Frontocentral delta-beta amplitude coupling in endometriosis-related chronic pelvic pain.

Chronic pelvic pain Electroencephalography (EEG) Endometriosis Eyes closed resting Frequency principal components analysis (fPCA)

Journal

Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology
ISSN: 1872-8952
Titre abrégé: Clin Neurophysiol
Pays: Netherlands
ID NLM: 100883319

Informations de publication

Date de publication:
05 2023
Historique:
received: 03 11 2022
revised: 08 02 2023
accepted: 13 02 2023
medline: 17 4 2023
pubmed: 26 3 2023
entrez: 25 3 2023
Statut: ppublish

Résumé

Endometriosis is associated with neuroplastic changes in cognitive control and pain processing networks. This was the first study to assess eyes-closed resting electroencephalogram (EEG) oscillatory amplitudes in women with endometriosis compared to healthy controls, and explore the relationship with chronic pelvic pain. Women with endometriosis-related chronic pelvic pain and individually age-matched pain-free controls (N = 20 per group) documented pelvic pain for 28 days before having continuous EEG recorded during a 2 min eyes closed resting state. Natural frequency components were extracted for each group using frequency principal components analysis. Corresponding components were assessed for group differences and correlated with pain scores. Relative to controls, the endometriosis group had greater component amplitudes in delta (0.5 Hz) and beta (∼28 Hz), and reduced alpha (∼10 Hz). Delta and beta amplitudes were positively associated with pain severity, but only beta maintained this association after delta-beta amplitude coupling was controlled. Enhanced resting delta and beta amplitudes were seen in women with endometriosis experiencing chronic pelvic pain. This delta-beta coupling varied with pelvic pain severity, perhaps reflecting altered cholinergic tone and/or stress reactivity. Endometriosis-related changes in central pain processing demonstrate a distinct neuronal oscillatory signature detectable at rest.

Identifiants

pubmed: 36965467
pii: S1388-2457(23)00220-1
doi: 10.1016/j.clinph.2023.02.173
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

146-156

Informations de copyright

Copyright © 2023 International Federation of Clinical Neurophysiology. Published by Elsevier B.V. All rights reserved.

Auteurs

Frances M De Blasio (FM)

NICM Health Research Institute and Translational Health Research Institute (THRI), Western Sydney University, Penrith, NSW 2751, Australia; Brain & Behaviour Research Institute and School of Psychology, University of Wollongong, Wollongong, NSW 2522, Australia.

Sapphire Love (S)

Brain & Behaviour Research Institute and School of Psychology, University of Wollongong, Wollongong, NSW 2522, Australia.

Robert J Barry (RJ)

Brain & Behaviour Research Institute and School of Psychology, University of Wollongong, Wollongong, NSW 2522, Australia.

Katherine Wassink (K)

Brain & Behaviour Research Institute and School of Psychology, University of Wollongong, Wollongong, NSW 2522, Australia.

Adele E Cave (AE)

NICM Health Research Institute and Translational Health Research Institute (THRI), Western Sydney University, Penrith, NSW 2751, Australia.

Mike Armour (M)

NICM Health Research Institute and Translational Health Research Institute (THRI), Western Sydney University, Penrith, NSW 2751, Australia.

Genevieve Z Steiner-Lim (GZ)

NICM Health Research Institute and Translational Health Research Institute (THRI), Western Sydney University, Penrith, NSW 2751, Australia. Electronic address: G.Steiner@westernsydney.edu.au.

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Classifications MeSH