ArticleScientific reports2025
Structural-functional fingerprinting for abnormalities investigation in glioma patients.
Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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.
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.
Who cites it
2 citing papers in PubMed.
- Machine-Learning-Based Survival Prediction in Glioblastoma Using Graph-Theoretical Analysis of Structural Network Alterations.Cancers · 2026Article
- Anomaly Detection for Structural and Functional Connectivity in Glioma Patients.NMR in biomedicine · 2026Article
Corrections and comments
- Update of
Authors and funding
6 authors.
Funding
Abstract
Gliomas alter brain function and integrity, but these disruptions are often studied separately. This study utilised a novel approach that integrated functional, structural and microstructural connectivity information to investigate glioma-induced brain network changes and their clinical implications. It focused on the impact of gliomas on key brain networks, with a particular emphasis on the relationship between tumour topology and its effect on homotopic areal-level parcellation. The investigation was grounded in a unique clinical dataset comprising functional and diffusion images of forty-one newly diagnosed glioma patients. Connectivity matrices (functional, structural, and microstructural) were generated using homotopic parcellations and combined into an integration connectivity matrix. A linear regression model compared patient data to pseudo-healthy references. This identified affected regions as those falling in the left tail of the distribution across patients and parcellations. The study revealed that lateralized gliomas affect networks in both hemispheres, with left hemisphere lesions primarily altering homotopic homolateral and contralateral networks in healthy tissues. Abnormalities were more easily detected in regions distant from the lesion using functional connectivity rather than structural measures. The approach highlighted the heterogeneity of functional and structural alterations and emphasised that a comprehensive understanding of glioma abnormalities requires integrating multiple connectivity modalities.
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Registered trials
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.