Diagnostic Utility of Spinal Cord Axial MRI T2-weighted Sequences in Multiple Sclerosis and Other Inflammatory Myelopathies

ObjectiveTo assess the utility of axial T2-weighted spinal cord images at multiple sclerosis (MS) diagnosis and in other inflammatory myelopathies. BackgroundMRI international guidelines from 2021 recommended including >=2 sagittal MRI spinal cord T2-weighted (T2) sequences for MS diagnosis but axial T2-images were considered optional, given a paucity of data on their additive benefit. Design/MethodsThis population-based study included incident people with MS (pwMS) from Olmsted County (01/01/2003-12/31/2018) with brain and cervico/thoracic spine MRI (both sagittal and axial-T2 images) at diagnosis. We compared to 90 other myelopathies (NMOSD, 20; MOGAD, 20; sarcoid, 20; spondylotic, 15; infarct, 15). The presence and number of cord lesions were independently evaluated on sagittal/axial T2, and sagittal short tau inversion recovery (STIR) by two blinded raters and compared using chi-squared or Wilcoxon signed-rank tests. Inter-rater agreement was measured with Cohen’s Kappa. ResultsWe included 136 pwMS. There was substantial agreement on presence of spinal cord lesions between the two raters (Cohen’s kappa range=0.70-0.77; agreement, 88-93%). Among pwMS, ≥1 spinal cord lesion was noted on: T2 (axial, 103/136[75%]; sagittal, 76/136[56%]; STIR, 72/109[66%]). T2-lesion detection rates showed an advantage of axial-T2 versus sagittal-T2 (p=0.001) but not sagittal STIR (p=0.10) in MS but not in other myelopathy groups (p range 0.43-1.00). The mean[standard deviation] number of cord T2-lesions/patient was higher on axial-T2 (2.1[2.5]) than sagittal-T2 (1.1[1.6], p<0.001) and sagittal STIR (1.4[1.7], p<0.001). Overall, axial-T2 detected 280 lesions vs 147 on sagittal-T2 (+90%) and 226 vs 154 on STIR (+47%). In 31 pwMS, spinal cord MRI was needed to fulfill dissemination in space, and axial-T2 images led to fulfillment of MS criteria in 3/31 additional patients (10%) than sagittal images alone. ConclusionsAxial-T2 images increase the sensitivity for spinal cord lesion detection beyond sagittal-T2 and STIR in MS, but not in the other myelopathies.

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Journal
Neurology
Published
2024-10-08
DOI
https://doi.org/10.1212/01.wnl.0001051292.17016.4a
Primary Topic
Multiple Sclerosis Research Studies
Type
article
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article

Diagnostic Utility of Spinal Cord Axial MRI T2-weighted Sequences in Multiple Sclerosis and Other Inflammatory Myelopathies

Massimo Filippi, Ajay A. Madhavan, Orhun H. Kantarci, Laura Cacciaguerra et al.
Neurology
Multiple Sclerosis Research Studies
article

Diagnostic Utility of Spinal Cord Axial MRI T2-weighted Sequences in Multiple Sclerosis and Other Inflammatory Myelopathies

Massimo Filippi, Ajay A. Madhavan, Orhun H. Kantarci, Laura Cacciaguerra, Eoin P. Flanagan, Brian G. Weinshenker, Burcu Zeydan, Karl N. Krecke, W. Oliver Tobin, John Jing-Wei Chen, Maria Assunta Rocca, Jan‐Mendelt Tillema, Mark Keegan, Sean J Pittock
article en

Abstract

ObjectiveTo assess the utility of axial T2-weighted spinal cord images at multiple sclerosis (MS) diagnosis and in other inflammatory myelopathies. BackgroundMRI international guidelines from 2021 recommended including >=2 sagittal MRI spinal cord T2-weighted (T2) sequences for MS diagnosis but axial T2-images were considered optional, given a paucity of data on their additive benefit. Design/MethodsThis population-based study included incident people with MS (pwMS) from Olmsted County (01/01/2003-12/31/2018) with brain and cervico/thoracic spine MRI (both sagittal and axial-T2 images) at diagnosis. We compared to 90 other myelopathies (NMOSD, 20; MOGAD, 20; sarcoid, 20; spondylotic, 15; infarct, 15). The presence and number of cord lesions were independently evaluated on sagittal/axial T2, and sagittal short tau inversion recovery (STIR) by two blinded raters and compared using chi-squared or Wilcoxon signed-rank tests. Inter-rater agreement was measured with Cohen’s Kappa. ResultsWe included 136 pwMS. There was substantial agreement on presence of spinal cord lesions between the two raters (Cohen’s kappa range=0.70-0.77; agreement, 88-93%). Among pwMS, ≥1 spinal cord lesion was noted on: T2 (axial, 103/136[75%]; sagittal, 76/136[56%]; STIR, 72/109[66%]). T2-lesion detection rates showed an advantage of axial-T2 versus sagittal-T2 (p=0.001) but not sagittal STIR (p=0.10) in MS but not in other myelopathy groups (p range 0.43-1.00). The mean[standard deviation] number of cord T2-lesions/patient was higher on axial-T2 (2.1[2.5]) than sagittal-T2 (1.1[1.6], p<0.001) and sagittal STIR (1.4[1.7], p<0.001). Overall, axial-T2 detected 280 lesions vs 147 on sagittal-T2 (+90%) and 226 vs 154 on STIR (+47%). In 31 pwMS, spinal cord MRI was needed to fulfill dissemination in space, and axial-T2 images led to fulfillment of MS criteria in 3/31 additional patients (10%) than sagittal images alone. ConclusionsAxial-T2 images increase the sensitivity for spinal cord lesion detection beyond sagittal-T2 and STIR in MS, but not in the other myelopathies.

NeurologyVol. 103(7_Supplement_1)
Advisory Board Company (United States) (US)
Good health and well-being
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Multiple Sclerosis Research Studies
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