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Cenobamate and Clobazam Combination as Personalized Medicine in Autoimmune-Associated Epilepsy With Anti-Gad65 Antibodies

BACKGROUND AND OBJECTIVES: Autoimmune-associated epilepsy (AAE) with antiglutamic acid decarboxylase 65 (GAD65) antibodies is considered a T-cell–mediated encephalitis that evolves to drug-resistant epilepsy. We do not have an effective therapeutic strategy for these patients. Because the GAD enzyme...

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Autores principales: Serrano-Castro, Pedro J., Rodríguez-Uranga, Juan J., Cabezudo-García, Pablo, García-Martín, Guillermina, Romero-Godoy, Jorge, Estivill-Torrús, Guillermo, Ciano-Petersen, Nicolás Lundahl, Oliver, Begoña, Ortega-Pinazo, Jesús, López-Moreno, Yolanda, Aguilar-Castillo, Maria J., Gutierrez-Cardo, Antonio L., Ramírez-García, Teresa, Sanchez-Godoy, Lorenzo, Carreño, Mar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10443460/
https://www.ncbi.nlm.nih.gov/pubmed/37607753
http://dx.doi.org/10.1212/NXI.0000000000200151
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author Serrano-Castro, Pedro J.
Rodríguez-Uranga, Juan J.
Cabezudo-García, Pablo
García-Martín, Guillermina
Romero-Godoy, Jorge
Estivill-Torrús, Guillermo
Ciano-Petersen, Nicolás Lundahl
Oliver, Begoña
Ortega-Pinazo, Jesús
López-Moreno, Yolanda
Aguilar-Castillo, Maria J.
Gutierrez-Cardo, Antonio L.
Ramírez-García, Teresa
Sanchez-Godoy, Lorenzo
Carreño, Mar
author_facet Serrano-Castro, Pedro J.
Rodríguez-Uranga, Juan J.
Cabezudo-García, Pablo
García-Martín, Guillermina
Romero-Godoy, Jorge
Estivill-Torrús, Guillermo
Ciano-Petersen, Nicolás Lundahl
Oliver, Begoña
Ortega-Pinazo, Jesús
López-Moreno, Yolanda
Aguilar-Castillo, Maria J.
Gutierrez-Cardo, Antonio L.
Ramírez-García, Teresa
Sanchez-Godoy, Lorenzo
Carreño, Mar
author_sort Serrano-Castro, Pedro J.
collection PubMed
description BACKGROUND AND OBJECTIVES: Autoimmune-associated epilepsy (AAE) with antiglutamic acid decarboxylase 65 (GAD65) antibodies is considered a T-cell–mediated encephalitis that evolves to drug-resistant epilepsy. We do not have an effective therapeutic strategy for these patients. Because the GAD enzyme is primarily responsible for the conversion of glutamate to GABA, the mechanism of epileptogenesis in this condition predicts decreased levels of GABA content in synaptic vesicles. Cenobamate (CNB) acts as a positive allosteric modulator at synaptic and extra synaptic GABAA receptors, producing increased inhibitory neurotransmission in the brain. This mechanism could be especially beneficial in AAE with anti-GAD65 antibodies because it would be able to correct the imbalance due to the GABAergic stimulation deficit in postsynaptic neurons. METHODS: We recruit a retrospective multicentric consecutive case series of AAE with anti-GAD65 antibodies from 5 epilepsy units in Spain who have received treatment with CNB. RESULTS: A total of 8 patients were recruited. This cohort of highly refractory patients have failed a mean of 9.50 (SD = 3.20) ASM without control of seizures for sustained periods of time. The average number of seizures per month during the previous 3 months before CNB treatment was 19.63 (SD = 17.03). After the introduction of CNB improvement was achieved in all our patients, with a median reduction in the number of seizures of 92.22% (interquartile range [IQR]: 57.25–98.75). The mean follow-up was 156.75 days (SD = 68.23). In patients with concomitant treatment with clobazam (CLB), the median percentage of seizure reduction was higher than those not taking CLB: 94.72% (IQR: 87.25–100) vs 41.50% (p = 0.044) and also higher than the control group of patients with refractory epilepsy not related to anti-GAD65 treated with the same combination: 94.72% (IQR: 87.25–100) vs 45.00% (IQR: 25.00–87.00) (p = 0.019). DISCUSSION: Treatment with the combination CNB + CLB could be a type of personalized medicine in patients with AAE with anti-GAD65. Our preliminary data will need to be endorsed with new prospective and controlled studies.
