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Recognition of seizure semiology and semiquantitative FDG‐PET analysis of anti‐LGI1 encephalitis

AIMS: Anti‐leucine‐rich glioma‐inactivated 1 (LGI1) autoimmune encephalitis (AE) is characterized by complex manifestations of seizures. Here, we report a new seizure semiology, attempt to classify the disease by semiology type, and explore the metabolic pattern of each group. METHODS: Anti‐LGI1 AE...

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Autores principales: Li, Tao‐Ran, Zhang, Yu‐Di, Wang, Qun, Shao, Xiao‐Qiu, Lv, Rui‐Juan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8446218/
https://www.ncbi.nlm.nih.gov/pubmed/34291554
http://dx.doi.org/10.1111/cns.13707
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author Li, Tao‐Ran
Zhang, Yu‐Di
Wang, Qun
Shao, Xiao‐Qiu
Lv, Rui‐Juan
author_facet Li, Tao‐Ran
Zhang, Yu‐Di
Wang, Qun
Shao, Xiao‐Qiu
Lv, Rui‐Juan
author_sort Li, Tao‐Ran
collection PubMed
description AIMS: Anti‐leucine‐rich glioma‐inactivated 1 (LGI1) autoimmune encephalitis (AE) is characterized by complex manifestations of seizures. Here, we report a new seizure semiology, attempt to classify the disease by semiology type, and explore the metabolic pattern of each group. METHODS: Anti‐LGI1 AE patients were retrospectively screened between May 2014 and September 2019 in our tertiary epilepsy center. All enrolled patients had seizures during long‐range video electroencephalogram (EEG) recordings, and all patients (except one) underwent [(18)F] fluoro‐2‐deoxyglucose (FDG) positron emission tomography (PET) scans. Voxel‐based metabolic analysis and z‐distribution analysis were carried out to determine the metabolic pattern. RESULTS: Thirty‐three patients were enrolled. According to the patients’ seizure semiology, we divided the patients into four groups: focal impaired awareness seizures (FIAS, n = 17), faciobrachial dystonic seizures (FBDS)‐only (n = 6), FBDS‐plus (n = 8), and focal aware motor seizures (FAMS) (n = 2). No significant differences were found in the clinical manifestations or accessory tests except for the onset age (FIAS < FBDS‐plus) and seizure semiology. This was the first study to extensively describe the clinical manifestations and EEG of FAMS in anti‐LGI1 AE patients. In addition, we found that the patients with different semiologies all showed a wide range of abnormal metabolism, which is not limited to the temporal regions and basal ganglia, and extends far beyond our previous interpretation of FDG‐PET data. CONCLUSION: Our results showed that FAMS can serve as a rare indicative seizure semiology of anti‐LGI1 AE and that individuals with this disease exhibited widespread functional network alterations.
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spelling pubmed-84462182021-09-22 Recognition of seizure semiology and semiquantitative FDG‐PET analysis of anti‐LGI1 encephalitis Li, Tao‐Ran Zhang, Yu‐Di Wang, Qun Shao, Xiao‐Qiu Lv, Rui‐Juan CNS Neurosci Ther Original Articles AIMS: Anti‐leucine‐rich glioma‐inactivated 1 (LGI1) autoimmune encephalitis (AE) is characterized by complex manifestations of seizures. Here, we report a new seizure semiology, attempt to classify the disease by semiology type, and explore the metabolic pattern of each group. METHODS: Anti‐LGI1 AE patients were retrospectively screened between May 2014 and September 2019 in our tertiary epilepsy center. All enrolled patients had seizures during long‐range video electroencephalogram (EEG) recordings, and all patients (except one) underwent [(18)F] fluoro‐2‐deoxyglucose (FDG) positron emission tomography (PET) scans. Voxel‐based metabolic analysis and z‐distribution analysis were carried out to determine the metabolic pattern. RESULTS: Thirty‐three patients were enrolled. According to the patients’ seizure semiology, we divided the patients into four groups: focal impaired awareness seizures (FIAS, n = 17), faciobrachial dystonic seizures (FBDS)‐only (n = 6), FBDS‐plus (n = 8), and focal aware motor seizures (FAMS) (n = 2). No significant differences were found in the clinical manifestations or accessory tests except for the onset age (FIAS < FBDS‐plus) and seizure semiology. This was the first study to extensively describe the clinical manifestations and EEG of FAMS in anti‐LGI1 AE patients. In addition, we found that the patients with different semiologies all showed a wide range of abnormal metabolism, which is not limited to the temporal regions and basal ganglia, and extends far beyond our previous interpretation of FDG‐PET data. CONCLUSION: Our results showed that FAMS can serve as a rare indicative seizure semiology of anti‐LGI1 AE and that individuals with this disease exhibited widespread functional network alterations. John Wiley and Sons Inc. 2021-07-22 /pmc/articles/PMC8446218/ /pubmed/34291554 http://dx.doi.org/10.1111/cns.13707 Text en © 2021 The Authors. CNS Neuroscience & Therapeutics published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Li, Tao‐Ran
Zhang, Yu‐Di
Wang, Qun
Shao, Xiao‐Qiu
Lv, Rui‐Juan
Recognition of seizure semiology and semiquantitative FDG‐PET analysis of anti‐LGI1 encephalitis
title Recognition of seizure semiology and semiquantitative FDG‐PET analysis of anti‐LGI1 encephalitis
title_full Recognition of seizure semiology and semiquantitative FDG‐PET analysis of anti‐LGI1 encephalitis
title_fullStr Recognition of seizure semiology and semiquantitative FDG‐PET analysis of anti‐LGI1 encephalitis
title_full_unstemmed Recognition of seizure semiology and semiquantitative FDG‐PET analysis of anti‐LGI1 encephalitis
title_short Recognition of seizure semiology and semiquantitative FDG‐PET analysis of anti‐LGI1 encephalitis
title_sort recognition of seizure semiology and semiquantitative fdg‐pet analysis of anti‐lgi1 encephalitis
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8446218/
https://www.ncbi.nlm.nih.gov/pubmed/34291554
http://dx.doi.org/10.1111/cns.13707
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