<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Auvin S</submitter><funding>National Institute of Neurological Disorders and Stroke</funding><funding>Eunice Kennedy Shriver National Institute of Child Health and Human Development</funding><funding>Consejo Nacional de Ciencia y Tecnología</funding><funding>NICHD NIH HHS</funding><funding>Deutsche Forschungsgemeinschaft</funding><funding>University College London</funding><funding>NINDS NIH HHS</funding><funding>Institut Universitaire de France</funding><funding>Defense Human Resources Activity</funding><funding>American Epilepsy Society</funding><pagination>2891-2908</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10836613</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>64(11)</volume><pubmed_abstract>Despite progress in the development of anti-seizure medications (ASMs), one third of people with epilepsy have drug-resistant epilepsy (DRE). The working definition of DRE, proposed by the International League Against Epilepsy (ILAE) in 2010, helped identify individuals who might benefit from presurgical evaluation early on. As the incidence of DRE remains high, the TASK1 workgroup on DRE of the ILAE/American Epilepsy Society (AES) Joint Translational Task Force discussed the heterogeneity and complexity of its presentation and mechanisms, the confounders in drawing mechanistic insights when testing treatment responses, and barriers in modeling DRE across the lifespan and translating across species. We propose that it is necessary to revisit the current definition of DRE, in order to transform the preclinical and clinical research of mechanisms and biomarkers, to identify novel, effective, precise, pharmacologic treatments, allowing for earlier recognition of drug resistance and individualized therapies.</pubmed_abstract><journal>Epilepsia</journal><pubmed_title>Revisiting the concept of drug-resistant epilepsy: A TASK1 report of the ILAE/AES Joint Translational Task Force.</pubmed_title><pmcid>PMC10836613</pmcid><funding_grant_id>R37 NS043209</funding_grant_id><funding_grant_id>A3‐S‐26782</funding_grant_id><funding_grant_id>W81XWH‐22‐1‐0510</funding_grant_id><funding_grant_id>U54 NS100064</funding_grant_id><funding_grant_id>PO 681/12‐1</funding_grant_id><funding_grant_id>NS43209</funding_grant_id><funding_grant_id>W81XWH‐22‐1‐0210</funding_grant_id><funding_grant_id>P50 HD105352</funding_grant_id><funding_grant_id>R01 NS043209</funding_grant_id><funding_grant_id>R01 NS127524</funding_grant_id><pubmed_authors>Auvin S</pubmed_authors><pubmed_authors>Galanopoulou AS</pubmed_authors><pubmed_authors>TASK1 workgroup on drug-resistant epilepsy of the ILAE/AES Joint Translational Task Force</pubmed_authors><pubmed_authors>Rocha L</pubmed_authors><pubmed_authors>Moshe SL</pubmed_authors><pubmed_authors>Potschka H</pubmed_authors><pubmed_authors>Walker MC</pubmed_authors></additional><is_claimable>false</is_claimable><name>Revisiting the concept of drug-resistant epilepsy: A TASK1 report of the ILAE/AES Joint Translational Task Force.</name><description>Despite progress in the development of anti-seizure medications (ASMs), one third of people with epilepsy have drug-resistant epilepsy (DRE). The working definition of DRE, proposed by the International League Against Epilepsy (ILAE) in 2010, helped identify individuals who might benefit from presurgical evaluation early on. As the incidence of DRE remains high, the TASK1 workgroup on DRE of the ILAE/American Epilepsy Society (AES) Joint Translational Task Force discussed the heterogeneity and complexity of its presentation and mechanisms, the confounders in drawing mechanistic insights when testing treatment responses, and barriers in modeling DRE across the lifespan and translating across species. We propose that it is necessary to revisit the current definition of DRE, in order to transform the preclinical and clinical research of mechanisms and biomarkers, to identify novel, effective, precise, pharmacologic treatments, allowing for earlier recognition of drug resistance and individualized therapies.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Nov</publication><modification>2025-04-04T02:25:05.581Z</modification><creation>2025-04-04T02:25:05.581Z</creation></dates><accession>S-EPMC10836613</accession><cross_references><pubmed>37676719</pubmed><doi>10.1111/epi.17751</doi></cross_references></HashMap>