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Magnetom trio 3t scanner

Manufactured by Siemens
Sourced in Germany, Australia

The Magnetom Trio 3T scanner is a magnetic resonance imaging (MRI) system produced by Siemens. It operates at a field strength of 3 Tesla, which allows for high-resolution imaging of the human body. The Magnetom Trio 3T scanner is designed to provide detailed anatomical and functional information to aid in medical diagnosis and research.

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68 protocols using magnetom trio 3t scanner

1

Multimodal MRI Data Collection Protocol

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MRI data were collected between three scanners. Participants were either scanned at Penn State Hershey Medical Center Department of Radiology on a Philips Achieve 3T scanner or a Siemens Magnetom Trio 3T scanner, or on an identical Siemens Magnetom Trio 3T scanner at Penn State University in the Social, Life, and Engineering Sciences Imaging Center (SLEIC).
During the MRI scan, structural and functional data were collected. Data were collected consistent with two prior studies in our laboratory (Roy, Campbell, Bernier, & Hillary, 2016 (link); Roy et al., 2017 ). Briefly, anatomical structural scans were collected using an MPRAGE sequence at a spatial resolution of 1.0 × 1.0 × 1.0 mm voxels, 2300ms repetition time, echo time of 2.98, flip angle of 9 degrees, and slices were collected interleaved. The MRI protocol included data collection for diffusion, inverse recovery and functional MRI data, but for the purposes of this paper, analyses are limited to structural imaging data.
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2

Imaging of Traumatic Brain Injury

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Data were collected on one of two scanners at one of the following sites: Penn State Hershey Medical Center Department of Radiology on a Siemens Magnetom Trio 3T scanner (n=20; 17 TBI and 3 HC), or on an identical Siemens Magnetom Trio 3T scanner in University Park at the Social, Life, and Engineering Sciences Imaging Center (n=24; 4 TBI and 20 HC). Significant efforts were made to monitor data fidelity and reliability. Data collection was consistent with previous studies in our laboratory (Roy et al., 2017 (link); Roy, Campbell, Bernier, & Hillary, 2016 (link); Bernier et al., 2017 (link); Grossner et al., 2018 (link)).
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3

MEG, MRI, and Cortical Mesh Reconstruction

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MEG data were acquired using a 306-channel Neuromag MEG device (Vectorview, Elekta). A structural T1 brain scan was acquired for source reconstruction using a Siemens MAGNETOM Trio 3 T scanner. MEG sensors were co-registered with anatomical MRI data by matching the digitized head-shape data with surface data from the structural scan (Jenkinson and Smith, 2001 (link)). For each participant, a cortical mesh was constructed using Freesurfer v5.3 (Fischl, 2012 (link)), and registered to a standard fs_LR mesh (Van Essen, 2012 (link)). For more detailed instructions, see the online Supplementary material.
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4

T2-weighted MRI Acquisition Protocol

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T2-weighted images were acquired using standard pulse sequences on a Magnetom Trio 3T scanner (Siemens AG, Erlangen, Germany). The T2-weighted image parameters included TR = 5800 ms, TE = 110 ms, flip angle = 150°, field of view = 240 × 188 mm2, and voxel size = 0.6 × 0.6 × 5 mm3.
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5

Structural MRI Brain Imaging Protocol

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A structural T1 brain scan was acquired for source reconstruction using a Siemens MAGNETOM Trio 3T scanner with a 32-channel head coil (TE = 2.18 ms, TR = 2,300 ms, TI = 1,100 ms, flip angle = 9°, 192 or 208 slices depending on head size, voxel-size = 0.8 × 0.8 × 0.8 cm).
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6

