Seizure specificities in patients with antibody-mediated autoimmune encephalitis.

autoimmune diseases electroencephalography encephalitis epilepsy paraneoplastic syndromes seizures

Journal

Epilepsia
ISSN: 1528-1167
Titre abrégé: Epilepsia
Pays: United States
ID NLM: 2983306R

Informations de publication

Date de publication:
08 2019
Historique:
received: 28 03 2019
revised: 15 06 2019
accepted: 18 06 2019
pubmed: 10 7 2019
medline: 16 4 2020
entrez: 9 7 2019
Statut: ppublish

Résumé

Accumulating data on patients with autoimmune encephalitis have shed light on specificities concerning clinical presentation and outcomes, which are dependent on the antigen targeted by the autoantibodies found in the patients' cerebrospinal fluid or sera. Such specificities include seizure-related clinical manifestations as well as the responsiveness to antiepileptic drugs. Although increased enthusiasm accompanies the discovery of novel antibodies and their associated clinical syndromes, several issues remain unsettled. First, it appears that therapy needs to be personalized in the view of the severity of each antibody-mediated syndrome, patient-related characteristics, and timing of treatment. Second, the lack of randomized controlled trials is a major drawback in the formulation of an appropriate immunotherapeutic strategy. In this review, we discuss the novel developments and challenges for the diagnosis and treatment of epilepsy in patients with well-characterized autoimmune encephalitis, and delineate the principles for a rational approach toward precision medicine in this emerging field.

Identifiants

pubmed: 31283859
doi: 10.1111/epi.16282
doi:

Substances chimiques

Autoantibodies 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

1508-1525

Informations de copyright

Wiley Periodicals, Inc. © 2019 International League Against Epilepsy.

Auteurs

Alberto Vogrig (A)

French Reference Center for Paraneoplastic Neurological Syndromes, Hospital for Neurology and Neurosurgery Pierre Wertheimer, Lyon University Hospital, Lyon, France.
SynatAc Team, NeuroMyoGene Institute, INSERM U1217/CNRS, UMR5310, Lyon, France.
University Claude Bernard Lyon 1, University of Lyon, Lyon, France.
Clinical Neurology Unit, Santa Maria della Misericordia University Hospital, Udine, Italy.

Bastien Joubert (B)

French Reference Center for Paraneoplastic Neurological Syndromes, Hospital for Neurology and Neurosurgery Pierre Wertheimer, Lyon University Hospital, Lyon, France.
SynatAc Team, NeuroMyoGene Institute, INSERM U1217/CNRS, UMR5310, Lyon, France.
University Claude Bernard Lyon 1, University of Lyon, Lyon, France.

Nathalie André-Obadia (N)

Department of Functional Neurology and Epileptology, Hospital for Neurology and Neurosurgery Pierre Wertheimer, Lyon University Hospital, Lyon, France.
Lyon's Neurosciences Research Center, INSERM U1028/CNRS, UMR 5292, University of Lyon, Lyon, France.

Gian Luigi Gigli (GL)

Clinical Neurology Unit, Santa Maria della Misericordia University Hospital, Udine, Italy.
Department of Medicine (DAME), University of Udine Medical School, Udine, Italy.
Department of Mathematics, Informatics and Physics (DMIF), University of Udine, Udine, Italy.

Sylvain Rheims (S)

Department of Functional Neurology and Epileptology, Hospital for Neurology and Neurosurgery Pierre Wertheimer, Lyon University Hospital, Lyon, France.
Lyon's Neurosciences Research Center, INSERM U1028/CNRS, UMR 5292, University of Lyon, Lyon, France.

Jérome Honnorat (J)

French Reference Center for Paraneoplastic Neurological Syndromes, Hospital for Neurology and Neurosurgery Pierre Wertheimer, Lyon University Hospital, Lyon, France.
SynatAc Team, NeuroMyoGene Institute, INSERM U1217/CNRS, UMR5310, Lyon, France.
University Claude Bernard Lyon 1, University of Lyon, Lyon, France.

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