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Electro-Clinical Features and Functional Connectivity Analysis in SYN1-Related Epilepsy.
Moya Quiros, Vincent; Adham, Ahmed; Convers, Philippe; Lesca, Gaetan; Mauguiere, François; Soulier, Hugo; Arzimanoglou, Alexis; Bayat, Allan; Braakman, Hilde; Camdessanche, Jean-Philippe; Casenave, Philippe; Chaton, Laurence; Chaix, Yves; Chochoi, Maxime; Depienne, Christel; Desportes, Vincent; De Ridder, Jessie; Dinkelacker, Vera; Gardella, Elena; Kluger, Gerhard J; Jung, Julien; Lemesle Martin, Martine; Mancardi, Maria Margherita; Mueller, Markus; Poulat, Anne-Lise; Platzer, Konrad; Roubertie, Agathe; Stokman, Marijn F; Vulto-van Silfhout, Anneke T; Wiegand, Gert; Mazzola, Laure.
Afiliación
  • Moya Quiros V; Neurology Department, University Hospital, Saint-Etienne, France.
  • Adham A; Physical Medicine and Rehabilitation Department, University Hospital of Saint-Étienne, Saint-Étienne, France.
  • Convers P; CEA, LETI, CLINATEC, University Grenoble Alpes, Grenoble, France.
  • Lesca G; Neurology Department, University Hospital, Saint-Etienne, France.
  • Mauguiere F; NeuroPain Lab, Lyon Neuroscience Research Centre, CRNL-INSERM U 1028/CNRS UMR 5292, University of Lyon, Lyon, France.
  • Soulier H; Department of Genetics, Member of the ERN EpiCARE, Hospices Civils de Lyon, Bron, France.
  • Arzimanoglou A; 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.
  • Bayat A; NeuroPain Lab, Lyon Neuroscience Research Centre, CRNL-INSERM U 1028/CNRS UMR 5292, University of Lyon, Lyon, France.
  • Braakman H; Department of Functional Neurology and Epileptology, Member of the ERN EpiCARE, Hospices Civils de Lyon, Université de Lyon, Lyon, France.
  • Camdessanche JP; Neurology Department, University Hospital, Saint-Etienne, France.
  • Casenave P; Department of Clinical Epileptology, Sleep Disorders and Functional Pediatric Neurology, coordinating member of the ERN EpiCARE, University Hospitals of Lyon (HCL), Lyon, France.
  • Chaton L; Sección Epilepsia, Sueño y Neurofisiología, Department of Neurology, coordinating member of the ERN EpiCARE, Hospital Sant Joan de Déu Barcelona, Barcelona, Spain.
  • Chaix Y; Institute for Regional Health Services, University of Southern Denmark, Odense, Denmark.
  • Chochoi M; Department of Epilepsy Genetics and Personalized Medicine, Danish Epilepsy Center, Member of the ERN EpiCARE, Dianalund, Denmark.
  • Depienne C; Department of Drug Design and Pharmacology, University of Copenhagen, Copenhagen, Denmark.
  • Desportes V; Department of Clinical Genetics, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.
  • De Ridder J; Department of Paediatric Neurology, Radboud University Medical Centre, Amalia Children's Hospital, Nijmegen, The Netherlands.
  • Dinkelacker V; Neurology Department, University Hospital, Saint-Etienne, France.
  • Gardella E; Department of Neurology, Hospital Libourne, Libourne, France.
  • Kluger GJ; Department of Neurology, Neurophysiology Unit, CHU Lille, Lille, France.
  • Jung J; Toulouse NeuroImaging Center, University of Toulouse, INSERM, Université Paul Sabatier, Toulouse, France.
  • Lemesle Martin M; Pediatric Neurology Unit, Children's Hospital, Toulouse-Purpan University Hospital, Toulouse, France.
  • Mancardi MM; Department of Neurology, Neurophysiology Unit, CHU Lille, Lille, France.
  • Mueller M; Institute of Human Genetics, University Hospital Essen, University Duisburg-Essen, Essen, Germany.
  • Poulat AL; Hospices Civils de Lyon, Department of Pediatric Neurology, Member of the ERN EpiCARE, Hôpital Femme Mère Enfant, Lyon, France.
  • Platzer K; Department of Neurology, Academic Center for Epileptology, Kempenhaeghe, Heeze, The Netherlands.
  • Roubertie A; Department of Neurology, University Hospital Strasbourg, Strasbourg, France.
  • Stokman MF; Institute for Regional Health Services, University of Southern Denmark, Odense, Denmark.
  • Vulto-van Silfhout AT; Department of Epilepsy Genetics and Personalized Medicine, Danish Epilepsy Center, Member of the ERN EpiCARE, Dianalund, Denmark.
  • Wiegand G; Schön Klinik Vogtareuth, Center for Pediatric Neurology, Neurorehabilitation and Epileptology, Collaborating Partner of the ERN EpiCARE, PMU, Vogtareuth, Salzburg, Germany.
  • Mazzola L; Department of Functional Neurology and Epileptology, Member of the ERN EpiCARE, Hospices Civils de Lyon, Université de Lyon, Lyon, France.
Ann Neurol ; 2024 Aug 23.
Article en En | MEDLINE | ID: mdl-39177219
ABSTRACT

OBJECTIVE:

There 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.

METHODS:

In 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.

RESULTS:

The 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.

INTERPRETATION:

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

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Ann Neurol Año: 2024 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Ann Neurol Año: 2024 Tipo del documento: Article País de afiliación: Francia