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Clinical Trials/NCT05825690
NCT05825690
Completed
N/A

Investigating the Prognostic Role of Brain MRI in Anti-LGI1 Encephalitis

Hospices Civils de Lyon1 site in 1 country50 target enrollmentJune 20, 2022

Overview

Phase
N/A
Intervention
Not specified
Conditions
Autoimmune Encephalitis
Sponsor
Hospices Civils de Lyon
Enrollment
50
Locations
1
Primary Endpoint
Cognitive dysfunction and disability
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

The term "autoimmune encephalitis" denotes an heterogenous group of diseases commonly associated with autoantibodies targeting neural or glial antigens. Patients harboring antibodies against the leucine-rich glioma-inactivated protein 1 (LGI1) usually respond well to immunotherapy, but a significant percentage develop cognitive sequelae and disability nonetheless. These patients would likely benefit for more aggressive and prolonged immunotherapy, aiming to prevent permanent neurological deficits. Identifying features predicting poor outcome would be crucial to guide treatment decisions. Brain magnetic resonance imaging is a key diagnostic tool in the acute phase, but radiological changes may also appear in follow-up studies, including global brain atrophy, hippocampal atrophy and mesial temporal sclerosis. We hypothesize that specific changes identifiable in the acute and chronic phase underlie a higher risk of poor outcome and persistent neurological deficits.

Registry
clinicaltrials.gov
Start Date
June 20, 2022
End Date
December 20, 2022
Last Updated
3 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • - Patients with a definite diagnosis of LGI1-antibody-associated encephalitis
  • available MRI records
  • Ascertained positivity for LGI1-antibodies in serum and/or CSF

Exclusion Criteria

  • - Positivity for another antibody against neural or glial antigens
  • MRI images not available
  • Not enough clinical data to ascertain outcome

Outcomes

Primary Outcomes

Cognitive dysfunction and disability

Time Frame: 12 months

Main outcome measures will include cognitive dysfunction measured by appropriate neuropsychological evaluations, and psychiatric symptoms; it will be "none", "light", "moderate", "severe"

Study Sites (1)

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