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spelling pubmed-104434602023-08-23 Cenobamate and Clobazam Combination as Personalized Medicine in Autoimmune-Associated Epilepsy With Anti-Gad65 Antibodies Serrano-Castro, Pedro J. Rodríguez-Uranga, Juan J. Cabezudo-García, Pablo García-Martín, Guillermina Romero-Godoy, Jorge Estivill-Torrús, Guillermo Ciano-Petersen, Nicolás Lundahl Oliver, Begoña Ortega-Pinazo, Jesús López-Moreno, Yolanda Aguilar-Castillo, Maria J. Gutierrez-Cardo, Antonio L. Ramírez-García, Teresa Sanchez-Godoy, Lorenzo Carreño, Mar Neurol Neuroimmunol Neuroinflamm Research Article BACKGROUND AND OBJECTIVES: Autoimmune-associated epilepsy (AAE) with antiglutamic acid decarboxylase 65 (GAD65) antibodies is considered a T-cell–mediated encephalitis that evolves to drug-resistant epilepsy. We do not have an effective therapeutic strategy for these patients. Because the GAD enzyme is primarily responsible for the conversion of glutamate to GABA, the mechanism of epileptogenesis in this condition predicts decreased levels of GABA content in synaptic vesicles. Cenobamate (CNB) acts as a positive allosteric modulator at synaptic and extra synaptic GABAA receptors, producing increased inhibitory neurotransmission in the brain. This mechanism could be especially beneficial in AAE with anti-GAD65 antibodies because it would be able to correct the imbalance due to the GABAergic stimulation deficit in postsynaptic neurons. METHODS: We recruit a retrospective multicentric consecutive case series of AAE with anti-GAD65 antibodies from 5 epilepsy units in Spain who have received treatment with CNB. RESULTS: A total of 8 patients were recruited. This cohort of highly refractory patients have failed a mean of 9.50 (SD = 3.20) ASM without control of seizures for sustained periods of time. The average number of seizures per month during the previous 3 months before CNB treatment was 19.63 (SD = 17.03). After the introduction of CNB improvement was achieved in all our patients, with a median reduction in the number of seizures of 92.22% (interquartile range [IQR]: 57.25–98.75). The mean follow-up was 156.75 days (SD = 68.23). In patients with concomitant treatment with clobazam (CLB), the median percentage of seizure reduction was higher than those not taking CLB: 94.72% (IQR: 87.25–100) vs 41.50% (p = 0.044) and also higher than the control group of patients with refractory epilepsy not related to anti-GAD65 treated with the same combination: 94.72% (IQR: 87.25–100) vs 45.00% (IQR: 25.00–87.00) (p = 0.019). DISCUSSION: Treatment with the combination CNB + CLB could be a type of personalized medicine in patients with AAE with anti-GAD65. Our preliminary data will need to be endorsed with new prospective and controlled studies. Lippincott Williams & Wilkins 2023-08-21 /pmc/articles/PMC10443460/ /pubmed/37607753 http://dx.doi.org/10.1212/NXI.0000000000200151 Text en Copyright © 2023 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits downloading and sharing the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
spellingShingle Research Article
Serrano-Castro, Pedro J.
Rodríguez-Uranga, Juan J.
Cabezudo-García, Pablo
García-Martín, Guillermina
Romero-Godoy, Jorge
Estivill-Torrús, Guillermo
Ciano-Petersen, Nicolás Lundahl
Oliver, Begoña
Ortega-Pinazo, Jesús
López-Moreno, Yolanda
Aguilar-Castillo, Maria J.
Gutierrez-Cardo, Antonio L.
Ramírez-García, Teresa
Sanchez-Godoy, Lorenzo
Carreño, Mar
Cenobamate and Clobazam Combination as Personalized Medicine in Autoimmune-Associated Epilepsy With Anti-Gad65 Antibodies
title Cenobamate and Clobazam Combination as Personalized Medicine in Autoimmune-Associated Epilepsy With Anti-Gad65 Antibodies
title_full Cenobamate and Clobazam Combination as Personalized Medicine in Autoimmune-Associated Epilepsy With Anti-Gad65 Antibodies
title_fullStr Cenobamate and Clobazam Combination as Personalized Medicine in Autoimmune-Associated Epilepsy With Anti-Gad65 Antibodies
title_full_unstemmed Cenobamate and Clobazam Combination as Personalized Medicine in Autoimmune-Associated Epilepsy With Anti-Gad65 Antibodies
title_short Cenobamate and Clobazam Combination as Personalized Medicine in Autoimmune-Associated Epilepsy With Anti-Gad65 Antibodies
title_sort cenobamate and clobazam combination as personalized medicine in autoimmune-associated epilepsy with anti-gad65 antibodies
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10443460/
https://www.ncbi.nlm.nih.gov/pubmed/37607753
http://dx.doi.org/10.1212/NXI.0000000000200151
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