Table 2.
Authors (year) |
Title | Subjects | B0; vendor |
Anatomical region |
Pulse sequence; contrast |
Voxel size; TR/TE (ms); cardiac gating |
Clinical outcome measure |
Key results |
---|---|---|---|---|---|---|---|---|
Barry et al. (2014) (42) | Resting state functional connectivity in the human spinal cord | HCs (22) | 7 T; Philips | C2 – C5 | 3D multi-shot GE-EPI | 0.91 × 0.91 × 4 mm3; 18/7.8; no | n/a | Low-frequency BOLD fluctuations are inherent in the spinal cord as well as the brain |
Kong et al. (2014) (43) | Intrinsically organized resting state networks in the human spinal cord | HCs (24) | 3 T; Siemens | C4 – T1 | GE-EPI | 1 × 1 × 5 mm3; 1890/44; no | n/a | Spatially distinct RSNs in the human spinal cord were identified, that were clearly separated into dorsal and ventral components |
Vahdat et al. (2015) (44) | Simultaneous Brain-Cervical Cord fMRI Reveals Intrinsic Spinal Cord Plasticity during Motor Sequence Learning | HC (25) | 3 T Siemens | Brain – T1 | GE-EPI | 2.5 × 2.5 × 4 mm3; 2500/30; no | n/a | Learning-related modulation of activity in the C6–C8 spinal region that is independent from that of related supraspinal sensorimotor structures is observed. |
Liu et al. (2016) (45) | Amplitude of Low Frequency Fluctuation (ALFF) in the Cervical Spinal Cord with Stenosis: A Resting State fMRI Study | Cervical spondylotic myelopathy (25) and HCs (18) | 3 T; Philips | C1 – C7 | GE-EPI | 1.25 × 1.25 × 4 mm3; 2000/30; no | JOA score | Amplitude of low frequency fluctuation values were higher in the CSM patients at all cervical segments |
Eippert et al. (2017) (46) | Investigating resting-state functional connectivity in the cervical spinal cord at 3T | HCs (20) | 3 T Siemens | C6 – T1 | GE-EPI | 1 × 1x 5 mm3; 1890/44; no; | n/a | Robust resting-state signals were observed at the clinically more prevalent field strength of 3 T. |
HC: healthy control; GE: gradient echo; BOLD: blood oxygenation level dependent; GE-EPI: gradient echo echo planar imaging; RSN: resting state networks; CSM: cervical spondylotic myelopathy; JOA: Japanese orthopedic association