Ignite Creation Date:
2025-12-24 @ 5:08 PM
Ignite Modification Date:
2025-12-24 @ 5:08 PM
Study NCT ID:
NCT04463550
Status:
UNKNOWN
Last Update Posted:
2020-07-09
First Post:
2020-04-17
Is NOT Gene Therapy:
False
Has Adverse Events:
False
Brief Title:
GFAP Auto-immunity : a French Cohort Study
Sponsor:
Organization:
Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}}, 'protocolSection': {'designModule': {'studyType': 'OBSERVATIONAL', 'designInfo': {'timePerspective': 'RETROSPECTIVE', 'observationalModel': 'COHORT'}, 'enrollmentInfo': {'type': 'ESTIMATED', 'count': 38}, 'patientRegistry': False}, 'statusModule': {'overallStatus': 'UNKNOWN', 'lastKnownStatus': 'RECRUITING', 'startDateStruct': {'date': '2019-09-01', 'type': 'ACTUAL'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2020-06', 'completionDateStruct': {'date': '2020-11-01', 'type': 'ESTIMATED'}, 'lastUpdateSubmitDate': '2020-07-03', 'studyFirstSubmitDate': '2020-04-17', 'studyFirstSubmitQcDate': '2020-07-03', 'lastUpdatePostDateStruct': {'date': '2020-07-09', 'type': 'ACTUAL'}, 'studyFirstPostDateStruct': {'date': '2020-07-09', 'type': 'ACTUAL'}, 'primaryCompletionDateStruct': {'date': '2020-01-01', 'type': 'ACTUAL'}}, 'outcomesModule': {'otherOutcomes': [{'measure': 'demographic data of patients GFAP-IgG positive : phenotype', 'timeFrame': '13 months', 'description': 'Report if caucasian (yes or no) retrospectively provided by the treating\n\nphysicians using a structured questionnaire'}, {'measure': 'demographic data of patients GFAP-IgG positive : sex', 'timeFrame': '13 months', 'description': 'Report if female sex (yes or no) retrospectively provided by the treating\n\nphysicians using a structured questionnaire\n\nphysicians using a structured questionnaire'}, {'measure': 'associated conditions of patients GFAP-IgG positive', 'timeFrame': '13 months', 'description': 'Report if neoplastic and dysimmune associated diseases and T cell dysregulation condition (yes or no)\n\nphysicians using a structured questionnaire\n\nphysicians using a structured questionnaire'}, {'measure': 'Report cerebrospinal fluid white cell count', 'timeFrame': '13 months', 'description': 'white cell count (/mm3)'}, {'measure': 'Report cerebrospinal fluid protein level', 'timeFrame': '13 months', 'description': 'protein level (g/L)'}, {'measure': 'Report cerebrospinal fluid glucose level', 'timeFrame': '13 months', 'description': 'glucose level (mmol/L)'}, {'measure': 'Report number of oligoclonal bands in cerebrospinal fluid', 'timeFrame': '13 months', 'description': 'number of oligoclonal bands'}, {'measure': 'Describe MRI features.', 'timeFrame': '13 months', 'description': 'Head and medullar MRI at diagnostic and follow up were reviewed by a neuroradiologist. scale) at each relapse and last follow up.'}, {'measure': 'Report other paraclinic findings : electroencephalographic results.', 'timeFrame': '13 months', 'description': 'Describe electroencephalographic results at diagnostic and follow up when done .'}, {'measure': 'Report other paraclinic findings : electromyographic results.', 'timeFrame': '13 months', 'description': 'Describe electromyographic results at diagnostic and follow up when done .'}, {'measure': 'Report ophthalmic exam : visual acuity', 'timeFrame': '13 months', 'description': 'Describe visual acuity (/10) at diagnostic and follow up when done .'}, {'measure': 'Report ophthalmic exam : ocular fundus.', 'timeFrame': '13 months', 'description': 'Describe ocular fundus at diagnostic and follow up results when done .'}, {'measure': 'Report ophthalmic exam : visual field.', 'timeFrame': '13 months', 'description': 'Describe visual field at diagnostic and follow up when done .'}, {'measure': 'Report ophthalmic exam : optical coherence tomography.', 'timeFrame': '13 months', 'description': 'Describe optical coherence tomography (RNFL thickness) at diagnostic and follow up when done .'}, {'measure': 'Report histologic findings.', 'timeFrame': '13 months', 'description': 'Describe histologic results at diagnostic and follow up when done .'}, {'measure': 'Report treatments and response.', 'timeFrame': '13 months', 'description': 'Describe acute and long-term treatments administered and response.'}, {'measure': 'Report outcome.', 'timeFrame': '13 months', 'description': 'Describe outcome (modified Rankin scale) at each relapse and last follow up.'}], 'primaryOutcomes': [{'measure': 'Report retrospectively clinical data of patients GFAP-IgG positive.', 'timeFrame': '13 months', 'description': 'Describe prodromes (yes or no), neurologic signs and clinical course (acute/subacute - yes or\n\nno - or progressive onset - yes or no), if admitted in intensive care units (yes or no), retrospectively provided by\n\nthe treating physicians using a structured questionnaire.or progressive onset), if admitted in intensive care units, neoplastic and dysimmune associated diseases and T cell dysregulation condition .'}], 'secondaryOutcomes': [{'measure': 'Describe GFAP-antibody test results.', 'timeFrame': '13 months', 'description': 'positivity of GFAP α -IgG in cerebrospinal fluid, in serum and isoform type at diagnostic and follow up.