Evidence map›Paper›PMID 39400557›Full record

ArticleActa neuropathologica2024

Neuropathological spectrum of anti-IgLON5 disease and stages of brainstem tau pathology: updated neuropathological research criteria of the disease-related tauopathy.

Ellen Gelpi, Raphael Reinecke, Carles Gaig, Alex Iranzo, Lidia Sabater, Laura Molina-Porcel, Iban Aldecoa, Verena Endmayr, Birgit Högl, Erich Schmutzhard and 43 more

Abstract read
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Article in Acta neuropathologica, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

17 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Prognostic Determinants of Presentation and Outcome in Anti-IgLON5 Disease.Neurology(R) neuroimmunology & neuroinflammation · 2026
    Observational
  4. Article
  5. Article
  6. Review
  7. Brain atrophy patterns in anti-IgLON5 disease.Brain : a journal of neurology · 2026
    Article
  8. Article
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  12. Article
  13. Article
  14. Neuroinflammation distinguishes HLA haplotypes in progressive supranuclear palsy.medRxiv : the preprint server for health sciences · 2025
    Article
  15. Article
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  17. 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

53 authors.

Ellen Gelpi *Division of Neuropathology and Neurochemistry, Department of Neurology, Medical University of Vienna, Waehringer Guertel 18-20, 1090, Vienna, Austria.ORCID 0000-0003-2948-4187
Raphael Reinecke *Division of Neuropathology and Neurochemistry, Department of Neurology, Medical University of Vienna, Waehringer Guertel 18-20, 1090, Vienna, Austria.
Carles GaigSleep Unit, Neurology Department, Hospital Clinic de Barcelona, IDIBAPS/FCRB, Barcelona, Spain.
Alex IranzoSleep Unit, Neurology Department, Hospital Clinic de Barcelona, IDIBAPS/FCRB, Barcelona, Spain.
Lidia SabaterInstitut d'Investigacions Biomèdiques August Pi i Sunyer (FCRB-IDIBAPS), Neuroimmunology Program, Barcelona, Spain.
Laura Molina-PorcelInstitut d'Investigacions Biomediques August Pi i Sunyer (IDIBAPS/FCRB), Neurological Tissue Bank of the Biobanc, Hospital Clinic, Barcelona, Spain.
Iban AldecoaInstitut d'Investigacions Biomediques August Pi i Sunyer (IDIBAPS/FCRB), Neurological Tissue Bank of the Biobanc, Hospital Clinic, Barcelona, Spain.
Verena EndmayrDivision of Neuropathology and Neurochemistry, Department of Neurology, Medical University of Vienna, Waehringer Guertel 18-20, 1090, Vienna, Austria.
Birgit HöglDepartment of Neurology, Medical University of Innsbruck, Innsbruck, Austria.
Erich SchmutzhardNeuro-Critical Care Unit, Department of Neurology, Medical University of Innsbruck, Innsbruck, Austria.
Werner PoeweDepartment of Neurology, Medical University of Innsbruck, Innsbruck, Austria.
Bettina PfauslerNeuro-Critical Care Unit, Department of Neurology, Medical University of Innsbruck, Innsbruck, Austria.
Mara PopovicInstitute of Pathology, Faculty of Medicine, University of Ljubljana, Ljubljana, Slovenia.
Janja Pretnar-OblakDepartment for Vascular Neurology and Intensive Neurological Therapy, University Medical Centre Ljubljana, Ljubljana, Slovenia.
Frank LeypoldtNeuroimmunology, Institute of Clinical Chemistry and Laboratory Medicine, Department of Neurology, Kiel University, Kiel, Germany.
Jakob MatschkeInstitute of Neuropathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Markus GlatzelInstitute of Neuropathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Elena Maria ErroNeurology Department, University Hospital Pamplona, Navarra, Spain.
Ivonne JericoNeurology Department, University Hospital Pamplona, Navarra, Spain.
Maria Cristina CaballeroNavarra Biomed Research Institute, Pamplona, Spain.
