Evidence map›Paper›PMID 41222674›Full record

ArticleNeuroradiology2025

Prospective clinical evaluation of automatic lesion assessment in patients with multiple sclerosis.

Amalie Monberg Hindsholm, Annika Reynberg Langkilde, Jonathan Frederik Carlsen, Dorthea Nørregaard, Thomas Axelsen, Aya Bakhtyar Baram, Natalia Grundtvig, Abdullah Shafique, Jette Lautrup Frederiksen, Flemming Littrup Andersen and 5 more

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Article in Neuroradiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

15 authors.

Amalie Monberg HindsholmDepartment of Clinical Physiology and Nuclear Medicine, Copenhagen University Hospital - Rigshospitalet, Copenhagen, Denmark. amalie.monberg.hindsholm@regionh.dk.
Annika Reynberg LangkildeDepartment of Radiology, Copenhagen University Hospital - Rigshospitalet, Copenhagen, Denmark.
Jonathan Frederik CarlsenDepartment of Radiology, Copenhagen University Hospital - Rigshospitalet, Copenhagen, Denmark.
Dorthea NørregaardDepartment of Radiology, Copenhagen University Hospital - Rigshospitalet, Copenhagen, Denmark.
Thomas AxelsenDepartment of Radiology, Copenhagen University Hospital - Rigshospitalet, Copenhagen, Denmark.
Aya Bakhtyar BaramDepartment of Radiology, Copenhagen University Hospital - Rigshospitalet, Copenhagen, Denmark.
Natalia GrundtvigDepartment of Radiology, Copenhagen University Hospital - Rigshospitalet, Copenhagen, Denmark.
Abdullah ShafiqueDepartment of Radiology, Copenhagen University Hospital - Rigshospitalet, Copenhagen, Denmark.
Jette Lautrup FrederiksenDanish Multiple Sclerosis Center, Department of Neurology, Copenhagen University Hospital - Rigshospitalet, Glostrup, Denmark.
Flemming Littrup AndersenDepartment of Clinical Physiology and Nuclear Medicine, Copenhagen University Hospital - Rigshospitalet, Copenhagen, Denmark.
Henrik Bw LarssonDepartment of Clinical Physiology and Nuclear Medicine, Copenhagen University Hospital - Rigshospitalet, Copenhagen, Denmark.
Adam Espe HansenDepartment of Radiology, Copenhagen University Hospital - Rigshospitalet, Copenhagen, Denmark.
Martin Lundsgaard HansenDepartment of Radiology, Copenhagen University Hospital - Rigshospitalet, Copenhagen, Denmark.
Claes Nøhr LadefogedDepartment of Clinical Physiology and Nuclear Medicine, Copenhagen University Hospital - Rigshospitalet, Copenhagen, Denmark.
Ulrich LindbergDepartment of Clinical Physiology and Nuclear Medicine, Copenhagen University Hospital - Rigshospitalet, Copenhagen, Denmark.

Funding

Rigshospitalet R233-A10076Scleroseforeningen A41569
6 · The paper itself

Abstract

purposeTo perform a real-world clinical validation of a commercial AI tool for automatic MRI assessment in multiple sclerosis (MS) patients, evaluating its impact on assessment time, workflow, and accuracy in detecting new and enlarging lesions.

methodsWe prospectively enrolled MS patients undergoing routine follow-up MRI from September-December 2024. Current and prior MRI examinations were anonymized and assessed independently by four neuroradiologists with and without AI assistance (mdbrain v.4.11.0). Assessment times were recorded, and radiologists completed utility questionnaires. Lesion quantification was compared between radiologist alone, radiologist with AI, and AI alone. Performance metrics including sensitivity, specificity, and predictive values were calculated case-level for detecting new and enlarging lesions.

resultsThe cohort included 112 MS patients scanned on 8 different MRI scanner models with varying protocols. Mean assessment time was reduced by 27 s when using AI versus without (p = 0.317). Radiologists found AI helpful in 87% of cases and reported difficulties in 11%. AI obtained negative predictive values of 0.89 for detecting new lesions when comparing to assessment without AI. Positive predictive values were low (0.35-0.65) due to false positive tendencies.

conclusionWe prospectively validated an AI tool for MS MRI follow-up in a real-world setting. It showed modest, non-significant time savings and low positive predictive value, limiting research use. High negative predictive value supports triaging potential. Radiologists found the AI tool helpful for lesion counting and detecting small new lesions. Findings highlight the need for thorough clinical evaluation, especially in areas lacking definitive ground truth.

Indexed as

Artificial IntelligenceImage Interpretation, Computer-AssistedMagnetic Resonance ImagingMultiple SclerosisAdultFemaleHumansMaleMiddle AgedPredictive Value of TestsProspective StudiesSensitivity and SpecificityArtificial intelligenceClinical validationLesion detectionMagnetic resonance imagingMultiple sclerosisRadiologist workflow

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Registered trials

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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.