Evidence map›Paper›PMID 39226702›Full record

ArticleNeuroImage. Clinical2024

The imprint of dissociative seizures on the brain.

S G Mueller, N Garga, P Garcia, S Rossi, A Vu, T Neylan, K D Laxer

Abstract read
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Article in NeuroImage. Clinical, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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0cells of the map it votes in
2citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

S G MuellerCenter for Imaging of Neurodegenerative Diseases, VAMC, San Francisco, CA, USA; Dept of Radiology and Biomedical Imaging, University of California, San Francisco, CA, USA. Electronic address: susanne.mueller@ucsf.edu.
N GargaVA Epilepsy Center of Excellence, VAMC, San Francisco, CA, USA; Dept. of Neurology, University of California, San Francisco, CA, USA.
P GarciaDept. of Neurology, University of California, San Francisco, CA, USA.
S RossiCenter for Imaging of Neurodegenerative Diseases, VAMC, San Francisco, CA, USA.
A VuCenter for Imaging of Neurodegenerative Diseases, VAMC, San Francisco, CA, USA; Dept of Radiology and Biomedical Imaging, University of California, San Francisco, CA, USA.
T NeylanVA Mental Health, VAMC San Francisco, CA, USA.
K D LaxerSutter Pacific Epilepsy Program, California Pacific Medical Center, San Francisco, CA, USA.

Funding

Individual Variation in Effects of Traumatic Stress on Gray Matter MyelinR01MH115020 · NIMH · NORTHERN CALIFORNIA INSTITUTE/RES/EDU · PI KAUFER, DANIELA, NEYLAN, THOMAS C · 2019 to 2023
$3.9M
Investigating Fear System Myelination in PTSD Using In Vivo and Post Mortem DataR01MH132617 · NIMH · NORTHERN CALIFORNIA INSTITUTE/RES/EDU · PI HUBER, BERTRAND R, NEYLAN, THOMAS C · 2023 to 2025
$2.1M
NIMH NIH HHS R01 MH115020NIMH NIH HHS R01 MH132617US Department of Defense W81XWH-17–1-0336
6 · The paper itself

Abstract

backgroundIncreased resting state functional connectivity between regions involved in emotion control with regions with other specializations, e.g. motor control (emotional hyperconnectivity) is one of the most consistent imaging findings in persons suffering from dissociative seizures (DS). The overall goal of this study was to better characterize DS-related emotional hyperconnectivity using dynamic resting state analysis combined with brainstem volumetry to investigate 1. If emotional hyperconnectivity is restricted to a single state. 2. How volume losses within the modulatory and emotional motor subnetworks of the neuromodulatory system influence the expression of the emotional hyperconnectivity.

methods13 persons with dissociative seizures (PDS) (f/m:10/3, mean age (SD) 44.6 (11.5)) and 15 controls (CON) (f/m:10/5, mean age (SD) 41.7 (13.0)) underwent a mental health test battery and structural and functional imaging at 3 T. Deformation based morphometry was used to assess brain volume loss by extracting the mean Jacobian determinants from 457 brain, forebrain and brainstem structures. The bold signals from 445 brainstem and brain rois were extracted with CONN and a dynamic fMRI analysis combined with graph and hierarchical analysis was used to identify and characterize 9 different brain states. Welch's t tests and Kendall tau tests were used for group comparisons and correlation analyses.

resultsThe duration of Brain state 6 was longer in PDS than in CON (93.1(88.3) vs. 23.4(31.2), p = 0.01) and positively correlated with higher degrees of somatization, depression, PTSD severity and dissociation. Its global connectivity was higher in PDS than CON (90.4(3.2) vs 86.5(4.2) p = 0.01) which was caused by an increased connectivity between regions involved in emotion control and regions involved in sense of agency/body control. The brainstem and brainstem-forebrain modulatory and emotional motor subnetworks of the neuromodulatory system were atrophied in PDS. Atrophy severity within the brainstem-forebrain subnetworks was correlated with state 6 dwell time (modulatory: tau = -0.295, p = 0.03; emotional motor: tau = -0.343, p = 0.015) and atrophy severity within the brainstem subnetwork with somatization severity (modulatory: tau = -0.25, p = 0.036; emotional motor: tau = -0.256, p = 0.033).

conclusionDS-related emotional hyperconnectivity was restricted to state 6 episodes. The remaining states were not different between PDS and CON. The modulatory subnetwork synchronizes brain activity across brain regions. Atrophy and dysfunction within that subnetwork could facilitate the abnormal interaction between regions involved in emotion control with those controlling sense of agency/body ownership during state 6 and contribute to the tendency for somatization in PDS. The emotional motor subnetwork controls the activity of spinal motoneurons. Atrophy and dysfunction within this subnetwork could impair that control resulting in motor symptoms during DS. Taken together, these findings indicate that DS have a neurophysiological underpinning.

Indexed as

BrainDissociative DisordersMagnetic Resonance ImagingSeizuresAdultBrain StemEmotionsFemaleHumansMaleMiddle AgedBrainstemDissociative seizureResting state fMRIVolumetry

Identifiers

PMID39226702
PMCPMC11403518

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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.