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1.5t system

Manufactured by Siemens
Sourced in Germany

The 1.5T system is a magnetic resonance imaging (MRI) system that operates at a magnetic field strength of 1.5 Tesla. It is designed to produce high-quality images of the human body for diagnostic and research purposes. The core function of the 1.5T system is to generate detailed images of the internal structures and organs, enabling medical professionals to assess and diagnose various medical conditions.

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20 protocols using 1.5t system

1

PET/CT and MRI Imaging Protocol

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Two integrated PET/CT scanners (Biograph 40 mCT; Siemens Healthcare and Gemini TF64; Philips) were used. All patients were on a low carbohydrate-fat allowed diet 24 h before 18F–FDG-PET/CT was performed, and they fasted 6 h before 18F–FDG-injection. Blood glucose levels were required to be less than 12 mmol/l in all patients, including in diabetic patients. One hour after intravenous injection of a 3.3 MBq/kg average dose of 18F–FDG (Mallinckrodt Pharmaceuticals, Petten, the Netherlands or IBA Molecular, Amsterdam, the Netherlands), whole-body low-dose CT scan was acquired for anatomic correlation and attenuation correction of the PET data. MRI of the spine was performed using 1.5 T systems (Siemens, Erlangen, Germany, and Philips, Best, the Netherlands).
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2

Longitudinal Brain Imaging and Diffusion Analysis

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At time 1 and time 2, structural magnetic resonance images were acquired on Siemens 1.5 T systems. Cortical reconstruction and volumetric segmentation were performed with the FreeSurfer image analysis suite (http://surfer.nmr.mgh.harvard.edu). Diffusion-weighted data were analyzed using TRActs Constrained by UnderLying Anatomy [TRACULA; (64 (link))], an automatic reconstruction tool for identifying major white matter tracts from diffusion-weighted images and measuring the diffusion within these tracts at a set number of locations. The acquisition sequences for gray matter data differed in minor ways across acquisitions. Following recommendations (60 (link), 65 (link)), we documented that there was no evidence of heteroskedasticity before completing our longitudinal analysis. Please see the Supplementary Materials for details about data acquisition, analysis, and tests of heteroskedasticity.
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3

Functional MRI Acquisition Protocol

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The experiment was performed on a 1.5-T Siemens system (Siemens Medical Systems, Erlangen, Germany). In the functional MRI (fMRI) sessions, imaging consisted of a single shot gradient Echo Planar Imaging (EPI) sequence (repetition time/echo time/flip angle = 3600 ms/50 ms/90°, field of view = 192 mm, matrix = 64 × 64, 40 axial slices, 2 mm thick with a 1-mm gap). Functional scanning was always preceded by 14.4 s of dummy scans to ensure tissue steady-state magnetization. A generalised reconstruction algorithm was used for data pre-processing to avoid ghost-EPI artefacts. An anatomical scan was also acquired for each subject and used for spatial normalisation. This was a 3D T1-weighted, modified equilibrium Fourier transform sequence with the following parameters: TR = 12.24 ms, TE = 3.56 ms, TI = 530 ms, FOV = 256 mm × 224 mm, acquisition matrix = 256 × 224, 1 mm slice thickness for 1 mm isotropic voxels.
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4

Quantifying Intramyocellular and Extramyocellular Lipids

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Each participant underwent a 1 H-MRS scan on a 1.5T Siemens system to assess IMCL and EMCL of the soleus muscle of the calf. Participants were scanned in the supine position with their right leg placed within an extremity RF coil to obtain images of the soleus muscle in which a voxel (1.3x1.3x3.0 mm 3 ) was positioned while avoiding gross marbling. Localised proton spectra were acquired using a PRESS sequence (TR 2000 ms; TE 30 ms) to obtain two spectra: a water-suppressed lipid spectra and a lipid-suppressed water spectra. The water resonance was set to 4.7ppm, the IMCL resonance was set to 1.3ppm and the EMCL resonance was set to 1.5ppm. MRS spectra were analysed on the Java-Based Magnetic Resonance User Interface (jMRUI) software with the inclusion of prior knowledge to assist in identification of the 4 lipid peaks, methyl and methylene IMCL and EMCL peaks [21] . IMCL and EMCL were expressed in arbitrary units as the ratio of the methylene IMCL or EMCL peaks to internal water.
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5

Breast MRI Imaging Protocol for NAC

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All MRI scans were conducted with patients in the prone position with a 1.5T system (Siemens, Erlangen, Germany) and a dedicated breast coil. Multiple contiguous axial and sagittal T1-weighted unenhanced and contrast-enhanced images (with and without fat suppression) and axial and sagittal images T2-weighted images were obtained. Reconstructed 3D maximum intensity and subtraction imaging were also performed. Residual tumors were defined based upon observed reductions in tumor enhancement and/or size when comparing MRI scans to those collected prior to NAC. Complete response (CR) was defined by total interval resolution of the previously detected lesion. MRI scans were evaluated by two radiologists based upon BI-RADS classification criteria, with any inconsistencies in their evaluations being resolved via discussion and consensus.
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6

