Evidence map›Paper›PMID 42226149›Full record

Observational studyBMC medical imaging2026

Deep learning-based neuroanatomical profiling reveals population-specific brain changes in multiple sclerosis: a large-scale Middle Eastern study.

Mahdi Bashiri Bawil, Mousa Shamsi, Abolhassan Shakeri Bavil

Abstract readObservational Study
In one paragraph

Observational study in BMC medical imaging, 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

3 authors.

Mahdi Bashiri BawilBiomedical Engineering Faculty, Sahand University of Technology, Tabriz, Iran.ORCID 0009-0002-2029-3245
Mousa ShamsiBiomedical Engineering Faculty, Sahand University of Technology, Tabriz, Iran. shamsi@sut.ac.ir.ORCID 0000-0003-4670-0531
Abolhassan Shakeri BavilRadiology Department, Tabriz University of Medical Sciences, Tabriz, Iran.ORCID 0000-0001-9397-0484

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMultiple sclerosis (MS) affects 2.8 million individuals worldwide, with Middle Eastern populations remaining underrepresented in neuroimaging research despite elevated regional prevalence rates. Large-scale comparative studies between MS patients and healthy controls (HC) are essential for characterizing disease-specific brain changes and establishing normative biomarkers. This study aimed to perform comprehensive statistical characterization of brain structural changes in MS patients compared to HC using automated deep learning-based segmentation, establishing population-specific reference ranges for a Middle Eastern cohort.

methodsThis retrospective observational study analyzed 1,381 subjects (1,000 HC, 381 MS patients) from Northwest Iran. Four deep learning architectures were evaluated on multi-center training data (local cohort plus MSSEG dataset), with U-Net selected for automated FLAIR sequence segmentation. Neuroanatomically-informed lesion classification identified periventricular, deep, and juxtacortical white matter hyperintensities. Statistical analyses employed age group- and gender-stratified comparisons with comprehensive correlation assessments across ventricular and lesion load measures.

resultsU-Net achieved optimal segmentation performance (DSC = 88.8%, HD95 = 2.8 mm), supporting its selection for population-level analysis. Compared to healthy controls, MS patients exhibited markedly elevated structural burden across all age strata: ventricular load was 1.7-fold higher (normalized ratios: 1.39%→2.37%; t = - 18.92, Cohen's d = 1.139) and white matter lesion load was 2.4-fold higher (normalized ratios: 0.315%→0.749%; U = 11,963.0, rank-biserial r = 0.310), both with p < 10⁻⁶. Among lesion subtypes, periventricular lesions predominated (53.91 ± 20.62% of total burden), while anatomical distribution patterns showed no significant gender differences. Age-related structural changes were more pronounced in MS patients than in controls, with stronger correlations observed for both ventricular load (r = 0.403, p = 2.50 × 10⁻¹⁶) and lesion load (r = 0.266, p = 1.33 × 10⁻⁷).

conclusionsThis study provides preliminary population-specific reference ranges for MS neuroimaging biomarkers in Middle Eastern populations, revealing lesion accumulation patterns with periventricular predominance. The automated segmentation and statistical framework address gaps in global MS research demographics.

Indexed as

BrainDeep LearningMultiple SclerosisNeuroimagingAdultFemaleHumansIranMagnetic Resonance ImagingMaleMiddle AgedMiddle Eastern PeopleRetrospective StudiesYoung AdultDeep learningFLAIR segmentationMRIMultiple sclerosis (MS)NeuroimagingPopulation-specific biomarkers

Identifiers

PMID42226149
PMCPMC13449394

What Socratic holds

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LicenceCC BY-NC-ND
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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 Socratic graph.