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Extent of Cord Pathology in the Lumbosacral Enlargement in Non-Traumatic versus Traumatic Spinal Cord Injury
被引:13
作者:
David, Gergely
[1
,2
]
Vallotton, Kevin
[1
]
Hupp, Markus
[1
]
Curt, Armin
[1
]
Freund, Patrick
[1
,3
,4
,5
]
Seif, Maryam
[1
,5
]
机构:
[1] Univ Zurich, Balgrist Univ Hosp, Spinal Cord Injury Ctr, Zurich, Switzerland
[2] Univ Med Ctr Hamburg Eppendorf, Dept Syst Neurosci, Hamburg, Germany
[3] UCL Inst Neurol, Dept Brain Repair & Rehabil, London, England
[4] UCL Inst Neurol, Wellcome Trust Ctr Human Neuroimaging, London, England
[5] Max Planck Inst Human Cognit & Brain Sci, Dept Neurophys, Leipzig, Germany
基金:
英国惠康基金;
欧盟地平线“2020”;
关键词:
degenerative cervical myelopathy;
diffusion tensor imaging;
magnetic resonance imaging;
neurodegeneration;
traumatic spinal cord injury;
CERVICAL SPONDYLOTIC MYELOPATHY;
OF-THE-ART;
MATTER SEGMENTATION;
EXPERIMENTAL-MODEL;
GREY-MATTER;
IN-VIVO;
DIFFUSION;
PATHOPHYSIOLOGY;
DEATH;
STATE;
D O I:
10.1089/neu.2021.0389
中图分类号:
R4 [临床医学];
学科分类号:
1002 ;
100602 ;
摘要:
This study compares remote neurodegenerative changes caudal to a cervical injury in degenerative cervical myelopathy (DCM; i.e., non-traumatic) and incomplete traumatic spinal cord injury (tSCI) patients, using magnetic resonance imaging (MRI)-based tissue area measurements and diffusion tensor imaging (DTI). Eighteen mild-to-moderate DCM patients with sensory impairments (modified Japanese Orthopedic score: 16.2 +/- 1.9), 14 incomplete tetraplegic tSCI patients (American Spinal Injury Association Impairment Scale C and D), and 20 healthy controls were recruited. All participants received DTI and T2*-weighted scans in the lumbosacral enlargement (caudal to injury) and at C2/C3 (rostral to injury). MRI readouts included DTI metrics in the white matter (WM) columns and cross-sectional WM and gray matter area. One-way analysis of variance with Tukey's post hoc comparison (p < 0.05) was used to assess group differences. In the lumbosacral enlargement, compared with DCM, tSCI patients exhibited decreased fractional anisotropy in the lateral (tSCI vs. DCM, -11.9%, p = 0.007) and ventral WM column (-8.0%, p = 0.021), and showed a trend toward lower values in the dorsal column (-8.9%, p = 0.068). At C2/C3, compared with controls, fractional anisotropy was lower in both groups in the dorsal (DCM vs. controls, -7.9%, p = 0.024; tSCI vs. controls, -10.0%, p = 0.007) and in the lateral column (DCM: -6.2%, p = 0.039; tSCI: -13.3%, p < 0.001), while tSCI patients had lower fractional anisotropy than DCM patients in the lateral column (-7.6%, p = 0.029). WM areas were not different between patient groups but were lower compared with controls in the lumbosacral enlargement (DCM: -16.9%, p < 0.001; tSCI: -10.5%, p = 0.043) and at C2/C3 (DCM: -16.0%, p < 0.001; tSCI: -18.1%, p < 0.001). In conclusion, mild-to-moderate DCM and incomplete tSCI lead to similar degree of degeneration of the dorsal and lateral columns at C2/C3, but tSCI results in more widespread white matter damage in the lumbosacral enlargement. These remote changes are likely to contribute to the patients' impairment and recovery. DTI is a sensitive tool to assess remote pathological changes in DCM and tSCI patients.
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页码:639 / 650
页数:12
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