Evidence map›Paper›PMID 40869047›Full record

ArticleInternational journal of molecular sciences2025

Transparent Machine Learning Reveals Diagnostic Glycan Biomarkers in Subarachnoid Hemorrhage and Vasospasm.

Attila Garami, Máté Czabajszki, Béla Viskolcz, Csaba Oláh, Csaba Váradi

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. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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.

Attila GaramiInstitute of Energy, Ceramic and Polymer Technology, University of Miskolc, 3515 Miskolc, Hungary.
Máté CzabajszkiDepartment of Neurosurgery, Borsod-Abaúj-Zemplén County Center Hospital and University Teaching Hospital, 3526 Miskolc, Hungary.ORCID 0009-0005-5863-3753
Béla ViskolczInstitute of Chemistry, Faculty of Materials Science and Engineering, University of Miskolc, 3515 Miskolc, Hungary.ORCID 0000-0002-0777-9569
Csaba OláhDepartment of Neurosurgery, Borsod-Abaúj-Zemplén County Center Hospital and University Teaching Hospital, 3526 Miskolc, Hungary.ORCID 0000-0001-9598-9322
Csaba VáradiInstitute of Chemistry, Faculty of Materials Science and Engineering, University of Miskolc, 3515 Miskolc, Hungary.ORCID 0000-0002-2672-095X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Subarachnoid hemorrhage (SAH) and its major complication, cerebral vasospasm (CVS), present significant challenges for early diagnosis and risk stratification. In this study, we developed interpretable decision tree models to differentiate between healthy controls, SAH patients, and SAH patients with vasospasm using serum N-glycomic data. Building on previously published glycomic profiles, we introduced a refined modeling approach combining systematic preprocessing, feature selection, and interpretable machine learning. Our methodology included outlier removal, standard scaling, and a novel correlation-based feature reduction guided by feature importance scores derived from preliminary decision trees. Binary classification tasks (Control vs. SAH and Control vs. CVS, and SAH vs. CVS) were evaluated through stratified repeated cross-validation and hyperparameter optimization. Models achieved high accuracy (up to 0.91) and stable F1-scores across configurations. Key glycans such as FA2(6)G1 (bi-antennary, fucosylated, monogalactosylated), A4G4S3(2) (tetra-antennary, tetra-galactosylated, tri-sialylated), and A3G3S3(5) (tri-antennary, tri-galactosylated, tri-sialylated) emerged as the most discriminative. Visualizations that combine joint feature distributions and decision boundaries provided intuitive insight into the classifier's logic. These findings support the integration of interpretable glycomics-based models into clinical workflows.

Indexed as

BiomarkersMachine LearningPolysaccharidesSubarachnoid HemorrhageVasospasm, IntracranialDecision TreesFemaleGlycomicsHumansMaleMiddle AgedBiomarkersPolysaccharidescerebral vasospasmdecision treeinterpretable machine learningliquid chromatographymass spectrometryN-glycansserum glycosylationsubarachnoid hemorrhage

Identifiers

PMID40869047
PMCPMC12386729

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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 OpenQuestion graph.