Reduced left amygdala volume in patients with dissociative seizures (psychogenic nonepileptic seizures).


Journal

Seizure
ISSN: 1532-2688
Titre abrégé: Seizure
Pays: England
ID NLM: 9306979

Informations de publication

Date de publication:
Feb 2020
Historique:
received: 31 10 2019
revised: 09 12 2019
accepted: 17 12 2019
pubmed: 25 12 2019
medline: 18 11 2020
entrez: 25 12 2019
Statut: ppublish

Résumé

This study specifically investigated differences of amygdalar and hippocampal volumes between patients with dissociative seizures (DS), mesial temporal lobe sclerosis (MTS), and normal controls (NC). Between 2003 and 2018, 127 patients diagnosed with DS and 278 with MTS were recruited. An additional 52 NC subjects were recruited between 2015 and 2018. We retrospectively selected 29 patients with DS (male:female, 6:23) with absence of structural confounding factors and obtained sex- and age-matched MTS and NC. We used Neuroreader to assess the volume of the amygdala and hippocampus as a percentage of total intracranial volume based on thin-slice (0.9-1.2 mm) T1-weighted images. Statistical analyses controlled for psychiatric comorbidity and logistic regression were used to evaluate efficacy of these values for individual-level diagnosis. The left amygdala and right hippocampus were significantly smaller in DS compared to NC (both p = 0.04), which was not explained by differences in psychiatric comorbidity. When controlling for ipsilateral hippocampal or amygdala volume, which was seen equally in all groups (Spearman, p < 0.02), these differences were no longer significant (amygdala, p = 0.16, hippocampus, p = 0.18), suggesting that amygdalar and hippocampal atrophy may reflect network or regional changes rather than focal abnormalities. The three-way accuracy for differentiating DS, MTS, and NC using these data was 64 % (95 % confidence interval: 54-74 %). Volumetric analysis demonstrates smaller left amygdalar and right hippocampal volumes in patients with DS compared to NC, which may mirror abnormalities in functional networks seen in conversion disorders and post-traumatic stress disorder.

Identifiants

pubmed: 31874358
pii: S1059-1311(19)30746-0
doi: 10.1016/j.seizure.2019.12.014
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

43-48

Informations de copyright

Copyright © 2019 British Epilepsy Association. Published by Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declarations of Competing Interest None.

Auteurs

Hiroyuki Tatekawa (H)

Department of Radiology, David Geffen School of Medicine, University of California, 10833 Le Conte Ave., Los Angeles, CA, 90095, USA. Electronic address: htatekawa@med.osaka-cu.ac.jp.

Wesley T Kerr (WT)

Department of Neurology, David Geffen School of Medicine, University of California, 10833 Le Conte Ave., Los Angeles, CA, 90095, USA.

Ivanka Savic (I)

Department of Neurology, David Geffen School of Medicine, University of California, 10833 Le Conte Ave., Los Angeles, CA, 90095, USA; Department of Women's and Children's Health, Karolinska Institute and Neurology Clinic, Karolinska University Hospital, Karolinska Universitetssjukhuset, Eugeniavägen 3, 171 76, Solna, Stockholm, Sweden.

Jerome Engel (J)

Department of Neurology, David Geffen School of Medicine, University of California, 10833 Le Conte Ave., Los Angeles, CA, 90095, USA; Department of Neurobiology, David Geffen School of Medicine, University of California, 10833 Le Conte Ave., Los Angeles, CA, 90095, USA; Department of Psychiatry and Biobehavioral Sciences, David Geffen School of Medicine, University of California, 10833 Le Conte Ave., Los Angeles, CA, 90095, USA; Department of the Brain Research Institute, David Geffen School of Medicine, University of California, 10833 Le Conte Ave., Los Angeles, CA, 90095, USA.

Noriko Salamon (N)

Department of Radiology, David Geffen School of Medicine, University of California, 10833 Le Conte Ave., Los Angeles, CA, 90095, USA.

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