Evidence map›Paper›PMID 39177219›Full record

ArticleAnnals of neurology2024

Electro-Clinical Features and Functional Connectivity Analysis in SYN1-Related Epilepsy.

Vincent Moya Quiros, Ahmed Adham, Philippe Convers, Gaetan Lesca, François Mauguiere, Hugo Soulier, Alexis Arzimanoglou, Allan Bayat, Hilde Braakman, Jean-Philippe Camdessanche and 21 more

Abstract read
In one paragraph

Article in Annals of neurology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

31 authors.

Vincent Moya QuirosNeurology Department, University Hospital, Saint-Etienne, France.ORCID https://orcid.org/0009-0006-7789-9933
Ahmed AdhamPhysical Medicine and Rehabilitation Department, University Hospital of Saint-Étienne, Saint-Étienne, France.
Philippe ConversNeurology Department, University Hospital, Saint-Etienne, France.
Gaetan LescaDepartment of Genetics, Member of the ERN EpiCARE, Hospices Civils de Lyon, Bron, France.ORCID https://orcid.org/0000-0001-7691-9492
François MauguiereNeuroPain Lab, Lyon Neuroscience Research Centre, CRNL-INSERM U 1028/CNRS UMR 5292, University of Lyon, Lyon, France.
Hugo SoulierNeurology Department, University Hospital, Saint-Etienne, France.
Alexis ArzimanoglouDepartment of Clinical Epileptology, Sleep Disorders and Functional Pediatric Neurology, coordinating member of the ERN EpiCARE, University Hospitals of Lyon (HCL), Lyon, France.
Allan BayatInstitute for Regional Health Services, University of Southern Denmark, Odense, Denmark.
Hilde BraakmanDepartment of Paediatric Neurology, Radboud University Medical Centre, Amalia Children's Hospital, Nijmegen, The Netherlands.ORCID https://orcid.org/0000-0001-8053-5918
Jean-Philippe CamdessancheNeurology Department, University Hospital, Saint-Etienne, France.
Philippe CasenaveDepartment of Neurology, Hospital Libourne, Libourne, France.
Laurence ChatonDepartment of Neurology, Neurophysiology Unit, CHU Lille, Lille, France.
Yves ChaixToulouse NeuroImaging Center, University of Toulouse, INSERM, Université Paul Sabatier, Toulouse, France.
Maxime ChochoiDepartment of Neurology, Neurophysiology Unit, CHU Lille, Lille, France.
Christel DepienneInstitute of Human Genetics, University Hospital Essen, University Duisburg-Essen, Essen, Germany.
Vincent DesportesHospices Civils de Lyon, Department of Pediatric Neurology, Member of the ERN EpiCARE, Hôpital Femme Mère Enfant, Lyon, France.
Jessie De RidderDepartment of Neurology, Academic Center for Epileptology, Kempenhaeghe, Heeze, The Netherlands.
Vera DinkelackerDepartment of Neurology, University Hospital Strasbourg, Strasbourg, France.
Elena GardellaInstitute for Regional Health Services, University of Southern Denmark, Odense, Denmark.ORCID https://orcid.org/0000-0002-7138-6022
Gerhard J KlugerSchön Klinik Vogtareuth, Center for Pediatric Neurology, Neurorehabilitation and Epileptology, Collaborating Partner of the ERN EpiCARE, PMU, Vogtareuth, Salzburg, Germany.
Julien JungDepartment of Functional Neurology and Epileptology, Member of the ERN EpiCARE, Hospices Civils de Lyon, Université de Lyon, Lyon, France.ORCID https://orcid.org/0000-0002-9274-0086
Martine Lemesle MartinDepartment of Neurophysiology, University Hospital Dijon, Dijon, France.
Maria Margherita MancardiUnit of Child Neuropsychiatry, Epilepsy Center, Member of the ERN EpiCARE, Istituto Giannina Gaslini, Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics and Maternal and Child Health, University of Genoa, Genoa, Italy.
Markus MuellerDepartment of Epileptology, Krankenhaus Mara, Bethel Epilepsy Center, Bielefeld University, Bielefeld, Germany.
Anne-Lise PoulatHospices Civils de Lyon, Department of Pediatric Neurology, Member of the ERN EpiCARE, Hôpital Femme Mère Enfant, Lyon, France.
Konrad PlatzerInstitute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.ORCID https://orcid.org/0000-0001-6127-6308
Agathe RoubertieDepartment of Pediatric Neurology, INSERM, University Hospital Montpellier, Montpellier, France.ORCID https://orcid.org/0000-0002-8180-4857
Marijn F StokmanDepartment of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
Anneke T Vulto-van SilfhoutDepartment of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
Gert WiegandDivision of Pediatric Neurology, Department of Pediatrics, Asklepios Klinik Nord-Heidberg, Hamburg, Germany.
Laure MazzolaNeurology Department, University Hospital, Saint-Etienne, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThere is currently scarce data on the electroclinical characteristics of epilepsy associated with synapsin 1 (SYN1) pathogenic variations. We examined clinical and electro-encephalographic (EEG) features in patients with epilepsy and SYN1 variants, with the aim of identifying a distinctive electroclinical pattern.

methodsIn this retrospective multicenter study, we collected and reviewed demographic, genetic, and epilepsy data of 19 male patients with SYN1 variants. Specifically, we analyzed interictal EEG data for all patients, and electro-clinical data from 10 epileptic seizures in 5 patients, using prolonged video-EEG monitoring recordings. Inter-ictal EEG functional connectivity parameters and frequency spectrum of the 10 patients over 12 years of age, were computed and compared with those of 56 age- and sex-matched controls.

resultsThe main electroclinical features of epilepsy in patients with SYN1 were (1) EEG background and organization mainly normal; (2) interictal abnormalities are often rare or not visible on EEG; (3) more than 60% of patients had reflex seizures (cutaneous contact with water and defecation being the main triggers) isolated or associated with spontaneous seizures; (4) electro-clinical semiology of seizures was mainly temporal or temporo-insulo/perisylvian with a notable autonomic component; and (5) ictal EEG showed a characteristic rhythmic theta/delta activity predominating in temporo-perisylvian regions at the beginning of most seizures. Comparing patients with SYN1 to healthy subjects, we observed a shift to lower frequency bands in power spectrum of interictal EEG and an increased connectivity in both temporal regions.

interpretationA distinct epilepsy syndrome emerges in patients with SYN1, with a rather characteristic clinical and EEG pattern suggesting predominant temporo-insular involvement. ANN NEUROL 2024.

Identifiers

PMID39177219
PMCPMC11683167

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