Epilepsy is one of the most common neurological disorders, affecting as many as 1 in 26 individuals. The childhood epileptic encephalopathies (CEE) are the most severe types of epilepsy, characterized by refractory seizures, cognitive arrest or regression associated with ongoing epileptic activity, and a poor prognosis. Identifying the genetic causes of CEE is the initial step toward developing more effective diagnostic tests, prognosis counseling and treatments. Despite significant advances in gene discovery in recent years, the majority of patient with CEE remain undiagnosed. Our recent work (R01NS069605) to investigate the genetic basis of epilepsy helped establish the role of copy number variants (CNVs) in CEE. More recently, we use a high-throughput targeted sequencing strategy to screen 73 known and candidate CEE genes for mutations in a cohort of >500 CEE probands, identifying pathogenic mutations in >10% of patients. Our studies identified CHD2 and SYNGAP1 as novel and important causes of CEE, GRIN2A as a cause of epilepsy-aphasia syndromes and GABRA1 and STXBP1 as causes of a subset of SCN1A- negative Dravet syndrome. In this proposal, we build upon these successes and propose three lines of investigation. First, we will use trio exome sequencing in 150 patients with CEE who have already been screened for mutations in a large number of CEE genes and are therefore enriched for gene discovery. Second, we will use high-throughput targeted of a panel of CEE and ID genes to investigate the role of these genes in several related neurodevelopmental disorders including intellectual disability, autism spectrum disorder and schizophrenia. Finally, we will investigate the role of the chromatin remodeling pathway in epileptogenesis, highlighted by the discovery of CHD2 mutations in a subset of CEE patients. Successful completion of our aims will lead to improved genetic diagnosis of patients, better prognosis and recurrence risk counseling for families, and novel targets for development of therapeutics.
Public Health Relevance Statement Epilepsy is one of the most common neurological disorders in humans, affecting up to 3% of the population. Childhood epileptic encephalopathies are the most severe form of epilepsy with onset in early childhood, multiple seizure types that are difficult to treat, and poor developmental outcomes. There is considerable evidence that genetic mutations cause childhood epileptic encephalopathies, and our recent research has identified several new genetic causes. However, most cases are still not explained. This research will identify new genes and genetic pathways in epilepsy. Furthermore, we will study the specific genetic changes disrupt normal brain function. Our results and will directly benefit individuals with epilepsy and their families through improved diagnostic, prognostic and recurrence risk information. Greater understanding of the genes involved in normal development and function of the brain will facilitate improved therapies for this common disorder and benefit society as a whole.
| Myers, Candace T; Hollingsworth, Georgina; Muir, Alison M et al. (2018) Parental Mosaicism in ""De Novo"" Epileptic Encephalopathies. N Engl J Med 378:1646-1648 |
| Chatron, Nicolas; Møller, Rikke S; Champaigne, Neena L et al. (2018) The epilepsy phenotypic spectrum associated with a recurrent CUX2 variant. Ann Neurol 83:926-934 |
| Carvill, Gemma L; Liu, Aijie; Mandelstam, Simone et al. (2018) Severe infantile onset developmental and epileptic encephalopathy caused by mutations in autophagy gene WDR45. Epilepsia 59:e5-e13 |
| Johannesen, Katrine M; Gardella, Elena; Linnankivi, Tarja et al. (2018) Defining the phenotypic spectrum of SLC6A1 mutations. Epilepsia 59:389-402 |
| Ottman, Ruth; Freyer, Catharine; Mefford, Heather C et al. (2018) Return of individual results in epilepsy genomic research: A view from the field. Epilepsia 59:1635-1642 |
| Howell, Katherine B; Eggers, Stefanie; Dalziel, Kim et al. (2018) A population-based cost-effectiveness study of early genetic testing in severe epilepsies of infancy. Epilepsia 59:1177-1187 |
| Jansen, Sandra; Hoischen, Alexander; Coe, Bradley P et al. (2018) A genotype-first approach identifies an intellectual disability-overweight syndrome caused by PHIP haploinsufficiency. Eur J Hum Genet 26:54-63 |
| Myers, Candace T; Stong, Nicholas; Mountier, Emily I et al. (2017) De Novo Mutations in PPP3CA Cause Severe Neurodevelopmental Disease with Seizures. Am J Hum Genet 101:516-524 |
| EuroEPINOMICS-RES Consortium. Electronic address: euroepinomics-RES@ua.ac.be; Epilepsy Phenome/Genome Project; Epi4K Consortium et al. (2017) De Novo Mutations in Synaptic Transmission Genes Including DNM1 Cause Epileptic Encephalopathies. Am J Hum Genet 100:179 |
| Sadleir, Lynette G; Mountier, Emily I; Gill, Deepak et al. (2017) Not all SCN1A epileptic encephalopathies are Dravet syndrome: Early profound Thr226Met phenotype. Neurology 89:1035-1042 |
Showing the most recent 10 out of 36 publications
