Cargando…
Early predictors of new-onset immune-related seizures: a preliminary study
BACKGROUND: Approximately 60% of patients with autoimmune encephalitis (AE) exhibit secondary acute symptomatic seizures and showed highly sensitive to immunotherapy. However, it is difficult for many patients to receive early immunotherapy since the early identification of the cause in AE is more c...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9798624/ https://www.ncbi.nlm.nih.gov/pubmed/36581882 http://dx.doi.org/10.1186/s12883-022-03042-0 |
_version_ | 1784860942946795520 |
---|---|
author | Shi, Xiangsong Cai, Weiwei Zhang, Xiulin Pan, Heyue Huang, Chengbing Wang, Shouyong Xu, Jianyang |
author_facet | Shi, Xiangsong Cai, Weiwei Zhang, Xiulin Pan, Heyue Huang, Chengbing Wang, Shouyong Xu, Jianyang |
author_sort | Shi, Xiangsong |
collection | PubMed |
description | BACKGROUND: Approximately 60% of patients with autoimmune encephalitis (AE) exhibit secondary acute symptomatic seizures and showed highly sensitive to immunotherapy. However, it is difficult for many patients to receive early immunotherapy since the early identification of the cause in AE is more complex. This study aimed to investigate the early predictors of initial immune-related seizures and to guide the evaluation of treatment and prognosis. METHODS: One hundred and fifty-four patients with new-onset “unknown etiology” seizures with a course of disease less than 6 months were included. Serum and/or cerebrospinal fluid neuron-specific autoantibodies (NSAbs), including N-methyl-D-aspartate receptor (NMDAR), α-amino-3-hydroxy-5- Methyl-4-isoxazole propionic acid receptor 1 (AMPAR1), AMPAR2, anti-leucine rich glioma inactivated 1 antibody (LGI1), anti-gamma-aminobutyric acid type B receptor (GABABR), anti-contact protein-related protein-2 (CASPR2) were used to screen for immune etiology of the seizures. In addition, patients with epilepsy and encephalopathy were also examined via brain MRI, long-term video EEG, antibody prevalence in epilepsy and encephalopathy (APE2) score, and modified Rankin Scale (mRS). A logistic regression model was used to analyze the early predictors of immune etiology. RESULTS: Thirty-four cases (22.1%) were positive for NSAbs. Among all 154 patients, 23 cases of autoimmune encephalitis (AE) (21 cases of NSAbs positive), 1 case of ganglionic glioma (NSAbs positive), 130 cases of epilepsy or seizures (12 cases of NSAbs positive) were recorded. Also, there were 17 patients (11.0%) with APE2 ≥ 4 points, and all of them met the clinical diagnosis of AE. The sensitivity and specificity of APE2 ≥ 4 points for predicting AE were 73.9% and 100%. The results of multivariate analysis showed that the NSAbs and APE2 scores independently influenced the early prediction of initial immune-related seizures (P < 0.05). CONCLUSION: NSAbs and APE2 scores could act as early predictors of initial immune-related seizures. |
format | Online Article Text |
id | pubmed-9798624 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-97986242022-12-30 Early predictors of new-onset immune-related seizures: a preliminary study Shi, Xiangsong Cai, Weiwei Zhang, Xiulin Pan, Heyue Huang, Chengbing Wang, Shouyong Xu, Jianyang BMC Neurol Research BACKGROUND: Approximately 60% of patients with autoimmune encephalitis (AE) exhibit secondary acute symptomatic seizures and showed highly sensitive to immunotherapy. However, it is difficult for many patients to receive early immunotherapy since the early identification of the cause in AE is more complex. This study aimed to investigate the early predictors of initial immune-related seizures and to guide the evaluation of treatment and prognosis. METHODS: One hundred and fifty-four patients with new-onset “unknown etiology” seizures with a course of disease less than 6 months were included. Serum and/or cerebrospinal fluid neuron-specific autoantibodies (NSAbs), including N-methyl-D-aspartate receptor (NMDAR), α-amino-3-hydroxy-5- Methyl-4-isoxazole propionic acid receptor 1 (AMPAR1), AMPAR2, anti-leucine rich glioma inactivated 1 antibody (LGI1), anti-gamma-aminobutyric acid type B receptor (GABABR), anti-contact protein-related protein-2 (CASPR2) were used to screen for immune etiology of the seizures. In addition, patients with epilepsy and encephalopathy were also examined via brain MRI, long-term video EEG, antibody prevalence in epilepsy and encephalopathy (APE2) score, and modified Rankin Scale (mRS). A logistic regression model was used to analyze the early predictors of immune etiology. RESULTS: Thirty-four cases (22.1%) were positive for NSAbs. Among all 154 patients, 23 cases of autoimmune encephalitis (AE) (21 cases of NSAbs positive), 1 case of ganglionic glioma (NSAbs positive), 130 cases of epilepsy or seizures (12 cases of NSAbs positive) were recorded. Also, there were 17 patients (11.0%) with APE2 ≥ 4 points, and all of them met the clinical diagnosis of AE. The sensitivity and specificity of APE2 ≥ 4 points for predicting AE were 73.9% and 100%. The results of multivariate analysis showed that the NSAbs and APE2 scores independently influenced the early prediction of initial immune-related seizures (P < 0.05). CONCLUSION: NSAbs and APE2 scores could act as early predictors of initial immune-related seizures. BioMed Central 2022-12-29 /pmc/articles/PMC9798624/ /pubmed/36581882 http://dx.doi.org/10.1186/s12883-022-03042-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Shi, Xiangsong Cai, Weiwei Zhang, Xiulin Pan, Heyue Huang, Chengbing Wang, Shouyong Xu, Jianyang Early predictors of new-onset immune-related seizures: a preliminary study |
title | Early predictors of new-onset immune-related seizures: a preliminary study |
title_full | Early predictors of new-onset immune-related seizures: a preliminary study |
title_fullStr | Early predictors of new-onset immune-related seizures: a preliminary study |
title_full_unstemmed | Early predictors of new-onset immune-related seizures: a preliminary study |
title_short | Early predictors of new-onset immune-related seizures: a preliminary study |
title_sort | early predictors of new-onset immune-related seizures: a preliminary study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9798624/ https://www.ncbi.nlm.nih.gov/pubmed/36581882 http://dx.doi.org/10.1186/s12883-022-03042-0 |
work_keys_str_mv | AT shixiangsong earlypredictorsofnewonsetimmunerelatedseizuresapreliminarystudy AT caiweiwei earlypredictorsofnewonsetimmunerelatedseizuresapreliminarystudy AT zhangxiulin earlypredictorsofnewonsetimmunerelatedseizuresapreliminarystudy AT panheyue earlypredictorsofnewonsetimmunerelatedseizuresapreliminarystudy AT huangchengbing earlypredictorsofnewonsetimmunerelatedseizuresapreliminarystudy AT wangshouyong earlypredictorsofnewonsetimmunerelatedseizuresapreliminarystudy AT xujianyang earlypredictorsofnewonsetimmunerelatedseizuresapreliminarystudy |