Evidence map›Paper›PMID 42793946›Full record

ArticleEntropy (Basel, Switzerland)2026

Impact of Recording Conditions and Feature Fusion on Dementia Classification Using Spectral, Entropy, and Complexity EEG Features.

Kerimay Sari, Samaneh Kouchaki, Daniel Abasolo

Abstract read
In one paragraph

Article in Entropy (Basel, Switzerland), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Kerimay SariCentre for Environmental and Biomedical Engineering, School of Engineering, University of Surrey, Guildford GU2 7XH, UK.ORCID 0009-0005-1921-0360
Samaneh KouchakiCentre for Vision, Speech and Signal Processing (CVSSP), University of Surrey, Guildford GU2 7XH, UK.ORCID 0000-0002-5870-4030
Daniel AbasoloCentre for Environmental and Biomedical Engineering, School of Engineering, University of Surrey, Guildford GU2 7XH, UK.ORCID 0000-0002-4268-2885

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Resting-state electroencephalography (EEG) is a promising low-cost, non-invasive modality for supporting differential classification of Alzheimer's disease (AD), mild cognitive impairment (MCI), and healthy controls (HCs). However, it remains unclear whether the combination of different EEG feature families consistently improves classification and whether their utility varies with recording condition. We compared spectral, entropy-based, and complexity-based features, both individually and in combination, for AD-HC, AD-MCI, and MCI-HC classification under eyes-closed (EC) and eyes-open (EO) conditions using an age-matched paired subset of the CAUEEG data set. Classification was evaluated using nested leave-one-subject-out cross-validation with two-stage hierarchical LightGBM gain-based feature selection. Under the EC condition, the highest balanced accuracies (BAs) were obtained with spectral features for AD-HC (79.99%), spectral-entropy for AD-MCI (68.33%), and spectral-entropy-complexity for MCI-HC (63.15%). Under the EO condition, spectral features performed best for AD-HC (84.91%) and AD-MCI (66.90%), whereas entropy performed best for MCI-HC (70.14%). Feature fusion therefore showed task-dependent rather than consistent benefits. Although numerical EC-EO differences were observed, none remained significant after paired permutation testing. Overall, the results suggest that the relative usefulness of EEG feature families varies across diagnostic comparisons and recording conditions.

Indexed as

Alzheimer’s diseasecomplexityEEGentropymild cognitive impairmentrecording conditionsspectral features

Identifiers

PMID42793946
PMCPMC13605554

What OpenQuestion holds

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Registered trials

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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.