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3t achieva x series mri scanner

Manufactured by Philips
Sourced in United States, Netherlands

The 3T Achieva X-series MRI scanner is a high-field magnetic resonance imaging system designed and manufactured by Philips. It operates at a magnetic field strength of 3 Tesla, which enables the acquisition of detailed and high-quality medical images. The core function of this scanner is to generate and detect radio frequency signals from the body to create cross-sectional images, allowing healthcare professionals to diagnose and monitor various medical conditions.

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13 protocols using 3t achieva x series mri scanner

1

3T MRI Acquisition Protocol for Brain Imaging

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Participants were scanned using a Philips 3T Achieva X-series MRI scanner (Philips Healthcare, USA). Anatomic images were acquired with a magnetization prepared gradient echo (MPRAGE) sequence (matrix=256×256, 160 sagittal slices, repetition time (TR)=2600ms, echo time (TE)=3.05ms, flip angle (FA)= 8°, final resolution=1×1×1mm3). Functional images were acquired for the first 22 participants using an 8-channel head coil with an echo planar imaging sequence [TR/TE/FA= 2000ms/30ms/90°, field of view= 240×240mm, matrix= 80×80, 37 oblique slices (parallel to orbitofrontal cortex to reduce sinus artifact), slice thickness= 4mm, interleaved slice acquisition, final resolution 3×3×4mm3]. Functional data were acquired on remaining 14 participants after an equipment upgrade to a 32-channel head coil using the same parameters, except thinner slices (slice thickness=2.5mm with 0.5mm gap) and sequential ascending slice acquisition to reduce orbitofrontal signal loss due to sinus cavity artifact.
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2

Optimized Neuroimaging Protocol for 3T MRI

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We acquired imaging data using a Philips 3T Achieva X-series MRI scanner (Philips Healthcare, Eindhoven, Netherlands). Anatomic images were acquired with a MPRAGE sequence (matrix = 256 × 256, 220 sagittal slices, TR/TE/FA = shortest/shortest/8°, final resolution = 0.94 × 0.94 × 1 mm3. Functional images were acquired using a 32-channel head coil with the following EPI sequence parameters: TR/TE/FA = 2000 ms/30 ms/90°, FOV = 240 × 240 mm, matrix = 80 × 80, 37 oblique slices, ascending sequential slice acquisition, slice thickness = 2.5 mm with 0.5 mm gap, final resolution 3.0 × 3.0 × 3.0 mm3. Parameters for the 32-channel coil were selected to reduce orbitofrontal cortex signal loss due to sinus artifact.
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3

Multimodal Neuroimaging Protocol for Brain Mapping

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Imaging data were acquired using a Philips 3T Achieva X-series MRI scanner (Philips Healthcare, Eindhoven, The Netherlands). Anatomic images were acquired with a MPRAGE sequence (matrix = 256 × 256, 220 sagittal slices, TR/TE/FA = shortest/shortest/8°, final resolution =0.94 × 0.94 × 1 mm3 resolution). Functional images were acquired using a 32-channel head coil with the following EPI sequence parameters: TR/TE/FA = 2000 msec/30 msec/90°, FOV = 240 × 240 mm, matrix = 80 × 80, 37 oblique slices, ascending sequential slice acquisition, slice thickness = 2.5 mm with 0.5 mm gap, final resolution 3.0 × 3.0 × 3.0 mm3. Parameters for the 32-channel coil (at an angle 30 degrees from the AC-PC line) were selected to reduce orbitofrontal signal loss due to sinus artifact.
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4

Multimodal Brain Imaging Protocol

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Imaging data were acquired using a Philips 3T Achieva X-series MRI scanner. Anatomic images were acquired with a MPRAGE sequence with the following parameters: matrix = 256 × 256; 22 sagittal slices; TR = shortest; TE = shortest; FA = 8°; resolution = 0.94 × 0.94 × 1 mm3. Functional images for the early participants (1–50) were acquired using an 8-channel head coil with an echo planar imaging (EPI) sequence and the following parameters: TR = 2000 msec; TE = 30 msec; FA = 90°; FOV = 240 × 240 mm2; matrix = 80 × 80, 37 oblique slices parallel to orbitofrontal cortex; “Philips interleaved” for participants 1–28 and interleaved for participants 29–49; resolution = 3.0 × 3.0 × 4.0 mm3. Functional images for the remaining participants (51–79) were acquired using a 32-channel head coil with the following parameters: TR = 2000 msec; TE = 30 msec; FA = 90°; FOV = 240 × 240 mm; matrix = 80 × 80, 37 oblique axial slices parallel to orbitofrontal cortex; sequential ascending acquisition; slice thickness = 2.5 mm with a 0.5 mm gap, resolution = 3.0 × 3.0 × 3.0 mm3. Three image volumes (6s) at the beginning of each functional run were discarded to allow the spin lattice magnetization to stabilize.
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5

