Evidence map›Paper›PMID 40076709›Full record

ArticleInternational journal of molecular sciences2025

Machine Learning Methods for Classifying Multiple Sclerosis and Alzheimer's Disease Using Genomic Data.

Magdalena Arnal Segura, Giorgio Bini, Anastasia Krithara, Georgios Paliouras, Gian Gaetano Tartaglia

Abstract read
In one paragraph

Article in International journal of molecular sciences, 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

5 authors.

Magdalena Arnal SeguraCentre for Human Technologies, Istituto Italiano di Tecnologia, Via Enrico Melen, 83, 16152 Genova, Italy.ORCID 0000-0001-8647-9232
Giorgio BiniCentre for Human Technologies, Istituto Italiano di Tecnologia, Via Enrico Melen, 83, 16152 Genova, Italy.
Anastasia KritharaInstitute of Informatics and Telecommunications, National Center for Scientific Research "Demokritos", 15341 Athens, Greece.ORCID 0000-0003-0491-4507
Georgios PaliourasInstitute of Informatics and Telecommunications, National Center for Scientific Research "Demokritos", 15341 Athens, Greece.
Gian Gaetano TartagliaCentre for Human Technologies, Istituto Italiano di Tecnologia, Via Enrico Melen, 83, 16152 Genova, Italy.

Funding

Alzheimer's Disease Neuroimaging Initiative - SupplementU01AG024904 · NIA · NORTHERN CALIFORNIA INSTITUTE RES &EDUC · PI WEINER, MICHAEL W · 2004 to 2015
$121.0M
European Research Council 855923NIA NIH HHS U01 AG024904
6 · The paper itself

Abstract

Complex diseases pose challenges in prediction due to their multifactorial and polygenic nature. This study employed machine learning (ML) to analyze genomic data from the UK Biobank, aiming to predict the genomic predisposition to complex diseases like multiple sclerosis (MS) and Alzheimer's disease (AD). We tested logistic regression (LR), ensemble tree methods, and deep learning models for this purpose. LR displayed remarkable stability across various subsets of data, outshining deep learning approaches, which showed greater variability in performance. Additionally, ML methods demonstrated an ability to maintain optimal performance despite correlated genomic features due to linkage disequilibrium. When comparing the performance of polygenic risk score (PRS) with ML methods, PRS consistently performed at an average level. By employing explainability tools in the ML models of MS, we found that the results confirmed the polygenicity of this disease. The highest-prioritized genomic variants in MS were identified as expression or splicing quantitative trait loci located in non-coding regions within or near genes associated with the immune response, with a prevalence of human leukocyte antigen (HLA) gene annotations. Our findings shed light on both the potential and the challenges of employing ML to capture complex genomic patterns, paving the way for improved predictive models.

Indexed as

Alzheimer DiseaseGenomicsMachine LearningMultiple SclerosisGenetic Predisposition to DiseaseHumansLinkage DisequilibriumMultifactorial InheritancePolymorphism, Single NucleotideQuantitative Trait LociAlzheimer’s diseasedeep learningextremely randomized treesgradient-boosted decision treeslogistic regressionmachine learningmultiple sclerosispolygenic risk score

Identifiers

PMID40076709
PMCPMC11900513

What OpenQuestion holds

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Registered trials

None linked

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.