Evidence map›Paper›PMID 35696452›Full record

ArticleBrain : a journal of neurology2022

The gain of function SCN1A disorder spectrum: novel epilepsy phenotypes and therapeutic implications.

Andreas Brunklaus, Tobias Brünger, Tony Feng, Carmen Fons, Anni Lehikoinen, Eleni Panagiotakaki, Mihaela-Adela Vintan, Joseph Symonds, James Andrew, Alexis Arzimanoglou and 25 more

Abstract read
In one paragraph

Article in Brain : a journal of neurology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed, 2 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

73 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
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  3. Review
  4. Review
  5. Article
  6. Article
  7. Holistic management of epilepsy in adults with intellectual development disorders.Epileptic disorders : international epilepsy journal with videotape · 2026
    Article
  8. Article
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  12. Review
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  14. Heterogeneity of monogenic epilepsy in loci, phenotypes, and treatment approaches.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2026
    Review
  15. CharacterizingmedRxiv : the preprint server for health sciences · 2026
    Article
  16. Review
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  20. Review

13 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

35 authors.

Andreas BrunklausInstitute of Health and Wellbeing, University of Glasgow, Glasgow, UK.ORCID 0000-0002-7728-6903
Tobias BrüngerCologne Center for Genomics, University of Cologne, Cologne, Germany.
Tony FengInstitute of Health and Wellbeing, University of Glasgow, Glasgow, UK.
Carmen FonsPediatric Neurology Department, CIBERER-ISCIII, Sant Joan de Déu Universitary Hospital, Institut de Recerca Sant Joan de Déu, Member of the ERN EpiCARE, Barcelona, Spain.
Anni LehikoinenPediatric Neurology Department, Kuopio University Hospital, Member of the ERN EpiCARE, Kuopio, Finland.
Eleni PanagiotakakiDepartment of Paediatric Clinical Epileptology, sleep disorders and functional neurology, Member of the ERN EpiCARE, University Hospitals of Lyon (HCL) and Inserm U1028/CNRS UMR5292, Lyon, France.
Mihaela-Adela Vintan'Iuliu Hatieganu' University of Medicine and Pharmacy, Faculty of Medicine, Department of Neuroscience, Neurology and Pediatric Neurology, Victor Babes, 43, 400012 Cluj-Napoca, Romania.
Joseph SymondsInstitute of Health and Wellbeing, University of Glasgow, Glasgow, UK.ORCID 0000-0002-2141-4216
James AndrewThe Paediatric Neurosciences Research Group, Royal Hospital for Children, Member of the ERN EpiCARE, Glasgow, UK.
Alexis ArzimanoglouPediatric Neurology Department, CIBERER-ISCIII, Sant Joan de Déu Universitary Hospital, Institut de Recerca Sant Joan de Déu, Member of the ERN EpiCARE, Barcelona, Spain.
Sarah DelimaIndiana University School of Medicine, IU Health Riley Hospital for Children, Department of Neurology, Division of Pediatric Neurology, Indianapolis, IN, USA.
Julie GalloisLouisiana State University Health Sciences Center School of Medicine, New Orleans, LA, USA.
Donncha HanrahanDepartment of Paediatric Neurology, Royal Belfast Hospital for Sick Children, Belfast, UK.
Gaetan LescaDepartment of Medical Genetics, Lyon University Hospital, Member of the ERN EpiCARE, Université Claude Bernard Lyon 1, Lyon, France.
Stewart MacLeodThe Paediatric Neurosciences Research Group, Royal Hospital for Children, Member of the ERN EpiCARE, Glasgow, UK.
Dragan MarjanovicThe Danish Epilepsy Centre, Member of the ERN EpiCARE, Dianalund, Denmark.
Amy McTagueDevelopmental Neurosciences, UCL Great Ormond Street Institute of Child Health, London, UK.
Noemi Nuñez-EnamoradoPediatric Neurology Department, 12 Octubre Universitary Hospital, Madrid, Spain.
Eduardo Perez-PalmaUniversidad del Desarrollo, Centro de Genética y Genómica, Facultad de Medicina Clínica Alemana, Santiago, Chile.
M Scott PerryJane and John Justin Neurosciences Center, Cook Children's Medical Center, Ft Worth, TX, USA.
Karen PysdenPaediatric Neurology Department, Leeds Teaching Hospitals, Leeds General Infirmary, Leeds, UK.
Sophie J Russ-HallEpilepsy Research Centre, Department of Medicine, University of Melbourne, Austin Health, Melbourne, Australia.
Ingrid E SchefferEpilepsy Research Centre, Department of Medicine, University of Melbourne, Austin Health, Melbourne, Australia.
Krystal SullyBaylor College of Medicine, Houston, TX, USA.
Steffen SyrbeDivision of Pediatric Epileptology, Center for Pediatrics and Adolescent Medicine, University Hospital Heidelberg, Heidelberg, Germany.
Ulvi VaherChildren's Clinic of Tartu University Hospital, Faculty of Medicine of Tartu University, Member of the ERN EpiCARE, Tartu, Estonia.
Murugan VelayuthamBirmingham Children's Hospital, Birmingham, UK.
Julie VogtWest Midlands Regional Genetics Service, Birmingham Women's and Children's Hospital, Birmingham, UK.
Shelly WeissDivision of Neurology, SickKids, University of Toronto, Toronto, Canada.
Elaine WirrellDivisions of Epilepsy and Child and Adolescent Neurology, Department of Neurology, Mayo Clinic, Rochester, MN, USA.
Sameer M ZuberiInstitute of Health and Wellbeing, University of Glasgow, Glasgow, UK.ORCID 0000-0002-4489-4697
Dennis LalCologne Center for Genomics, University of Cologne, Cologne, Germany.
Rikke S MøllerThe Danish Epilepsy Centre, Member of the ERN EpiCARE, Dianalund, Denmark.
Massimo MantegazzaUniversité Côte d'Azur, 06560 Valbonne-Sophia Antipolis, France.ORCID 0000-0002-1070-7929
Sandrine CestèleUniversité Côte d'Azur, 06560 Valbonne-Sophia Antipolis, France.

