KCNQ2 R144 variants cause neurodevelopmental disability with language impairment and autistic features without neonatal seizures through a gain-of-function mechanism.


Journal

EBioMedicine
ISSN: 2352-3964
Titre abrégé: EBioMedicine
Pays: Netherlands
ID NLM: 101647039

Informations de publication

Date de publication:
Jul 2022
Historique:
received: 22 01 2022
revised: 08 06 2022
accepted: 10 06 2022
pubmed: 4 7 2022
medline: 20 7 2022
entrez: 3 7 2022
Statut: ppublish

Résumé

Prior studies have revealed remarkable phenotypic heterogeneity in KCNQ2-related disorders, correlated with effects on biophysical features of heterologously expressed channels. Here, we assessed phenotypes and functional properties associated with KCNQ2 missense variants R144W, R144Q, and R144G. We also explored in vitro blockade of channels carrying R144Q mutant subunits by amitriptyline. Patients were identified using the RIKEE database and through clinical collaborators. Phenotypes were collected by a standardized questionnaire. Functional and pharmacological properties of variant subunits were analyzed by whole-cell patch-clamp recordings. Detailed clinical information on fifteen patients (14 novel and 1 previously published) was analyzed. All patients had developmental delay with prominent language impairment. R144Q patients were more severely affected than R144W patients. Infantile to childhood onset epilepsy occurred in 40%, while 67% of sleep-EEGs showed sleep-activated epileptiform activity. Ten patients (67%) showed autistic features. Activation gating of homomeric Kv7.2 R144W/Q/G channels was left-shifted, suggesting gain-of-function effects. Amitriptyline blocked channels containing Kv7.2 and Kv7.2 R144Q subunits. Patients carrying KCNQ2 R144 gain-of-function variants have developmental delay with prominent language impairment, autistic features, often accompanied by infantile- to childhood-onset epilepsy and EEG sleep-activated epileptiform activity. The absence of neonatal seizures is a robust and important clinical differentiator between KCNQ2 gain-of-function and loss-of-function variants. The Kv7.2/7.3 channel blocker amitriptyline might represent a targeted treatment. Supported by FWO, GSKE, KCNQ2-Cure, Jack Pribaz Foundation, European Joint Programme on Rare Disease 2020, the Italian Ministry for University and Research, the Italian Ministry of Health, the European Commission, the University of Antwerp, NINDS, and Chalk Family Foundation.

Sections du résumé

BACKGROUND BACKGROUND
Prior studies have revealed remarkable phenotypic heterogeneity in KCNQ2-related disorders, correlated with effects on biophysical features of heterologously expressed channels. Here, we assessed phenotypes and functional properties associated with KCNQ2 missense variants R144W, R144Q, and R144G. We also explored in vitro blockade of channels carrying R144Q mutant subunits by amitriptyline.
METHODS METHODS
Patients were identified using the RIKEE database and through clinical collaborators. Phenotypes were collected by a standardized questionnaire. Functional and pharmacological properties of variant subunits were analyzed by whole-cell patch-clamp recordings.
FINDINGS RESULTS
Detailed clinical information on fifteen patients (14 novel and 1 previously published) was analyzed. All patients had developmental delay with prominent language impairment. R144Q patients were more severely affected than R144W patients. Infantile to childhood onset epilepsy occurred in 40%, while 67% of sleep-EEGs showed sleep-activated epileptiform activity. Ten patients (67%) showed autistic features. Activation gating of homomeric Kv7.2 R144W/Q/G channels was left-shifted, suggesting gain-of-function effects. Amitriptyline blocked channels containing Kv7.2 and Kv7.2 R144Q subunits.
INTERPRETATION CONCLUSIONS
Patients carrying KCNQ2 R144 gain-of-function variants have developmental delay with prominent language impairment, autistic features, often accompanied by infantile- to childhood-onset epilepsy and EEG sleep-activated epileptiform activity. The absence of neonatal seizures is a robust and important clinical differentiator between KCNQ2 gain-of-function and loss-of-function variants. The Kv7.2/7.3 channel blocker amitriptyline might represent a targeted treatment.
FUNDING BACKGROUND
Supported by FWO, GSKE, KCNQ2-Cure, Jack Pribaz Foundation, European Joint Programme on Rare Disease 2020, the Italian Ministry for University and Research, the Italian Ministry of Health, the European Commission, the University of Antwerp, NINDS, and Chalk Family Foundation.

Identifiants

pubmed: 35780567
pii: S2352-3964(22)00311-5
doi: 10.1016/j.ebiom.2022.104130
pmc: PMC9254340
pii:
doi:

Substances chimiques

KCNQ2 Potassium Channel 0
KCNQ2 protein, human 0
Amitriptyline 1806D8D52K

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

104130

Informations de copyright

Copyright © 2022 The Authors. Published by Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of interests SW received consultancy and speaker fees from UCB, Biocodex, Xenon, Zogenix, Lundbeck, Knopp Biosciences, Encoded MT received consultancy fees from Xenon. ECC received consultancy fees from Xenon, Knopp, these activities have been reviewed and approved by Baylor College of Medicine according to its policy on disclosure of outside interests. RSM received consultancy and speaker fees from EISAI and UCB. The remaining authors have no conflicts of interest.

Auteurs

Francesco Miceli (F)

Department of Neuroscience, University of Naples "Federico II", Naples, Italy.

Charissa Millevert (C)

Applied & Translational Neurogenomics Group, VIB Center for Molecular Neurology, VIB, Antwerp, Belgium; Department of Neurology, University Hospital, Antwerp, Belgium.

