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Antibodies Contributing to Focal Epilepsy Signs and Symptoms Score
OBJECTIVE: Diagnosing autoimmune encephalitis (AIE) is difficult in patients with less fulminant diseases such as epilepsy. However, recognition is important, as patients require immunotherapy. This study aims to identify antibodies in patients with focal epilepsy of unknown etiology, and to create...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8048471/ https://www.ncbi.nlm.nih.gov/pubmed/33427313 http://dx.doi.org/10.1002/ana.26013 |
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author | de Bruijn, Marienke A. A. M. Bastiaansen, Anna E. M. Mojzisova, Hana van Sonderen, Agnes Thijs, Roland D. Majoie, Marian J. M. Rouhl, Rob P. W. van Coevorden‐Hameete, Marleen H. de Vries, Juna M. Muñoz Lopetegi, Amaia Roozenbeek, Bob Schreurs, Marco W. J. Sillevis Smitt, Peter A. E. Titulaer, Maarten J. |
author_facet | de Bruijn, Marienke A. A. M. Bastiaansen, Anna E. M. Mojzisova, Hana van Sonderen, Agnes Thijs, Roland D. Majoie, Marian J. M. Rouhl, Rob P. W. van Coevorden‐Hameete, Marleen H. de Vries, Juna M. Muñoz Lopetegi, Amaia Roozenbeek, Bob Schreurs, Marco W. J. Sillevis Smitt, Peter A. E. Titulaer, Maarten J. |
author_sort | de Bruijn, Marienke A. A. M. |
collection | PubMed |
description | OBJECTIVE: Diagnosing autoimmune encephalitis (AIE) is difficult in patients with less fulminant diseases such as epilepsy. However, recognition is important, as patients require immunotherapy. This study aims to identify antibodies in patients with focal epilepsy of unknown etiology, and to create a score to preselect patients requiring testing. METHODS: In this prospective, multicenter cohort study, adults with focal epilepsy of unknown etiology, without recognized AIE, were included, between December 2014 and December 2017, and followed for 1 year. Serum, and if available cerebrospinal fluid, were analyzed using different laboratory techniques. The ACES score was created using factors favoring an autoimmune etiology of seizures (AES), as determined by multivariate logistic regression. The model was externally validated and evaluated using the Concordance (C) statistic. RESULTS: We included 582 patients, with median epilepsy duration of 8 years (interquartile range = 2–18). Twenty patients (3.4%) had AES, of whom 3 had anti–leucine‐rich glioma inactivated 1, 3 had anti–contactin‐associated protein‐like 2, 1 had anti–N‐methyl‐D‐aspartate receptor, and 13 had anti–glutamic acid decarboxylase 65 (enzyme‐linked immunosorbent assay concentrations >10,000IU/ml). Risk factors for AES were temporal magnetic resonance imaging hyperintensities (odds ratio [OR] = 255.3, 95% confidence interval [CI] = 19.6–3332.2, p < 0.0001), autoimmune diseases (OR = 13.31, 95% CI = 3.1–56.6, p = 0.0005), behavioral changes (OR 12.3, 95% CI = 3.2–49.9, p = 0.0003), autonomic symptoms (OR = 13.3, 95% CI = 3.1–56.6, p = 0.0005), cognitive symptoms (OR = 30.6, 95% CI = 2.4–382.7, p = 0.009), and speech problems (OR = 9.6, 95% CI = 2.0–46.7, p = 0.005). The internally validated C statistic was 0.95, and 0.92 in the validation cohort (n = 128). Assigning each factor 1 point, an antibodies contributing to focal epilepsy signs and symptoms (ACES) score ≥ 2 had a sensitivity of 100% to detect AES, and a specificity of 84.9%. INTERPRETATION: Specific signs point toward AES in focal epilepsy of unknown etiology. The ACES score (cutoff ≥ 2) is useful to select patients requiring antibody testing. ANN NEUROL 2021;89:698–710 |
format | Online Article Text |
