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Benchmarking Synolitic Graphs for Autism Classification from Multisite Resting-State fMRI.

Overview

  1. Department of Mathematics and Women’s Cancer, University College London, London WC1E 6BT, UK
  2. Institute of Biogerontology, Lobachevsky State University, Nizhny Novgorod 603022, Russia
  3. Institute for Cognitive Neuroscience, University Higher School of Economics, Moscow 101000, Russia; (D.V.)
  4. Academician A.P. Nesterov Department of Ophthalmology of the Institute of Clinical Medicine, Pirogov Russian National Research Medical University, Moscow 117437, Russia
  5. Centre for Cancer Screening, Prevention and Early Diagnosis, Wolfson Institute of Population Health, Queen Mary University of London, London EC1M 6BQ, UK
  6. Department of Paediatrics and Paediatric Infectious Diseases, Institute of Child’s Health, I.M. Sechenov First Moscow State Medical University (Sechenov University), Moscow 119991, Russia
Journal: Diagnostics (Basel, Switzerland), volume 16, issue 17, article 2746
Dates: received 4 August 2026; accepted 24 August 2026; published online 27 August 2026
Type: Research article · Language: English
License: CC BY
Identifiers: DOI 10.3390/diagnostics16172746 · PMID 42739176 · PMCID PMC13565625 · OpenAlex W7204457728
Open access: gold, a free copy (OpenAlex)
Status: code on request
Categories: fMRI (modality), human (organism), autism (population), methods / tools (subfield)
Methods: Spectral & time-frequency, Statistics, Machine learning, Preprocessing, Connectivity, fMRI & imaging
Keywords: autism spectrum disorder, resting-state fMRI, synolitic graphs, functional connectivity, ABIDE, multisite classification, benchmark study
Topic: Functional Brain Connectivity Studies (Cognitive Neuroscience, Neuroscience), according to OpenAlex
Funding: Barts Charity (G-001522)
Citations: not cited yet (Europe PMC); 28 references in the paper

Abstract

Background/Objectives: Synolitic graphs (SGs) were developed for task-based fMRI, where edge weights encode the discriminative power of pairwise regional features; whether similar information can be recovered from resting-state data was untested. We benchmarked SGs for autism spectrum disorder (ASD) classification using the multisite ABIDE-I dataset (871 subjects: 403 subjects with ASD, 468 typical controls; 17 sites; CC200 atlas). Methods: Using 5-fold cross-validation with 10 repeats and balanced accuracy as the primary metric, we compared SGs with eight baselines including correlation matrices, tangent space connectivity, elastic net logistic regression, SVM, and XGBoost. Results: The vectorised correlation matrix achieved 67.9% balanced accuracy (AUC = 0.743), the combined model 68.0% (AUC = 0.744), and SGs 57.0% (AUC = 0.598). SGs performed above chance (permutation p = 0.001), but their performance was not significantly different from that of direct logistic regression (Nadeau–Bengio p = 0.82). After covariate residualisation, correlation-based methods retained 66.9–67.1% balanced accuracy, while SGs achieved 55.6%. Leave-one-site-out validation yielded 66.0–66.2% for correlation-based models and 55.0% for SGs, with similar declines of approximately 2 percentage points from standard cross-validation. SG-derived ROI rankings were unstable, and ADOS severity prediction among 193 ASD participants was underpowered and inconclusive. Conclusions: Conventional connectivity representations substantially outperformed SGs for resting-state ASD classification, contrasting with previously reported task-fMRI advantages. No evaluated method achieved performance suitable for stand-alone clinical screening or diagnosis; this study should therefore be interpreted as a methodological benchmark rather than a validation of a clinically deployable tool.

Reproduced under the paper's license (CC BY), from the paper cited above.

Code

The paper says that its authors' code is available on request: it was not published with the paper, so there is nothing to verify.

The paper's code and data availability statement is in the Data section.

Tracing map

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Data

No dataset and no data link were found in the paper.

