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BRIEF TITLE * (in English and Sufficiently Descriptive) Role of MRI in Anti-LGI1 Encephalitis

Completed
Conditions
Autoimmune Encephalitis
Interventions
Other: Retrospective evaluation of specific brain MRI features
Registration Number
NCT05825690
Lead Sponsor
Hospices Civils de Lyon
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.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
50
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

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
LGI1- PatientsRetrospective evaluation of specific brain MRI featuresPatients affected by autoimmune encephalitis with antibodies against LGI1
Primary Outcome Measures
NameTimeMethod
Cognitive dysfunction and disability12 months

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

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Centre de référence des syndromes neurologiques paranéoplasiques et encéphalites autoimmunes

🇫🇷

Lyon, France

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