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Clinical and electrophysiological features of SCN8A variants causing episodic or chronic ataxia

BACKGROUND: Variants in SCN8A are associated with a spectrum of epilepsies and neurodevelopmental disorders. Ataxia as a predominant symptom of SCN8A variation has not been well studied. We set out to investigate disease mechanisms and genotype–phenotype correlations of SCN8A-related ataxia. METHODS...

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Autores principales: Lyu, Hang, Boßelmann, Christian M., Johannesen, Katrine M., Koko, Mahmoud, Ortigoza-Escobar, Juan Dario, Aguilera-Albesa, Sergio, Garcia-Navas Núñez, Deyanira, Linnankivi, Tarja, Gaily, Eija, van Ruiten, Henriette J.A., Richardson, Ruth, Betzler, Cornelia, Horvath, Gabriella, Brilstra, Eva, Geerdink, Niels, Orsucci, Daniele, Tessa, Alessandra, Gardella, Elena, Fleszar, Zofia, Schöls, Ludger, Lerche, Holger, Møller, Rikke S., Liu, Yuanyuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10628346/
http://dx.doi.org/10.1016/j.ebiom.2023.104855
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author Lyu, Hang
Boßelmann, Christian M.
Johannesen, Katrine M.
Koko, Mahmoud
Ortigoza-Escobar, Juan Dario
Aguilera-Albesa, Sergio
Garcia-Navas Núñez, Deyanira
Linnankivi, Tarja
Gaily, Eija
van Ruiten, Henriette J.A.
Richardson, Ruth
Betzler, Cornelia
Horvath, Gabriella
Brilstra, Eva
Geerdink, Niels
Orsucci, Daniele
Tessa, Alessandra
Gardella, Elena
Fleszar, Zofia
Schöls, Ludger
Lerche, Holger
Møller, Rikke S.
Liu, Yuanyuan
author_facet Lyu, Hang
Boßelmann, Christian M.
Johannesen, Katrine M.
Koko, Mahmoud
Ortigoza-Escobar, Juan Dario
Aguilera-Albesa, Sergio
Garcia-Navas Núñez, Deyanira
Linnankivi, Tarja
Gaily, Eija
van Ruiten, Henriette J.A.
Richardson, Ruth
Betzler, Cornelia
Horvath, Gabriella
Brilstra, Eva
Geerdink, Niels
Orsucci, Daniele
Tessa, Alessandra
Gardella, Elena
Fleszar, Zofia
Schöls, Ludger
Lerche, Holger
Møller, Rikke S.
Liu, Yuanyuan
author_sort Lyu, Hang
collection PubMed
description BACKGROUND: Variants in SCN8A are associated with a spectrum of epilepsies and neurodevelopmental disorders. Ataxia as a predominant symptom of SCN8A variation has not been well studied. We set out to investigate disease mechanisms and genotype–phenotype correlations of SCN8A-related ataxia. METHODS: We collected genetic and electro-clinical data of ten individuals from nine unrelated families carrying novel SCN8A variants associated with chronic progressive or episodic ataxia. Electrophysiological characterizations of these variants were performed in ND7/23 cells and cultured neurons. FINDINGS: Variants associated with chronic progressive ataxia either decreased Na(+) current densities and shifted activation curves towards more depolarized potentials (p.Asn995Asp, p.Lys1498Glu and p.Trp1266Cys) or resulted in a premature stop codon (p.Trp937Ter). Three variants (p.Arg847Gln and biallelic p.Arg191Trp/p.Asp1525Tyr) were associated with episodic ataxia causing loss-of-function by decreasing Na(+) current densities or a hyperpolarizing shift of the inactivation curve. Two additional episodic ataxia-associated variants caused mixed gain- and loss-of function effects in ND7/23 cells and were further examined in primary murine hippocampal neuronal cultures. Neuronal firing in excitatory neurons was increased by p.Arg1629His, but decreased by p.Glu1201Lys. Neuronal firing in inhibitory neurons was decreased for both variants. No functional effect was observed for p.Arg1913Trp. In four individuals, treatment with sodium channel blockers exacerbated symptoms. INTERPRETATION: We identified episodic or chronic ataxia as predominant phenotypes caused by variants in SCN8A. Genotype-phenotype correlations revealed a more pronounced loss-of-function effect for variants causing chronic ataxia. Sodium channel blockers should be avoided under these conditions. FUNDING: BMBF, 10.13039/501100001659DFG, the 10.13039/501100003196Italian Ministry of Health, University of Tuebingen.
