Evidence map›Paper›PMID 39891731›Full record

ArticleJournal of neurology2025

Hippocampal dysfunction after autoimmune encephalitis depending on the antibody type.

Martin Hänsel, Heinz Reichmann, Antje Haehner, Henning Schmitz-Peiffer, Hauke Schneider

Abstract read
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Article in Journal of neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Martin HänselDepartment of Neurology, University of Dresden, Fetscherstraße 74, 01307, Dresden, Germany.ORCID http://orcid.org/0000-0001-9300-1130
Heinz ReichmannDepartment of Neurology, University of Dresden, Fetscherstraße 74, 01307, Dresden, Germany.
Antje HaehnerDepartment of Otorhinolaryngology, Medical Faculty Carl-Gustav Carus, Smell and Taste Clinic, Technical University of Dresden, Dresden, Germany.
Henning Schmitz-Peiffer *Department of Neurology, University of Dresden, Fetscherstraße 74, 01307, Dresden, Germany.
Hauke Schneider *Department of Neurology, University of Dresden, Fetscherstraße 74, 01307, Dresden, Germany. hauke.schneider@uk-augsburg.de.ORCID http://orcid.org/0000-0002-9641-0922

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundComprehensive neurocognitive function analyses of autoimmune encephalitis (AE) patients, especially long-term ones, are rare. This study aims to measure cognitive function in patients diagnosed with AE.

methodsThis case-control study included AE patients (n = 11) with antibodies against NMDA receptor (NMDAR) (n = 4), VGKC (n = 3), GAD (3), and one antibody-negative patient. The control group contained 12 pneumococcal meningo-encephalitis patients (PC). Subgroup analyses compared AE patients with and without NMDAR antibodies. Neurocognitive tests were performed to evaluate verbal and visual memory, face recognition, attentional capacity, incidental learning capacity, and overall cognitive function (Montreal cognitive assessment, MoCA). Limbic structural involvement was assessed through magnetic resonance imaging (MRI). Statistical analyses investigated correlations between antibody status, results of neurocognitive tests, and MRI findings.

resultsFollow-up (AE vs. PC) was 33 (11-95) vs. 96 (26-132) months after diagnosis. Neurocognitive functions were normal in both AE and PC groups in all tests except face recognition, which was pathological in both groups. The overall/recognition/long-delay visual memory (p = 0.009/0.008/0.005) and incidental learning (p = 0.017) scores were significantly higher in NMDAR patients compared to non-NMDAR patients. Non-NMDAR patients with right-sided limbic MRI pathologies had significantly lower overall/recognition/long-delay visual memory (p = 0.006/0.044/0.024) and incidental learning (p = 0.009) scores compared to NMDAR patients.

conclusionsWe observed mainly normal neurocognitive functions after autoimmune and bacterial encephalitis. However, compared to NMDAR patients, patients with non-NMDAR autoimmune encephalitis showed a significant and material-specific association between a right-sided hippocampal lesion and limitations in figural-mnestic and incidental learning capacities. Neurocognitive functions in AE patients should be further evaluated prospectively and in more detail.

Indexed as

AutoantibodiesEncephalitisHashimoto DiseaseHippocampusAdultCase-Control StudiesFemaleFollow-Up StudiesHumansMagnetic Resonance ImagingMaleMiddle AgedNeuropsychological TestsReceptors, N-Methyl-D-AspartateYoung AdultAutoantibodiesReceptors, N-Methyl-D-AspartateAutoimmune encephalitisCaspr2GADHippocampusIncidental learningLGI1MoCANeurocognitionNMDARVDLTVLMT

Identifiers

PMID39891731
PMCPMC11787161

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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.