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Trio mri system

Manufactured by Siemens
Sourced in Germany

The Trio MRI system is a magnetic resonance imaging (MRI) device manufactured by Siemens. It is designed to generate high-quality images of the human body for diagnostic purposes. The Trio MRI system utilizes a superconducting magnet to create a strong, uniform magnetic field, which is essential for the MRI imaging process. It is capable of producing detailed images of the body's internal structures, including organs, tissues, and anatomical features.

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28 protocols using trio mri system

1

Functional Neuroimaging Data Acquisition

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Functional imaging data were acquired using a 3‐T TRIO MRI system (Siemens, Erlangen, Germany) and T2*‐weighted EPI sequences (repetition time = 2.2 s and echo time = 30 ms). For the experiment, a total of 874 volumes of 36 axial slices were acquired using an interleaved slice mode (thickness = 3 mm, distance factor = 10%, field of view = 200 mm, 64 × 64 matrix, in‐plane voxel size = 3.1 × 3.1 mm2).
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2

Resting-State fMRI Acquisition Protocol

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Functional magnetic resonance imaging (fMRI) was performed on a 3-T Siemens Trio MRI system, with 152 resting-state T2*-weighted, echoplanar images (EPI) acquired (slice thickness = 4 mm; 34 slices; TR = 2 s; TE = 30 ms; flip angle = 90°; matrix = 64 × 64; fov = 200 mm). Resting-state images were acquired for 5 min, while participants viewed a black screen. High-resolution, T2-weighted, matched-bandwidth (MBW) and T1-weighted magnetization-prepared rapid-acquisition gradient echo (MPRAGE) scans were also acquired. The orientation for these scans was oblique axial to maximize brain coverage and to optimize signal from ventromedial PFC.
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3

MRI data preprocessing protocol for fMRI analysis

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The MRI data were collected on 3 T MRI systems (Experiment 1: Trio MRI system, Experiment 2: Prisma-Fit MRI system; Siemens) using 12-channel (Experiment 1) and 32-channel (Experiment 2) head coils. Anatomical images were acquired using T1-weighted sequences (Experiment 1: MPRAGE sequence, FoV = 256 mm, TR = 2530 ms, TE = 1.74 ms, 176 slices, flip angle = 7˚, voxel size = 1.0 × 1.0 × 1.0 mm3; Experiment 2: MEMPRAGE sequence, FoV = 256 mm; TR = 2530 ms; TE = 1.69 ms; 176 slices; flip angle = 7˚; voxel size = 1.0 × 1.0 × 1.0 mm3). Functional images were acquired using T2*-weighted gradient echo-planar imaging sequences (Experiment 1: FoV = 220 mm, TR = 1780 ms, TE = 24 ms, 37 descending slices, flip angle = 70˚, voxel size = 3.0 × 3.0 × 3.5 mm3; Experiment 2: FoV = 220 mm; TR = 1200 ms; TE = 30 ms; 51 slices; flip angle = 65˚; voxel size = 2.5 × 2.5 × 2.5 mm3).
We used SPM12 (Wellcome Department of Imaging Neuroscience, London, UK) to analyze the MRI data. The first two volumes of each run were removed to allow for scanner equilibration. Functional images were first converted from DICOM to NIFTI and then preprocessed with the following steps: de-spiking, slice-timing correction, realignment, segmentation, coregistration, and normalization. The functional images were smoothened with 6 mm full-width-half-maximum (FWHM) Gaussian kernels.
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4

Functional and Structural Brain Imaging

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Functional images were acquired at a 3 T Siemens Trio MRI system (Siemens, Erlangen, Germany) using a 3D EPI sequence with an isotropic voxel size of 2 mm and a TR of 1800 ms (TE = 25 ms, 64 slices, distance factor 50%, flip angle 15°, field of view 224 × 224 × 128 mm). Four runs corresponding to the four task blocks were collected. The duration of each run depended on the time required by the participant to complete the task block. On average, a run lasted 11.76 min (± 1.63 SD min). T1-weighted structural images were acquired with an MPRAGE sequence (TR = 2300 ms, TE = 3.03 ms, flip angle 8°, in-plane resolution = 256 × 256 mm, voxel size 1 mm isotropic).
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5

Resting-state fMRI Acquisition Protocol

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Resting-state fMRI images were acquired over 5 minutes using a 3-T Siemens AG Trio MRI system with a 12-channel coil while participants viewed a black screen (152 T2*-weighted echoplanar images; repetition time = 2 seconds; echo time = 30 milliseconds; slice thickness = 4 mm; flip angle = 90°; matrix: 64 × 64; field of view = 192 mm). A T2-weighted matched-bandwidth anatomical scan was acquired for initial registration, and a T1-weighted magnetization-prepared rapid-acquisition gradient echo (MPRAGE) scan was acquired for further registration, including spatial normalization to standard space (Montreal Neurological Institute [MNI]).
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6

