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Higher incidence of acute symptomatic seizures in probable antibody-negative pediatric autoimmune encephalitis than in major antibody-positive autoimmune encephalitis.
Yamada, Naoki; Inoue, Takeshi; Kuki, Ichiro; Yamamoto, Naohiro; Fukuoka, Masataka; Nukui, Megumi; Okuno, Hideo; Ishikawa, Junichi; Amo, Kiyoko; Togawa, Masao; Sakuma, Hiroshi; Okazaki, Shin.
Afiliação
  • Yamada N; Department of Pediatric Neurology and Logopedics, Osaka City General Hospital, Osaka, Japan.
  • Inoue T; Department of Pediatric Neurology and Logopedics, Osaka City General Hospital, Osaka, Japan.
  • Kuki I; Department of Pediatric Neurology and Logopedics, Osaka City General Hospital, Osaka, Japan.
  • Yamamoto N; Department of Pediatric Neurology and Logopedics, Osaka City General Hospital, Osaka, Japan.
  • Fukuoka M; Department of Pediatric Neurology and Logopedics, Osaka City General Hospital, Osaka, Japan.
  • Nukui M; Department of Pediatric Neurology and Logopedics, Osaka City General Hospital, Osaka, Japan.
  • Okuno H; Department of Pediatric Emergency, Infectious Disease Internal Medicine, Osaka City General Hospital, Osaka, Japan.
  • Ishikawa J; Department of Pediatric Emergency, Infectious Disease Internal Medicine, Osaka City General Hospital, Osaka, Japan.
  • Amo K; Department of Pediatric Emergency, Infectious Disease Internal Medicine, Osaka City General Hospital, Osaka, Japan.
  • Togawa M; Department of Pediatric Emergency, Infectious Disease Internal Medicine, Osaka City General Hospital, Osaka, Japan.
  • Sakuma H; Department of Brain and Neuroscience, Tokyo Metropolitan Institute of Medical Science, Tokyo, Japan.
  • Okazaki S; Department of Pediatric Neurology and Logopedics, Osaka City General Hospital, Osaka, Japan.
Front Neurol ; 15: 1418083, 2024.
Article em En | MEDLINE | ID: mdl-39099783
ABSTRACT

Purpose:

To delineate the characteristics of probable antibody-negative pediatric autoimmune encephalitis (probable Ab-negative AE), we compared the clinical features of probable Ab-negative AE to those of major antibody-positive AE.

Methods:

We retrospectively reviewed the clinical features of 18 patients with probable Ab-negative AE, 13 with anti-N-methyl-D-aspartate receptor encephalitis (NMDARE), and 13 with myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD). Clinical characteristics, neuroimaging findings, treatments, and outcomes were analyzed.

Results:

The age of onset and length of hospital stay were significantly higher in the NMDARE group than in the other groups (p = 0.02 and p < 0.01). Regarding initial neurological symptoms, acute symptomatic seizures in the probable Ab-negative AE group (67%) were significantly more frequent than in the NMDARE (15%) and MOGAD (23%) groups (p < 0.01). Paraclinical evidence of neuroinflammation within 1 month of disease onset revealed that single-photon emission computed tomography (SPECT) detected abnormal alterations in 14/14 (100%), cerebrospinal fluid (CSF) analysis in 15/18 (83%), and magnetic resonance imaging (MRI) in 11/18 (61%) in patients with probable Ab-negative AE. In the probable Ab-negative AE group, seven patients (39%) developed autoimmune-associated epilepsy, whereas one patient (8%) had both NMDARE and MOGAD (not statistically significant, p = 0.07).

Conclusion:

Patients with probable Ab-negative AE exhibited acute symptomatic seizures as initial neurological symptoms significantly more frequently. They developed autoimmune-associated epilepsy more frequently than those with NMDARE and MOGAD, which was not statistically significant. SPECT within 1 month of disease onset might be a valuable surrogate marker of ongoing neuroinflammation and neuronal dysfunction, even in patients with negative MRI findings.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Front Neurol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Front Neurol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Japão