Cargando…
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...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , |
---|---|
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 |
_version_ | 1785131737342279680 |
---|---|
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. |
format | Online Article Text |
id | pubmed-10628346 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT lyuhang clinicalandelectrophysiologicalfeaturesofscn8avariantscausingepisodicorchronicataxia AT boßelmannchristianm clinicalandelectrophysiologicalfeaturesofscn8avariantscausingepisodicorchronicataxia AT johannesenkatrinem clinicalandelectrophysiologicalfeaturesofscn8avariantscausingepisodicorchronicataxia AT kokomahmoud clinicalandelectrophysiologicalfeaturesofscn8avariantscausingepisodicorchronicataxia AT ortigozaescobarjuandario clinicalandelectrophysiologicalfeaturesofscn8avariantscausingepisodicorchronicataxia AT aguileraalbesasergio clinicalandelectrophysiologicalfeaturesofscn8avariantscausingepisodicorchronicataxia AT garcianavasnunezdeyanira clinicalandelectrophysiologicalfeaturesofscn8avariantscausingepisodicorchronicataxia AT linnankivitarja clinicalandelectrophysiologicalfeaturesofscn8avariantscausingepisodicorchronicataxia AT gailyeija clinicalandelectrophysiologicalfeaturesofscn8avariantscausingepisodicorchronicataxia AT vanruitenhenrietteja clinicalandelectrophysiologicalfeaturesofscn8avariantscausingepisodicorchronicataxia AT richardsonruth clinicalandelectrophysiologicalfeaturesofscn8avariantscausingepisodicorchronicataxia AT betzlercornelia clinicalandelectrophysiologicalfeaturesofscn8avariantscausingepisodicorchronicataxia AT horvathgabriella clinicalandelectrophysiologicalfeaturesofscn8avariantscausingepisodicorchronicataxia AT brilstraeva clinicalandelectrophysiologicalfeaturesofscn8avariantscausingepisodicorchronicataxia AT geerdinkniels clinicalandelectrophysiologicalfeaturesofscn8avariantscausingepisodicorchronicataxia AT orsuccidaniele clinicalandelectrophysiologicalfeaturesofscn8avariantscausingepisodicorchronicataxia AT tessaalessandra clinicalandelectrophysiologicalfeaturesofscn8avariantscausingepisodicorchronicataxia AT gardellaelena clinicalandelectrophysiologicalfeaturesofscn8avariantscausingepisodicorchronicataxia AT fleszarzofia clinicalandelectrophysiologicalfeaturesofscn8avariantscausingepisodicorchronicataxia AT scholsludger clinicalandelectrophysiologicalfeaturesofscn8avariantscausingepisodicorchronicataxia AT lercheholger clinicalandelectrophysiologicalfeaturesofscn8avariantscausingepisodicorchronicataxia AT møllerrikkes clinicalandelectrophysiologicalfeaturesofscn8avariantscausingepisodicorchronicataxia AT liuyuanyuan clinicalandelectrophysiologicalfeaturesofscn8avariantscausingepisodicorchronicataxia |