Evidence map›Paper›PMID 39105896›Full record

ArticleJournal of neurology2024

LGI1 encephalitis: potentially complement-activating anti-LGI1-IgG subclasses 1/2/3 are associated with the development of hippocampal sclerosis.

Christian G Bien, Anna Rada, Markus Mertens, Corinna I Bien, Jan Bauer, Anne Hagemann, Friedrich G Woermann

Abstract read
In one paragraph

Article in Journal of neurology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Review
  3. Persistent Bilateral [Annals of clinical and translational neurology · 2026
    Article
  4. Plasma proteome in LGI-1 autoimmune encephalitis.Journal of neuroinflammation · 2026
    Article
  5. Observational
  6. Article
  7. Autoimmune encephalitis-associated epilepsy.Nature reviews. Neurology · 2025
    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

7 authors.

Christian G BienDepartment of Epileptology, Krankenhaus Mara, Bethel Epilepsy Center, Medical School OWL, Bielefeld University, Maraweg 21, 33617, Bielefeld, Germany. christian.bien@gmx.de.ORCID http://orcid.org/0000-0003-2225-8654
Anna RadaDepartment of Epileptology, Krankenhaus Mara, Bethel Epilepsy Center, Medical School OWL, Bielefeld University, Maraweg 21, 33617, Bielefeld, Germany.ORCID http://orcid.org/0000-0003-2538-0786
Markus MertensSociety for Epilepsy Research, Bielefeld, Germany.
Corinna I BienLaboratory Krone, Bad Salzuflen, Germany.
Jan BauerDepartment of Neuroimmunology, Center for Brain Research, Medical University of Vienna, Vienna, Austria.ORCID http://orcid.org/0000-0001-5802-8047
Anne HagemannSociety for Epilepsy Research, Bielefeld, Germany.ORCID http://orcid.org/0000-0002-8158-7442
Friedrich G WoermannDepartment of Epileptology, Krankenhaus Mara, Bethel Epilepsy Center, Medical School OWL, Bielefeld University, Maraweg 21, 33617, Bielefeld, Germany.ORCID http://orcid.org/0009-0007-9502-0491

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Two-thirds of published patients with anti-leucine rich, glioma inactivated 1 (LGI1) encephalitis develop hippocampal sclerosis (HS). It is likely that this contributes to residual cognitive long-term deficits and the risk of epilepsy. Almost all patients harbor anti-LGI1-immunoglobulin G-(IgG-) subclass 4, which is considered a "benign", non-destructive subclass. In contrast, neuropathological case studies have suggested that the classical complement cascade may contribute to mediotemporal cell death in patients with LGI1 antibodies. IgG subclasses 1, 2, or 3 are required to initiate this cascade. We hypothesized that patients with these anti-LGI1-IgG1/2/3 in addition to IgG4 have a higher risk of developing HS than patients with anti-LGI1-IgG4 alone. We retrospectively assessed all anti-LGI1 encephalitis patients from this center with anti-LGI1-IgG-subclass information and follow-up MRI available. Nine out of 20 patients had developed HS (45%). Volumetric FreeSurfer analysis confirmed the visual HS diagnoses. HS and a lower hippocampal volume were associated with anti-LGI1-IgG1/2/3. All six patients with this IgG subclass status developed HS. There was no association with older or younger age at onset, female sex, longer latency from disease onset to start of immunotherapy, less intense immunotherapy, higher serum titers of LGI1 antibodies, LGI1 antibodies in CSF or higher LGI1-specific antibody indices. There was no association between anti-LGI1-IgG1/2/3 status and neuropsychological performance, epilepsy, or general neurological performance. This confirms our hypothesis that anti-LGI1-IgG1/2/3 in serum puts patients at risk of developing HS. If these findings can be confirmed and clinically corroborated, patients with anti-LGI1-IgG1/2/3 might become candidates for anti-complement-directed immunological treatments.

Indexed as

AutoantibodiesHippocampusImmunoglobulin GIntracellular Signaling Peptides and ProteinsSclerosisAdultAgedEncephalitisFemaleHippocampal SclerosisHumansMagnetic Resonance ImagingMaleMiddle AgedRetrospective Studiesanti-leucine-rich glioma-inactivated 1 autoantibodyAutoantibodiesImmunoglobulin GIntracellular Signaling Peptides and ProteinsLGI1 protein, humanHippocampal sclerosisImmunoglobulin G subclassesLGI1 antibodiesRisk factors

Identifiers

PMID39105896
PMCPMC11377613

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Registered trials

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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.