MRI Imaging Protocol for Brain Analysis

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We acquired all imaging data using a Philips 3T Achieva X-series MRI scanner (Philips Healthcare, Eindhoven, The Netherlands) with a 32-channel head coil. We acquired anatomic images using an MPRAGE sequence (matrix = 256 x 256, 220 sagittal slices, TR/TE/FA = 8.0844/3.7010/8°, final resolution = 0.94 x 0.94 x 1 mm3). We acquired functional images using the following EPI sequence parameters: TR/TE/FA = 2000 ms/30 ms/90°, FOV = 240 x 240 mm, matrix = 80 x 80, 37 oblique slices, ascending sequential slice acquisition, slice thickness = 2.5 mm with 0.5 mm gap, final resolution 3.0 x 3.0 x 3.0 mm3.
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6

Neuroimaging Data Preprocessing Protocol

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Images were acquired using a Philips 3T Achieva X-series MRI scanner (Philips Healthcare, Eindhoven, the Netherlands) with a 32-channel head coil. Data preprocessing was performed using SPM12 (University College London, http://www.fil.ion.ucl.ac.uk/spm/) and the CONN toolbox v20b (https://www.nitrc.org/projects/conn) using standard processing steps. See Supplementary Information for complete details.
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7

Multimodal MRI Acquisition Protocol

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Imaging data were acquired using a Philips 3T Achieva X-series MRI scanner (Philips Healthcare, Eindhoven, The Netherlands). Anatomic images were acquired with a MPRAGE sequence (matrix = 256 × 256, 220 sagittal slices, TR/TE/FA = shortest/shortest/8°, final resolution = 0.94 × 0.94 × 1 mm3 resolution). Resting state images were acquired using a 32-channel head coil with the following echo-planar imaging sequence parameters: TR/TE/FA = 2000 ms/30 ms/90°, FOV = 240 × 240 mm, matrix = 80 × 80, 37 oblique slices, ascending sequential slice acquisition, slice thickness = 2.5 mm with 0.5 mm gap, final resolution 3.0 × 3.0 × 3.0 mm3 for 7.5 minutes. Parameters for the 32-channel coil were selected to reduce orbitofrontal signal loss due to sinus artifact.
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8

3-T fMRI Acquisition and Analysis

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A Philips 3-T Achieva X-series MRI scanner (Philips Medical Systems, Andover, MA) with a SENSE 8 channel head coil was used for data collection at the Ann Arbor Veterans Affairs Hospital. The scanning parameters and analysis methods are consistent with those previously reported by our lab (Duval et al., 2018 (link); Liberzon et al., 2015 (link)) and other fMRI aims in this study (to be reported elsewhere). A 3D FFE-TFE sequence (field of view (FOV)= 256 × 256 mm, slice thickness= 1 mm, 0 mm gap) was used to acquire T1-weighted anatomic images and slice localization, transformation, and co-registration were conducted using axial slices aligned with the AC-PC plane. EPI single shot sequence was used (EPI factor= 43, repetition time/echo time (TR/TE)= 2000/25 ms, flip angle= 90°, field of view (FOV)= 220 × 220 mm, slice thickness= 2.8 mm, 0 mm gap, 42 data points, 150 dynamic scan). Gradient echo blood oxygen level dependent (BOLD) scans were used to acquire functional data.
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9

3T MRI Acquisition Protocol for BOLD Imaging

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MRI assessment was conducted in a single Philips 3-T Achieva X-series MRI scanner (Philips Medical Systems, Andover, MA), with an 8-channel SENSE Head coil. T1-weighted anatomic images were acquired with a 3D fast field echo-turbo field echo sequence (field of view (FOV) = 256 × 256 mm, slice thickness = 1 mm, 0 mm gap). Axial slices aligned with the anterior commisure- posterior commisure plane were used for slice localization, transformation, and co-registration. Functional images were acquired with gradient-echo blood oxygen level-dependent scans. Echo planar imaging (EPI) single-shot sequence was used (EPI factor = 43, repetition time/echo time (TR/TE) = 2,000/25 ms, flip angle = 90°, FOV = 220 × 220 mm, slice thickness = 2.8 mm, 0 mm gap, 42 data points, 150 dynamic scan).
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10

MRI Acquisition Protocols for Multisite Neuroimaging

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MRI data were acquired using one of three instrument configurations. Among 67 used subjects, 28 subjects were acquired using a Siemens 3T TIM Trio (Siemens Healthcare, Munich, Germany) with a 12-channel head-coil. 39 subjects were acquired using a Philips 3T Achieva X-series MRI scanner (Philips Healthcare, Eindhoven, The Netherlands). Of the subjects scanned on the Philips instrument 36 subjects were acquired using an 8-channel head coil and 3 subjects were acquired using a 32-channel head coil. Anatomic images were acquired with a MPRAGE sequence (matrix = 256 x 256, 220 sagittal slices, volume/TE/FA = shortest/shortest/8°, final resolution = 0.94 x 0.94 x 1 mm3. Functional images were acquired with the following EPI sequence parameters: volume/TE/FA = 2000 ms/30 ms/90°, FOV = 240 x 240 mm, matrix = 80 x 80 (64 x 64 on the Siemens scanner), 37 oblique slices (32 oblique slices on the Siemens scanner), ascending sequential slice acquisition, slice thickness = 2.5 mm with 0.5 mm gap, final resolution 3.0 x 3.0 x 3.0 mm3.
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