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Towards a Treatment for Neuroinflammation in Epilepsy: Interleukin-1 Receptor Antagonist, Anakinra, as a Potential Treatment in Intractable Epilepsy

Febrile Infection-Related Epilepsy Syndrome (FIRES) is a unique catastrophic epilepsy syndrome, and the development of drug-resistant epilepsy (DRE) is inevitable. Recently, anakinra, an interleukin-1 receptor antagonist (IL-1RA), has been increasingly used to treat DRE due to its potent anticonvuls...

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Autores principales: Yamanaka, Gaku, Ishida, Yu, Kanou, Kanako, Suzuki, Shinji, Watanabe, Yusuke, Takamatsu, Tomoko, Morichi, Shinichiro, Go, Soken, Oana, Shingo, Yamazaki, Takashi, Kawashima, Hisashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8230637/
https://www.ncbi.nlm.nih.gov/pubmed/34208064
http://dx.doi.org/10.3390/ijms22126282
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author Yamanaka, Gaku
Ishida, Yu
Kanou, Kanako
Suzuki, Shinji
Watanabe, Yusuke
Takamatsu, Tomoko
Morichi, Shinichiro
Go, Soken
Oana, Shingo
Yamazaki, Takashi
Kawashima, Hisashi
author_facet Yamanaka, Gaku
Ishida, Yu
Kanou, Kanako
Suzuki, Shinji
Watanabe, Yusuke
Takamatsu, Tomoko
Morichi, Shinichiro
Go, Soken
Oana, Shingo
Yamazaki, Takashi
Kawashima, Hisashi
author_sort Yamanaka, Gaku
collection PubMed
description Febrile Infection-Related Epilepsy Syndrome (FIRES) is a unique catastrophic epilepsy syndrome, and the development of drug-resistant epilepsy (DRE) is inevitable. Recently, anakinra, an interleukin-1 receptor antagonist (IL-1RA), has been increasingly used to treat DRE due to its potent anticonvulsant activity. We here summarized its effects in 38 patients (32 patients with FIRES and six with DRE). Of the 22 patients with FIRES, 16 (73%) had at least short-term seizure control 1 week after starting anakinra, while the remaining six suspected anakinra-refractory cases were male and had poor prognoses. Due to the small sample size, an explanation for anakinra refractoriness was not evident. In all DRE patients, seizures disappeared or improved, and cognitive function improved in five of the six patients following treatment. Patients showed no serious side effects, although drug reactions with eosinophilia and systemic symptoms, cytopenia, and infections were observed. Thus, anakinra has led to a marked improvement in some cases, and functional deficiency of IL-1RA was indicated, supporting a direct mechanism for its therapeutic effect. This review first discusses the effectiveness of anakinra for intractable epileptic syndromes. Anakinra could become a new tool for intractable epilepsy treatment. However, it does not currently have a solid evidence base.
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spelling pubmed-82306372021-06-26 Towards a Treatment for Neuroinflammation in Epilepsy: Interleukin-1 Receptor Antagonist, Anakinra, as a Potential Treatment in Intractable Epilepsy Yamanaka, Gaku Ishida, Yu Kanou, Kanako Suzuki, Shinji Watanabe, Yusuke Takamatsu, Tomoko Morichi, Shinichiro Go, Soken Oana, Shingo Yamazaki, Takashi Kawashima, Hisashi Int J Mol Sci Review Febrile Infection-Related Epilepsy Syndrome (FIRES) is a unique catastrophic epilepsy syndrome, and the development of drug-resistant epilepsy (DRE) is inevitable. Recently, anakinra, an interleukin-1 receptor antagonist (IL-1RA), has been increasingly used to treat DRE due to its potent anticonvulsant activity. We here summarized its effects in 38 patients (32 patients with FIRES and six with DRE). Of the 22 patients with FIRES, 16 (73%) had at least short-term seizure control 1 week after starting anakinra, while the remaining six suspected anakinra-refractory cases were male and had poor prognoses. Due to the small sample size, an explanation for anakinra refractoriness was not evident. In all DRE patients, seizures disappeared or improved, and cognitive function improved in five of the six patients following treatment. Patients showed no serious side effects, although drug reactions with eosinophilia and systemic symptoms, cytopenia, and infections were observed. Thus, anakinra has led to a marked improvement in some cases, and functional deficiency of IL-1RA was indicated, supporting a direct mechanism for its therapeutic effect. This review first discusses the effectiveness of anakinra for intractable epileptic syndromes. Anakinra could become a new tool for intractable epilepsy treatment. However, it does not currently have a solid evidence base. MDPI 2021-06-11 /pmc/articles/PMC8230637/ /pubmed/34208064 http://dx.doi.org/10.3390/ijms22126282 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Yamanaka, Gaku
Ishida, Yu
Kanou, Kanako
Suzuki, Shinji
Watanabe, Yusuke
Takamatsu, Tomoko
Morichi, Shinichiro
Go, Soken
Oana, Shingo
Yamazaki, Takashi
Kawashima, Hisashi
Towards a Treatment for Neuroinflammation in Epilepsy: Interleukin-1 Receptor Antagonist, Anakinra, as a Potential Treatment in Intractable Epilepsy
title Towards a Treatment for Neuroinflammation in Epilepsy: Interleukin-1 Receptor Antagonist, Anakinra, as a Potential Treatment in Intractable Epilepsy
title_full Towards a Treatment for Neuroinflammation in Epilepsy: Interleukin-1 Receptor Antagonist, Anakinra, as a Potential Treatment in Intractable Epilepsy
title_fullStr Towards a Treatment for Neuroinflammation in Epilepsy: Interleukin-1 Receptor Antagonist, Anakinra, as a Potential Treatment in Intractable Epilepsy
title_full_unstemmed Towards a Treatment for Neuroinflammation in Epilepsy: Interleukin-1 Receptor Antagonist, Anakinra, as a Potential Treatment in Intractable Epilepsy
title_short Towards a Treatment for Neuroinflammation in Epilepsy: Interleukin-1 Receptor Antagonist, Anakinra, as a Potential Treatment in Intractable Epilepsy
title_sort towards a treatment for neuroinflammation in epilepsy: interleukin-1 receptor antagonist, anakinra, as a potential treatment in intractable epilepsy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8230637/
https://www.ncbi.nlm.nih.gov/pubmed/34208064
http://dx.doi.org/10.3390/ijms22126282
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