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spelling pubmed-106283462023-11-08 Clinical and electrophysiological features of SCN8A variants causing episodic or chronic ataxia Lyu, Hang Boßelmann, Christian M. Johannesen, Katrine M. Koko, Mahmoud Ortigoza-Escobar, Juan Dario Aguilera-Albesa, Sergio Garcia-Navas Núñez, Deyanira Linnankivi, Tarja Gaily, Eija van Ruiten, Henriette J.A. Richardson, Ruth Betzler, Cornelia Horvath, Gabriella Brilstra, Eva Geerdink, Niels Orsucci, Daniele Tessa, Alessandra Gardella, Elena Fleszar, Zofia Schöls, Ludger Lerche, Holger Møller, Rikke S. Liu, Yuanyuan eBioMedicine Articles BACKGROUND: Variants in SCN8A are associated with a spectrum of epilepsies and neurodevelopmental disorders. Ataxia as a predominant symptom of SCN8A variation has not been well studied. We set out to investigate disease mechanisms and genotype–phenotype correlations of SCN8A-related ataxia. METHODS: We collected genetic and electro-clinical data of ten individuals from nine unrelated families carrying novel SCN8A variants associated with chronic progressive or episodic ataxia. Electrophysiological characterizations of these variants were performed in ND7/23 cells and cultured neurons. FINDINGS: Variants associated with chronic progressive ataxia either decreased Na(+) current densities and shifted activation curves towards more depolarized potentials (p.Asn995Asp, p.Lys1498Glu and p.Trp1266Cys) or resulted in a premature stop codon (p.Trp937Ter). Three variants (p.Arg847Gln and biallelic p.Arg191Trp/p.Asp1525Tyr) were associated with episodic ataxia causing loss-of-function by decreasing Na(+) current densities or a hyperpolarizing shift of the inactivation curve. Two additional episodic ataxia-associated variants caused mixed gain- and loss-of function effects in ND7/23 cells and were further examined in primary murine hippocampal neuronal cultures. Neuronal firing in excitatory neurons was increased by p.Arg1629His, but decreased by p.Glu1201Lys. Neuronal firing in inhibitory neurons was decreased for both variants. No functional effect was observed for p.Arg1913Trp. In four individuals, treatment with sodium channel blockers exacerbated symptoms. INTERPRETATION: We identified episodic or chronic ataxia as predominant phenotypes caused by variants in SCN8A. Genotype-phenotype correlations revealed a more pronounced loss-of-function effect for variants causing chronic ataxia. Sodium channel blockers should be avoided under these conditions. FUNDING: BMBF, 10.13039/501100001659DFG, the 10.13039/501100003196Italian Ministry of Health, University of Tuebingen. Elsevier 2023-10-28 /pmc/articles/PMC10628346/ http://dx.doi.org/10.1016/j.ebiom.2023.104855 Text en © 2023 The Authors. Published by Elsevier B.V. https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Articles
Lyu, Hang
Boßelmann, Christian M.
Johannesen, Katrine M.
Koko, Mahmoud
Ortigoza-Escobar, Juan Dario
Aguilera-Albesa, Sergio
Garcia-Navas Núñez, Deyanira
Linnankivi, Tarja
Gaily, Eija
van Ruiten, Henriette J.A.
Richardson, Ruth
Betzler, Cornelia
Horvath, Gabriella
Brilstra, Eva
Geerdink, Niels
Orsucci, Daniele
Tessa, Alessandra
Gardella, Elena
Fleszar, Zofia
Schöls, Ludger
Lerche, Holger
Møller, Rikke S.
Liu, Yuanyuan
Clinical and electrophysiological features of SCN8A variants causing episodic or chronic ataxia
title Clinical and electrophysiological features of SCN8A variants causing episodic or chronic ataxia
title_full Clinical and electrophysiological features of SCN8A variants causing episodic or chronic ataxia
title_fullStr Clinical and electrophysiological features of SCN8A variants causing episodic or chronic ataxia
title_full_unstemmed Clinical and electrophysiological features of SCN8A variants causing episodic or chronic ataxia
title_short Clinical and electrophysiological features of SCN8A variants causing episodic or chronic ataxia
title_sort clinical and electrophysiological features of scn8a variants causing episodic or chronic ataxia
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10628346/
http://dx.doi.org/10.1016/j.ebiom.2023.104855
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