Evidence map›Paper›PMID 41491449›Full record

ArticleJournal of neuro-oncology2026

BOLD complexity characterizes glioblastoma survival via voxel-wise and localized sample entropy.

Mengqi Gu, Patrick H Luckett, Michael Olufawo, Donna Dierker, Gabriel T Verastegui, Joshua S Shimony, Eric C Leuthardt

Abstract read
In one paragraph

Article in Journal of neuro-oncology, 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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0cells of the map it votes in
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

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.

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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

7 authors.

Mengqi GuDepartment of Biomedical Engineering, Washington University School of Medicine, St. Louis, MO, 63110, USA. alex.gu@wustl.edu.ORCID http://orcid.org/0009-0006-0891-3105
Patrick H LuckettDepartment of Neurological Surgery, Washington University School of Medicine, St. Louis, MO, 63110, USA.ORCID http://orcid.org/0000-0003-2262-6605
Michael OlufawoDepartment of Neurological Surgery, Washington University School of Medicine, St. Louis, MO, 63110, USA.ORCID http://orcid.org/0009-0006-7214-0207
Donna DierkerMallinckrodt Institute of Radiology, Washington University School of Medicine, St. Louis, MO, 63110, USA.ORCID http://orcid.org/0000-0001-9791-8384
Gabriel T VerasteguiDepartment of Neurological Surgery, Washington University School of Medicine, St. Louis, MO, 63110, USA.ORCID http://orcid.org/0000-0003-2462-9324
Joshua S ShimonyMallinckrodt Institute of Radiology, Washington University School of Medicine, St. Louis, MO, 63110, USA.ORCID http://orcid.org/0000-0002-6228-776X
Eric C LeuthardtDepartment of Neurological Surgery, Washington University School of Medicine, St. Louis, MO, 63110, USA.ORCID http://orcid.org/0000-0003-4154-3135

Funding

Training and DisseminationP41EB018783 · NIBIB · WADSWORTH CENTER · PI Jonathan Rickel Wolpaw · 2014 to 2026
$15.4M
Augmented Neurosurgical Navigation Software Using Resting State MRIR01CA203861 · NCI · WASHINGTON UNIVERSITY · PI Eric CLAUDE Leuthardt, JOSHUA S SHIMONY · 2017 to 2026
$5.8M
BCI2000: Software Resource for Adaptive Neurotechnology ResearchU24NS109103 · NINDS · WASHINGTON UNIVERSITY · PI BRUNNER, PETER · 2019 to 2024
$2.8M
BCI2000+: A Software Platform for Adaptive NeurotechnologiesR01EB026439 · NIBIB · WASHINGTON UNIVERSITY · PI BRUNNER, PETER · 2018 to 2022
$1.5M
NCI NIH HHS R01 CA203861NIBIB NIH HHS P41 EB018783NIBIB NIH HHS R01 EB026439NINDS NIH HHS U24 NS109103
6 · The paper itself

Abstract

purposeGlioblastoma (GBM) is the most prevalent and lethal primary brain tumor. Non-invasive presurgical biomarkers are urgently needed to predict patients’ overall survival (OS). Here we demonstrated a nuanced prognostic tool using sample entropy to assess Blood-Oxygen-Level-Dependent (BOLD) complexity and predict survival outcome, which is computationally efficient, reproducible, robust to noise, and readily transferable across cohorts.

methodsResting-state fMRI from 205 treatment-naïve GBM patients and 1148 cognitively stable healthy controls were evaluated. Sample entropy (SampEn), a complexity metric, was evaluated in relation to OS at four levels: whole brain voxel-wise, 15 resting state networks (RSNs), a 64-feature autoencoded latent space, and complexity dynamics along contrast-enhancing (CE) boundary.

resultsGBM patients showed a significant reduction in global SampEn versus controls (p < 0.001). Among RSNs, medial temporal lobe (MTL) and basal ganglia (BGA) SampEn correlated inversely with OS (R² = 0.033 and 0.034; p = 0.008 and 0.006). The latent-space-dependent Cox risk score stratifies patients into high and low survival populations (p < 0.001). The number of SampEn peaks at the CE boundary also correlated negatively with OS (R² = 0.020, p = 0.037).

conclusionsVoxel-wise SampEn revealed widespread loss of BOLD complexity in GBM. It identifies influences at RSNs and tumor-edge, characterizing survival. Latent space analysis revealed whole-brain SampEn characteristics, which provide a compact, data-driven biomarker that augments conventional Cox modelling and stratifies the patient survival. These findings show fMRI-derived SampEn measures are efficient and robust for risk stratification and mechanistic insight in glioblastoma.

Indexed as

BrainBrain NeoplasmsGlioblastomaMagnetic Resonance ImagingOxygenAdultAgedBrain MappingEntropyFemaleHumansImage Processing, Computer-AssistedMaleMiddle AgedPrognosisOxygenBiomarkerFunctional MRIGlioblastomaNeuroimagingSurvival

Identifiers

PMID41491449
PMCPMC12769512

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.