Evidence map›Paper›PMID 40101271›Full record

ArticleJournal of Alzheimer's disease : JAD2025

EEG biomarkers for Alzheimer's disease: A novel automated pipeline for detecting and monitoring disease progression.

Leif Er Simmatis, Emma E Russo, Tayo Steininger, Haleigh Riddell, Evelyn Chen, Queenny Chiu, Michelle Lin, Donghun Oh, Porsha Taheri, Irene E Harmsen and 1 more

Abstract read
In one paragraph

Article in Journal of Alzheimer's disease : JAD, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
–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

4 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Interactive and open educational resources for advanced EEG analysis.Epileptic disorders : international epilepsy journal with videotape · 2026
    Article
  4. 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

11 authors.

Leif Er SimmatisFaculty of Medicine, University of Toronto, Toronto, Ontario, Canada.
Emma E RussoFaculty of Medicine, University of Toronto, Toronto, Ontario, Canada.ORCID 0009-0006-1102-8553
Tayo SteiningerCove Neurosciences Inc., Toronto, Ontario, Canada.ORCID 0009-0000-9513-0569
Haleigh RiddellCove Neurosciences Inc., Toronto, Ontario, Canada.
Evelyn ChenCove Neurosciences Inc., Toronto, Ontario, Canada.ORCID 0009-0001-8192-7363
Queenny ChiuCove Neurosciences Inc., Toronto, Ontario, Canada.ORCID 0009-0008-4425-165X
Michelle LinCove Neurosciences Inc., Toronto, Ontario, Canada.
Donghun OhCove Neurosciences Inc., Toronto, Ontario, Canada.
Porsha TaheriCove Neurosciences Inc., Toronto, Ontario, Canada.ORCID 0009-0001-3536-7916
Irene E HarmsenFaculty of Medicine, University of Toronto, Toronto, Ontario, Canada.ORCID 0000-0001-9056-1706
Nardin SamuelFaculty of Medicine, University of Toronto, Toronto, Ontario, Canada.ORCID 0000-0002-5007-4134

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BackgroundAlzheimer's disease (AD) is a neurodegenerative disorder that profoundly alters brain function and organization. Currently, there is a lack of validated functional biomarkers to aid in diagnosing and classifying AD. Therefore, there is a pressing need for early, accurate, non-invasive, and accessible methods to detect and characterize disease progression. Electroencephalography (EEG) has emerged as a minimally invasive technique to quantify functional changes in neural activity associated with AD. However, challenges such as poor signal-to-noise ratio-particularly for resting-state (rsEEG) recordings-and issues with standardization have hindered its broader application.ObjectiveTo conduct a pilot analysis of our custom automated preprocessing and feature extraction pipeline to identify indicators of AD and correlates of disease progression.MethodsWe analyzed data from 36 individuals with AD and 29 healthy participants recorded using a standard 19-channel EEG and features were processed using our custom end-t-end pipeline. Various features encompassing amplitude, power, connectivity, complexity, and microstates were extracted. Unsupervised machine learning (uniform manifold approximation and projection) and supervised learning (random forest classifiers with nested cross-validation) were used to characterize the dataset and identify differences between AD and healthy groups.ResultsOur pipeline successfully detected several new and previously established EEG-based measures indicative of AD status and progression, demonstrating strong external validity.ConclusionsOur findings suggest that this automated approach provides a promising initial framework for implementing EEG biomarkers in the AD patient population, paving the way for improved diagnostic and monitoring strategies.

Indexed as

Alzheimer DiseaseBrainDisease ProgressionElectroencephalographyAgedAged, 80 and overBiomarkersFemaleHumansMachine LearningMaleMiddle AgedPilot ProjectsBiomarkersAlzheimer’s diseasebiomarkerselectroencephalographymachine learning

Identifiers

PMID40101271
PMCPMC12583641

What Socratic holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.