Please use this identifier to cite or link to this item: http://ahro.austin.org.au/austinjspui/handle/1/22880
Title: Antiepileptic drug teratogenicity and de novo genetic variation load.
Authors: Perucca, Piero;Anderson, Alison;Jazayeri, Dana;Hitchcock, Alison;Graham, Janet;Todaro, Marian;Tomson, Torbjörn;Battino, Dina;Perucca, Emilio;Martinez Ferri, Meritxell;Rochtus, Anne;Lagae, Lieven;Canevini, Maria Paola;Zambrelli, Elena;Campbell, Ellen;Koeleman, Bobby P C;Scheffer, Ingrid E;Berkovic, Samuel F;Kwan, Patrick;Sisodiya, Sanjay M;Goldstein, David B;Petrovski, Slavé;Craig, John;Vajda, Frank J E;O'Brien, Terence J
Affiliation: Institute of Genomic Medicine, Columbia University, New York, USA
Belfast Health and Social Care Trust, Belfast, UK
Chalfont Centre for Epilepsy, Chalfont-St-Peter, UK
Centre for Genomic Research, AstraZeneca, Cambridge, UK
Department of Neuroscience, Central Clinical School, Monash University
Department of Health Sciences, University of Milan, Italy
Epilepsy Center, Department of Neurophysiology and Experimental Epileptology, I.R.C.C.S. Neurological Institute "Carlo Besta" Foundation, Milan, Italy
Department of Internal Medicine and Therapeutics, University of Pavia, and Clinical Trial Center, IRCCS Mondino Foundation, Pavia, Italy
Child Neuropsychiatry Unit-Epilepsy Center, San Paolo Hospital, Milan, Italy
Departments of Medicine and Neurology, The University of Melbourne, The Royal Melbourne Hospital, Melbourne, Australia
Department of Clinical and Experimental Epilepsy, UCL Queen Square Institute of Neurology, London, UK
Epilepsy Research Centre, Department of Medicine, Austin Health, The University of Melbourne, Heidelberg, Victoria, Australia
Child Neuropsychiatry Unit-Epilepsy Center, San Paolo Hospital, Milan, Italy
Department of Paediatrics, The University of Melbourne, Royal Children's Hospital, Florey and Murdoch Children's Research Institutes, Melbourne, Australia
Department of Neurology, Alfred Health, Melbourne, Australia
Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden..
Servicio de Neurología, Hospital Mútua de Terrassa, Barcelona, Spain..
Department of Development and Regeneration, Section of Pediatric Neurology, University Hospitals Leuven, Leuven, Belgium..
Department of Genetics, Center for Molecular Medicine, University Medical Center Utrecht, The Netherlands..
Issue Date: 25-Mar-2020
EDate: 2020
Citation: Annals of neurology 2020; online first: 25 March
Abstract: The mechanisms by which antiepileptic drugs (AEDs) cause birth defects (BDs) are unknown. Data suggest that AED-induced BDs may result from a genome-wide increase of de novo variants in the embryo, a mechanism which we investigated. Whole-exome sequencing data from child-parent trios were interrogated for de novo single-nucleotide variants/indels (dnSNVs/indels) and copy number variants (dnCNVs). Generalized linear models were applied to assess de novo variant burdens in: children exposed prenatally to AEDs (AED-exposed children) vs children without BDs not exposed prenatally to AEDs (AED-unexposed unaffected children), and AED-exposed children with BDs vs those without BDs, adjusting for confounders. Fisher's exact test was used to compare categorical data. 67 child-parent trios were included: 10 with AED-exposed children with BDs; 46 with AED-exposed unaffected children; 11 with AED-unexposed unaffected children. The dnSNV/indel burden did not differ between AED-exposed children and AED-unexposed unaffected children [median dnSNV/indel number/child (range): 3 (0-7) vs 3 (1-5), p = 0.50]. Among AED-exposed children, there were no significant differences between those with BDs and those unaffected. Likely deleterious dnSNVs/indels were detected in 9/67 (13%) children, none of whom had BDs. The proportion of cases harbouring likely deleterious dnSNVs/indels did not differ significantly between AED-unexposed and AED-exposed children. The dnCNV burden was not associated with AED exposure or birth outcome. Our study indicates that prenatal AED exposure does not increase the burden of de novo variants, and that this mechanism is not a major contributor to AED-induced BDs. These results can be incorporated in routine patient counselling. This article is protected by copyright. All rights reserved.
URI: http://ahro.austin.org.au/austinjspui/handle/1/22880
DOI: 10.1002/ana.25724
ORCID: 0000-0002-7855-7066
0000-0002-2311-2174
0000-0003-4580-841X
PubMed URL: 32215971
Type: Journal Article
Appears in Collections:Journal articles

Files in This Item:
There are no files associated with this item.


Items in AHRO are protected by copyright, with all rights reserved, unless otherwise indicated.