Epileptic phenotypes in autoimmune encephalitis: from acute symptomatic seizures to autoimmune-associated epilepsy.
AUTOIMMUNE ENCEPHALITIS
EPILEPSY
Journal
Journal of neurology, neurosurgery, and psychiatry
ISSN: 1468-330X
Titre abrégé: J Neurol Neurosurg Psychiatry
Pays: England
ID NLM: 2985191R
Informations de publication
Date de publication:
25 Jul 2022
25 Jul 2022
Historique:
received:
19
03
2022
accepted:
06
07
2022
entrez:
25
7
2022
pubmed:
26
7
2022
medline:
26
7
2022
Statut:
aheadofprint
Résumé
To describe the clinical and paraclinical findings, treatment options and long-term outcomes in autoimmune encephalitis (AE), with a close look to epilepsy. In this retrospective observational cohort study, we enrolled patients with new-onset seizures in the context of AE. We compared clinical and paraclinical findings in patients with and without evidence of antibodies. Overall, 263 patients (138 females; median age 55 years, range 4-86) were followed up for a median time of 30 months (range 12-120). Antineuronal antibodies were detected in 63.50%.Antibody-positive patients had multiple seizure types (p=0.01) and prevalent involvement of temporal regions (p=0.02). A higher prevalence of episodes of SE was found in the antibody-negative group (p<0.001).Immunotherapy was prescribed in 88.60%, and effective in 61.80%. Independent predictors of favourable outcome of the AE were early immunotherapy (p<0.001) and the detection of antineuronal surface antibodies (p=0.01).Autoimmune-associated epilepsy was the long-term sequela in 43.73%, associated with cognitive and psychiatric disturbances in 81.73%. Independent predictors of developing epilepsy were difficult to treat seizures at onset (p=0.04), a high number of antiseizure medications (p<0.001), persisting interictal epileptiform discharges at follow-up (p<0.001) and poor response to immunotherapy during the acute phase (p<0.001). The recognition of seizures secondary to AE represents a rare chance for aetiology-driven seizures management. Early recognition and treatment at the pathogenic level may reduce the risk of long-term irreversible sequelae. However, the severity of seizures at onset is the major risk factor for the development of chronic epilepsy.This study provides class IV evidence for management recommendations.
Identifiants
pubmed: 35879055
pii: jnnp-2022-329195
doi: 10.1136/jnnp-2022-329195
pii:
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Investigateurs
Umberto Aguglia
(U)
Vincenzo Belcastro
(V)
Luana Benedetti
(L)
Simone Beretta
(S)
Stefania Maria Bova
(SM)
Claudia Cagnetti
(C)
Susanna Casellato
(S)
Lorenzo Celli
(L)
Elisabetta Cesaroni
(E)
Eduard Cesnick
(E)
Giangennaro Coppola
(G)
Edvige Correnti
(E)
Giuseppe Didato
(G)
Giuseppe D'Orsi
(G)
Elena Fallica
(E)
Alessandra Ferrari
(A)
Alessandro Ferretti
(A)
Carlo Andrea Galimberti
(CA)
Annateresa Giallonardo
(A)
Loretta Giuliano
(L)
Angela La Neve
(A)
Claudio Liguori
(C)
Carla Marini
(C)
Federico Massa
(F)
Massimo Mastrangelo
(M)
Laura Mumoli
(L)
Carlotta Mutti
(C)
Francesca Felicia Operto
(FF)
Elena Pasini
(E)
Chiara Pastori
(C)
Daniela Passarelli
(D)
Giada Pauletto
(G)
Chiara Pizzanelli
(C)
Francesca Ragona
(F)
Patrizia Riguzzi
(P)
Romana Rizzi
(R)
Marta Elena Santarone
(ME)
Delia Simula
(D)
Vito Sofia
(V)
Maria Tappatà
(M)
Elena Tartara
(E)
Francesca Vanadia
(F)
Alberto Verrotti
(A)
Laura Tassi
(L)
Lucia Zinno
(L)
Informations de copyright
© Author(s) (or their employer(s)) 2022. No commercial re-use. See rights and permissions. Published by BMJ.
Déclaration de conflit d'intérêts
Competing interests: None declared.