Observational studyFrontiers in immunology2026
Systemic and organ-specific autoantibodies and worse outcomes in autoimmune encephalitis: a multicenter cohort study.
Observational study in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
10 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Objective: Autoimmune encephalitis (AE) is a group of neuroinflammatory disorders with variable clinical outcomes. Despite the identification of specific neuronal autoantibodies, their clinical presentation and outcomes were significantly variable in clinical practice, suggesting the influence of additional factors beyond the primary autoantibody. Systemic and Organ-Specific autoantibodies (SAOS-Ab) are frequently detected in AE patients, but their clinical role remains incompletely characterized. We hypothesized that the coexistence of SAOS-Ab in AE was associated with a more severe disease course and higher relapse risk. Methods: In this multicenter, retrospective cohort study, we analyzed 218 AE patients from four Chinese tertiary centers (January 2018-October 2022). AE patients were stratified into SAOS-Ab-positive and SAOS-Ab-negative groups based on serological testing. We compared demographic, clinical, and immunological features. The primary outcomes were disease severity at onset (measured by clinical assessment scale in autoimmune encephalitis [CASE] scores), short-term functional outcome (measured by modified Rankin scale [mRS] scores), and 24-month relapse risk. Multivariable logistic and Cox regression analyses were employed to identify independent predictors of poor outcome and relapse. Results: A high prevalence (57.3%, 125/218) of SAOS-Ab was observed. The SAOS-Ab-positive group had a higher female proportion (55.2% vs 35.5%, Conclusion: SAOS-Ab is a prevalent and clinically relevant biomarker in AE, associated with distinct immunologic profiles, more severe disease, and significantly increased relapse risk. These findings support the integration of SAOS-Ab testing into AE management to facilitate early risk stratification and more frequent follow-up.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.