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Scalp EEG spikes predict impending epilepsy in TSC infants: A longitudinal observational study
OBJECTIVE: To determine if routine electroencephalography (EEG) in seizure‐naive infants with tuberous sclerosis complex (TSC) can predict epilepsy and subsequent neurocognitive outcomes. METHODS: Forty infants 7 months of age or younger and meeting the genetic or clinical diagnostic criteria for tu...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6910957/ https://www.ncbi.nlm.nih.gov/pubmed/31691264 http://dx.doi.org/10.1111/epi.16379 |
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author | Wu, Joyce Y. Goyal, Monisha Peters, Jurriaan M. Krueger, Darcy Sahin, Mustafa Northrup, Hope Au, Kit S. O’Kelley, Sarah Williams, Marian Pearson, Deborah A. Hanson, Ellen Byars, Anna W. Krefting, Jessica Beasley, Mark Cutter, Gary Limdi, Nita Bebin, E. Martina |
author_facet | Wu, Joyce Y. Goyal, Monisha Peters, Jurriaan M. Krueger, Darcy Sahin, Mustafa Northrup, Hope Au, Kit S. O’Kelley, Sarah Williams, Marian Pearson, Deborah A. Hanson, Ellen Byars, Anna W. Krefting, Jessica Beasley, Mark Cutter, Gary Limdi, Nita Bebin, E. Martina |
author_sort | Wu, Joyce Y. |
collection | PubMed |
description | OBJECTIVE: To determine if routine electroencephalography (EEG) in seizure‐naive infants with tuberous sclerosis complex (TSC) can predict epilepsy and subsequent neurocognitive outcomes. METHODS: Forty infants 7 months of age or younger and meeting the genetic or clinical diagnostic criteria for tuberous sclerosis were enrolled. Exclusion criteria included prior history of seizures or treatment with antiseizure medications. At each visit, seizure history and 1‐hour awake and asleep video‐EEG, standardized across all sites, were obtained until 2 years of age. Developmental assessments (Mullen and Vineland‐II) were completed at 6, 12, and 24 months of age. RESULTS: Of 40 infants enrolled (mean age of 82.4 days), 32 completed the study. Two were lost to follow‐up and six were treated with antiepileptic drugs (AEDs) due to electrographic seizures and/or interictal epileptiform discharges (IEDs) on their EEG studies prior to the onset of clinical seizures. Seventeen of the 32 remaining children developed epilepsy at a mean age of 7.5 months (standard deviation [SD] = 4.4). Generalized/focal slowing, hypsarrhythmia, and generalized/focal attenuation were not predictive for the development of clinical seizures. Presence of IEDs had a 77.3% positive predictive value and absence a 70% negative predictive value for developing seizures by 2 years of age. IEDs preceded clinical seizure onset by 3.6 months (mean). Developmental testing showed significant decline, only in infants with ongoing seizures, but not infants who never developed seizures or whose seizures came under control. SIGNIFICANCE: IEDs identify impending epilepsy in the majority (77%) of seizure‐naive infants with TSC. The use of a 1‐hour awake and asleep EEG can be used as a biomarker for ongoing epileptogenesis in most, but not all, infants with TSC. Persistent seizures, but not history of interictal epileptiform activity or history of well‐controlled seizures, correlated with low scores on the Vineland and Mullen tests at 2 years of age. |
format | Online Article Text |
id | pubmed-6910957 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-69109572020-01-27 Scalp EEG spikes predict impending epilepsy in TSC infants: A longitudinal observational study Wu, Joyce Y. Goyal, Monisha Peters, Jurriaan M. Krueger, Darcy Sahin, Mustafa Northrup, Hope Au, Kit S. O’Kelley, Sarah Williams, Marian Pearson, Deborah A. Hanson, Ellen Byars, Anna W. Krefting, Jessica Beasley, Mark Cutter, Gary Limdi, Nita Bebin, E. Martina Epilepsia Full‐length Original Research OBJECTIVE: To determine if routine electroencephalography (EEG) in seizure‐naive infants with tuberous sclerosis complex (TSC) can predict epilepsy and subsequent neurocognitive outcomes. METHODS: Forty infants 7 months of age or younger and meeting the genetic or clinical diagnostic criteria for tuberous sclerosis were enrolled. Exclusion criteria included prior history of seizures or treatment with antiseizure medications. At each visit, seizure history and 1‐hour awake and asleep video‐EEG, standardized across all sites, were obtained until 2 years of age. Developmental assessments (Mullen and Vineland‐II) were completed at 6, 12, and 24 months of age. RESULTS: Of 40 infants enrolled (mean age of 82.4 days), 32 completed the study. Two were lost to follow‐up and six were treated with antiepileptic drugs (AEDs) due to electrographic seizures and/or interictal epileptiform discharges (IEDs) on their EEG studies prior to the onset of clinical seizures. Seventeen of the 32 remaining children developed epilepsy at a mean age of 7.5 months (standard deviation [SD] = 4.4). Generalized/focal slowing, hypsarrhythmia, and generalized/focal attenuation were not predictive for the development of clinical seizures. Presence of IEDs had a 77.3% positive predictive value and absence a 70% negative predictive value for developing seizures by 2 years of age. IEDs preceded clinical seizure onset by 3.6 months (mean). Developmental testing showed significant decline, only in infants with ongoing seizures, but not infants who never developed seizures or whose seizures came under control. SIGNIFICANCE: IEDs identify impending epilepsy in the majority (77%) of seizure‐naive infants with TSC. The use of a 1‐hour awake and asleep EEG can be used as a biomarker for ongoing epileptogenesis in most, but not all, infants with TSC. Persistent seizures, but not history of interictal epileptiform activity or history of well‐controlled seizures, correlated with low scores on the Vineland and Mullen tests at 2 years of age. John Wiley and Sons Inc. 2019-11-05 2019-12 /pmc/articles/PMC6910957/ /pubmed/31691264 http://dx.doi.org/10.1111/epi.16379 Text en © 2019 The Authors. Epilepsia published by Wiley Periodicals, Inc. on behalf of International League Against Epilepsy. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Full‐length Original Research Wu, Joyce Y. Goyal, Monisha Peters, Jurriaan M. Krueger, Darcy Sahin, Mustafa Northrup, Hope Au, Kit S. O’Kelley, Sarah Williams, Marian Pearson, Deborah A. Hanson, Ellen Byars, Anna W. Krefting, Jessica Beasley, Mark Cutter, Gary Limdi, Nita Bebin, E. Martina Scalp EEG spikes predict impending epilepsy in TSC infants: A longitudinal observational study |
title | Scalp EEG spikes predict impending epilepsy in TSC infants: A longitudinal observational study |
title_full | Scalp EEG spikes predict impending epilepsy in TSC infants: A longitudinal observational study |
title_fullStr | Scalp EEG spikes predict impending epilepsy in TSC infants: A longitudinal observational study |
title_full_unstemmed | Scalp EEG spikes predict impending epilepsy in TSC infants: A longitudinal observational study |
title_short | Scalp EEG spikes predict impending epilepsy in TSC infants: A longitudinal observational study |
title_sort | scalp eeg spikes predict impending epilepsy in tsc infants: a longitudinal observational study |
topic | Full‐length Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6910957/ https://www.ncbi.nlm.nih.gov/pubmed/31691264 http://dx.doi.org/10.1111/epi.16379 |
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