Evidence map›Paper›PMID 40341391›Full record

ArticleNPJ Parkinson's disease2025

Characterizing the heterogeneity of neurodegenerative diseases through EEG normative modeling.

Judie Tabbal, Aida Ebadi, Ahmad Mheich, Aya Kabbara, Bahar Güntekin, Görsev Yener, Veronique Paban, Ute Gschwandtner, Peter Fuhr, Marc Verin and 3 more

Abstract read
In one paragraph

Article in NPJ Parkinson's disease, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 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.

Judie TabbalMINDIG, F-35000, Rennes, France.
Aida EbadiMINDIG, F-35000, Rennes, France.
Ahmad MheichMINDIG, F-35000, Rennes, France.
Aya KabbaraMINDIG, F-35000, Rennes, France.
Bahar GüntekinDepartment of Biophysics, School of Medicine, Istanbul Medipol University, Istanbul, Turkey.
Görsev YenerIzmir University of Economics, Faculty of Medicine, Izmir, Turkey.
Veronique PabanAix Marseille Univ, CNRS-UMR 7077, CRPN, Marseille, France.ORCID http://orcid.org/0000-0001-7758-3302
Ute GschwandtnerDepartments of Clinical Research and of Neurology, University Hospital of Basel, Basel, Switzerland.
Peter FuhrDepartments of Clinical Research and of Neurology, University Hospital of Basel, Basel, Switzerland.
Marc VerinCentre Hospitalier Université d'Orléans, Service de Neurologie, Orléans, France.
Claudio BabiloniDepartment of Physiology and Pharmacology "Vittorio Erspamer", Sapienza University of Rome, Rome, Italy.
Sahar AllouchMINDIG, F-35000, Rennes, France.
Mahmoud HassanMINDIG, F-35000, Rennes, France. mahmoud.hassan.work@gmail.com.ORCID http://orcid.org/0000-0003-0307-5086

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neurodegenerative diseases like Parkinson's (PD) and Alzheimer's (AD) exhibit considerable heterogeneity of functional brain features within patients, complicating diagnosis and treatment. Here, we use electroencephalography (EEG) and normative modeling to investigate neurophysiological mechanisms underpinning this heterogeneity. Resting-state EEG data from 14 clinical units included healthy adults (n = 499) and patients with PD (n = 237) and AD (n = 197), aged over 40. Spectral and source connectivity analyses provided features for normative modeling, revealing significant, frequency-dependent EEG deviations with high heterogeneity in PD and AD. Around 30% of patients exhibited spectral deviations, while ~80% showed functional source connectivity deviations. Notably, the spatial overlap of deviant features did not exceed 60% for spectral and 25% for connectivity analysis. Furthermore, patient-specific deviations correlated with clinical measures, with greater deviations linked to worse UPDRS for PD (⍴ = 0.24, p = 0.025) and MMSE for AD (⍴ = -0.26, p = 0.01). These results suggest that EEG deviations could enrich individualized clinical assessment in Precision Neurology.

Identifiers

PMID40341391
PMCPMC12062460

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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.