Potential thresholds of critically increased cardiac-related spinal cord motion in degenerative cervical myelopathy.
Front Neurol
; 15: 1411182, 2024.
Article
em En
| MEDLINE
| ID: mdl-38978814
ABSTRACT
Introduction:
New diagnostic techniques are a substantial research focus in degenerative cervical myelopathy (DCM). This cross-sectional study determined the significance of cardiac-related spinal cord motion and the extent of spinal stenosis as indicators of mechanical strain on the cord.Methods:
Eighty-four DCM patients underwent MRI/clinical assessments and were classified as MRI+ [T2-weighted (T2w) hyperintense lesion in MRI] or MRI- (no T2w-hyperintense lesion). Cord motion (displacement assessed by phase-contrast MRI) and spinal stenosis [adapted spinal canal occupation ratio (aSCOR)] were related to neurological (sensory/motor) and neurophysiological readouts [contact heat evoked potentials (CHEPs)] by receiver operating characteristic (ROC) analysis.Results:
MRI+ patients (N = 31; 36.9%) were more impaired compared to MRI- patients (N = 53; 63.1%) based on the modified Japanese Orthopedic Association (mJOA) subscores for upper {MRI+ [median (Interquartile range)] 4 (4-5); MRI- 5 (5-5); p < 0.01} and lower extremity [MRI+ 6 (6-7); MRI- 7 (6-7); p = 0.03] motor dysfunction and the monofilament score [MRI+ 21 (18-23); MRI- 24 (22-24); p < 0.01]. Both patient groups showed similar extent of cord motion and stenosis. Only in the MRI- group displacement identified patients with pathologic assessments [trunk/lower extremity pin prick score (T/LEPP) AUC = 0.67, p = 0.03; CHEPs AUC = 0.73, p = 0.01]. Cord motion thresholds T/LEPP 1.67 mm (sensitivity 84.6%, specificity 52.5%); CHEPs 1.96 mm (sensitivity 83.3%, specificity 65.6%). The aSCOR failed to show any relation to the clinical assessments.Discussion:
These findings affirm cord motion measurements as a promising additional biomarker to improve the clinical workup and to enable timely surgical treatment particularly in MRI- DCM patients. Clinical trial registration www.clinicaltrials.gov, NCT02170155.
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Base de dados:
MEDLINE
Idioma:
En
Ano de publicação:
2024
Tipo de documento:
Article