MRI investigation of the sensorimotor cortex and the corticospinal tract after acute spinal cord injury: a prospective longitudinal study

被引:226
作者
Freund, Patrick [1 ,3 ,4 ]
Weiskopf, Nikolaus [4 ]
Ashburner, John [4 ]
Wolf, Katharina [1 ]
Sutter, Reto [2 ]
Altmann, Daniel R. [5 ,6 ]
Friston, Karl J. [4 ]
Thompson, Alan [3 ,7 ]
Curt, Armin [1 ]
机构
[1] Univ Zurich, Univ Zurich Hosp, Spinal Cord Injury Ctr Balgrist, CH-8008 Zurich, Switzerland
[2] Univ Zurich, Univ Hosp Balgrist, Dept Radiol, CH-8008 Zurich, Switzerland
[3] UCL, UCL Inst Neurol, Dept Brain Repair & Rehabil, London, England
[4] UCL, UCL Inst Neurol, Wellcome Trust Ctr Neuroimaging, London, England
[5] UCL, UCL Inst Neurol, Queen Sq Multiple Sclerosis Ctr, NMR Res Unit, London, England
[6] London Sch Hyg & Trop Med, Dept Med Stat, London WC1, England
[7] UCL Hosp Biomed Res Ctr, Natl Inst Hlth Res, London, England
基金
英国惠康基金; 瑞士国家科学基金会;
关键词
VOXEL-BASED MORPHOMETRY; MULTIPLE-SCLEROSIS; ANTI-NOGO; RECOVERY; ATROPHY; MAPS; SEGMENTATION; DISABILITY; OUTCOMES; MYELIN;
D O I
10.1016/S1474-4422(13)70146-7
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background In patients with chronic spinal cord injury, imaging of the spinal cord and brain above the level of the lesion provides evidence of neural degeneration; however, the spatial and temporal patterns of progression and their relation to clinical outcomes are uncertain. New interventions targeting acute spinal cord injury have entered clinical trials but neuroimaging outcomes as responsive markers of treatment have yet to be established. We aimed to use Mill to assess neuronal degeneration above the level of the lesion after acute spinal cord injury. Methods In our prospective longitudinal study, we enrolled patients with acute traumatic spinal cord injury and healthy controls. We assessed patients clinically and by MRI at baseline, 2 months, 6 months, and 12 months, and controls by Mill at the same timepoints. We assessed atrophy in white matter in the cranial corticospinal tracts and grey matter in sensorimotor cortices by tensor-based analyses of T1-weighted MRI data. We used cross-sectional spinal cord area measurements to assess atrophy at cervical level C2/C3. We used myelin-sensitive magnetisation transfer (MT) and longitudinal relaxation rate (R1) maps to assess microstructural changes associated with myelin. We also assessed associations between MRI parameters and clinical improvement. All analyses of brain scans done with statistical parametric mapping were corrected for family-wise error. Findings Between Sept 17,2010, and Dec 31,2012, we recruited 13 patients and 18 controls. In the 12 months from baseline, patients recovered by a mean of 5-27 points per log month (95% CI 1.91-8.63) on the international standards for the neurological classification of spinal cord injury (ISNCSCI) motor score (p=0.002) and by 10-93 points per log month (6-20-15.66) on the spinal cord independence measure (SCIM) score (p<0.0001). Compared with controls, patients showed a rapid decline in cross-sectional spinal cord area (patients declined by 0.46 mm per month compared with a stable cord area in controls; p<0.0001). Patients had faster rates than controls of volume decline of white matter in the cranial corticospinal tracts at the level of the internal capsule (right Z score 5.21, p=0.0081; left Z score 4.12, p=0-0004) and right cerebral peduncle (Z score 3-89, p=0.0302) and of grey matter in the left primary motor cortex (Z score 4.23, p=0.041). Volume changes were paralleled by significant reductions of MT and R1 in the same areas and beyond. Improvements in SCIM scores at 12 months were associated with a reduced loss in cross-sectional spinal cord area over 12 months (Pearson's correlation 0-77, p=0.004) and reduced white matter volume of the corticospinal tracts at the level of the right internal capsule (Z score 4-30, p=0.0021), the left internal capsule (Z score 4.27, p=0.0278), and left cerebral pedunde (Z score 4.05, p=0.0316). Improvements in ISNCSCI motor scores were associated with less white matter volume change encompassing the corticospinal tract at the level of the right internal capsule (Z score 4.01, p<0.0001). Interpretation Extensive upstream atrophic and microstructural changes of corticospinal axons and sensorimotor cortical areas occur in the first months after spinal cord injury, with faster degenerative changes relating to poorer recovery. Structural volumetric and microstructural MRI protocols remote from the site of spinal cord injury could serve as neuroimaging biomarkers in acute spinal cord injury.
引用
收藏
页码:873 / 881
页数:9
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