Evidence map›Paper›PMID 40610223›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2025

Unveiling Cortical Criticality Changes along the Prodromal to the Overt Continuum of Alpha-Synucleinopathy.

Monica Roascio, Sheng H Wang, Vladislav Myrov, Felix Siebenhühner, Rosella Trò, Pietro Mattioli, Francesco Famà, Silvia D Morbelli, Matteo Pardini, Beatrice Orso and 3 more

Abstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

13 authors.

Monica RoascioDepartment of Informatics, Bioengineering, Robotics and System Engineering (DIBRIS), University of Genoa, Genoa 16145, Italy monica.roascio@edu.unige.it gabriele.arnulfo@unige.it.ORCID 0000-0002-4522-1574
Sheng H WangNeuroscience Center, Helsinki Institute of Life Science (HiLife), University of Helsinki, Helsinki FI-00014, Finland.ORCID 0000-0002-6226-6213
Vladislav MyrovDepartment of Neuroscience and Biomedical Engineering, Aalto University, Espoo FI-00076, Finland.ORCID 0000-0001-5147-2727
Felix SiebenhühnerNeuroscience Center, Helsinki Institute of Life Science (HiLife), University of Helsinki, Helsinki FI-00014, Finland.ORCID 0000-0002-2621-9145
Rosella TròDepartment of Informatics, Bioengineering, Robotics and System Engineering (DIBRIS), University of Genoa, Genoa 16145, Italy.ORCID 0000-0002-4915-5295
Pietro MattioliDepartment of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Children's Sciences (DINOGMI), University of Genoa, Genoa 16132, Italy.ORCID 0000-0003-2563-5830
Francesco FamàDepartment of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Children's Sciences (DINOGMI), University of Genoa, Genoa 16132, Italy.ORCID 0000-0002-9084-9037
Silvia D MorbelliNuclear Medicine Unit, Città della Salute e della Scienza di Torino, Turin 10126, Italy.ORCID 0000-0002-7833-6095
Matteo PardiniDepartment of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Children's Sciences (DINOGMI), University of Genoa, Genoa 16132, Italy.ORCID 0000-0002-4740-1982
Beatrice OrsoDepartment of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Children's Sciences (DINOGMI), University of Genoa, Genoa 16132, Italy.ORCID 0000-0001-9983-7940
J Matias PalvaNeuroscience Center, Helsinki Institute of Life Science (HiLife), University of Helsinki, Helsinki FI-00014, Finland.ORCID 0000-0003-1885-2749
Dario ArnaldiDepartment of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Children's Sciences (DINOGMI), University of Genoa, Genoa 16132, Italy.ORCID 0000-0001-6823-6069
Gabriele ArnulfoDepartment of Informatics, Bioengineering, Robotics and System Engineering (DIBRIS), University of Genoa, Genoa 16145, Italy monica.roascio@edu.unige.it gabriele.arnulfo@unige.it.ORCID 0000-0002-1140-0320

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Patients with idiopathic/isolated REM sleep behavior disorder (iRBD) are in the prodromal stage of alpha-synucleinopathies. Neurodegeneration early affects subcortical structures, including the substantia nigra, in iRBD patients. However, it remains unclear whether there is also an early neurodegeneration process affecting the cerebral cortex. We investigated whether EEG-derived metrics for aberrant cortical dynamics and imbalanced excitation-inhibition (E/I) correlate with disease severity in iRBD patients, aiming to better understand the pathophysiology progression from the prodromal to the overt stage of alpha-synucleinopathies. We retrospectively analyzed resting-state EEG recordings, as a marker of cortical function, and presynaptic dopaminergic imaging, a marker of subcortical function from 59 iRBD patients (9 female) who underwent longitudinal clinical evaluation alongside 46 age-matched healthy controls (22 female). We assessed power-law scaling in long-range temporal correlations (LRTCs), neuronal bistability, and functional E/I balance from the resting-state sensor EEG data and then correlated these to large-scale synchrony, nigrostriatal dopaminergic function, and clinical data. Compared with the control group, patients showed higher LRTCs and bistability in 2-7 Hz oscillations. Patients who developed parkinsonism/dementia exhibited hyperexcitability in 5-7 Hz compared with those who did not. This was also correlated with stronger phase synchrony. Both hyperexcitability in 5-7 Hz and bistability in 2-4 Hz negatively associated with nigrostriatal dopaminergic impairment. The iRBD patients, especially those closer to phenoconversion to parkinsonism or dementia, show clear aberrant cortical dynamics and hyperexcitability alongside substantia nigra impairment, suggesting that neurodegeneration in the prodromal stages affects both subcortical structures and cortical dynamics.

Indexed as

Cerebral CortexProdromal SymptomsREM Sleep Behavior DisorderSynucleinopathiesAdultAgedDisease ProgressionElectroencephalographyFemaleHumansMaleMiddle AgedRetrospective Studiescortical excitation–inhibition balancecritical cortical dynamicsidiopathic REM sleep behavior disorderpathophysiology

Identifiers

PMID40610223
PMCPMC12311758

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.