Multimodal Neuroimaging Acquisition Protocol

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A 3-T Siemens Trio MRI system was used to collect echoplanar imaging data (repetition time = 2.0 s, echo time = 30 ms, flip angle = 81°; 36 axial slices: matrix = 64 × 64, 3.7-mm3 resolution, collected in two separate scans including 184 and 178 volumes), a high-resolution T1-weighted MPRAGE anatomical volume (192 sagittal slices, matrix = 224 × 256, field of view = 224 × 256 mm2, slice thickness = 1 mm, no gap, TE=2.56ms, TI=1100ms, TR=2100ms) and a fieldmap for geometric distortion correction. The only difference in acquisition parameters across the two data collection sites was that the MPRAGE had TE=2.38 ms at the Medical University of South Carolina site. Otherwise, scanning parameters were identical as was the version of the hardware (TrioTim) and software (Syngo MRB17). Stimuli were presented using a high-resolution rear-projection system (Avotec, Stuart, FL), and responses were recorded using a fiber-optic response pad (MRA Inc., Washington, PA). A computer running E-Prime (Version 1.1 SP3, Psychology Software Tools, Pittsburgh, PA) controlled stimulus presentation, which was synchronized with the collection of brain volumes via trigger pulses from the magnet.
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7

Neuroimaging and Trauma Disclosure

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In screening sessions, medical history and psychiatric symptoms were assessed (see the Supporting Information for inclusion criteria and Figure S1, Supporting Information, for a design overview). The testing session consisted of an fMRI scan containing a high‐resolution structural scan, a fear COND/EXT paradigm,[73] and a well‐established emotional face‐matching paradigm.[74] All magnetic resonance imaging (MRI) data were acquired using a 3T Siemens TRIO MRI system (Siemens AG, Erlangen, Germany) with a Siemens 32‐channel head coil. Following fMRI acquisition, the participants completed an experimental trauma paradigm.[28] To measure trauma disclosure and intrusive thoughts, subjects completed online diaries during the following three days after trauma exposure. Saliva samples were collected before the fMRI scan as baseline measure, and before and after the experimental trauma paradigm to measure oxytocin levels. In addition, blood samples were taken before the fMRI scan to measure the levels of gonadal steroids including estradiol and testosterone, as control variables. For a detailed list of the questionnaires and neuroendocrine parameters see the Supporting Information.
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8

Resting-State fMRI Acquisition Protocol

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Functional magnetic resonance imaging (fMRI) was performed on a 3-T Siemens Trio MRI system, with 152 resting-state T2*-weighted, echoplanar images (EPI) acquired (slice thickness = 4 mm; 34 slices; TR = 2 s; TE = 30 ms; flip angle = 90°; matrix = 64 × 64; fov = 200 mm). Resting-state images were acquired for 5 min, while participants viewed a black screen. High-resolution, T2-weighted, matched-bandwidth (MBW) and T1-weighted magnetization-prepared rapid-acquisition gradient echo (MPRAGE) scans were also acquired. The orientation for these scans was oblique axial to maximize brain coverage and to optimize signal from ventromedial PFC.
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9

Multimodal Brain Imaging Protocol for fMRI Studies

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During a 1.5-hour MRI session, MRI data were acquired using a 3T Siemens Trio MRI system equipped with a standard quadrature head coil, using T2*-sensitive gradient-recalled single shot echo planar pulse sequence. Anatomical images were collected with spin echo imaging in the axial plane parallel to the AC-PC line with TR = 300 msec, TE = 2.5 msec, bandwidth = 300 Hz/pixel, flip angle = 60 degrees, field of view = 220 × 220 mm, matrix = 256 × 256, 32 slices with slice thickness = 4mm with no gap. A slice thickness of 4 mm was utilized to consider the optimum level of signal-to-noise ratio; this is common in other fMRI studies, but could cause suboptimal tissue specificity. Functional MRI images were obtained using a single-shot gradient echo planar imaging (EPI) sequence. Thirty-two axial slices parallel to the AC-PC line covering the whole brain were acquired with TR = 2,000 msec, TE = 25 msec, bandwidth = 2004 Hz/pixel, flip angle = 85 degrees, field of view = 220×220 mm, matrix = 64×64, 32 slices with slice thickness = 4mm and no gap. Finally, a high-resolution 3D Magnetization Prepared Rapid Gradient Echo (MPRAGE) sequence was used to obtain sagittal images for multi-subject registration (TR = 2530 ms; echo time (TE) = 3.34 ms; bandwidth = 180 Hz/pixel; flip angle (FA) = 7°; slice thickness = 1mm; field of view = 256×256 mm; matrix = 256 × 256).
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10

Resting-state and Task-based fMRI in Methamphetamine Users

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Task-based scans were collected from 26 Methamphetamine and 27 Control subjects. One Methamphetamine subject was excluded due to excessive head motion (> 2 mm translational displacement, > 1.5 degrees rotation), leaving a final sample of 25. Eighteen Control and 15 Methamphetamine subjects underwent resting-state fMRI in the same session while viewing a black screen for 5 min. Imaging was performed on a 3-T Siemens Trio MRI system, with 302 functional task-based and 152 resting-state T2*-weighted, echoplanar images (EPI) acquired (slice thickness = 4 mm; 34 slices; TR = 2 s; TE = 30 ms; flip angle = 90°; matrix = 64 x 64; fov = 200 mm). High-resolution, T2-weighted, matched-bandwidth (MBW) and magnetization-prepared rapid-acquisition gradient echo (MPRAGE) scans were also acquired. The orientation for these scans was oblique axial to maximize brain coverage and to optimize signal from ventromedial PFC.
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