Cervical Spine Prospective Feasibility Study : Dynamic Flexion-Extension Diffusion-Tensor Weighted Magnetic Resonance Imaging.
Adult
Anisotropy
Case-Control Studies
Cervical Vertebrae
Diffusion Magnetic Resonance Imaging
Diffusion Tensor Imaging
/ methods
Feasibility Studies
Female
Healthy Volunteers
Humans
Male
Middle Aged
Observer Variation
Patient Positioning
/ methods
Posture
Prospective Studies
Range of Motion, Articular
Reproducibility of Results
Sensitivity and Specificity
Spinal Cord Diseases
/ diagnostic imaging
Cervical myelopathy
Diffusion tensor imaging
Dynamic magnetic resonance imaging
Extension
Flexion
Journal
Clinical neuroradiology
ISSN: 1869-1447
Titre abrégé: Clin Neuroradiol
Pays: Germany
ID NLM: 101526693
Informations de publication
Date de publication:
Sep 2019
Sep 2019
Historique:
received:
22
01
2018
accepted:
30
03
2018
pubmed:
20
4
2018
medline:
7
2
2020
entrez:
20
4
2018
Statut:
ppublish
Résumé
Diffusion tensor imaging (DTI) in flexion-extension may serve as a diagnostic tool to improve the sensitivity for detection of myelopathy. In this study, the feasibility and reproducibility of dynamic DTI in the cervical spinal cord was assessed in healthy volunteers and patients. All subjects were examined in maximum neck flexion-extension in a 3T magnetic resonance imaging (MRI) scanner. Range of motion, space available for the spinal cord, fractional anisotropy (FA) and apparent diffusion coefficient (ADC) were measured and compared between the neck positions. Volunteers showed no variation in ADC and FA. In patients, extension produced higher ADC in the diseased than in the control segments (p = 0.0045). The ADC of the affected segments was higher in extension than in the neutral position (p = 0.0030) or in flexion (p = 0.0002). The FA was significantly lower in extension in patients at both the control level C2/3 (p = 0.0154) and the affected segment (p = 0.0187). Dynamic DTI of the cervical spine is feasible and ADC increased in the patient group in extension. This finding may open a previously unexplored avenue to attempt an earlier identification of myelopathy.
Identifiants
pubmed: 29671001
doi: 10.1007/s00062-018-0686-0
pii: 10.1007/s00062-018-0686-0
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
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