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Locus coeruleus co-activation patterns at rest show higher state persistence in patients with dissociative seizures: A Pilot Study.

Samantha Weber, Johannes Jungilligens, Selma Aybek, Stoyan Popkirov

Epilepsia open December 1, 2024 DOI: 10.1002/epi4.13050 via PubMed

Summary

AI-generated from the abstract

Patients with dissociative seizures tend to remain in specific brain states linked to the locus coeruleus rather than switching between them, suggesting that arousal-related impairments in network switching may be a neural mechanism of dissociation. A co-activation pattern analysis of resting-state fMRI in 14 patients and 14 healthy controls identified three locus-coeruleus-related brain states. Patients showed higher state persistence for two of these states compared to controls (Cohen's d = -0.55 and -0.57; p = 0.01 for both). No significant group differences were found when using the red nucleus as a control seed.

Study at a glance

Characteristics Preliminary co-activation pattern analysis of resting-state fMRI Pilot study Peer reviewed
Sample size 28
Population 14 patients with dissociative seizures and 14 healthy controls
Keywords Co‐activation pattern Pnes Conversion disorder Coupling Dynamic functional connectivity
Citations 7
Key finding Patients with dissociative seizures show higher persistence in locus-coeruleus-dependent brain states compared to healthy controls.

Abstract

Dissociative seizures are paroxysmal disruptions of awareness and behavioral control in the context of affective arousal. Alterations in stress-related endocrine function have been demonstrated, but the timescale of dissociation suggests that the central locus coeruleus (LC) noradrenergic system is likely pivotal. Here, we investigate whether LC activation at rest is associated with altered brain network dynamics. A preliminary co-activation pattern (CAP) analysis of resting-state functional magnetic resonance imaging (fMRI) in 14 patients with dissociative seizures and 14 healthy controls was performed by using the LC as a seeding region. The red nucleus served as a control condition. Entry rates, durations, and state transition probabilities of identified CAPs were calculated. Analyses were corrected for demographic, technical, and clinical confounders including depression and anxiety. Three LC-related CAPs were identified, with the dominant two showing inverse activations and deactivations of the default mode network and the attention networks, respectively. Analysis of transition probabilities between and within the three CAPs revealed higher state persistence in patients compared to healthy controls for both CAP2LC (Cohen's d = -0.55; p = 0.01) and CAP3LC (Cohen's d = -0.57; p = 0.01). The control analysis using the red nucleus as a seed yielded similar CAPs, but no significant between-group differences in transition probabilities. Higher state persistence of LC-CAPs in patients with dissociative seizures generates the novel hypothesis that arousal-related impairments of network switching might be a candidate neural mechanism of dissociation. Dissociative seizures often arise during high affective arousal. The locus coeruleus is a brain structure involved in managing such acute arousal states. We investigated whether the activity of the locus coeruleus correlates with activity in other regions of the brain (which we refer to as "brain states"), and whether those brain states were different between patients with dissociative seizures and healthy controls. We found that patients tended to stay in certain locus coeruleus-dependent brain states instead of switching between them. This might be related to the loss of awareness and disruptions of brain functions ("dissociation") that patients experience during seizures.

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