Evidence map›Paper›PMID 38635129›Full record

ArticleActa neurologica Belgica2024

Clinical features, cerebrospinal fluid changes, and prognosis in Chinese patients with autoimmune encephalitis.

Wu Yan, Wang Mengke, Su Zhiqiang, Gu Jiaao, Guan Fulin

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Article in Acta neurologica Belgica, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Predictors for identifying autoimmune encephalitis in pediatric patients.Frontiers in cellular and infection microbiology · 2026
    Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Wu YanFirst Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang, China.
Wang MengkeFirst Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang, China.
Su ZhiqiangFirst Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang, China.
Gu JiaaoFirst Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang, China. jiaaogu@outlook.com.
Guan FulinFirst Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang, China. fulinguancn@outlook.com.ORCID http://orcid.org/0000-0003-4693-8208

Funding

First affiliated hospital of Harbin Medical University 2016B004
6 · The paper itself

Abstract

introductionAutoimmune encephalitis (AE) is a rare, treatable disease of the central nervous system (CNS) caused by an antibody-related immune response. This study is to investigate the correlation of clinical features, cerebrospinal fluid (CSF) characteristics, and prognosis in patients with AE.

methodsA total of 71 patients diagnosed with antibody-positive AE were retrospectively analyzed. The patients were divided into three groups: anti-NMDAR group, anti-LGI1 group, and other types. Clinical data were collected to analyze clinical features and CSF results, and prognosis was determined by modified Rankin Scale (mRS).

resultsThere was statistical difference in the incidences of decreased consciousness level (P < 0.001), memory loss (P = 0.017), speech disorders (P = 0.035), and dyskinesia (P = 0.001) in different antibodies groups. Younger age (P = 0.018), elevated CSF chloride content (P = 0.006), and white blood cells > 50/mm

conclusionThere are differences in age, gender, clinical characteristics, and CSF results in different subtypes of AE. First-line therapy failure would have poor functional recovery, and delayed therapy would increase the risk of relapse. Chloride ion content and white blood cell count in cerebrospinal fluid are positively correlated with the patient's exacerbation and admission to ICU. These indicators have certain clinical value for the prognosis of AE patients.

Indexed as

AutoantibodiesEncephalitisHashimoto DiseaseAdolescentAdultAgedChildChinaEast Asian PeopleFemaleHumansMaleMiddle AgedPrognosisRetrospective StudiesYoung Adultanti-leucine-rich glioma-inactivated 1 autoantibodyAutoantibodiesAutoimmune encephalitisCerebrospinal fluidClinical manifestationsICU admissionPrognosis

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.