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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2021
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
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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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