Evidence map›Paper›PMID 40427951›Full record

ArticleHealthcare (Basel, Switzerland)2025

Integrative Machine Learning Framework for Enhanced Subgroup Classification in Medulloblastoma.

Kaung Htet Hein, Wai Lok Woo, Gholamreza Rafiee

Abstract read
In one paragraph

Article in Healthcare (Basel, Switzerland), 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

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Kaung Htet HeinSchool of Electronics, Electrical Engineering, and Computer Science, Queen's University Belfast, Belfast BT9 5BN, UK.ORCID 0009-0003-0426-250X
Wai Lok WooDepartment of Computer and Information Sciences, Northumbria University, Newcastle NE1 8ST, UK.ORCID 0000-0002-8698-7605
Gholamreza RafieeSchool of Electronics, Electrical Engineering, and Computer Science, Queen's University Belfast, Belfast BT9 5BN, UK.ORCID 0000-0002-1268-031X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMedulloblastoma is the most common malignant brain tumor in children, classified into four primary molecular subgroups: WNT, SHH, Group 3, and Group 4, each exhibiting significant molecular heterogeneity and varied survival outcomes. Accurate classification of these subgroups is crucial for optimizing treatments and improving patient outcomes. DNA methylation profiling is a promising approach for subgroup classification; however, its application is still evolving, with ongoing efforts to improve accessibility and develop more accurate classification methods.

objectivesThis study aims to develop a supervised machine learning-based framework using Illumina 450K methylation data to classify medulloblastoma into seven molecular subgroups: WNT, SHH-Infant, SHH-Child, Group3-LowRisk, Group3-HighRisk, Group4-LowRisk, and Group4-HighRisk, incorporating age and risk factors for enhanced subgroup differentiation.

methodsThe proposed model leverages six metagenes, capturing the underlying patterns of the top 10,000 probes with the highest variances from Illumina 450K data, thus enhancing methylation data representation while reducing computational demands.

resultsAmong the models evaluated, the SVM achieved the highest performance, with a mean balanced accuracy 98% and a macro-averaged AUC of 0.99 in an independent validation. This suggests that the model effectively captures the relevant methylation patterns for medulloblastoma subgroup classification.

conclusionsThe developed SVM-based model provides a robust framework for accurate classification of medulloblastoma subgroups using DNA methylation data. Integrating this model into clinical decision making could enhance subgroup-directed therapies and improve patient outcomes.

Indexed as

450 K methylation datamachine learningmedulloblastomasubgroup classificationsubgroup-directed therapies

Identifiers

PMID40427951
PMCPMC12111120

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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.