Suscribirse

Drug-resistant juvenile myoclonic epilepsy: A literature review - 25/04/24

Doi : 10.1016/j.neurol.2024.02.385 
A. Nica a, b,
a Epilepsy Unit, Reference Center for Rare Epilepsies, Neurology Department, Clinical Investigation Center 1414, Rennes University Hospital, Rennes, France 
b Signal and Image Processing Laboratory (LTSI), INSERM, Rennes University, Rennes, France 

*Correspondence at: Service de Neurologie, Hôpital Pontchaillou, CHU de Rennes, 2, rue Henri-le-Guilloux, 35033 Rennes cedex, France.Service de Neurologie, Hôpital Pontchaillou, CHU de Rennes2, rue Henri-le-GuillouxRennes cedex35033France

Highlights

DR can affect one third of JME patients, but pseudoresistance must be ruled out.
Absence seizures, young age at onset, and catamenial seizures are DR risk factors.
Photosensitivity may be a protective factor, at least in femaless.
VPA is the best ASM, but has teratogenic risks, possibly affecting males too.
Alternative ASMs (e.g., LEV and LTG) and neuromodulation are available for DR-JME.

El texto completo de este artículo está disponible en PDF.

Abstract

The ILAE's Task Force on Nosology and Definitions revised in 2022 its definition of juvenile myoclonic epilepsy (JME), the most common idiopathic generalized epilepsy disorder, but this definition may well change again in the future. Although good drug response could almost be a diagnostic criterion for JME, drug resistance (DR) is observed in up to a third of patients. It is important to distinguish this from pseudoresistance, which is often linked to psychosocial problems or psychiatric comorbidities. After summarizing these aspects and the various definitions applied to JME, the present review lists the risk factors for DR-JME that have been identified in numerous studies and meta-analyses. The factors most often cited are absence seizures, young age at onset, and catamenial seizures. By contrast, photosensitivity seems to favor good treatment response, at least in female patients. Current hypotheses on DR mechanisms in JME are based on studies of either simple (e.g., cortical excitability) or more complex (e.g., anatomical and functional connectivity) neurophysiological markers, bearing in mind that JME is regarded as a neural network disease. This research has revealed correlations between the intensity of some markers and DR, and above all shed light on the role of these markers in associated neurocognitive and neuropsychiatric disorders in both patients and their siblings. Studies of neurotransmission have mainly pointed to impaired GABAergic inhibition. Genetic studies have generally been inconclusive. Increasing restrictions have been placed on the use of valproate, the standard antiseizure medication for this syndrome, owing to its teratogenic and developmental risks. Levetiracetam and lamotrigine are prescribed as alternatives, as is vagal nerve stimulation, and there are several other promising antiseizure drugs and neuromodulation methods. The development of better alternative treatments is continuing to take place alongside advances in our knowledge of JME, as we still have much to learn and understand.

El texto completo de este artículo está disponible en PDF.

Keywords : Juvenile myoclonic epilepsy, Drug resistance


Esquema


© 2024  Elsevier Masson SAS. Reservados todos los derechos.
Añadir a mi biblioteca Eliminar de mi biblioteca Imprimir
Exportación

    Exportación citas

  • Fichero

  • Contenido

Vol 180 - N° 4

P. 271-289 - avril 2024 Regresar al número
Artículo precedente Artículo precedente
  • The landscape of drug resistant absence seizures in adolescents and adults: Pathophysiology, electroclinical spectrum and treatment options
  • G. Daquin, F. Bonini
| Artículo siguiente Artículo siguiente
  • Drug-resistant generalized epilepsies: Revisiting the frontiers of idiopathic generalized epilepsies
  • L. Gauer, S. Baer, M.-P. Valenti-Hirsch, A. De Saint-Martin, E. Hirsch

Bienvenido a EM-consulte, la referencia de los profesionales de la salud.
El acceso al texto completo de este artículo requiere una suscripción.

¿Ya suscrito a @@106933@@ revista ?

Mi cuenta


Declaración CNIL

EM-CONSULTE.COM se declara a la CNIL, la declaración N º 1286925.

En virtud de la Ley N º 78-17 del 6 de enero de 1978, relativa a las computadoras, archivos y libertades, usted tiene el derecho de oposición (art.26 de la ley), el acceso (art.34 a 38 Ley), y correcta (artículo 36 de la ley) los datos que le conciernen. Por lo tanto, usted puede pedir que se corrija, complementado, clarificado, actualizado o suprimido información sobre usted que son inexactos, incompletos, engañosos, obsoletos o cuya recogida o de conservación o uso está prohibido.
La información personal sobre los visitantes de nuestro sitio, incluyendo su identidad, son confidenciales.
El jefe del sitio en el honor se compromete a respetar la confidencialidad de los requisitos legales aplicables en Francia y no de revelar dicha información a terceros.


Todo el contenido en este sitio: Copyright © 2025 Elsevier, sus licenciantes y colaboradores. Se reservan todos los derechos, incluidos los de minería de texto y datos, entrenamiento de IA y tecnologías similares. Para todo el contenido de acceso abierto, se aplican los términos de licencia de Creative Commons.