Epilepsia

Amitriptyline use in individuals with KCNQ2/3 gain‐of‐function variants: A retrospective cohort study

Matthias De Wachter 1, 2
Charissa Millevert 3, 4
Joost Nicolai 5
Elisabeth Cats 6
Gerhard Kluger 7, 8
Mathieu Milh 9
Robin Cloarec 10
Steffen Syrbe 11
Katrijn Arts 12
Katrien Jansen 12
Magdalena Krygier 13
Robert Smigiel 14
S. Auvin 15, 16, 17
Kern Olofson 18
Cathrine E. Gjerulfsen 2
Berten Ceulemans 1
Rikke S. Møller 2, 19
Allan Bayat 2, 18, 19
S. Weckhuysen 3, 4, 20, 21
Show full list: 19 authors
2
 
Department of Epilepsy Genetics and Personalized Medicine Danish Epilepsy Center (EpiCARE member) Dianalund Denmark
3
 
Department of Neurology Antwerp University Hospital, University of Antwerp Edegem Belgium
4
 
Vlaams Instituut voor Biotechnologie (VIB) Center for Molecular Neurology Antwerp Belgium
6
 
Gelre Hospitals Apeldoorn the Netherlands
7
 
Clinic for Neuropediatrics and Neurological Rehabilitation, Epilepsy Center for Children and Adolescents Schön Klinik Vogtareuth Vogtareuth Germany
9
 
Department of Child Neurology Aix‐Marseille University, AP‐HM, La Timone Children's Hospital Marseille France
10
 
Center de Référence Déficiences Intellectuelles et Polyhandicaps de Causes Rares APHM, Hôpital de la Timone‐Enfants Marseille France
11
 
Center for Child and Adolescent Medicine, Clinic 1, Division of Pediatric Epileptology Heidelberg University, Medical Faculty of Heidelberg Heidelberg Germany
14
 
Department of Pediatrics, Endocrinology, Diabetology, and Metabolic Diseases Wrocław Medical University Wrocław Poland
15
 
Pediatric Neurology Department, CRMR Epilepsies Rares (EpiCARE member) APHP, Robert Debré University Hospital Paris France
18
 
Department of Child Neurology Danish Epilepsy Center Dianalund Denmark
Publication typeJournal Article
Publication date2025-02-17
Journal: Epilepsia
scimago Q1
SJR2.227
CiteScore10.9
Impact factor6.6
ISSN00139580, 15281167, 15281157
Abstract
Objective

Heterozygous gain‐of‐function (GOF) variants in KCNQ2 and KCNQ3, encoding the voltage‐gated potassium channel subunits Kv7.2 and Kv7.3, lead to neurodevelopmental disorders for which no established treatments are available. Amitriptyline, an antidepressant, blocks Kv7.2/Kv7.3 and has previously been reported to be effective in a single individual with a KCNQ2 GOF variant. We designed a retrospective, single‐arm, multicenter study to investigate the effects of amitriptyline in a real‐world setting.

Methods

We used a 7‐point Likert scale to measure seizure frequency, clinical examination, motor function, alertness, skill acquisition, communication, mood, behavior, self‐care, sleep, tiredness, and electroencephalogram at baseline, after a minimum of 6 weeks of intervention, and, if applicable, after discontinuation. Adverse events were assessed in all participants, and the effectiveness of the treatment was evaluated in 11 individuals who received a minimum dosage of .5 mg/kg/day for at least 6 weeks. Data were collected from October 2023 to August 2024.

Results

Thirteen individuals, eight with a pathogenic KCNQ2 GOF variant and five with a pathogenic KCNQ3 GOF variant, were included. Nine were female, and the median age at start of amitriptyline was 7.1 years (range = 1.5–20 years). Eleven individuals received a minimum dosage of .5 mg/kg/day for at least 6 weeks. The median dosage of amitriptyline administered was 1 mg/kg/day, with a median treatment duration of 29 weeks. Although amitriptyline was ineffective in two individuals (18%), eight (72%) demonstrated at least minimal improvement in two or more domains, with improvements in alertness and communication being the most frequently reported. In those with reported improvements, amitriptyline was discontinued in four individuals, but continued improvements were seen, to the same or greater extent compared to treatment. The remaining five individuals are on continued treatment because of perceived benefits.

Significance

Overall, the effect of amitriptyline remains unclear, and formal n‐of‐1 trials are needed to investigate the precise effects of amitriptyline in KCNQ GOF‐related neurodevelopmental disorders.

  • We do not take into account publications without a DOI.
  • Statistics recalculated only for publications connected to researchers, organizations and labs registered on the platform.
  • Statistics recalculated weekly.

Are you a researcher?

Create a profile to get free access to personal recommendations for colleagues and new articles.
Share
Cite this
GOST | RIS | BibTex
Found error?