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Mutations in GABRB3: From febrile seizures to epileptic encephalopathies

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

  • Rikke S Møller
  • Thomas V Wuttke
  • Ingo Helbig
  • Carla Marini
  • Katrine M Johannesen
  • Eva H Brilstra
  • Ulvi Vaher
  • Ingo Borggraefe
  • Inga Talvik
  • Tiina Talvik
  • Gerhard Kluger
  • Laurence L Francois
  • Gaetan Lesca
  • Julitta de Bellescize
  • Susanne Blichfeldt
  • Nicolas Chatron
  • Nils Holert
  • Julia Jacobs
  • Marielle Swinkels
  • Cornelia Betzler
  • Steffen Syrbe
  • Marina Nikanorova
  • Candace T Myers
  • Line H G Larsen
  • Sabina Vejzovic
  • Manuela Pendziwiat
  • Sarah von Spiczak
  • Sarah Hopkins
  • Holly Dubbs
  • Konstantin Mukhin
  • Hans Holthausen
  • Koen L van Gassen
  • Hans A Dahl
  • Heather C Mefford
  • Renzo Guerrini
  • Johannes R Lemke
  • Holger Lerche
  • Hiltrud Muhle
  • Snezana Maljevic

OBJECTIVE: To examine the role of mutations in GABRB3 encoding the β3 subunit of the GABAA receptor in individual patients with epilepsy with regard to causality, the spectrum of genetic variants, their pathophysiology, and associated phenotypes.

METHODS: We performed massive parallel sequencing of GABRB3 in 416 patients with a range of epileptic encephalopathies and childhood-onset epilepsies and recruited additional patients with epilepsy with GABRB3 mutations from other research and diagnostic programs.

RESULTS: We identified 22 patients with heterozygous mutations in GABRB3, including 3 probands from multiplex families. The phenotypic spectrum of the mutation carriers ranged from simple febrile seizures, genetic epilepsies with febrile seizures plus, and epilepsy with myoclonic-atonic seizures to West syndrome and other types of severe, early-onset epileptic encephalopathies. Electrophysiologic analysis of 7 mutations in Xenopus laevis oocytes, using coexpression of wild-type or mutant β3, together with α5 and γ2s subunits and an automated 2-microelectrode voltage-clamp system, revealed reduced GABA-induced current amplitudes or GABA sensitivity for 5 of 7 mutations.

CONCLUSIONS: Our results indicate that GABRB3 mutations are associated with a broad phenotypic spectrum of epilepsies and that reduced receptor function causing GABAergic disinhibition represents the relevant disease mechanism.

OriginalsprogEngelsk
TidsskriftNeurology
Vol/bind88
Udgave nummer5
Sider (fra-til)483-492
Antal sider10
ISSN0028-3878
DOI
StatusUdgivet - 31 jan. 2017

ID: 172131366