Multimodal Brain Imaging Protocol

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Imaging data were collected on a Siemens MAGNETOM Trio 3T scanner as described in a previous publication (Gullett et al, 2018 (link)). Briefly, whole-brain T1-weighted images were collected in 255 interleaved axial 1-mm slices with TR=1.90 s, TE=2.98 s, and field of view=256×256 mm. Structural T1 images were processed using the Freesurfer automated pipeline (Fischl et al, 2002 (link)). Whole-brain DTI were collected in 69 interleaved axial 2-mm slices with TR=1.10 s, TE=103 ms, and field of view=128×128 mm. Diffusion data were collated into a dataset with 64 b=1000m/s2 volumes, 10 b=5 mm/s2 volumes, and 1 b=0 volume, for a total of 75 volumes per scan.
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7

MRI Protocol for Functional Brain Imaging

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MRI data were acquired using a Siemens Magnetom Trio 3T scanner. Two MPRAGE structural sequences were acquired (192 axial slices with isotropic spatial resolution of 0.9 mm) for registering each participant’s functional data to standard space while participants completed the practice block and were averaged together to increase the signal-to-noise ratio. Gradient field-maps were collected to correct for distortions caused by magnetic field inhomogeneities in the functional data (Jezzard & Balaban, 1995 (link)). During each of the three task blocks, 331 functional imaging volumes were collected using a Siemens gradient echo-planar imaging sequence (repetition time [TR] 3000 ms, echo time [TE] 25 ms, flip angle 90°, field of view [FOV] 256 mm). Each image consisted of 50 oblique axial slices (slice thickness 2.40 mm, in-plane voxel size 2.13 mm x 2.13 mm) acquired parallel to the plane containing the anterior and posterior commissures. Three volumes at the beginning of each task block were discarded to allow the scanner to reach steady state.
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8

High-Resolution T1-Weighted Brain Scans

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A high‐resolution T1‐weighted structural brain scan was acquired for each participant and used to segment and delineate brain regions. Participants were scanned on one of two magnetic resonance imaging (MRI) scanners, a Siemens Magnetom Trio 3 T scanner (n = 38) or a Siemens Verio 3T scanner (Siemens, Erlangen, Germany) (n = 60).
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9

Preterm Infants' Neurological Outcomes

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Infant medical records were obtained and a medical risk index score (range: 0–10) was created from dichotomized (present= 1, absent= 0) factors: intrauterine growth restriction, did not receive antenatal steroids, received dexamethasone, oxygen at 36 weeks, necrotizing enterocolitis, confirmed sepsis, patent ductus arteriosus, retinopathy of prematurity, ≥3 standard deviation (SD) decrease in weight-for-height/length from birth to term-equivalent age, and >75th percentile for duration of parenteral nutrition.11 (link) Based upon previous findings in this cohort,21 (link) NICU room type (private room or open ward) was also examined as a potential covariate of interest. VPT infants underwent magnetic resonance imaging (MRI) at term-equivalent postmenstrual age using a Siemens Magnetom Trio 3T scanner with previously documented sequences.22 (link) MRI images were qualitatively scored for the presence and severity of cystic lesions, focal signal abnormality, myelination delay, thinning of the corpus callosum, lateral ventricle dilatation, and cerebral volume reduction.23 (link) Total WMA scores (range: 0–15) were categorized into none (0–2), mild (3–4), moderate (5–6), and severe (≥7).23 (link) Mothers reported the use of physical, occupational or speech/language intervention services from birth to 5 years on a customized questionnaire.
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10

Resting-state fMRI Preprocessing and Connectivity

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Resting state fMRI (6 minutes; 180 volumes) and high resolution T1 scans were acquired on a Siemens Magnetom Trio 3T scanner, followed by standard preprocessing in SPM8 and connectivity analyses in the CONN toolbox (see Supplemental Materials) 50 (link). Participants were excluded if they exceeded absolute thresholds for translation (3mm) or framewise displacement (FD; more than 1/3 of the time series exceeding 0.5mm FD) 9 (link),51 (link). Within the BI and BN groups, the included versus excluded participants did not significantly differ (p's > 0.20) in age, sex, BIQ scores (Total, Social novelty, or Situational novelty scales), social phobia symptoms, or IQ (block design, vocabulary, or full scale).
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