Data Availability Statement

ABIDE-I raw imaging and phenotypic data are publicly available from the International Neuroimaging Data-sharing Initiative (INDI) 1000 Functional Connectomes Project at http://fcon_1000.projects.nitrc.org/indi/abide/abide_I.html (accessed on 11 July 2026). C-PAC-preprocessed derivatives (filt_noglobal strategy, CC200 parcellation) are available from the Preprocessed Connectomes Project at http://preprocessed-connectomes-project.org/abide/cpac.html (accessed on 11 July 2026), also mirrored on NITRC and as a public Amazon Web Services S3 bucket, as described by Craddock et al. [10]. All ABIDE-I data are fully anonymised and contain no protected health information, in accordance with HIPAA guidelines and 1000 Functional Connectomes Project/INDI data-sharing protocols; consequently, no separate data use agreement is required, although users must register with NITRC and the 1000 Functional Connectomes Project to obtain access. The original data collection, including clinical/diagnostic assessment, was approved and conducted by the institutional review boards and clinical teams at each of the 17 contributing acquisition sites, as described by the ABIDE consortium [3]. Raw ABIDE-I data are distributed under a Creative Commons Attribution-NonCommercial-ShareAlike licence and the C-PAC-preprocessed derivatives under a permissive BSD-style licence; our use of both datasets for non-commercial academic research complies with these terms. Analysis code is available from the authors upon reasonable request.

Reproduced under the paper's license (CC BY), from the paper cited above.

Versions

The history of this record: each version stored by the harvester or made by a correction of its authors or of the maintainers of its code, and what changed in its facts. The texts of the paper (its abstract, its availability statements) are not part of it; versions that changed only those are not listed.

Version 1, 27 September 2026: the first record

Recorded: type, language, journal, volume, issue, pages, dates, 7 authors, 7 keywords, 1 funder, 21 references.

Cite

This paper

Zaikin, A., Vlasenko, D., Zakharov, D., Oganezova, J. G., Krivonosov, M. I., Ivanchenko, M., & Blyuss, O. (2026). Benchmarking Synolitic Graphs for Autism Classification from Multisite Resting-State fMRI. Diagnostics (Basel, Switzerland), 16(17), 2746. https://doi.org/10.3390/diagnostics16172746

BibTeX

@article{zaikin2026benchmarking,
author = {Zaikin, Alexey and Vlasenko, Daniil and Zakharov, Denis and Oganezova, Janna G and Krivonosov, Mikhail I and Ivanchenko, Mikhail and Blyuss, Oleg},
title = {{Benchmarking Synolitic Graphs for Autism Classification from Multisite Resting-State fMRI}},
journal = {Diagnostics (Basel, Switzerland)},
year = {2026},
month = aug,
volume = {16},
number = {17},
pages = {2746},
publisher = {Multidisciplinary Digital Publishing Institute (MDPI)},
issn = {2075-4418},
doi = {10.3390/diagnostics16172746},
url = {https://doi.org/10.3390/diagnostics16172746},
pmid = {42739176},
pmcid = {PMC13565625}
}

RIS

TY - JOUR
AU - Zaikin, Alexey
AU - Vlasenko, Daniil
AU - Zakharov, Denis
AU - Oganezova, Janna G
AU - Krivonosov, Mikhail I
AU - Ivanchenko, Mikhail
AU - Blyuss, Oleg
TI - Benchmarking Synolitic Graphs for Autism Classification from Multisite Resting-State fMRI
T2 - Diagnostics (Basel, Switzerland)
J2 - Diagnostics (Basel)
PY - 2026
DA - 2026/08/27
VL - 16
IS - 17
SP - 2746
SN - 2075-4418
PB - Multidisciplinary Digital Publishing Institute (MDPI)
DO - 10.3390/diagnostics16172746
UR - https://doi.org/10.3390/diagnostics16172746
LA - en
ER -

CSL-JSON

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