Evidence map›Paper›PMID 38855641›Full record

ArticleFrontiers in psychiatry2024

Utilizing portable electroencephalography to screen for pathology of Alzheimer's disease: a methodological advancement in diagnosis of neurodegenerative diseases.

Masahiro Hata, Yuki Miyazaki, Kohji Mori, Kenji Yoshiyama, Shoshin Akamine, Hideki Kanemoto, Shiho Gotoh, Hisaki Omori, Atsuya Hirashima, Yuto Satake and 3 more

Abstract read
In one paragraph

Article in Frontiers in psychiatry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

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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

13 authors.

Masahiro Hata *Department of Psychiatry, Osaka University Graduate School of Medicine, Osaka, Japan.
Yuki Miyazaki *Department of Psychiatry, Osaka University Graduate School of Medicine, Osaka, Japan.
Kohji MoriDepartment of Psychiatry, Osaka University Graduate School of Medicine, Osaka, Japan.
Kenji YoshiyamaDepartment of Psychiatry, Osaka University Graduate School of Medicine, Osaka, Japan.
Shoshin AkamineDepartment of Psychiatry, Osaka University Graduate School of Medicine, Osaka, Japan.
Hideki KanemotoDepartment of Psychiatry, Osaka University Graduate School of Medicine, Osaka, Japan.
Shiho GotohDepartment of Psychiatry, Osaka University Graduate School of Medicine, Osaka, Japan.
Hisaki OmoriDepartment of Psychiatry, Osaka University Graduate School of Medicine, Osaka, Japan.
Atsuya HirashimaDepartment of Psychiatry, Osaka University Graduate School of Medicine, Osaka, Japan.
Yuto SatakeDepartment of Psychiatry, Osaka University Graduate School of Medicine, Osaka, Japan.
Takashi SuehiroDepartment of Psychiatry, Osaka University Graduate School of Medicine, Osaka, Japan.
Shun TakahashiDepartment of Psychiatry, Osaka University Graduate School of Medicine, Osaka, Japan.
Manabu IkedaDepartment of Psychiatry, Osaka University Graduate School of Medicine, Osaka, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The current biomarker-supported diagnosis of Alzheimer's disease (AD) is hindered by invasiveness and cost issues. This study aimed to address these challenges by utilizing portable electroencephalography (EEG). We propose a novel, non-invasive, and cost-effective method for identifying AD, using a sample of patients with biomarker-verified AD, to facilitate early and accessible disease screening. Methods: This study included 35 patients with biomarker-verified AD, confirmed via cerebrospinal fluid sampling, and 35 age- and sex-balanced healthy volunteers (HVs). All participants underwent portable EEG recordings, focusing on 2-minute resting-state EEG epochs with closed eyes state. EEG recordings were transformed into scalogram images, which were analyzed using "vision Transformer(ViT)," a cutting-edge deep learning model, to differentiate patients from HVs. Results: The application of ViT to the scalogram images derived from portable EEG data demonstrated a significant capability to distinguish between patients with biomarker-verified AD and HVs. The method achieved an accuracy of 73%, with an area under the receiver operating characteristic curve of 0.80, indicating robust performance in identifying AD pathology using neurophysiological measures. Conclusions: Our findings highlight the potential of portable EEG combined with advanced deep learning techniques as a transformative tool for screening of biomarker-verified AD. This study not only contributes to the neurophysiological understanding of AD but also opens new avenues for the development of accessible and non-invasive diagnostic methods. The proposed approach paves the way for future clinical applications, offering a promising solution to the limitations of advanced diagnostic practices for dementia.

Indexed as

Alzheimer’s diseaseamyloid betadeep learningdementiaEEG

Identifiers

PMID38855641
PMCPMC11157607

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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.