Utility of genetic testing for therapeutic decision-making in adults with epilepsy
- PMID: 32427350
- DOI: 10.1111/epi.16533
Utility of genetic testing for therapeutic decision-making in adults with epilepsy
Abstract
Objective: Genetic testing has become a routine part of the diagnostic workup in children with early onset epilepsies. In the present study, we sought to investigate a cohort of adult patients with epilepsy, to determinate the diagnostic yield and explore the gain of personalized treatment approaches in adult patients.
Methods: Two hundred patients (age span = 18-80 years) referred for diagnostic gene panel testing at the Danish Epilepsy Center were included. The vast majority (91%) suffered from comorbid intellectual disability. The medical records of genetically diagnosed patients were mined for data on epilepsy syndrome, cognition, treatment changes, and seizure outcome following the genetic diagnosis.
Results: We found a genetic diagnosis in 46 of 200 (23%) patients. SCN1A, KCNT1, and STXBP1 accounted for the greatest number of positive findings (48%). More rare genetic findings included SLC2A1, ATP6A1V, HNRNPU, MEF2C, and IRF2BPL. Gene-specific treatment changes were initiated in 11 of 46 (17%) patients (one with SLC2A1, 10 with SCN1A) following the genetic diagnosis. Ten patients improved, with seizure reduction and/or increased alertness and general well-being.
Significance: With this study, we show that routine diagnostic testing is highly relevant in adults with epilepsy. The diagnostic yield is similar to previously reported pediatric cohorts, and the genetic findings can be useful for therapeutic decision-making, which may lead to better seizure control, ultimately improving quality of life.
Keywords: NGS; adults; gene panel; genetic testing.
© 2020 International League Against Epilepsy.
Comment in
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Gene tests in adults with epilepsy and intellectual disability.Nat Rev Neurol. 2020 Oct;16(10):527-528. doi: 10.1038/s41582-020-0388-5. Nat Rev Neurol. 2020. PMID: 32616899 No abstract available.
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Epilepsy gene panel yield and impact on outcomes for adults with unexplained seizures.Epilepsia. 2020 Aug;61(8):1797-1798. doi: 10.1111/epi.16606. Epub 2020 Jul 11. Epilepsia. 2020. PMID: 32652572 No abstract available.
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The prevalence of genetically diagnosable epilepsies in young adulthood: How many should we be looking for?Epilepsia. 2020 Sep;61(9):2053-2054. doi: 10.1111/epi.16640. Epub 2020 Aug 12. Epilepsia. 2020. PMID: 32783195 No abstract available.
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Genetic testing in adult epilepsy patients: A call to action for clinicians.Epilepsia. 2020 Sep;61(9):2055-2056. doi: 10.1111/epi.16639. Epub 2020 Aug 12. Epilepsia. 2020. PMID: 32783210 No abstract available.
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