Why we urgently need improved epilepsy therapies for adult patients.
Anti-Seizure drugs
Epilepsy genetics
Epilepsy surgery
Neuromodulation
Treatment refractory epilepsy
Journal
Neuropharmacology
ISSN: 1873-7064
Titre abrégé: Neuropharmacology
Pays: England
ID NLM: 0236217
Informations de publication
Date de publication:
15 06 2020
15 06 2020
Historique:
received:
28
03
2019
revised:
12
11
2019
accepted:
15
11
2019
pubmed:
22
11
2019
medline:
4
6
2021
entrez:
22
11
2019
Statut:
ppublish
Résumé
Up to a third of patients with epilepsy suffer from recurrent seizures despite therapeutic advances. Current epilepsy treatments are limited by experiential data from treating different types of epilepsy. For example, we lack evidence-based approaches to efficacious multi-drug therapies or identifying potentially serious or disabling adverse events before medications are initiated. Despite advances in neuroscience and genetics, our understanding of epilepsy pathogenesis and mechanisms of treatment-resistance remains limited. For most patients with epilepsy, precision medicine for improved seizure control and reduced toxicity remains a future goal. A third of epilepsy patients suffer from ongoing seizures and even more suffer from adverse effects of treatment. There is a critical need for more effective and safer therapies for epilepsy patients with frequent comorbitidies, including depression, anxiety, migraine, and cognitive impairments, as well as special populations (e.g., women, elderly). Advances from genomic sequencing techniques may identify new genes and regulatory elements that influence both the depth of the epilepsies' roots within brain circuitry as well as ASD resistance. Improved understanding of epilepsy mechanisms, identification of potential new therapeutic targets, and their assessment in randomized controlled trials are needed to reduce the burden of refractory epilepsy. This article is part of the special issue entitled 'New Epilepsy Therapies for the 21st Century - From Antiseizure Drugs to Prevention, Modification and Cure of Epilepsy'.
Identifiants
pubmed: 31751547
pii: S0028-3908(19)30421-6
doi: 10.1016/j.neuropharm.2019.107855
pii:
doi:
Substances chimiques
Anticonvulsants
0
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
107855Informations de copyright
Published by Elsevier Ltd.
Déclaration de conflit d'intérêts
Declaration of competing interest Santoshi Billakota has no COI. Kyung-Wha Kim has no COI. Orrin Devinsky serves on the scientific and/or medical advisory boards, and has equity interest and/or receives compensation from Receptor Life Sciences, Privateer Holdings/Tilray, and Egg Rock Holdings/Papa & Barkley. He has also been an investigator and consultant for GW Pharmaceuticals. He has also consulted for Zogenix. He also compensated serves on the scientific and/or medical advisory boards, and has equity interest and/or receives compensation from Tevard, Rettco, Engage Pharmaceuticals, Pairnomix and Empatica.