Quantitative MRI Analysis of Lumbar Discs

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The lumbar spine was imaged using a 1.5 T System (Siemens, Germany) with a surface coil. Midsagittal T2-weighted MRIs were used for the evaluation of the discs. The signal intensity of the discs on the images was analysed by Vue PACS (Virtual Reading Profile, Carestream Health, Inc.). Multiplanar virtual reading (MPVR) was used to reconstruct three-dimensional (3D) colour MRI images.
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7

MRI Brain Imaging Protocol for ALS

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Structural high-resolution 3D T1-weighted MR images of head were obtained on a 1.5 T system (Siemens Symphony, Erlangen, Germany) using magnetization-prepared rapid gradient echo (MPRAGE) sequence. Imaging parameters were as follows: 160 slices, 1 mm thick, with 1.0 × 1.0 mm in-plane resolution; pulse sequence parameters were as follows: TR = 1970 ms; TE = 4.38 ms; number of averages = 1; and scan time = 6.45 minutes. T2- and PD-weighted images were also obtained using dual-echo FSE sequence to assess hyperintense signal changes along corticospinal tract in ALS patients. Imaging parameters include the following: 40 contiguous slices; slice thickness = 4 mm; in-plane resolution = 0.9 × 0.9 mm; pulse sequence parameters were as follows: repetition time (TR) = 3900 ms; echo time (TE) = 26 ms and 104 ms; echo train length or turbo factor = 7; and number of averages = 1; total scan time = 3.5 minutes. Although this dataset was used in our previous VBM studies [9 (link)], we did not study brain parenchymal fraction and so applied it to this study.
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8

MRI and CT Myelography Protocol for Identifying Spontaneous Intracranial Hypotension

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The brain MRI was performed using a 1.5-T System (Siemens, Germany) with a head-sense-coil. Midsagittal T1-weighted MRIs were selected for the evaluation of brain sagging, which was defined as either cerebral aqueduct displacement ≥1.8 mm or cerebellar tonsil displacement ≥4.3 mm (Fig 1) [25 (link)]. The midportion of the dominant transverse sinus on sagittal T1-weighted MRIs was used for assessing the venous distension sign (VDS), as proposed by Farb et al. (Fig 2) [26 (link)]. Dural enhancement was evaluated on axial and coronal T1-weighted images with gadolinium enhancement (Fig 3).
CT myelography for detecting the sites of dural leakage was performed on a second-generation dual-source CT with tube voltages set at 100 kVp and 140 kVp (with tin filter). Leakage varied from a small amount of contrast tracking along a single nerve root to extensive bilateral collections of contrast within the paraspinal soft tissues (Fig 4) [7 (link)].
Two neuroradiologists (Q.Z. and D.W.) blinded to the study design reviewed all images to document the presence or absence of SDHs, and evaluated pachymeningeal enhancement, VDS, brain sagging, and the number of dural leaks. Inter-observer repeatability was calculated using the intra-class correlation coefficient, which ranged from 0.86 to 0.92 for the MRI evaluations and was 0.81 for the CT assessment, indicating good inter-observer reliability.
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9

Multimodal MRI Acquisition Protocol

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The T1-weighted MRI images of all subjects were acquired using a Siemens 1.5T system with the following scanning parameters: TR (Repetition Time)/TE (Echo Time) = 2000/3.1 ms, slice thickness = 1 mm, flip angle (FA) =8°, and field of view (FOV) =90.625. The ASL MRI images were obtained using the same scanner with the following parameters: TR/TE = 4600/15.9 ms, slice thickness = 3 mm, FA = 180°, and FOV = 100.
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10

Multimodal Imaging Evaluation of Ankle Disorders

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Conventional radiography was performed on the Luminos dRF MAX (Siemens, Erlangen, Germany). AP, lateral and Mortise view are the three standard images performed of the ankle. Additional axial image to visualize the hypertrophic tuberculum was performed. US images using EPIQ5G (Philips Health Systems, Bothell, WA 98021, USA) (Figure 3). Cone Beam CT (CBCT) imaging was performed on a Newtom 5G-system (QR, Verona, Italy), with a field of view of 8 × 8 cm, centered on the painful ankle region. MR examinations were performed on a 1.5T system (Siemens, Magnetom Aera, Erlangen, Germany). Our routine protocol consisted of sagittal, axial and coronal fat suppressed (FS) T2-Weighted Images (WI), coronal PD and axial T1-WI with a slice thickness of 3 mm. Only seven patients were examined by one imaging modality (MRI). The other patients had at least a combination of two imaging techniques of which the combination of MR and US was most frequent (6 patients or 26%).
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