Evidence map›Paper›PMID 42568677›Full record

ArticleFrontiers in neuroscience2026

Machine learning methods evaluation for identification of cognitive phenotypes in multiple sclerosis and their MRI correlates.

Patrycja Romaniszyn-Kania, Weronika Galus, Julia Wyszomirska, Katarzyna Zawiślak-Fornagiel, Oskar Bożek, Daniel Ledwoń, Damian Kania, Aleksandra Tuszy, Joanna Siuda, Andrzej W Mitas

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Article in Frontiers in neuroscience, 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

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Patrycja Romaniszyn-KaniaFaculty of Biomedical Engineering, Silesian University of Technology, Zabrze, Poland.
Weronika GalusDepartment of Neurology, Faculty of Medical Sciences in Katowice, Medical University of Silesia, Katowice, Poland.
Julia WyszomirskaDepartment of Psychology, Faculty of Health Sciences in Katowice, Medical University of Silesia, Katowice, Poland.
Katarzyna Zawiślak-FornagielDepartment of Neurology, Faculty of Medical Sciences in Katowice, Medical University of Silesia, Katowice, Poland.
Oskar BożekDepartment of Radiology and Nuclear Medicine, Faculty of Medical Sciences in Katowice, Medical University of Silesia, Katowice, Poland.
Daniel LedwońFaculty of Biomedical Engineering, Silesian University of Technology, Zabrze, Poland.
Damian KaniaInstitute of Physiotherapy and Health Sciences, The Jerzy Kukuczka Academy of Physical Education in Katowice, Katowice, Poland.
Aleksandra TuszyFaculty of Biomedical Engineering, Silesian University of Technology, Zabrze, Poland.
Joanna SiudaDepartment of Neurology, Faculty of Medical Sciences in Katowice, Medical University of Silesia, Katowice, Poland.
Andrzej W MitasFaculty of Biomedical Engineering, Silesian University of Technology, Zabrze, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Cognitive impairment (CI) is common in multiple sclerosis (MS) yet poorly captured by conventional disability scales. Although neuropsychological assessment and magnetic resonance imaging (MRI) are routinely used separately, there is no simple clinically applicable framework integrating cognitive performance with structural brain changes to identify patients at increased risk of cognitive decline. Integrating neuropsychological testing with MRI-based atrophy metrics may yield clinically useful cognitive phenotypes with differential patterns of brain atrophy measures. Methods: Data were collected from 79 patients with multiple sclerosis (PwMS) who underwent comprehensive neuropsychological assessment and brain MRI. Neuropsychological variables were subjected to a feature selection procedure based on variance and quartile coefficient of dispersion filtering, followed by Pearson correlation and mutual information (MI) analyses to generate reduced feature sets. These feature sets were used as input for unsupervised clustering with the Partitioning Around Medoids (PAM) algorithm to identify cognitive phenotypes. Differences between the resulting groups in the degree of brain atrophy measures were subsequently evaluated using appropriate statistical tests-one-way ANOVA or the Kruskal-Wallis test. Results: The feature selection procedure based on variance and mutual information identified neuropsychological features that were subsequently used for clustering. Based on these features, the PAM algorithm identified three distinct groups of PwMS that differed in their clinical characteristics, degree of brain atrophy measures, and cognitive phenotype, ranging from preserved cognition to global cognitive impairment. Conclusion: Three cognitive phenotypes with differential patterns of brain atrophy measures integrate neuropsychological testing with MRI measures into a clinically applicable framework that may help bridge the gap between structural imaging findings and everyday cognitive assessment in PwMS. This approach may improve screening, enable earlier detection of CI, improve monitoring, and provide valuable information for rehabilitation planning.

Indexed as

cognitive impairmentcognitive profile modelingmachine learningmultiple sclerosisneurodegenerative diseases

Identifiers

PMID42568677
PMCPMC13447364

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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.