id | pubmed-8048471 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-80484712021-04-16 Antibodies Contributing to Focal Epilepsy Signs and Symptoms Score de Bruijn, Marienke A. A. M. Bastiaansen, Anna E. M. Mojzisova, Hana van Sonderen, Agnes Thijs, Roland D. Majoie, Marian J. M. Rouhl, Rob P. W. van Coevorden‐Hameete, Marleen H. de Vries, Juna M. Muñoz Lopetegi, Amaia Roozenbeek, Bob Schreurs, Marco W. J. Sillevis Smitt, Peter A. E. Titulaer, Maarten J. Ann Neurol Research Articles OBJECTIVE: Diagnosing autoimmune encephalitis (AIE) is difficult in patients with less fulminant diseases such as epilepsy. However, recognition is important, as patients require immunotherapy. This study aims to identify antibodies in patients with focal epilepsy of unknown etiology, and to create a score to preselect patients requiring testing. METHODS: In this prospective, multicenter cohort study, adults with focal epilepsy of unknown etiology, without recognized AIE, were included, between December 2014 and December 2017, and followed for 1 year. Serum, and if available cerebrospinal fluid, were analyzed using different laboratory techniques. The ACES score was created using factors favoring an autoimmune etiology of seizures (AES), as determined by multivariate logistic regression. The model was externally validated and evaluated using the Concordance (C) statistic. RESULTS: We included 582 patients, with median epilepsy duration of 8 years (interquartile range = 2–18). Twenty patients (3.4%) had AES, of whom 3 had anti–leucine‐rich glioma inactivated 1, 3 had anti–contactin‐associated protein‐like 2, 1 had anti–N‐methyl‐D‐aspartate receptor, and 13 had anti–glutamic acid decarboxylase 65 (enzyme‐linked immunosorbent assay concentrations >10,000IU/ml). Risk factors for AES were temporal magnetic resonance imaging hyperintensities (odds ratio [OR] = 255.3, 95% confidence interval [CI] = 19.6–3332.2, p < 0.0001), autoimmune diseases (OR = 13.31, 95% CI = 3.1–56.6, p = 0.0005), behavioral changes (OR 12.3, 95% CI = 3.2–49.9, p = 0.0003), autonomic symptoms (OR = 13.3, 95% CI = 3.1–56.6, p = 0.0005), cognitive symptoms (OR = 30.6, 95% CI = 2.4–382.7, p = 0.009), and speech problems (OR = 9.6, 95% CI = 2.0–46.7, p = 0.005). The internally validated C statistic was 0.95, and 0.92 in the validation cohort (n = 128). Assigning each factor 1 point, an antibodies contributing to focal epilepsy signs and symptoms (ACES) score ≥ 2 had a sensitivity of 100% to detect AES, and a specificity of 84.9%. INTERPRETATION: Specific signs point toward AES in focal epilepsy of unknown etiology. The ACES score (cutoff ≥ 2) is useful to select patients requiring antibody testing. ANN NEUROL 2021;89:698–710 John Wiley & Sons, Inc. 2021-01-27 2021-04 /pmc/articles/PMC8048471/ /pubmed/33427313 http://dx.doi.org/10.1002/ana.26013 Text en © 2021 The Authors. Annals of Neurology published by Wiley Periodicals LLC on behalf of American Neurological Association. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Research Articles de Bruijn, Marienke A. A. M. Bastiaansen, Anna E. M. Mojzisova, Hana van Sonderen, Agnes Thijs, Roland D. Majoie, Marian J. M. Rouhl, Rob P. W. van Coevorden‐Hameete, Marleen H. de Vries, Juna M. Muñoz Lopetegi, Amaia Roozenbeek, Bob Schreurs, Marco W. J. Sillevis Smitt, Peter A. E. Titulaer, Maarten J. Antibodies Contributing to Focal Epilepsy Signs and Symptoms Score |
title | Antibodies Contributing to Focal Epilepsy Signs and Symptoms Score |
title_full | Antibodies Contributing to Focal Epilepsy Signs and Symptoms Score |
title_fullStr | Antibodies Contributing to Focal Epilepsy Signs and Symptoms Score |
title_full_unstemmed | Antibodies Contributing to Focal Epilepsy Signs and Symptoms Score |
title_short | Antibodies Contributing to Focal Epilepsy Signs and Symptoms Score |
title_sort | antibodies contributing to focal epilepsy signs and symptoms score |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8048471/ https://www.ncbi.nlm.nih.gov/pubmed/33427313 http://dx.doi.org/10.1002/ana.26013 |
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