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Epilepsy as a dynamic disease: A Bayesian model for differentiating seizure risk from natural variability
OBJECTIVE: A fundamental challenge in treating epilepsy is that changes in observed seizure frequencies do not necessarily reflect changes in underlying seizure risk. Rather, changes in seizure frequency may occur due to probabilistic variation around an underlying seizure risk state caused by norma...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5983137/ https://www.ncbi.nlm.nih.gov/pubmed/29881802 http://dx.doi.org/10.1002/epi4.12112 |
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author | Chiang, Sharon Vannucci, Marina Goldenholz, Daniel M. Moss, Robert Stern, John M. |
author_facet | Chiang, Sharon Vannucci, Marina Goldenholz, Daniel M. Moss, Robert Stern, John M. |
author_sort | Chiang, Sharon |
collection | PubMed |
description | OBJECTIVE: A fundamental challenge in treating epilepsy is that changes in observed seizure frequencies do not necessarily reflect changes in underlying seizure risk. Rather, changes in seizure frequency may occur due to probabilistic variation around an underlying seizure risk state caused by normal fluctuations from natural history, leading to seizure unpredictability and potentially suboptimal medication adjustments in epilepsy management. However, no rigorous statistical approach exists to systematically distinguish expected changes in seizure frequency due to natural variability from changes in underlying seizure risk. METHODS: Using data from SeizureTracker.com, a patient‐reported seizure diary tool containing over 1.2 million recorded seizures across 8 years, a novel epilepsy seizure risk assessment tool (EpiSAT) employing a Bayesian mixed‐effects hidden Markov model for zero‐inflated count data was developed to estimate changes in underlying seizure risk using patient‐reported seizure diary and clinical measurement data. Accuracy for correctly assessing underlying seizure risk was evaluated through a simulation comparison. Implications for the natural history of tuberous sclerosis complex (TSC) were assessed using data from SeizureTracker.com. RESULTS: EpiSAT led to significant improvement in seizure risk assessment compared to traditional approaches relying solely on observed seizure frequencies. Applied to TSC, four underlying seizure risk states were identified. The expected duration of each state was <12 months, providing a data‐driven estimate of the amount of time a person with TSC would be expected to remain at the same seizure risk level according to the natural course of epilepsy. SIGNIFICANCE: We propose a novel Bayesian statistical approach for evaluating seizure risk on an individual patient level using patient‐reported seizure diaries, which allows for the incorporation of external clinical variables to assess impact on seizure risk. This tool may improve the ability to distinguish true changes in seizure risk from natural variations in seizure frequency in clinical practice. Incorporation of systematic statistical approaches into antiepileptic drug (AED) management may help improve understanding of seizure unpredictability as well as timing of treatment interventions for people with epilepsy. |
format | Online Article Text |
id | pubmed-5983137 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-59831372018-06-07 Epilepsy as a dynamic disease: A Bayesian model for differentiating seizure risk from natural variability Chiang, Sharon Vannucci, Marina Goldenholz, Daniel M. Moss, Robert Stern, John M. Epilepsia Open Full‐length Original Research OBJECTIVE: A fundamental challenge in treating epilepsy is that changes in observed seizure frequencies do not necessarily reflect changes in underlying seizure risk. Rather, changes in seizure frequency may occur due to probabilistic variation around an underlying seizure risk state caused by normal fluctuations from natural history, leading to seizure unpredictability and potentially suboptimal medication adjustments in epilepsy management. However, no rigorous statistical approach exists to systematically distinguish expected changes in seizure frequency due to natural variability from changes in underlying seizure risk. METHODS: Using data from SeizureTracker.com, a patient‐reported seizure diary tool containing over 1.2 million recorded seizures across 8 years, a novel epilepsy seizure risk assessment tool (EpiSAT) employing a Bayesian mixed‐effects hidden Markov model for zero‐inflated count data was developed to estimate changes in underlying seizure risk using patient‐reported seizure diary and clinical measurement data. Accuracy for correctly assessing underlying seizure risk was evaluated through a simulation comparison. Implications for the natural history of tuberous sclerosis complex (TSC) were assessed using data from SeizureTracker.com. RESULTS: EpiSAT led to significant improvement in seizure risk assessment compared to traditional approaches relying solely on observed seizure frequencies. Applied to TSC, four underlying seizure risk states were identified. The expected duration of each state was <12 months, providing a data‐driven estimate of the amount of time a person with TSC would be expected to remain at the same seizure risk level according to the natural course of epilepsy. SIGNIFICANCE: We propose a novel Bayesian statistical approach for evaluating seizure risk on an individual patient level using patient‐reported seizure diaries, which allows for the incorporation of external clinical variables to assess impact on seizure risk. This tool may improve the ability to distinguish true changes in seizure risk from natural variations in seizure frequency in clinical practice. Incorporation of systematic statistical approaches into antiepileptic drug (AED) management may help improve understanding of seizure unpredictability as well as timing of treatment interventions for people with epilepsy. John Wiley and Sons Inc. 2018-04-20 /pmc/articles/PMC5983137/ /pubmed/29881802 http://dx.doi.org/10.1002/epi4.12112 Text en © 2018 The Authors. Epilepsia Open 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-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Full‐length Original Research Chiang, Sharon Vannucci, Marina Goldenholz, Daniel M. Moss, Robert Stern, John M. Epilepsy as a dynamic disease: A Bayesian model for differentiating seizure risk from natural variability |
title | Epilepsy as a dynamic disease: A Bayesian model for differentiating seizure risk from natural variability |
title_full | Epilepsy as a dynamic disease: A Bayesian model for differentiating seizure risk from natural variability |
title_fullStr | Epilepsy as a dynamic disease: A Bayesian model for differentiating seizure risk from natural variability |
title_full_unstemmed | Epilepsy as a dynamic disease: A Bayesian model for differentiating seizure risk from natural variability |
title_short | Epilepsy as a dynamic disease: A Bayesian model for differentiating seizure risk from natural variability |
title_sort | epilepsy as a dynamic disease: a bayesian model for differentiating seizure risk from natural variability |
topic | Full‐length Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5983137/ https://www.ncbi.nlm.nih.gov/pubmed/29881802 http://dx.doi.org/10.1002/epi4.12112 |
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