Evidence map›Paper›PMID 39648748›Full record

ArticleActa neuropsychiatrica2024

Uncovering key predictive channels and clinical variables in the gamma band auditory steady-state response in early-stage psychosis: a longitudinal study.

Kristina M Holton, Amy Higgins, Austin J Brockmeier, Mei-Hua Hall

Abstract read
In one paragraph

Article in Acta neuropsychiatrica, 2024. 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

4 authors.

Kristina M HoltonCenter for Bioinformatics and Computational Biology, University of Delaware, Newark, DE, USA.ORCID https://orcid.org/0000-0002-1002-2882
Amy HigginsPsychosis Neurobiology Laboratory, McLean Hospital, Belmont, MA, USA.
Austin J BrockmeierCenter for Bioinformatics and Computational Biology, University of Delaware, Newark, DE, USA.
Mei-Hua HallPsychosis Neurobiology Laboratory, McLean Hospital, Belmont, MA, USA.

Funding

Neurobiological Markers as Predictors of Later Functional Outcome in First Episode PsychosisR01MH109687 · NIMH · MCLEAN HOSPITAL · PI HALL, MEI-HUA · 2016 to 2021
$2.5M
NIMH NIH HHS R01 MH109687
6 · The paper itself

Abstract

objectivePsychotic disorders are characterised by abnormalities in the synchronisation of neuronal responses. A 40 Hz gamma band deficit during auditory steady-state response (ASSR) measured by electroencephalogram (EEG) is a robust observation in psychosis and is associated with symptoms and functional deficits. However, the majority of ASSR studies focus on specific electrode sites, while whole scalp analysis using all channels, and the association with clinical symptoms, are rare.

methodsIn this study, we use whole-scalp 40 Hz ASSR EEG measurements – power and phase-locking factor – to establish deficits in early-stage psychosis (ESP) subjects, classify ESP status using an ensemble of machine learning techniques, identify correlates with principal components obtained from clinical/demographic/functioning variables, and correlate functional outcome after a short-term follow-up.

resultsWe identified significant spatially-distributed group level differences for power and phase locking. The performance of different machine learning techniques and interpretation of the extracted feature importance indicate that phase locking has a more predictive and parsimonious pattern than power. Phase locking is also associated with principal components composed of measures of cognitive processes. Short-term functional outcome is associated with baseline 40 Hz ASSR signals from the FCz and other channels in both phase locking and power.

conclusionThis whole-scalp EEG study provides additional evidence to link deficits in 40 Hz ASSRs with cognition and functioning in ESP, and corroborates with prior studies of phase locking from a subset of EEG channels. Confirming 40 Hz ASSR deficits serves as a candidate phenotype to identify circuit dysfunctions and a biomarker for clinical outcomes in psychosis.

Indexed as

ElectroencephalographyEvoked Potentials, AuditoryGamma RhythmMachine LearningPsychotic DisordersAdolescentAdultFemaleHumansLongitudinal StudiesMaleYoung AdultEarly stage psychosiselectroencephalogramlongitudinalmachine learningschizophrenia spectrum disorder

Identifiers

PMID39648748
PMCPMC13130324

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.