Evidence map›Paper›PMID 40185925›Full record

ArticleEuropean radiology2025

Evaluation of a deep learning segmentation tool to help detect spinal cord lesions from combined T2 and STIR acquisitions in people with multiple sclerosis.

Baptiste Lodé, Burhan Rashid Hussein, Cédric Meurée, Ricky Walsh, Malo Gaubert, Nicolas Lassalle, Guilhem Courbon, Agathe Martin, Jeanne Le Bars, Françoise Durand-Dubief and 21 more

Abstract read
In one paragraph

Article in European radiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–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

5 citing papers in PubMed.

  1. Review
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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

31 authors.

Baptiste LodéDepartment of Neuroradiology, Rennes University Hospital, Rennes, France.
Burhan Rashid HusseinEMPENN Research Team, IRISA, CNRS‑INSERM‑INRIA, Rennes University, Rennes, France.
Cédric MeuréeEMPENN Research Team, IRISA, CNRS‑INSERM‑INRIA, Rennes University, Rennes, France.
Ricky WalshEMPENN Research Team, IRISA, CNRS‑INSERM‑INRIA, Rennes University, Rennes, France.
Malo GaubertEMPENN Research Team, IRISA, CNRS‑INSERM‑INRIA, Rennes University, Rennes, France.
Nicolas LassalleDepartment of Radiology, Rennes University Hospital, Rennes, France.
Guilhem CourbonNeurology Department, Rennes University Hospital, Rennes, France.
Agathe MartinNeurology Department, Rennes University Hospital, Rennes, France.
Jeanne Le BarsNeurology Department, Rennes University Hospital, Rennes, France.
Françoise Durand-DubiefNeurology A, Hôpital Neurologique Pierre Wertheimer, Hospices Civils de Lyon, University Lyon 1, Lyon, France.
Bertrand BourreCHU Rouen, Department of Neurology, Rouen, France.
Adil MaaroufCRMBM, CNRS, Aix-Marseille Université, Marseille, France/APHM Hôpital de la Timone, Marseille, France.
Olivier OutteryckUniversity of Lille, INSERM, Department of Neuroradiology, CHU Lille, Lille, France.
Clément MehierDepartment of Radiology, Rennes University Hospital, Rennes, France.
Alexandre PoulinDepartment of Radiology, Rennes University Hospital, Rennes, France.
Camille CathelineauDepartment of Radiology, Rennes University Hospital, Rennes, France.
Jeremy HongDepartment of Radiology, Rennes University Hospital, Rennes, France.
Guillaume CritonDepartment of Radiology, Lyon University Hospital, Lyon, France.
Sophie Motillon-AlonsoDepartment of Radiology, Rennes University Hospital, Rennes, France.
Augustin LeclerDepartment of Neuroradiology, Foundation Adolphe de Rothschild Hospital, Paris, France.
Frédérique CharbonneauDepartment of Neuroradiology, Foundation Adolphe de Rothschild Hospital, Paris, France.
Loïc DuronDepartment of Neuroradiology, Foundation Adolphe de Rothschild Hospital, Paris, France.
Alexandre Bani-SadrCREATIS - CNRS UMR 5220 & INSERM U1044, University Claude Bernard Lyon 1, Lyon, France.
Céline DelpierreDepartment of Neuroradiology, Rouen University Hospital, Rouen, France.
Jean-Christophe FerréDepartment of Radiology, Rennes University Hospital, Rennes, France.
Gilles EdanNeurology Department, Rennes University Hospital, Rennes, France.
François CottonCREATIS - CNRS UMR 5220 & INSERM U1044, University Claude Bernard Lyon 1, Lyon, France.
Romain CaseyUniv Lyon, Université Claude Bernard Lyon 1, Hospices Civils de Lyon, Fondation EDMUS, OFSEP, Centre de Recherche en Neurosciences de Lyon, Lyon, France.
Francesca GalassiEMPENN Research Team, IRISA, CNRS‑INSERM‑INRIA, Rennes University, Rennes, France.
Benoit Combès *EMPENN Research Team, IRISA, CNRS‑INSERM‑INRIA, Rennes University, Rennes, France.
Anne Kerbrat *EMPENN Research Team, IRISA, CNRS‑INSERM‑INRIA, Rennes University, Rennes, France. anne.kerbrat@chu-rennes.fr.ORCID http://orcid.org/0000-0002-4530-3553

Funding

Agence Nationale de la Recherche ANR-10-COHO-002 OFSEPAgence Nationale de la Recherche ANR-21-RHUS-0014
6 · The paper itself

Abstract

objectiveTo develop a deep learning (DL) model for the detection of spinal cord (SC) multiple sclerosis (MS) lesions from both sagittal T2 and short tau inversion recovery (STIR) sequences and to investigate whether such a model could improve the performance of clinicians in detecting SC lesions. MATERIALS AND

methodsA DL tool was developed based on SC sagittal T2 and STIR acquisitions from the imaging database of the French MS registry (OFSEP), including retrospective data from 40 different scanners. A multi-reader study based on retrospective data was performed between December 2023 and June 2024 to compare the performance of 20 clinicians in interpreting upper and lower SC acquisitions with and without the use of the tool. A ground truth was established by three experts. Sensitivity, precision, and inter-reader variability were evaluated.

resultsWe included 50 patients (39 females, median age: 41 years [range: 15-67]) with SC MRI acquired between February 2017 and December 2022. When reading with the tool, the clinicians' mean sensitivity to detect SC lesions improved (from 74.3% [95% CI = 67.8-80.6%] to 79.2% [95% CI: 73.5-85.0%]; p < 0.0001), with no evidence of difference in the mean precision: (69.0% [95% CI: 62.8-75.2%] vs 70.1% [95% CI: 64.3-75.9%]; p = 0.08). Inter-reader variability in lesion detection was slightly improved with the tool (Light's kappa = 0.55 vs 0.60), but without statistical difference (p = 0.056).

conclusionThe use of an automatic tool can help clinicians detect SC lesions in pwMS by increasing their sensitivity. KEY POINTS: Question No tool to help detect MS SC lesions is used in clinical practice despite their frequency and prognostic value. Findings This DL-based tool led to improvement in clinicians' sensitivity in detecting SC lesions from both sagittal T2 and STIR sequences, without decreasing precision. Clinical relevance Our study indicated the potential of a DL-based tool to assist clinicians in the challenging task of detecting SC lesions in people with MS on a combination of sequences commonly acquired in clinical practice.

Indexed as

Deep LearningImage Interpretation, Computer-AssistedMagnetic Resonance ImagingMultiple SclerosisSpinal CordAdolescentAdultAgedFemaleHumansMaleMiddle AgedReproducibility of ResultsRetrospective StudiesSensitivity and SpecificityYoung AdultDeep learning-based toolMRIMultiple sclerosisSpinal cordSTIR sequence

Identifiers

PMID40185925
PMCPMC12417267

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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.