Decreased uncinate fasciculus integrity in functional seizures following traumatic brain injury
Objective The uncinate fasciculus (UF) has been implicated previously in contributing to the pathophysiology of functional (nonepileptic) seizures (FS). FS are frequently preceded by adverse life events (ALEs) and present with comorbid psychiatric symptoms, yet neurobiological correlates of these fa...
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Veröffentlicht in: | Epilepsia (Copenhagen) 2024-04, Vol.65 (4), p.1060-1071 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Objective
The uncinate fasciculus (UF) has been implicated previously in contributing to the pathophysiology of functional (nonepileptic) seizures (FS). FS are frequently preceded by adverse life events (ALEs) and present with comorbid psychiatric symptoms, yet neurobiological correlates of these factors remain unclear. To address this gap, using advanced diffusion magnetic resonance imaging (dMRI), UF tracts in a large cohort of patients with FS and pre‐existing traumatic brain injury (TBI + FS) were compared to those in patients with TBI without FS (TBI‐only). We hypothesized that dMRI measures in UF structural connectivity would reveal UF differences when controlling for TBI status. Partial correlation tests assessed the potential relationships with psychiatric symptom severity measures.
Methods
Participants with TBI‐only (N = 46) and TBI + FS (N = 55) completed a series of symptom questionnaires and MRI scanning. Deterministic tractography via diffusion spectrum imaging (DSI) was implemented in DSI studio (https://dsi‐studio.labsolver.org) with q‐space diffeomorphic reconstruction (QSDR), streamline production, and manual segmentation to assess bilateral UF integrity. Fractional anisotropy (FA), radial diffusivity (RD), streamline counts, and their respective asymmetry indices (AIs) served as estimates of white matter integrity.
Results
Compared to TBI‐only, TBI + FS participants demonstrated decreased left hemisphere FA and RD asymmetry index (AI) for UF tracts (both p |
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ISSN: | 0013-9580 1528-1167 |
DOI: | 10.1111/epi.17896 |