The patient population consisted of 45 patients (19 males and 26 females, 63 ± 9 years and 71 ± 13 years, respectively) presenting with cognitive symptoms of possible neurodegenerative disease who underwent brain 18F-FDG PET/CT and MRI examinations collected between April 2017 and September 2019 at Geneva University Hospital. The detailed demographic information of the patients is summarized in Table Table1.1. The study protocol was approved by the institution’s ethics committee and all patients gave written informed content. PET/CT acquisitions were performed on a Biograph mCT scanner (Siemens Healthcare, Erlangen, Germany) about 35 min post-injection. A low-dose CT scan (120 kVp, 20 mAs) was performed for PET attenuation correction. The patients underwent a 20-min static brain PET scan after injection of 205 ± 10 MBq of 18F-FDG. PET data were acquired in list-mode format and reconstructed using the e7 tool (an offline reconstruction toolkit provided by Siemens Healthcare) to produce FD PET images. Subsequently, a subset of PET data containing 5% of the total events was extracted randomly from the list-mode data to produce the LD images using a validated code [25]. Both FD and LD PET images were reconstructed into a 200 × 200 × 109 image matrix (2.03 × 2.03 × 2.2 mm3 voxel size) using an ordinary Poisson ordered subsets-expectation maximization (OP-OSEM) algorithm (5 iterations, 21 subsets) with point spread function (PSF) modelling. PET images underwent post-reconstruction Gaussian filtering with 2 mm FWHM similar to the clinical protocol. MRI data acquisition was carried out on a 3T MAGNETOM Skyra (Siemens Healthcare, Erlangen, Germany) with a 64-channel head coil. The MRI scans included a 3D T1-weighted magnetization prepared rapid gradient-echo, MP-RAGE (TE/TR/TI, 2.3 ms/1930 ms/ 970 ms, flip angle 8°; NEX = 1, voxel size 0.8 × 0.8 × 1 mm3) and a 3D T2-weighted (TE/TR, 386 ms/5000 ms, NEX = 1; voxel size 0.5 × 0.5 × 1 mm3).
Demographics of patients included in this study protocol
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