Electro‐Clinical Features and Functional Connectivity Analysis in SYN1‐Related Epilepsy

Author:

Moya Quiros Vincent1ORCID,Adham Ahmed23,Convers Philippe14,Lesca Gaetan56ORCID,Mauguiere François47,Soulier Hugo1,Arzimanoglou Alexis89,Bayat Allan10111213,Braakman Hilde14ORCID,Camdessanche Jean‐Philippe1,Casenave Philippe15,Chaton Laurence16,Chaix Yves1718,Chochoi Maxime16,Depienne Christel19,Desportes Vincent20,De Ridder Jessie21,Dinkelacker Vera22,Gardella Elena1011ORCID,Kluger Gerhard J.23,Jung Julien724ORCID,Lemesle Martin Martine25,Mancardi Maria Margherita26,Mueller Markus27,Poulat Anne‐Lise20,Platzer Konrad28ORCID,Roubertie Agathe29ORCID,Stokman Marijn F.30,Vulto‐van Silfhout Anneke T.30,Wiegand Gert3132,Mazzola Laure14

Affiliation:

1. Neurology Department University Hospital Saint‐Etienne France

2. Physical Medicine and Rehabilitation Department University Hospital of Saint‐Étienne Saint‐Étienne France

3. CEA, LETI, CLINATEC University Grenoble Alpes Grenoble France

4. NeuroPain Lab, Lyon Neuroscience Research Centre, CRNL—INSERM U 1028/CNRS UMR 5292 University of Lyon Lyon France

5. Department of Genetics Member of the ERN EpiCARE, Hospices Civils de Lyon Bron France

6. Institute NeuroMyoGène, Laboratoire Physiopathologie et Génétique du Neurone et du Muscle, CNRS UMR 5261‐INSERM U1315 Université de Lyon—Université Claude Bernard Lyon 1 Lyon France

7. Department of Functional Neurology and Epileptology, Member of the ERN EpiCARE, Hospices Civils de Lyon Université de Lyon Lyon France

8. Department of Clinical Epileptology, Sleep Disorders and Functional Pediatric Neurology, coordinating member of the ERN EpiCARE University Hospitals of Lyon (HCL) Lyon France

9. Sección Epilepsia, Sueño y Neurofisiología, Department of Neurology, coordinating member of the ERN EpiCARE Hospital Sant Joan de Déu Barcelona Barcelona Spain

10. Institute for Regional Health Services University of Southern Denmark Odense Denmark

11. Department of Epilepsy Genetics and Personalized Medicine, Danish Epilepsy Center Member of the ERN EpiCARE Dianalund Denmark

12. Department of Drug Design and Pharmacology University of Copenhagen Copenhagen Denmark

13. Department of Clinical Genetics Copenhagen University Hospital, Rigshospitalet Copenhagen Denmark

14. Department of Paediatric Neurology, Radboud University Medical Centre Amalia Children's Hospital Nijmegen The Netherlands

15. Department of Neurology Hospital Libourne Libourne France

16. Department of Neurology Neurophysiology Unit, CHU Lille Lille France

17. Toulouse NeuroImaging Center, University of Toulouse, INSERM Université Paul Sabatier Toulouse France

18. Pediatric Neurology Unit, Children's Hospital Toulouse‐Purpan University Hospital Toulouse France

19. Institute of Human Genetics, University Hospital Essen University Duisburg‐Essen Essen Germany

20. Hospices Civils de Lyon, Department of Pediatric Neurology, Member of the ERN EpiCARE Hôpital Femme Mère Enfant Lyon France

21. Department of Neurology Academic Center for Epileptology, Kempenhaeghe Heeze The Netherlands

22. Department of Neurology University Hospital Strasbourg Strasbourg France

23. Schön Klinik Vogtareuth, Center for Pediatric Neurology, Neurorehabilitation and Epileptology Collaborating Partner of the ERN EpiCARE, PMU, Vogtareuth Salzburg Germany

24. Department of Neurology, University Hospital Lyon Neuroscience Research Center (CRNL), INSERM U1028, CNRS UMR5292 Lyon France

25. Department of Neurophysiology University Hospital Dijon Dijon France

26. Unit 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

27. Department of Epileptology, Krankenhaus Mara, Bethel Epilepsy Center Bielefeld University Bielefeld Germany

28. Institute of Human Genetics University of Leipzig Medical Center Leipzig Germany

29. Department of Pediatric Neurology, INSERM University Hospital Montpellier Montpellier France

30. Department of Human Genetics Radboud University Medical Center Nijmegen The Netherlands

31. Division of Pediatric Neurology, Department of Pediatrics Asklepios Klinik Nord‐Heidberg Hamburg Germany

32. Department of Pediatric and Adolescent Medicine II (Neuropediatrics, Social Pediatrics) University Medical Centre Schleswig‐Holstein Kiel Germany

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

Publisher

Wiley

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