Evidence map›Paper›PMID 41008314›Full record

ArticleBrain sciences2025

Interpretable Disorder Signatures: Probing Neural Latent Spaces for Schizophrenia, Alzheimer's, and Autism Stratification.

Zafar Iqbal, Md Mahfuzur Rahman, Qasim Zia, Pavel Popov, Zening Fu, Vince D Calhoun, Sergey Plis

Abstract read
In one paragraph

Article in Brain sciences, 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

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.

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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
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.

Zafar IqbalDepartment of Computer Science, Georgia State University, Atlanta, GA 30302, USA.ORCID 0009-0005-6139-0019
Md Mahfuzur RahmanDepartment of Computer Science, Georgia State University, Atlanta, GA 30302, USA.
Qasim ZiaDepartment of Computer Science, Georgia State University, Atlanta, GA 30302, USA.ORCID 0009-0004-2028-5960
Pavel PopovDepartment of Computer Science, Georgia State University, Atlanta, GA 30302, USA.ORCID 0000-0002-6407-4098
Zening FuDepartment of Computer Science, Georgia State University, Atlanta, GA 30302, USA.
Vince D CalhounDepartment of Computer Science, Georgia State University, Atlanta, GA 30302, USA.
Sergey PlisDepartment of Computer Science, Georgia State University, Atlanta, GA 30302, USA.ORCID 0000-0003-0040-0365

Funding

Multivariate methods for identifying multitask/multimodal brain imaging biomarkersR01EB006841 · NIBIB · THE MIND RESEARCH NETWORK · PI VINCE D CALHOUN, Sergey Plis · 2007 to 2026
$9.8M
COINSTAC: Decentralized, Scalable Analysis of Loosely Coupled DataR01DA040487 · NIDA · THE MIND RESEARCH NETWORK · PI CALHOUN, VINCE D, PLIS, SERGEY · 2015 to 2024
$7.1M
NIBIB NIH HHS R01 EB006841NIDA NIH HHS R01 DA040487
6 · The paper itself

Abstract

objectiveThis study aims to develop and validate an interpretable deep learning framework that leverages self-supervised time reversal (TR) pretraining to identify consistent, biologically plausible functional network biomarkers across multiple neurological and psychiatric disorders.

methodsWe pretrained a hierarchical LSTM model using a TR pretext task on the Human Connectome Project (HCP) dataset. The pretrained weights were transferred to downstream classification tasks on five clinical datasets (FBIRN, BSNIP, ADNI, OASIS, and ABIDE) spanning schizophrenia, Alzheimer's disease, and autism spectrum disorder. After fine-tuning, we extracted latent features and employed a logistic regression probing analysis to decode class-specific functional network contributions. Models trained from scratch without pretraining served as a baseline. Statistical tests (one-sample and two-sample

resultsTR pretraining consistently improved classification performance in four out of five datasets, with AUC gains of up to 5.3%, particularly in data-scarce settings. Probing analyses revealed biologically meaningful and consistent patterns: schizophrenia was associated with reduced auditory network activity, Alzheimer's with disrupted default mode and cerebellar networks, and autism with sensorimotor anomalies. TR-pretrained models produced more statistically significant latent features and demonstrated higher consistency across datasets (e.g., Pearson correlation = 0.9003 for schizophrenia probing vs. -0.67 for non-pretrained). In contrast, non-pretrained models showed unstable performance and inconsistent feature importance.

conclusionsTime Reversal pretraining enhances both the performance and interpretability of deep learning models for fMRI classification. By enabling more stable and biologically plausible representations, TR pretraining supports clinically relevant insights into disorder-specific network disruptions. This study demonstrates the utility of interpretable self-supervised models in neuroimaging, offering a promising step toward transparent and trustworthy AI applications in psychiatry.

Indexed as

Alzheimer’s diseaseautism spectrum disorderexplainabilityfMRIinterpretabilitylatent featurespretrainingschizophreniaself-supervisedtime reversal

Identifiers

PMID41008314
PMCPMC12469018

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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.