Continuous EEG Findings in Autoimmune Encephalitis.


Journal

Journal of clinical neurophysiology : official publication of the American Electroencephalographic Society
ISSN: 1537-1603
Titre abrégé: J Clin Neurophysiol
Pays: United States
ID NLM: 8506708

Informations de publication

Date de publication:
01 Mar 2021
Historique:
pubmed: 5 12 2019
medline: 4 5 2021
entrez: 5 12 2019
Statut: ppublish

Résumé

Autoimmune encephalitis (AE) is a cause of new-onset seizures, including new-onset refractory status epilepticus, yet there have been few studies assessing the EEG signature of AE. Multicenter retrospective review of patients diagnosed with AE who underwent continuous EEG monitoring. We identified 64 patients (male, 39%; white, 49%; median age, 44 years); of whom, 43 (67%) were antibody-proven AE patients. Of the patients with confirmed antibody AE, the following were identified: N-methyl-D-aspartate receptor (n = 17, 27%), voltage-gated potassium channel (n = 16, 25%), glutamic acid decarboxylase (n = 6, 9%), and other (n = 4, 6%). The remaining patients were classified as probable antibody-negative AE (n = 11, 17%), definite limbic encephalitis (antibody-negative) (n = 2, 3%), and Hashimoto encephalopathy (n = 8, 13%). Fifty-three percent exhibited electrographic seizures. New-onset refractory status epilepticus was identified in 19% of patients. Sixty-three percent had periodic or rhythmic patterns; of which, 38% had plus modifiers. Generalized rhythmic delta activity was identified in 33% of patients. Generalized rhythmic delta activity and generalized rhythmic delta activity plus fast activity were more common in anti-N-methyl-D-aspartate AE (P = 0.0001 and 0.0003, respectively). No other periodic or rhythmic patterns exhibited AE subtype association. Forty-two percent had good outcome on discharge. Periodic or rhythmic patterns, seizures, and new-onset refractory status epilepticus conferred an increased risk of poor outcome (OR, 6.4; P = 0.0012; OR, 3; P = 0.0372; OR, 12.3; P = 0.02, respectively). Our study confirms a signature EEG pattern in anti-N-methyl-D-aspartate AE, termed extreme delta brush, identified as generalized rhythmic delta activity plus fast activity in our study. We found no other pattern association with other AE subtypes. We also found a high incidence of seizures among patients with AE. Finally, periodic or rhythmic patterns, seizures, and new-onset refractory status epilepticus conferred an increased risk of poor outcome regardless of AE subtype.

Identifiants

pubmed: 31800465
pii: 00004691-202103000-00007
doi: 10.1097/WNP.0000000000000654
pmc: PMC7263965
mid: NIHMS1572004
doi:

Substances chimiques

Autoantibodies 0

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

124-129

Subventions

Organisme : NINDS NIH HHS
ID : R01 NS102190
Pays : United States
Organisme : NINDS NIH HHS
ID : R01 NS107291
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR000454
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR001863
Pays : United States

Informations de copyright

Copyright © 2019 by the American Clinical Neurophysiology Society.

Déclaration de conflit d'intérêts

The authors have no conflicts of interest to disclose.

Références

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Auteurs

Anna-Marieta Moise (AM)

Department of Neurology, Emory University School of Medicine, Atlanta, Georgia, U.S.A.
Mission Neurosciences Program, Epilepsy Department, Mission Health, Asheville, North Carolina, U.S.A.

Ioannis Karakis (I)

Department of Neurology, Emory University School of Medicine, Atlanta, Georgia, U.S.A.

Aline Herlopian (A)

Department of Neurology and Yale Comprehensive Epilepsy Center, Yale University, New Haven, Connecticut, U.S.A.

Monica Dhakar (M)

Department of Neurology, Emory University School of Medicine, Atlanta, Georgia, U.S.A.

Lawrence J Hirsch (LJ)

Department of Neurology and Yale Comprehensive Epilepsy Center, Yale University, New Haven, Connecticut, U.S.A.

George Cotsonis (G)

Department of Neurology, Emory University School of Medicine, Atlanta, Georgia, U.S.A.

Suzette LaRoche (S)

Mission Neurosciences Program, Epilepsy Department, Mission Health, Asheville, North Carolina, U.S.A.

Christian M Cabrera Kang (CM)

Neurology Division, Laureate Medical Group, Atlanta, Georgia, U.S.A.

Brandon Westover (B)

MGH Epilepsy Service and Division of Clinical Neurophysiology, Massachusetts General Hospital, Boston, Massachusetts, U.S.A.

Andres Rodriguez (A)

Department of Neurology, Emory University School of Medicine, Atlanta, Georgia, U.S.A.

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