OSCR

FUSION-AD: interpretable AI framework for risk assessment and subgroup discovery in Alzheimer's disease.

Overview

Authors: Abid Iqbal1, Saad Arif2, Ghassan Husnain3, Sarra Ayouni4
ORCID iDs: Saad Arif
  1. Department of Computer Engineering, College of Computer Sciences and Information Technology, King Faisal University, Al Ahsa, Saudi Arabia
  2. Department of Mechanical Engineering, College of Engineering, King Faisal University, Al-Ahsa, Saudi Arabia
  3. Department of Computer Science, CECOS University of IT and Emerging Sciences, Peshawar, Pakistan
  4. Department of Information Systems, College of Computer and Information Sciences, Princess Nourah bint Abdulrahman University, Riyadh, Saudi Arabia
Institutions: King Faisal University (Saudi Arabia); CECOS University (Pakistan); Princess Nourah bint Abdulrahman University (Saudi Arabia)
Journal: Frontiers in neuroinformatics, volume 20, article 1799307
Dates: received 29 January 2026; accepted 4 May 2026; published online 28 May 2026
Type: Research article · Language: English
License: CC BY
Identifiers: DOI 10.3389/fninf.2026.1799307 · PMID 42292927 · PMCID PMC13253770 · OpenAlex W7162694172
Open access: gold, a free copy (OpenAlex)
Status: data only
Categories: behavior only (modality), Alzheimer's / dementia (population)
Methods: Connectivity, Smoothing, state filtering, decompositions, Machine learning, Preprocessing, Statistics
Keywords: AI-driven diagnostics, Alzheimer's disease, clinical decision support, explainability, explainable boosting machine, interpretable AI, precision medicine, risk assessment
Topic: Dementia and Cognitive Impairment Research (Psychiatry and Mental health, Medicine), according to OpenAlex
Citations: not cited yet (Europe PMC); 61 references in the paper

Abstract

Introduction: Alzheimer's disease (AD) is difficult to treat because of its multifactorial causes and heterogeneous progression across individuals. This study introduces FUSION-AD, a user-friendly and interpretable artificial intelligence framework for AD risk assessment and subgroup discovery.

Methods: FUSION-AD integrates tree-based models, transformer-based neural networks, rule mining, and subgroup discovery to provide accurate and interpretable predictions. The framework was developed using the synthetic El Kharoua Alzheimer's Disease Dataset, which contains 2,149 structured clinical records from patients aged 60–90 years, with a mean age of 74.6 years and an average mini-mental state examination (MMSE) score of 21.7. The pipeline included data preprocessing, model benchmarking, feature-importance analysis, SHAP-based explanation, transformer attention analysis, association rule mining, and subgroup discovery.

Results: Within the evaluated dataset, TabNet achieved the strongest point-estimate performance among the standalone benchmark models on the primary evaluation split, with an area under the receiver operating characteristic curve (AUROC) of 0.95, followed by XGBoost at 0.93, Random Forest at 0.92, and Logistic Regression at 0.89. Feature importance, SHAP values, and transformer attention consistently identified MMSE, Functional Assessment, and Memory Complaints as the most influential predictors. Association rule mining further highlighted diabetes and high body mass index as important risk factors. Subgroup discovery identified four clinical clusters, with prevalence ranging from 21.3 to 28.4%. Cluster 0 showed notable declines in daily functioning, with Functional Assessment decreasing by 2.1 and activities of daily living decreasing by 1.5, whereas Cluster 1 maintained daily functioning but showed increased behavioral symptoms.

Discussion: FUSION-AD demonstrates that AD can be modeled in a way that balances predictive performance with interpretability within the studied dataset. The identified subgroup patterns suggest that lifestyle-driven profiles may benefit from preventive strategies, while cognitively impaired groups may require closer monitoring. These findings provide a foundation for future clinically oriented decision-support systems and require further validation using real-world clinical datasets.

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

Code

The paper links to its data, not to its authors' code: see the Data section.

Tracing map

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Data

Datasets cited

Data availability statement

Publicly available datasets were analyzed in this study. This data can be found here: https://www.kaggle.com/datasets/rabieelkharoua/alzheimers-disease-dataset.

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, 28 September 2026: the first record

Recorded: type, language, journal, volume, pages, dates, 4 authors, 8 keywords, 1 funder, 55 references.

Cite

This paper

Iqbal, A., Arif, S., Husnain, G., & Ayouni, S. (2026). FUSION-AD: interpretable AI framework for risk assessment and subgroup discovery in Alzheimer's disease. Frontiers in neuroinformatics, 20, 1799307. https://doi.org/10.3389/fninf.2026.1799307

BibTeX

@article{iqbal2026fusion,
author = {Iqbal, Abid and Arif, Saad and Husnain, Ghassan and Ayouni, Sarra},
title = {{FUSION-AD: interpretable AI framework for risk assessment and subgroup discovery in Alzheimer's disease}},
journal = {Frontiers in neuroinformatics},
year = {2026},
month = may,
volume = {20},
pages = {1799307},
publisher = {Frontiers Media SA},
issn = {1662-5196},
doi = {10.3389/fninf.2026.1799307},
url = {https://doi.org/10.3389/fninf.2026.1799307},
pmid = {42292927},
pmcid = {PMC13253770}
}

RIS

TY - JOUR
AU - Iqbal, Abid
AU - Arif, Saad
AU - Husnain, Ghassan
AU - Ayouni, Sarra
TI - FUSION-AD: interpretable AI framework for risk assessment and subgroup discovery in Alzheimer's disease
T2 - Frontiers in neuroinformatics
J2 - Front Neuroinform
PY - 2026
DA - 2026/05/28
VL - 20
SP - 1799307
SN - 1662-5196
PB - Frontiers Media SA
DO - 10.3389/fninf.2026.1799307
UR - https://doi.org/10.3389/fninf.2026.1799307
LA - en
ER -

CSL-JSON

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