Maria Virginia Soldovieri (MV)

Department of Medicine and Health Science "V. Tiberio", University of Molise, Campobasso, Italy.

Ilaria Mosca (I)

Department of Medicine and Health Science "V. Tiberio", University of Molise, Campobasso, Italy.

Paolo Ambrosino (P)

Department of Science and Technology (DST), University of Sannio, Benevento, Italy.

Lidia Carotenuto (L)

Department of Neuroscience, University of Naples "Federico II", Naples, Italy.

Dewi Schrader (D)

Division of Neurology, Department of Pediatrics, BC Children's Hospital, University of British Columbia, Vancouver, British Columbia, Canada.

Hyun Kyung Lee (HK)

Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, Canada.

James Riviello (J)

Section of Neurology and Developmental Neuroscience, Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA.

William Hong (W)

Section of Neurology and Developmental Neuroscience, Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA; Division of Epilepsy and Clinical Neurophysiology, Department of Neurology, Boston Children's Hospital, Boston, MA, USA.

Sarah Risen (S)

Section of Neurology and Developmental Neuroscience, Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA; Department of Pediatrics, Texas Children's Hospital, Houston, TX, USA.

Lisa Emrick (L)

Section of Neurology and Developmental Neuroscience, Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA; Department of Pediatrics, Texas Children's Hospital, Houston, TX, USA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.

Hitha Amin (H)

Pediatric Neurology at Cortica Care, Irvine, CA, USA.

Dorothée Ville (D)

Pediatric Neurology Department, Lyon University Hospital, France.

Patrick Edery (P)

Department of Genetics, Lyon University Hospital, France; Centre for Neuroscience Research Lyon, Lyon, France.

Julitta de Bellescize (J)

Department of Pediatric Clinical Epileptology, Sleep Disorders and Functional Neurology, Member of the European Reference Network EpiCARE, University Hospitals of Lyon (HCL), Lyon, France.

Vincent Michaud (V)

Reference Center for Rare "Neurogenetic" Diseases, Department of Medical Genetics, Pellegrin Hospital, Bordeaux University Hospital, France.

Julien Van-Gils (J)

Reference Center for Rare "Neurogenetic" Diseases, Department of Medical Genetics, Pellegrin Hospital, Bordeaux University Hospital, France.

Cyril Goizet (C)

Reference Center for Rare "Neurogenetic" Diseases, Department of Medical Genetics, Pellegrin Hospital, Bordeaux University Hospital, France; Rare Diseases Laboratory: Genetics and Metabolism (MRGM), Bordeaux University, Bordeaux, France.

Marjolein H Willemsen (MH)

Department of Human Genetics, Radboud University Medical Center, Nijmegen, the Netherlands.

Tjitske Kleefstra (T)

Department of Human Genetics, Radboud University Medical Center, Nijmegen, the Netherlands; Vincent Van Gogh Instituut, Center for Neuropsychiatry, Venray, Limburg, the Netherlands.

Rikke S Møller (RS)

Department of Epilepsy Genetics and Personalized Medicine, Danish Epilepsy Centre, Dianalund, Denmark; Department Regional Health Research, University of Southern Denmark, Odense, Denmark.

Allan Bayat (A)

Department of Epilepsy Genetics and Personalized Medicine, Danish Epilepsy Centre, Dianalund, Denmark; Department Regional Health Research, University of Southern Denmark, Odense, Denmark.

Orrin Devinsky (O)

Department of Neurology, NYU Langone Health and Grossman School of Medicine, New York, NY, USA.

Tristan Sands (T)

Department of Neurology, Columbia University Irving Medical Center, New York, NY, USA; Institute for Genomic Medicine, Columbia University Irving Medical Center, New York, NY, USA.

G Christoph Korenke (GC)

Department of Neuropediatrics, University Children's Hospital, Klinikum Oldenburg, Oldenburg, Germany.

Gerhard Kluger (G)

Neuropediatric Clinic and Clinic for Neurorehabilitation, Epilepsy Center for Children and Adolescents, Schön Klinik Vogtareuth, Vogtareuth, Germany; Research Institute for Rehabilitation, Transition and Palliation, Paracelsus Medical University Salzburg, Salzburg, Austria.

Heather C Mefford (HC)

Department of Pediatrics, Division of Genetic Medicine, University of Washington, Seattle, WA, USA.

Eva Brilstra (E)

Department of Medical Genetics, University Medical Center Utrecht, Utrecht, the Netherlands.

Gaetan Lesca (G)

Department of Medical Genetics, Lyon University Hospital, Lyon, France; Neuromyogene Institute, University of Lyon, Lyon, France.

Mathieu Milh (M)

Aix Marseille University, Pediatric neurology unit, Timone Children Hospital, Marseille, France.

Edward C Cooper (EC)

Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA; Departments of Neurology and Neuroscience, Baylor College of Medicine, Houston, TX, USA.

Maurizio Taglialatela (M)

Department of Neuroscience, University of Naples "Federico II", Naples, Italy. Electronic address: mtaglial@unina.it.

Sarah Weckhuysen (S)

Applied & Translational Neurogenomics Group, VIB Center for Molecular Neurology, VIB, Antwerp, Belgium; Department of Neurology, University Hospital, Antwerp, Belgium; µNEURO Research Centre of Excellence, University of Antwerp, Antwerp, Belgium; Translational Neurosciences, Faculty of Medicine and Health Science, University of Antwerp, Antwerp, Belgium. Electronic address: Sarah.Weckhuysen@uantwerpen.vib.be.

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