Neuropathy and Anti-GFAP Antibodies

NCT ID: NCT05742087

Last Updated: 2023-02-23

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

120 participants

Study Classification

OBSERVATIONAL

Study Start Date

2022-09-01

Study Completion Date

2023-05-01

Brief Summary

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Anti-Glial Fibrillary Acidic Protein (GFAP) are antibodies associated to inflammatory diseases of the central nervous system. The GFAP protein is highly expressed by astrocytes explaining these syndromes, but GFAP is also expressed by immature and non-myelinating Schwann cells. Thus, these antibodies could also lead to damages of the peripheral nervous system (PNS). Moreover, such damages have already been reported on small studies, and there is a need for larger cohorts.

The investigators will use the cohort of patients with neurological syndromes and anti-GFAP antibodies identified in the cerebrospinal fluid (CSF) of the "Reference center for paraneoplastic neurological syndromes and autoimmune encephalitis" to determine the frequency of the PNS involvement in these patients.

Detailed Description

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Conditions

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Neurological Diseases or Conditions Neurological Diseases Associated to Anti GFAP Antibodies

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

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Patients presenting with neurological symptoms and anti-GFAP antibodies in the CSF.

This is a non-interventional study involving biological samples. Samples are already stored in biobank repositories and collected as part of "good clinical practice" in the diagnostic process of patients with suspected autoimmune encephalitis, meaning that the standard diagnostic and therapeutic approaches will not be altered in the selected study population. Patients have already gave explicit written consent for biological specimens sampling and storage at the "iological Resource Center of the Hospices Civils de Lyon" (CRB-HCL) (including tissue, cells or biological fluids).

The group will be composed of patients included in the French cohort of patients with neurological syndromes and anti-GFAP antibodies in the CSF.

Clinical examination

Intervention Type OTHER

The examination performed by the clinician of the patient will be analyzed from the cohort as previously explained.

electroneuromyography (ENMG)

Intervention Type OTHER

Data from the ENMGs will be extracted from the cohort and analyzed.

Interventions

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Clinical examination

The examination performed by the clinician of the patient will be analyzed from the cohort as previously explained.

Intervention Type OTHER

electroneuromyography (ENMG)

Data from the ENMGs will be extracted from the cohort and analyzed.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* \- Age \> 18 years old
* Neurological symptoms
* Anti-GFAP antibodies identified in the CSF

Exclusion Criteria

* \- Uncomplete data in the medical records of patients
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Hospices Civils de Lyon

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Centre de référence des syndromes neurologiques paranéoplasiques et encéphalites autoimmunes

Lyon, , France

Site Status

Countries

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France

Other Identifiers

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22-5018

Identifier Type: -

Identifier Source: org_study_id

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