Evidence map›Paper›PMID 39906543›Full record

ArticleBMJ neurology open2025

Spinal cord demyelination predicts neurological deterioration in patients with mild degenerative cervical myelopathy.

Abdul Al-Shawwa, Michael Craig, Kalum Ost, David Anderson, Steve Casha, W Bradley Jacobs, Nathan Evaniew, Saswati Tripathy, Jacques Bouchard, Peter Lewkonia and 10 more

Abstract read
In one paragraph

Article in BMJ neurology open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors.

Abdul Al-ShawwaHotchkiss Brain Institute, University of Calgary Cumming School of Medicine, Calgary, Alberta, Canada.
Michael CraigCombined Orthopaedic and Neurosurgery Spine Program, University of Calgary Department of Surgery, Calgary, Alberta, Canada.
Kalum OstHotchkiss Brain Institute, University of Calgary Cumming School of Medicine, Calgary, Alberta, Canada.
David AndersonDepartment of Biochemistry and Molecular Biology, University of Calgary Cumming School of Medicine, Calgary, Alberta, Canada.
Steve CashaCombined Orthopaedic and Neurosurgery Spine Program, University of Calgary Department of Surgery, Calgary, Alberta, Canada.
W Bradley JacobsCombined Orthopaedic and Neurosurgery Spine Program, University of Calgary Department of Surgery, Calgary, Alberta, Canada.
Nathan EvaniewCombined Orthopaedic and Neurosurgery Spine Program, University of Calgary Department of Surgery, Calgary, Alberta, Canada.
Saswati TripathyCombined Orthopaedic and Neurosurgery Spine Program, University of Calgary Department of Surgery, Calgary, Alberta, Canada.
Jacques BouchardCombined Orthopaedic and Neurosurgery Spine Program, University of Calgary Department of Surgery, Calgary, Alberta, Canada.
Peter LewkoniaCombined Orthopaedic and Neurosurgery Spine Program, University of Calgary Department of Surgery, Calgary, Alberta, Canada.
Fred NichollsCombined Orthopaedic and Neurosurgery Spine Program, University of Calgary Department of Surgery, Calgary, Alberta, Canada.
Alex SoroceanuCombined Orthopaedic and Neurosurgery Spine Program, University of Calgary Department of Surgery, Calgary, Alberta, Canada.
Ganesh SwamyCombined Orthopaedic and Neurosurgery Spine Program, University of Calgary Department of Surgery, Calgary, Alberta, Canada.
Kenneth C ThomasCombined Orthopaedic and Neurosurgery Spine Program, University of Calgary Department of Surgery, Calgary, Alberta, Canada.
Stephan duPlessisCombined Orthopaedic and Neurosurgery Spine Program, University of Calgary Department of Surgery, Calgary, Alberta, Canada.
Michael Mh YangCombined Orthopaedic and Neurosurgery Spine Program, University of Calgary Department of Surgery, Calgary, Alberta, Canada.
Julien Cohen-AdadInstitute of Biomedical Engineering, Polytechnique Montreal, Montreal, Quebec, Canada.ORCID 0000-0003-3662-9532
Nicholas DeaCombined Neurosurgical and Orthopaedic Spine Program, The University of British Columbia Department of Surgery, Vancouver, British Columbia, Canada.
Jefferson R WilsonDivision of Neurosurgery, University of Toronto Department of Surgery, Toronto, Ontario, Canada.
David W CadotteHotchkiss Brain Institute, University of Calgary Cumming School of Medicine, Calgary, Alberta, Canada.ORCID 0000-0003-2581-5903

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Degenerative cervical myelopathy (DCM) is the most common form of atraumatic spinal cord injury globally. Clinical guidelines regarding surgery for patients with mild DCM and minimal symptoms remain uncertain. This study aims to identify imaging and clinical predictors of neurological deterioration in mild DCM and explore pathophysiological correlates to guide clinical decision-making. Methods: Patients with mild DCM underwent advanced MRI scans that included T2-weighted, diffusion tensor imaging and magnetisation transfer (MT) sequences, along with clinical outcome measures at baseline and 6-month intervals after enrolment. Quantitative MRI (qMRI) metrics were derived above and below maximally compressed cervical levels (MCCLs). Various machine learning (ML) models were trained to predict 6 month neurological deterioration, followed by global and local model interpretation to assess feature importance. Results: A total of 49 patients were followed for a maximum of 2 years, contributing 110 6-month data entries. Neurological deterioration occurred in 38% of cases. The best-performing ML model, combining clinical and qMRI metrics, achieved a balanced accuracy of 83%, and an area under curve-receiver operating characteristic of 0.87. Key predictors included MT ratio (demyelination) above the MCCL in the dorsal and ventral funiculi and moderate tingling in the arm, shoulder or hand. qMRI metrics significantly improved predictive performance compared to models using only clinical (bal. acc=68.1%) or imaging data (bal. acc=57.4%). Conclusions: Reduced myelin content in the dorsal and ventral funiculi above the site of compression, combined with sensory deficits in the hands and gait/balance disturbances, predicts 6-month neurological deterioration in mild DCM and may warrant early surgical intervention.

Indexed as

MRIMYELOPATHYNEURORADIOLOGYNEUROSURGERY

Identifiers

PMID39906543
PMCPMC11792293

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.