Evidence map›Paper›PMID 42076512›Full record

ArticleSensors (Basel, Switzerland)2026

A Functional Shape Framework for the Detection of Multiple Sclerosis Using Optical Coherence Tomography Images.

Homa Tahvilian, Raheleh Kafieh, Fereshteh Ashtari, M N S Swamy, M Omair Ahmad

Abstract read
In one paragraph

Article in Sensors (Basel, Switzerland), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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

5 authors.

Homa TahvilianDepartment of Electrical and Computer Engineering, Concordia University, Montréal, QC H3G 1M8, Canada.ORCID 0009-0004-3761-9066
Raheleh KafiehDepartment of Engineering, Durham University, Durham DH1 3LE, UK.ORCID 0000-0003-0087-9476
Fereshteh AshtariIsfahan Neurosciences Research Center, Isfahan University of Medical Sciences, Isfahan 81746-73461, Iran.ORCID 0000-0002-4881-958X
M N S SwamyDepartment of Electrical and Computer Engineering, Concordia University, Montréal, QC H3G 1M8, Canada.ORCID 0000-0002-3989-5476
M Omair AhmadDepartment of Electrical and Computer Engineering, Concordia University, Montréal, QC H3G 1M8, Canada.ORCID 0000-0002-2924-6659

Funding

Natural Sciences and Engineering Research Council of Canada 67543
6 · The paper itself

Abstract

Multiple sclerosis (MS) is an inflammatory and neurodegenerative disease. Optical coherence tomography (OCT) is a non-invasive imaging technique of the retina. The thickness of the ganglion cell-inner plexiform layer (GCIPL) obtained from an OCT image is a valuable biomarker for monitoring MS. Since the functional shape (F-shape)-based technique has proven to be an effective platform for detecting glaucoma using OCT images, in this paper, we develop an F-shape-based framework to distinguish MS subjects from healthy ones using the thickness of GCIPL. The thickness of the GCIPL layers in the macula region of OCT images in a selected region of interest (ROI) for a set of healthy and MS subjects is represented as F-shape objects, which are registered to a common template using atlas registration. The residual F-shapes, defined as the difference between the F-shape of this common template and the individual registered F-shapes, are used to train an support vector machine (SVM) classifier and subsequently to detect MS. Accuracy, sensitivity, specificity, and area under the curve (AUC) are used to evaluate and compare the classification performance of the proposed F-shape-based scheme and those of sectoral-based schemes. The proposed F-shape-based scheme is shown to significantly outperform the sectoral-based schemes. The superior performance of the proposed F-shape-based scheme can be attributed to the use of (i) a highly dense mesh formed on the ROI in the macula region, (ii) atlas registration that puts the F-shapes of all the subjects on a common platform, and (iii) residual thicknesses as input features for the classification.

Indexed as

Multiple SclerosisTomography, Optical CoherenceAlgorithmsHumansRetinal Ganglion CellsSupport Vector Machineatlas registrationfunctional shapemultiple sclerosisoptical coherence tomographysupport vector machine classifier

Identifiers

PMID42076512
PMCPMC13120478

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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.