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A case-control study of clinical features, immunotherapy and long-term prognosis of autoimmune encephalitis

A case-control study of clinical features, immunotherapy and long-term prognosis of autoimmune encephalitis

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100048563
Enrollment
Unknown
Registered
2021-07-10
Start date
2021-07-01
Completion date
Unknown
Last updated
2022-03-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

autoimmune encephalitis

Interventions

Case series:None

Sponsors

Shenzhen People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Clinical manifestations: acute or subacute onset; 2. Auxiliary examination: with one or more of the following auxiliary examination findings, or combined with related tumors. (1) Abnormal cerebrospinal fluid: leukocytosis of cerebrospinal fluid (>5x10^6/L); or cytology of cerebrospinal fluid shows lymphocytic inflammation; or oligoclonal zone of cerebrospinal fluid is positive; (2) Neuroimaging or electrophysiological abnormalities: abnormal T2 or FLAIR signal in MRI limbic system, unilateral or bilateral, or abnormal T2 or FLAIR signal in other regions (excluding non-specific white matter changes and stroke); or high limbic system on PET Metabolic alterations, or multiple cortical and/or basal ganglia hypermetabolism; or EEG abnormalities: focal epilepsy or epileptiform discharges (in or outside the temporal lobe), or diffuse or multifocal slow waves rhythm; (3) Specific types of tumors associated with AEs, such as limbic encephalitis with small cell lung cancer, anti-NMDAR encephalitis with teratoma. 3. Confirmatory test: positive for autoantibodies against neuronal surface antigens. Antibody detection mainly adopts indirect immunofluorescence assay (IIF). According to the antigen substrate, it is divided into two types: cell based assay (CBA) and tissue based assay (TBA). CBA uses transfected cells expressing neuronal cell surface antigens, and TBA uses animal brain tissue sections as antigen substrates. CBA has high specificity and sensitivity. The patient's paired cerebrospinal fluid and serum samples should be tested as much as possible, and the initial dilution titers of cerebrospinal fluid and serum are 1:1 and 1:10, respectively. 3. Exclude other possible causes; 4. Reasonably exclude other etiologies (refer to the differential diagnosis section of this consensus).

Exclusion criteria

Exclusion criteria: Undiagnosed, suspected autoimmune encephalitis.

Design outcomes

Primary

MeasureTime frame
Cerebrospinal fluid;Mental symptoms;

Countries

China

Contacts

Public ContactXu Qianhui

Department of Neurogy Shenzhen People's Hospital

qianhuixu.jnu.edu@hotmail.com+86 13723428937

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026