ArticlePloS one2026
FEDI-CODE: A federated and causally-informed framework for dementia risk prediction using multi-site patient data.
Article in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Early detection of dementia is critical for timely intervention and disease management, yet it remains a challenging task due to the fragmented nature of healthcare data and the need for privacy-preserving solutions. This paper proposes FEDI-CODE, a Federated and Causally Informed Dementia Estimation framework that integrates deep learning, federated learning, and counterfactual inference to predict dementia risk across distributed patient data sources. FEDI-CODE is designed to operate without centralizing sensitive medical data, enabling collaborative training across institutions while preserving privacy. It combines temporal modeling of longitudinal imaging and clinical data with individualized treatment effect estimation for modifiable risk factors such as alcohol consumption, weight, and cardiovascular indicators. A fusion module aggregates representations from each site to form a global prediction head. Extensive experiments on simulated multi-site dementia datasets demonstrate that FEDI-CODE achieves an accuracy of 83.7%, a precision of 83%, a recall of 81%, an F1-score of 82%, and an AUC-ROC of 0.86, outperforming standard federated models and deep learning baselines by notable margins. The model also generalizes well to external datasets, achieving 79.2% accuracy and 0.80 AUC-ROC, confirming its robustness. Furthermore, FEDI-CODE produces interpretable causal insights by estimating individual treatment effects, offering actionable clinical value. These results highlight FEDI-CODE as a scalable, interpretable, and privacy-aware solution for early dementia screening and personalized risk assessment.
Indexed as
Identifiers
What OpenQuestion holds
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 OpenQuestion graph.