conducted with a Siemens 962 HR+ ECAT PET scanner (Siemens/CTI, Knoxville KY) or on a Siemens Biograph 40 scanner. Structural MRIs were parcellated using FreeSurfer23 (link) (Martinos Center, Boston, MA) and, within each region, partial volume correction was applied24 (link). Standard uptake value ratios (SUVR) were calculated from regions of interest (ROI), with PIB-positivity defined as the mean cortical SUVR (from prefrontal, parietal and temporal ROIs) >1.42, a value commensurate with a mean cortical binding potential of 0.18 defined previously for a similar cohort17 (link), 22 (link). Cerebellar cortex, a region negative for amyloid in AD, was used as the reference region. Since the difference in spatial resolution between the two scanners used in this study is small (~0.01 SUVR unit), the same PIB cut-off was used for the entire dataset.
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