Evidence map›Paper›PMID 36002969›Full record

ArticleNeuroImage. Clinical2022

Spectral decomposition of EEG microstates in post-traumatic stress disorder.

Braeden A Terpou, Saurabh B Shaw, Jean Théberge, Victor Férat, Christoph M Michel, Margaret C McKinnon, Ruth A Lanius, Tomas Ros

Open access · goldAbstract read
In one paragraph

Article in NeuroImage. Clinical, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
3.6field-weighted citation impact, top 6% of its field
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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 33 citations in OpenAlex.

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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

8 authors at 5 institutions in 2 countries.

Braeden A TerpouDepartment of Psychiatry and Behavioural Neurosciences, McMaster University, Hamilton, Canada; Homewood Research Institute, Guelph, Canada. Electronic address: terpouba@mcmaster.ca.
Saurabh B ShawDepartment of Psychiatry, Western University, London, Canada; Homewood Research Institute, Guelph, Canada; Vector Institute, Toronto, Canada.
Jean ThébergeDepartment of Psychiatry, Western University, London, Canada; Department of Medical Biophysics, Western University, London, Canada; Imaging Division, Lawson Health Research Institute, London, Canada.
Victor FératDepartment of Basic Neurosciences, University of Geneva, Geneva, Switzerland.
Christoph M MichelDepartment of Basic Neurosciences, University of Geneva, Geneva, Switzerland; Centre for Biomedical Imaging (CIBM), Lausanne-Geneva, Switzerland.
Margaret C McKinnonDepartment of Psychiatry and Behavioural Neurosciences, McMaster University, Hamilton, Canada; Mood Disorders Program, St. Joseph's Healthcare Hamilton, Hamilton, Canada; Homewood Research Institute, Guelph, Canada.
Ruth A LaniusDepartment of Psychiatry, Western University, London, Canada; Imaging Division, Lawson Health Research Institute, London, Canada; Homewood Research Institute, Guelph, Canada.
Tomas RosDepartment of Basic Neurosciences, University of Geneva, Geneva, Switzerland; Centre for Biomedical Imaging (CIBM), Lausanne-Geneva, Switzerland.
Homewood Research Institute · CAWestern University · CACentre d'Imagerie BioMedicale · CHMcMaster University · CAUniversity of Geneva · CH

Funding

CIHR 148784
6 · The paper itself

Abstract

Microstates offer a promising framework to study fast-scale brain dynamics in the resting-state electroencephalogram (EEG). However, microstate dynamics have yet to be investigated in post-traumatic stress disorder (PTSD), despite research demonstrating resting-state alterations in PTSD. We performed microstate-based segmentation of resting-state EEG in a clinical population of participants with PTSD (N = 61) and a non-traumatized, healthy control group (N = 61). Microstate-based measures (i.e., occurrence, mean duration, time coverage) were compared group-wise using broadband (1-30 Hz) and frequency-specific (i.e., delta, theta, alpha, beta bands) decompositions. In the broadband comparisons, the centro-posterior maximum microstate (map E) occurred significantly less frequently (d = -0.64, pFWE = 0.03) and had a significantly shorter mean duration in participants with PTSD as compared to controls (d = -0.71, pFWE < 0.01). These differences were reflected in the narrow frequency bands as well, with lower frequency bands like delta (d = -0.78, pFWE < 0.01), theta (d = -0.74, pFWE = 0.01), and alpha (d = -0.65, pFWE = 0.02) repeating these group-level trends, only with larger effect sizes. Interestingly, a support vector machine classification analysis comparing broadband and frequency-specific measures revealed that models containing only alpha band features significantly out-perform broadband models. When classifying PTSD, the classification accuracy was 76 % and 65 % for the alpha band and the broadband model, respectively (p = 0.03). Taken together, we provide original evidence supporting the clinical utility of microstates as diagnostic markers of PTSD and demonstrate that filtering EEG into distinct frequency bands significantly improves microstate-based classification of a psychiatric disorder.

Indexed as

Stress Disorders, Post-TraumaticBrainBrain MappingElectroencephalographyHumansEEGMachine learningMicrostatesPTSDResting-state

Identifiers

PMID36002969
PMCPMC9421541
OpenAlexW4288739814

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.