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Signa hdx 1.5t mri scanner

Manufactured by GE Healthcare

The Signa HDx 1.5T MRI scanner is a magnetic resonance imaging system designed and manufactured by GE Healthcare. It utilizes a 1.5 Tesla superconducting magnet to generate high-quality images of the human body for diagnostic purposes.

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2 protocols using signa hdx 1.5t mri scanner

1

Codeine Pharmacokinetics and Brain Imaging

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Codeine phosphate (Qinghai Pharmaceutical Group Co., Ltd., Xining, China) has been previously reported to require 1 h to reach the peak plasma drug concentration in the brain (4 (link)). Thus, data from healthy participants were collected before and 1 h after oral administration of codeine phosphate (1.0 mg/kg). A Signa HDx 1.5T MRI scanner (GE Healthcare Life Sciences) was used for data acquisition. An echo-planar imaging (EPI) sequence was used for resting-state fMRI with the following conditions: Repetition time (TR), 2000 ms; echo time (TE), 25 ms; flip angle, 90°; number of slices, 39; and field of view, 192 mm.
Proton (1H) MRS involved the use of a point resolved spectroscopy sequence (also known as PRESS) with the following conditions: TE/TR, 35/1500 ms; total scan number, 128; volume of interest, 2 cm3; full wave at half maximum, <10; and water suppression, <98%. The voxels were placed in the symmetrical frontal lobe.
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2

HUNT MRI Exclusion Criteria and Imaging Protocol

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The exclusion criteria for HUNT MRI were the same as those for standard MRI: i.e. ferromagnetic foreign body, weight >150 kg and claustrophobia. All participants were scanned in a 1.5 T General Electric Signa HDx 1.5 T MRI scanner equipped with an eight-channel head coil (GE Healthcare) and software version pre-14.0 M. T1-weighted magnetization-prepared rapid acquisition with gradient echo (MPRAGE) volume, transverse T2, T2*, and fluid-attenuated inversion recovery (FLAIR) sequences, a time of flight threedimensional (3D) angio sequence, and diffusion-tensor imaging were obtained for each participant. The images were independently evaluated by two experienced neuroradiologists. Differences of opinion were resolved by consensus following discussion. White matter hyperintensities (WMH) were graded according to the Fazekas score (25) . The neuroradiologists were not provided with clinical information, but knew the participants' names and birth date. They were also able to access previous radiological assessments and clinical data in cases of abnormal findings. In addition, certain participants were interviewed by phone to verify a diagnosis of multiple sclerosis, cerebral contusion, or progressive supranuclear palsy, and to differentiate between silent and clinical infarctions of the brain.
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