Evidence map›Paper›PMID 40760473›Full record

ArticleBMC neurology2025

Efficacy of early rituximab treatment in anti-mGluR1 encephalitis: a case report.

Kazuki Yamada, Hiroaki Yaguchi, Shuntaro Nakamura, Kazuhiro Horiuchi, Shintaro Fujii, Taichi Nomura, Akihiko Kudo, Akira Takekoshi, Nobuaki Yoshikura, Akio Kimura and 2 more

Abstract readCase Reports
In one paragraph

Article in BMC neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. 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

12 authors.

Kazuki YamadaDepartment of Neurology, Hakodate Municipal Hospital, 1-10-1, Minatocho, Hakodate, Japan. yamak354546@gmail.com.
Hiroaki YaguchiDepartment of Neurology, Faculty of Medicine, Graduate School of Medicine, Hokkaido University, N-15 W-7, Kita-ku, Sapporo, Japan. yaguchi-h@pop.med.hokudai.ac.jp.
Shuntaro NakamuraDepartment of Neurology, Hakodate Municipal Hospital, 1-10-1, Minatocho, Hakodate, Japan.
Kazuhiro HoriuchiDepartment of Neurology, Hakodate Municipal Hospital, 1-10-1, Minatocho, Hakodate, Japan.
Shintaro FujiiDepartment of Neurology, Faculty of Medicine, Graduate School of Medicine, Hokkaido University, N-15 W-7, Kita-ku, Sapporo, Japan.
Taichi NomuraDepartment of Neurology, Faculty of Medicine, Graduate School of Medicine, Hokkaido University, N-15 W-7, Kita-ku, Sapporo, Japan.
Akihiko KudoDepartment of Neurology, Faculty of Medicine, Graduate School of Medicine, Hokkaido University, N-15 W-7, Kita-ku, Sapporo, Japan.
Akira TakekoshiDepartment of Neurology and Geriatrics, Gifu University Graduate School of Medicine, Gifu, Japan.
Nobuaki YoshikuraDepartment of Neurology and Geriatrics, Gifu University Graduate School of Medicine, Gifu, Japan.
Akio KimuraDepartment of Neurology and Geriatrics, Gifu University Graduate School of Medicine, Gifu, Japan.
Takayoshi ShimohataDepartment of Neurology and Geriatrics, Gifu University Graduate School of Medicine, Gifu, Japan.
Ichiro YabeDepartment of Neurology, Faculty of Medicine, Graduate School of Medicine, Hokkaido University, N-15 W-7, Kita-ku, Sapporo, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAnti-mGluR1 encephalitis is a form of autoimmune encephalitis, with limited reports globally and only two cases reported from Japan. There are uncertainties regarding the optimal immunosuppressive agents and individual drug responses. Herein, we report a case of anti-mGluR1 encephalitis from Japan, notable for a favorable outcome after an early rituximab initiation and an observed increase in cerebellar blood flow during the early disease stages. CASE PRESENTATION: The patient was a 65-year-old woman who experienced dizziness for 3 months, followed by worsening gait instability. She was referred to our department due to progressive difficulty standing and walking. Neurological examination revealed dysarthria, severe cerebellar ataxia, and impaired performance on the finger-to-nose and knee-to-heel tests. Blood tests were negative for rheumatologic autoantibodies, and cerebrospinal fluid (CSF) analysis showed a cell count of 4/µL and a protein level of 40.0 mg/dL. However, the IgG index was elevated at 1.35, and oligoclonal bands were positive. Brain magnetic resonance imaging showed no abnormalities, but ¹²³I-iodoamphetamine single-photon emission computed tomography revealed mild hyperperfusion in the bilateral cerebellar hemispheres. Based on the clinical presentation, immune-mediated cerebellar ataxia was suspected. The patient was treated with intravenous methylprednisolone, oral prednisolone, and intravenous immunoglobulin. Further diagnostic testing using tissue- and cell-based assays detected mGluR1 antibodies in pretreatment serum and CSF, confirming the diagnosis of anti-mGluR1 encephalitis. As the initial treatment was insufficient, rituximab was administered, leading to significant improvement, including the ability to walk unaided. At the most recent follow-up, >6 months postonset, she showed no symptom progression or cerebellar atrophy.

conclusionsWe experienced a case of anti-mGluR1 encephalitis with increased cerebellar blood flow, where early RTX administration led to a favorable outcome. Its early use, as an acute treatment and for maintenance, may help prevent recurrence and contribute to a positive prognosis.

Indexed as

Antibodies, Monoclonal, Murine-DerivedEncephalitisImmunologic FactorsAgedAutoantibodiesFemaleHumansReceptors, Metabotropic GlutamateRituximabTreatment OutcomeAntibodies, Monoclonal, Murine-DerivedAutoantibodiesImmunologic Factorsmetabotropic glutamate receptor type 1Receptors, Metabotropic GlutamateRituximabAnti-mGluR1 encephalitisCerebellar blood flowMGluR1 antibodyRituximab

Identifiers

PMID40760473
PMCPMC12323163

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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.