Study of Pathophysiology of Status Epilepticus and Dysimmune Encephalitis

Официальное название

COLETTE : Study of the Pathophysiology of Status Epilepticus and Dysimmune Encephalitis and Identification of Valuable Biomarkers

Обзор

COLETTE is an interventional study for which blood, cerebrospinal fluid and post-mortem tissues are collected in patients with status epilepticus or epilepsy associated to dysimmune encephalitis as well as in control patients, to better understand the pathophysiology of these severe epileptic disorders.

Подробное описание

Epilepsy is one of the most common neurological condition which concerns around 50 million people worldwide. Epilepsy is characterized by a lasting predisposition to generate seizures. Epilepsy can present as heterogenous set of clinical symptoms and is related to extremely varied etiologies. Some epilepsies are triggered by antineuronal autoantibodies and/or complicated by a status epilepticus. These conditions may induce brain atrophy, and severe neurological sequels.

The severity of these epilepsies requires significant efforts to (i) identify new therapeutic strategies able to control the evolution of dysimmune encephalitis and refractory status epilepticus, (ii) to identify their etiologies and (iii) to propose neuroprotective strategies.

Therefore, the investigators will organize a collection of biological samples (blood, cerebrospinal fluid, post-mortem brain tissues) and paraclinical data (electroencephalogram, evoked potential, CT, MRI) in patients with severe epilepsies, whether or not associated with autoantibodies, and/or evolving into status epilepticus.

This study should bring new insights allowing to better understand mechanisms that trigger the emergence of an epileptic brain (epileptogenesis) through :

(i) the identification and characterization of new pathophysiological pathways involving autoimmunity directed against the cerebral cortex and associated with severe epilepsy (ii) the identification and characterization of pathophysiological pathways participating in the excitotoxicity observed in status epilepticus.

Вмешательства

• Другое Blood sampling, cerebrospinal fluid , post-mortem cerebral tissues (NA for the Group 3)
  Collection of biological samples and clinical/paraclinical data
• Другое Blood sampling, cerebrospinal fluid, stool sampling post-mortem cerebral tissues (NA for the Group 3)
  Collection of biological samples and clinical/paraclinical data

Первичные конечные точки

• Identification of (i) antibodies in the plasma and in the cerebrospinal fluid of patients with dysimmune encephalitis and (ii) biomarkers for neuronal death in the plasma and in the cerebrospinal fluid of patients with status epilepticus [Срок оценки: 9 months and 24 months]

Вторичные конечные точки (4)

• Identification of new dysimmune abnormalities [Срок оценки: 9 months and 24 months]
• Identification of specific EEG patterns associated to dysimmune encephalitis and/or status epilepticus [Срок оценки: 9 months and 24 months]
• Identification of new genetic pathways associated to dysimmune encephalitis and status [Срок оценки: 9 months and 24 months]
• Identification of new metabolic pathway that may participate in the excitotoxicity observed in status epilepticus or dysimmune encephalitis [Срок оценки: 9 months and 24 months]

Критерии участия

Критерии включения

Group 1:

• Patients aged 2 years or above, with status epilepticus.
• Affiliation to a French social security system excluding "Aide Médicale" Etat (AME).
• Patients or relatives have been informed and given free informed and written consent to participate
• Patients under legal protection (guardianship, curatorship) or not

Group 2:

• Patients aged 2 years or above, with clinical signs of epilepsy associated to dysimmune encephalitis.
• Affiliation to a French social security system excluding "Aide Médicale" Etat (AME).
• Patients or relatives have been informed and given free informed and written consent to participate
• Patients under legal protection (guardianship, curatorship) or not

Group 3:

• Patients aged 18 years or above, without status epilepticus and/or dysimmune encephalitis.
• Affiliation to a French social security system excluding "Aide Médicale" Etat (AME).
• Patients or relatives have been informed and given free informed and written consent to participate
• Patients under legal protection (guardianship, curatorship) or not

Критерии исключения

Group 1:

• Women with known or clinically detected pregnancy.
• Patient deprived of liberty
• Patients with known neurodegenerative disease.

Group 2:

• Women with known or clinically detected pregnancy.
• Patient deprived of liberty
• Patients have been already treated by corticoids or IgIV.

Group 3:

• Women with known or clinically detected pregnancy.
• Patient deprived of liberty.
• Patients with status epilepticus.
• Patients with known neurodegenerative disease, brain tumor, severe head trauma, meningitis, subarachnoid hemorrhages, stroke.

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Распределение

Нерандомизированное

Модель

Параллельные группы

Маскирование

Открытое

Основная цель

Фундаментальное исследование

Центры проведения

Франция · 1 центр

• Hôpital de la Pitié Salpêtrière — Paris

Идентификаторы

NCT: NCT04421846 · APHP200306 · 2020-A00053-36

Первоисточники (государственные реестры)

• ClinicalTrials.gov (NIH, США)

Открыть это исследование на ClinicalTrials.gov ↗