Funding

Project 3 - Development and investigation of murine models of channelopathy-associated epilepsyU54NS108874 · NINDS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI GEORGE, ALFRED L. · 2018 to 2022
$12.1M
Medical Research Council MR/L001497/1Medical Research Council MR/T007087/1NINDS NIH HHS U54 NS108874
6 · The paper itself

Abstract

Brain voltage-gated sodium channel NaV1.1 (SCN1A) loss-of-function variants cause the severe epilepsy Dravet syndrome, as well as milder phenotypes associated with genetic epilepsy with febrile seizures plus. Gain of function SCN1A variants are associated with familial hemiplegic migraine type 3. Novel SCN1A-related phenotypes have been described including early infantile developmental and epileptic encephalopathy with movement disorder, and more recently neonatal presentations with arthrogryposis. Here we describe the clinical, genetic and functional evaluation of affected individuals. Thirty-five patients were ascertained via an international collaborative network using a structured clinical questionnaire and from the literature. We performed whole-cell voltage-clamp electrophysiological recordings comparing sodium channels containing wild-type versus variant NaV1.1 subunits. Findings were related to Dravet syndrome and familial hemiplegic migraine type 3 variants. We identified three distinct clinical presentations differing by age at onset and presence of arthrogryposis and/or movement disorder. The most severely affected infants (n = 13) presented with congenital arthrogryposis, neonatal onset epilepsy in the first 3 days of life, tonic seizures and apnoeas, accompanied by a significant movement disorder and profound intellectual disability. Twenty-one patients presented later, between 2 weeks and 3 months of age, with a severe early infantile developmental and epileptic encephalopathy and a movement disorder. One patient presented after 3 months with developmental and epileptic encephalopathy only. Associated SCN1A variants cluster in regions of channel inactivation associated with gain of function, different to Dravet syndrome variants (odds ratio = 17.8; confidence interval = 5.4-69.3; P = 1.3 × 10-7). Functional studies of both epilepsy and familial hemiplegic migraine type 3 variants reveal alterations of gating properties in keeping with neuronal hyperexcitability. While epilepsy variants result in a moderate increase in action current amplitude consistent with mild gain of function, familial hemiplegic migraine type 3 variants induce a larger effect on gating properties, in particular the increase of persistent current, resulting in a large increase of action current amplitude, consistent with stronger gain of function. Clinically, 13 out of 16 (81%) gain of function variants were associated with a reduction in seizures in response to sodium channel blocker treatment (carbamazepine, oxcarbazepine, phenytoin, lamotrigine or lacosamide) without evidence of symptom exacerbation. Our study expands the spectrum of gain of function SCN1A-related epilepsy phenotypes, defines key clinical features, provides novel insights into the underlying disease mechanisms between SCN1A-related epilepsy and familial hemiplegic migraine type 3, and identifies sodium channel blockers as potentially efficacious therapies. Gain of function disease should be considered in early onset epilepsies with a pathogenic SCN1A variant and non-Dravet syndrome phenotype.

Indexed as

ArthrogryposisEpilepsies, MyoclonicEpilepsyMigraine with AuraMovement DisordersSpasms, InfantileEpileptic SyndromesGain of Function MutationHumansInfantInfant, NewbornNAV1.1 Voltage-Gated Sodium ChannelPhenotypeNAV1.1 Voltage-Gated Sodium ChannelSCN1A protein, humanarthrogryposisepilepsygain of functionmovement disorderSCN1A

Identifiers

PMID35696452
PMCPMC9679167

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.