\n\npositivity of GFAP α -IgG in cerebrospinal fluid, in serum and isoform type at diagnostic and follow up.'}, {'measure': 'demographic data of patients GFAP-IgG positive : age at onset', 'timeFrame': '13 months', 'description': 'age at onset (years) retrospectively provided by the treating\n\nphysicians using a structured questionnaire'}]}, 'oversightModule': {'oversightHasDmc': False, 'isFdaRegulatedDrug': False, 'isFdaRegulatedDevice': False}, 'conditionsModule': {'keywords': ['Acidic Protein IgG', 'astrocytopathy', 'meningoencephalomyelitis', 'perivascular-radial parenchymal enhancement', 'autoimmune', 'paraneoplasic'], 'conditions': ['Autoimmune GFAP Astrocytopathy']}, 'descriptionModule': {'briefSummary': 'Glial fibrillary acidic protein (GFAP)-Immunoglobulin G (IgG) have recently been described as a biomarker of a novel inflammatory central nervous system (CNS) disorder, termed autoimmune GFAP astrocytopathy. Thus far, four major clinical series have been published (two from Mayo Clinic USA, one from Italy and one from China). GFAP-IgG detected in serum or in cerebrospinal fluid, by tissue-based assay and confirmed by cell-based assay, are associated with encephalitis or meningoencephalitis of acute or subacute onset, less frequently with myelitis or optic disk edema. The characteristic MRI feature is brain linear perivascular radial gadolinium enhancement in the white matter perpendicular to the ventricle, consistent with the immunohistochemical staining pattern of GFAP in rodent brain sections. Approximately 20% of reported cases are associated with a neoplasm (ovarian teratoma mostly). Coexisting neural autoantibodies are described in some patients, N-methyl-D-aspartate (NMDA)-receptor (R)-IgG mostly, followed by aquaporin 4 (AQP4)-IgG. The disease is usually corticosteroid responsive although relapse can occur. In contrast, Chinese patients display poorer outcomes. Pathophysiology is not well understood but the intracellular antigen location makes GFAP-IgG unlikely pathogenic whereas animal models and neuropathologic data suggest a T-cell immune-mediated disorder.\n\nThe aim of the investigators is to report the first French cohort of patients GFAP-IgG positive. Investigators retrospectively assessed clinical, immunological and radiological features, treatment response and outcomes.'}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['CHILD', 'ADULT', 'OLDER_ADULT'], 'samplingMethod': 'NON_PROBABILITY_SAMPLE', 'studyPopulation': 'Patients GFAP-IgG positive in serum and/or CSF', 'healthyVolunteers': False, 'eligibilityCriteria': 'Inclusion Criteria:\n\n* Positive GFAP-Ab in serum and/or CSF tested by immunohistochemistry on mouse brain slices and confirmed by cell-based assay (CBA) of HEK293 cells expressing GFAP.\n* Diagnosis and follow-up in France\n* No age limit : from 0 to unlimited age\n\nExclusion Criteria:\n\n* Patients GFAP-IgG negative in serum and CSF\n* Absence of complete clinicopathological data\n* Foreign follow-up'}, 'identificationModule': {'nctId': 'NCT04463550', 'acronym': 'GFAP', 'briefTitle': 'GFAP Auto-immunity : a French Cohort Study', 'organization': {'class': 'OTHER', 'fullName': 'Hospices Civils de Lyon'}, 'officialTitle': 'GFAP Auto-immunity : a French Cohort Study', 'orgStudyIdInfo': {'id': 'GFAP'}}, 'armsInterventionsModule': {'armGroups': [{'label': 'Patients GFAP-IgG positive in serum and/or CSF', 'description': 'Patients developing clinical autoimmune encephalitis or meningoencephalomyelitis with anti-GFAP antibodies, managed by the National Reference Center for Paraneoplastic Syndromes and Autoimmune Encephalitis or the National Reference Center for Centre de référence for Neuro-inflammatory diseases of the brain and the spinal cord at the Neurological Hospital of Bron.', 'interventionNames': ['Other: Description and analysis']}], 'interventions': [{'name': 'Description and analysis', 'type': 'OTHER', 'description': 'Retrospective, non-interventional study, using clinical, biological, radiological and therapeutic data collected during the initial diagnosis and follow-up.', 'armGroupLabels': ['Patients GFAP-IgG positive in serum and/or CSF']}]}, 'contactsLocationsModule': {'locations': [{'zip': '69250', 'city': 'Bron', 'status': 'RECRUITING', 'country': 'France', 'contacts': [{'name': 'Romain MARIGNIER', 'role': 'CONTACT', 'email': 'romain.marignier@chu-lyon.fr', 'phone': '04-72-35-75-22'}, {'name': 'Géraldine PICARD', 'role': 'CONTACT', 'email': 'geraldine.picard@chu-lyon.fr', 'phone': '04 72 35 58 42'}], 'facility': 'Hospices Civils de Lyon', 'geoPoint': {'lat': 45.73865, 'lon': 4.91303}}], 'centralContacts': [{'name': 'Romain MARIGNIER, Dr', 'role': 'CONTACT', 'email': 'romain.marignier@chu-lyon.fr', 'phone': '04-72-35-75-22'}, {'name': 'Géraldine PICARD', 'role': 'CONTACT', 'email': 'geraldine.picard@chu-lyon.fr', 'phone': '04 72 35 58 42'}], 'overallOfficials': [{'name': 'Romain MARIGNIER', 'role': 'STUDY_DIRECTOR', 'affiliation': 'Centre de référence des maladies inflammatoires rares du cerveau et de la moelle, Lyon, France'}]}, 'ipdSharingStatementModule': {'ipdSharing': 'NO'}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'Hospices Civils de Lyon', 'class': 'OTHER'}, 'responsibleParty': {'type': 'SPONSOR'}}}}