Evidence map›Paper›PMID 42247118›Full record

ArticleEuropean radiology experimental2026

Whole anterior visual pathway segmentation from high-resolution MRI using artificial intelligence.

Andrea Diociasi, Emanuele Pravatà, Luca Carmisciano, Oliver C Kiersnowski, Iester Michele, Kevin Klein Gunnewiek, Luigi Lorenzini, Lorenzo Gualco, Matteo Pardini, Luca Roccatagliata and 4 more

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In one paragraph

Article in European radiology experimental, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

14 authors.

Andrea DiociasiDepartment of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health (DINOGMI), University of Genova, Genova, Italy.
Emanuele PravatàDepartment of Neuroscience, Imaging and Clinical Sciences, Centro I.T.A.B., Università degli Studi G. D'Annunzio di Chieti-Pescara, Chieti, Italy. emanuele.pravata@unich.it.ORCID http://orcid.org/0000-0002-5225-2993
Luca CarmiscianoDepartment of Health Sciences, Section of Biostatistics, University of Genova, Genova, Italy.
Oliver C KiersnowskiIRCCS Ospedale Policlinico San Martino, Genova, Italy.
Iester MicheleDepartment of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health (DINOGMI), University of Genova, Genova, Italy.
Kevin Klein GunnewiekPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Luigi LorenziniDepartment of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health (DINOGMI), University of Genova, Genova, Italy.
Lorenzo GualcoDepartment of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health (DINOGMI), University of Genova, Genova, Italy.
Matteo PardiniDepartment of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health (DINOGMI), University of Genova, Genova, Italy.
Luca RoccatagliataDepartment of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health (DINOGMI), University of Genova, Genova, Italy.
Chiara ZeccaNeurocenter of Southern Switzerland, EOC, Lugano, Switzerland.
Claudio GobbiNeurocenter of Southern Switzerland, EOC, Lugano, Switzerland.
Roberto GuidottiDepartment of Neuroscience, Imaging and Clinical Sciences, Centro I.T.A.B., Università degli Studi G. D'Annunzio di Chieti-Pescara, Chieti, Italy.
Andrea ChincariniIstituto Nazionale di Fisica Nucleare, Genova, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveManual segmentation of the whole anterior visual pathway (aVP) from high-resolution magnetic resonance imaging (MRI) is time-consuming and prone to inter-rater variability. We developed and validated a fully automated deep learning framework, "aVP-seg," to perform rapid, multiclass segmentation of the optic nerves, chiasm, and optic tracts in healthy volunteers and multiple sclerosis (MS) patients. MATERIALS AND

methodsWe developed and validated a cascaded two-stage three-dimensional convolutional neural network (principal segmentation + refinement) for automated multiclass segmentation of the aVP from 0.6-mm isotropic three-dimensional constructive interference in steady state (CISS) MRI. The model was trained and evaluated in 34 healthy controls and 46 MS patients. Ground truth was derived from manual segmentations by two expert radiologists. Spatial agreement metrics included Dice similarity coefficient (DSC), 95th percentile Hausdorff distance (HD95), and volumetric similarity.

resultsAgreement with the ground truth for the whole aVP was high (DSC 0.86 ± 0.03, mean ± standard deviation; 95% confidence interval (CI) 0.85-0.86). Boundary alignment was strong (HD95 1.18 mm ± 0.54; 95% CI 1.06-1.30) and volumetric similarity was high (0.96 ± 0.04; 95% CI 0.95-0.97). Accuracy was consistent for the left and right optic nerves (DSC 0.85-0.86 ± 0.05-0.04) and chiasm (DSC 0.83 ± 0.09), but lower for the left and right optic tracts (DSC 0.74-0.75 ± 0.07-0.07).

conclusionThe aVP-seg provided accurate, automated multiclass segmentation of the whole aVP from high-resolution CISS MRI. This tool may standardize and accelerate the extraction of quantitative biomarkers of aVP integrity in neuro-ophthalmic conditions. RELEVANCE STATEMENT: Automated multiclass segmentation of the entire anterior visual pathway enables standardized and reproducible preparation of MRI data for quantitative analysis. This approach facilitates future assessment of optic pathway involvement in MS and other neuro-ophthalmic disorders. KEY POINTS: aVP-seg enabled fully automated segmentation of the entire anterior visual pathway from high-resolution CISS MRI data. Automated segmentation reduces processing time and operator-dependent variability. aVP-seg shows robust performance across both healthy subjects and MS patients.

Indexed as

Artificial IntelligenceConvolutional Neural NetworksImage Processing, Computer-AssistedMagnetic Resonance ImagingMultiple SclerosisVisual PathwaysAdultDeep LearningFemaleHumansMaleMiddle AgedOptic ChiasmOptic NerveArtificial intelligenceDeep learningMagnetic resonance imagingMultiple sclerosisVisual pathways

Identifiers

PMID42247118
PMCPMC13241553

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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.