Cargando…
Brain‐responsive neurostimulation treatment in patients with GAD65 antibody–associated autoimmune mesial temporal lobe epilepsy
Glutamic acid decarboxylase 65‐kilodalton isoform (GAD65) antibodies have been associated with multiple nonneurological and neurological syndromes including autoimmune epilepsy (AE). Although immunotherapy remains the cornerstone for the treatment of AE, those with GAD65 Ab‐associated AE (GAD65‐AE)...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7278537/ https://www.ncbi.nlm.nih.gov/pubmed/32524057 http://dx.doi.org/10.1002/epi4.12395 |
_version_ | 1783543354669137920 |
---|---|
author | Feyissa, Anteneh M Mirro, Emily A. Wabulya, Angela Tatum, William O. Wilmer‐Fierro, Kaitlyn E. Won Shin, Hae |
author_facet | Feyissa, Anteneh M Mirro, Emily A. Wabulya, Angela Tatum, William O. Wilmer‐Fierro, Kaitlyn E. Won Shin, Hae |
author_sort | Feyissa, Anteneh M |
collection | PubMed |
description | Glutamic acid decarboxylase 65‐kilodalton isoform (GAD65) antibodies have been associated with multiple nonneurological and neurological syndromes including autoimmune epilepsy (AE). Although immunotherapy remains the cornerstone for the treatment of AE, those with GAD65 Ab‐associated AE (GAD65‐AE) remain refractory to immunotherapy and antiseizure medication (ASM). Outcomes of epilepsy surgery in this patient population have also been unsatisfactory. The role of neuromodulation therapy, particularly direct brain‐responsive neurostimulation therapy, has not been previously examined in GAD65‐AE. Here, we describe four consecutive patients with refractory GAD‐65‐associated temporal lobe epilepsy (GAD65‐TLE) receiving bilateral hippocampal RNS System treatment. The RNS System treatment was well tolerated and effective in this study cohort. Three patients had a >50% clinical seizure reduction, and one patient became clinically seizure‐free following resective surgery informed by the RNS System data with continued RNS System treatment. In all four of our patients, the long‐term ambulatory data provided by the RNS System allowed us to gain objective insights on electrographic seizure lateralization, patterns, and burden as well as guided immunotherapy and ASM optimization. Our results suggest the potential utility of the RNS System in the management of ASM intractable GAD65‐AE. |
format | Online Article Text |
id | pubmed-7278537 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-72785372020-06-09 Brain‐responsive neurostimulation treatment in patients with GAD65 antibody–associated autoimmune mesial temporal lobe epilepsy Feyissa, Anteneh M Mirro, Emily A. Wabulya, Angela Tatum, William O. Wilmer‐Fierro, Kaitlyn E. Won Shin, Hae Epilepsia Open Short Research Article Glutamic acid decarboxylase 65‐kilodalton isoform (GAD65) antibodies have been associated with multiple nonneurological and neurological syndromes including autoimmune epilepsy (AE). Although immunotherapy remains the cornerstone for the treatment of AE, those with GAD65 Ab‐associated AE (GAD65‐AE) remain refractory to immunotherapy and antiseizure medication (ASM). Outcomes of epilepsy surgery in this patient population have also been unsatisfactory. The role of neuromodulation therapy, particularly direct brain‐responsive neurostimulation therapy, has not been previously examined in GAD65‐AE. Here, we describe four consecutive patients with refractory GAD‐65‐associated temporal lobe epilepsy (GAD65‐TLE) receiving bilateral hippocampal RNS System treatment. The RNS System treatment was well tolerated and effective in this study cohort. Three patients had a >50% clinical seizure reduction, and one patient became clinically seizure‐free following resective surgery informed by the RNS System data with continued RNS System treatment. In all four of our patients, the long‐term ambulatory data provided by the RNS System allowed us to gain objective insights on electrographic seizure lateralization, patterns, and burden as well as guided immunotherapy and ASM optimization. Our results suggest the potential utility of the RNS System in the management of ASM intractable GAD65‐AE. John Wiley and Sons Inc. 2020-04-14 /pmc/articles/PMC7278537/ /pubmed/32524057 http://dx.doi.org/10.1002/epi4.12395 Text en © 2020 The Authors. Epilepsia Open published by Wiley Periodicals Inc. on behalf of International League Against Epilepsy. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Short Research Article Feyissa, Anteneh M Mirro, Emily A. Wabulya, Angela Tatum, William O. Wilmer‐Fierro, Kaitlyn E. Won Shin, Hae Brain‐responsive neurostimulation treatment in patients with GAD65 antibody–associated autoimmune mesial temporal lobe epilepsy |
title | Brain‐responsive neurostimulation treatment in patients with GAD65 antibody–associated autoimmune mesial temporal lobe epilepsy |
title_full | Brain‐responsive neurostimulation treatment in patients with GAD65 antibody–associated autoimmune mesial temporal lobe epilepsy |
title_fullStr | Brain‐responsive neurostimulation treatment in patients with GAD65 antibody–associated autoimmune mesial temporal lobe epilepsy |
title_full_unstemmed | Brain‐responsive neurostimulation treatment in patients with GAD65 antibody–associated autoimmune mesial temporal lobe epilepsy |
title_short | Brain‐responsive neurostimulation treatment in patients with GAD65 antibody–associated autoimmune mesial temporal lobe epilepsy |
title_sort | brain‐responsive neurostimulation treatment in patients with gad65 antibody–associated autoimmune mesial temporal lobe epilepsy |
topic | Short Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7278537/ https://www.ncbi.nlm.nih.gov/pubmed/32524057 http://dx.doi.org/10.1002/epi4.12395 |
work_keys_str_mv | AT feyissaantenehm brainresponsiveneurostimulationtreatmentinpatientswithgad65antibodyassociatedautoimmunemesialtemporallobeepilepsy AT mirroemilya brainresponsiveneurostimulationtreatmentinpatientswithgad65antibodyassociatedautoimmunemesialtemporallobeepilepsy AT wabulyaangela brainresponsiveneurostimulationtreatmentinpatientswithgad65antibodyassociatedautoimmunemesialtemporallobeepilepsy AT tatumwilliamo brainresponsiveneurostimulationtreatmentinpatientswithgad65antibodyassociatedautoimmunemesialtemporallobeepilepsy AT wilmerfierrokaitlyne brainresponsiveneurostimulationtreatmentinpatientswithgad65antibodyassociatedautoimmunemesialtemporallobeepilepsy AT wonshinhae brainresponsiveneurostimulationtreatmentinpatientswithgad65antibodyassociatedautoimmunemesialtemporallobeepilepsy |