Evidence map›Paper›PMID 35715951›Full record

ArticleAnnals of clinical and translational neurology2022

Disease progression and brain atrophy in NMDAR encephalitis: Associated factor & clinical implication.

Woo-Jin Lee, Soon-Tae Lee, Do-Yong Kim, Soyun Kim, Kon Chu

Open access · goldAbstract read
In one paragraph

Article in Annals of clinical and translational neurology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.4field-weighted citation impact, top 18% of its field
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

8 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Review
  3. Autoimmune encephalitis.Nature reviews. Disease primers · 2025
    Review
  4. NMDAR Encephalitis: Identifying Prognostic Biomarkers.Journal of clinical neurology (Seoul, Korea) · 2025
    Article
  5. Article
  6. Article
  7. Outcome and Sequelae of Autoimmune Encephalitis.Journal of clinical neurology (Seoul, Korea) · 2024
    Review
  8. Review
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 at 1 institution in 1 country.

Woo-Jin LeeDepartment of Neurology, Seoul National University Hospital, Seoul, South Korea.ORCID 0000-0001-6090-7921
Soon-Tae LeeDepartment of Neurology, Seoul National University Hospital, Seoul, South Korea.ORCID 0000-0003-4767-7564
Do-Yong KimDepartment of Neurology, Seoul National University Hospital, Seoul, South Korea.
Soyun KimDepartment of Neurology, Seoul National University Hospital, Seoul, South Korea.
Kon ChuDepartment of Neurology, Seoul National University Hospital, Seoul, South Korea.ORCID 0000-0001-5863-0302
Seoul National University Hospital · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveWe investigated the longitudinal pattern, determining factors, and clinical implications of brain volume changes in N-methyl d-aspartate receptor-antibody (NMDAR) encephalitis.

methodsBaseline clinical profiles, treatment profiles, and outcome measured using the Clinical Assessment Scale in Autoimmune Encephalitis (CASE) and modified Rankin scale (mRS) were obtained from a long-term clinical database documenting an NMDAR encephalitis cohort. In serial MRI, the change in the normalized volume of different brain regions from the baseline evaluation was measured. At each MRI evaluation time point, the cumulative disease burden (CASE score × months) and the cumulative duration of status epilepticus were also evaluated.

resultsThirty-six patients were followed-up for 28.5 months (range 12-63 months). The volume ratio at last MRI to baseline was the lowest in the cerebellum (94.4 ± 5.7%, p < 0.001). Once developed, cerebellar volume reduction followed a progressive course until 2 years from disease onset. The degree of cerebellar volume reduction was positively correlated with mRS and total CASE scores (all, p < 0.001), and CASE scores in the domains of memory, language, and psychiatric problems, gait instability/ataxia, and weakness (all, p < 0.01). In linear mixed model analyses, the degree of cerebellar volume reduction was associated with cumulative disease burden up to 2 years (p < 0.001) and duration of status epilepticus (p < 0.001), and delayed removal of teratoma for ≥1 month (p = 0.006).

interpretationIn NMDAR encephalitis, cerebellar volume reduction was progressive once developed. Cerebellar volume reduction might reflect disease burden and extent of progression and be associated with poor outcomes in multiple functional domains.

Indexed as

Anti-N-Methyl-D-Aspartate Receptor EncephalitisCentral Nervous System DiseasesNeurodegenerative DiseasesStatus EpilepticusAtrophyAutoantibodiesBrainDisease ProgressionEncephalitisHashimoto DiseaseHumansAutoantibodies

Identifiers

PMID35715951
PMCPMC9268893
OpenAlexW4283077769

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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 Socratic graph.