Evidence map›Paper›PMID 41928193›Full record

Observational studyBMC psychiatry2026

Psychiatric symptoms as clinical warning signals of adult anti-LGI-1 encephalitis: an observational cohort study.

Yujie Yi, Xiaohong Fu, Yingzhu Zhao, Hong Zhou, Kaiye Xing, Ying Yu, Jie Wang

Abstract readObservational Study
In one paragraph

Observational study in BMC psychiatry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

1 citing paper in PubMed.

  1. 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

7 authors.

Yujie Yi *First Clinical Medical College of Shanxi Medical University, Taiyuan, China.
Xiaohong Fu *First Clinical Medical College of Shanxi Medical University, Taiyuan, China.
Yingzhu ZhaoFirst Clinical Medical College of Shanxi Medical University, Taiyuan, China.
Hong ZhouFirst Clinical Medical College of Shanxi Medical University, Taiyuan, China.
Kaiye XingFirst Clinical Medical College of Shanxi Medical University, Taiyuan, China.
Ying YuFirst Clinical Medical College of Shanxi Medical University, Taiyuan, China.
Jie WangDepartment of Neurology, First Hospital/First Clinical Medical College of Shanxi Medical University, No.85, Jiefang South Road, Yingze Street, Taiyuan, Shanxi, 030000, China. luwanglu2012@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesAnti-LGI-1 (Anti-leucine-rich glioma-inactivated 1) encephalitis is one of the most common types of autoimmune encephalitis, and psychiatric symptoms are among its important clinical manifestations. Relevant clinical studies are still in the minority. This study aimed to investigate the clinical features and disease outcomes of adult anti-LGI1 encephalitis patients with psychiatric symptoms.

methodsThis study retrospectively analyzed 68 patients with anti-LGI-1 encephalitis from January 2016 to August 2024, grouped by the presence of psychiatric symptoms. Comparisons included clinical features, laboratory findings, MRI features, treatment, and prognosis.

resultsThis study included 50 patients completing the 12-month follow-up. 64% of the patients developed psychiatric symptoms during the disease, with personality changes, hallucinations, and mood disorder being the most common manifestations. Patients with psychiatric symptoms had a higher rate of cerebrospinal fluid antibodies (p < 0.001), more severe blood-brain barrier damage indicated (p = 0.009), greater likelihood of cognitive decline (p = 0.016), electrolyte imbalances like hyponatremia (p = 0.02), worse mRS and CASE scores at onset (p < 0.001), higher rates of delayed immunotherapy initiation (p = 0.003) and second-line therapy (p = 0.042), as well as poorer prognosis after one year with more relapses (p = 0.016).

conclusionPatients with anti-LGI-1 encephalitis show a variety of psychiatric symptoms, often portending a more severe disease phenotype. This suggests that psychiatric symptoms may indicate the disease’s severity and prognosis early on. CLINICAL TRIAL NUMBER: Not applicable.

Indexed as

AutoantibodiesEncephalitisAdultAgedFemaleHumansIntracellular Signaling Peptides and ProteinsMaleMiddle AgedMood DisordersPrognosisRetrospective Studiesanti-leucine-rich glioma-inactivated 1 autoantibodyAutoantibodiesIntracellular Signaling Peptides and ProteinsLGI1 protein, humanAnti-LGI-1 encephalitisAutoimmune diseaseCognitive impairmentOutcomePsychiatric symptoms

Identifiers

PMID41928193
PMCPMC13188490

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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.