Maria Victoria ZelayaNavarra Biomed Research Institute, Pamplona, Spain.
Sara MariottoNeurology Unit, Department of Neurosciences, Biomedicine, and Movement Sciences, University of Verona, Verona, Italy.
Anna HeidbrederDepartment of Neurology, Kepler University Hospital Linz, and Clinical Research Institute for Neurosciences, Johannes Kepler University, Linz, Austria.
Ognian KalevDivision of Neuropathology, Department of Pathology and Molecular Pathology, Kepler University Hospital Linz, Austria and Clinical Research Institute for Neurosciences, Johannes Kepler University, Linz, Austria.
Serge WeisDivision of Neuropathology, Department of Pathology and Molecular Pathology, Kepler University Hospital Linz, Austria and Clinical Research Institute for Neurosciences, Johannes Kepler University, Linz, Austria.
Stefan MacherComprehensive Center for Clinical Neurosciences & Mental Health Vienna, Medical University of Vienna, Waehringer Guertel 18-20, 1090, Vienna, Austria.
Evelyn Berger-SieczkowskiComprehensive Center for Clinical Neurosciences & Mental Health Vienna, Medical University of Vienna, Waehringer Guertel 18-20, 1090, Vienna, Austria.
Julia FerrariDepartment of Neurology, St. John's of God Hospital, Vienna, Austria.
Christoph ReisingerCenter of Forensic Medicine, Medical University of Vienna, Vienna, Austria.
Nikolaus KluppCenter of Forensic Medicine, Medical University of Vienna, Vienna, Austria.
Pentti TienariTranslational Immunology, Research Programs Unit, Department of Neurology, University of Helsinki, Helsinki University Hospital, Helsinki, Finland.
Osma RautilaTranslational Immunology, Research Programs Unit, Department of Neurology, University of Helsinki, Helsinki University Hospital, Helsinki, Finland.
Marja NiemeläDepartment of Neurology, Helsinki University Hospital, Helsinki, Finland.
Deniz Yilmazer-HankeClinical Neuroanatomy, Department of Neurology, University Hospital, Ulm University, Ulm, Germany.
Mar GuaspSleep Unit, Neurology Department, Hospital Clinic de Barcelona, IDIBAPS/FCRB, Barcelona, Spain.
Bas BloemDepartment of Neurology, Donders Institute for Brain, Cognition, and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.
Judith Van GaalenDepartment of Neurology, Rijnstate Hospital, Arnhem, The Netherlands.
Benno KustersDepartment of Pathology, Radboud University Medical Centre, Nijmegen, The Netherlands.
Maarten TitulaerDepartment of Neurology, Erasmus University Medical Center, Rotterdam, The Netherlands.
Nina L FransenDepartment of Pathology, Amsterdam UMC, Amsterdam, The Netherlands.
Joan SantamariaSleep Unit, Neurology Department, Hospital Clinic de Barcelona, IDIBAPS/FCRB, Barcelona, Spain.
Thimoty DawsonNeuropathology, Lancashire Teaching Hospitals NHS Foundation Trust, Preston, UK.
Janice L HoltonQueen Square Brain Bank for Neurological Disorders, Department of Neurodegenerative Disease, UCL Institute of Neurology, University College London, London, UK.
Helen LingQueen Square Brain Bank for Neurological Disorders, Department of Neurodegenerative Disease, UCL Institute of Neurology, University College London, London, UK.
Tamas ReveszQueen Square Brain Bank for Neurological Disorders, Department of Neurodegenerative Disease, UCL Institute of Neurology, University College London, London, UK.
Liisa MyllykangasDepartment of Pathology, University of Helsinki, HUS Diagnostic Center, Helsinki University Hospital, Helsinki, Finland.
Herbert BudkaDivision of Neuropathology and Neurochemistry, Department of Neurology, Medical University of Vienna, Waehringer Guertel 18-20, 1090, Vienna, Austria.
Gabor G KovacsDepartment of Laboratory Medicine and Pathobiology and Tanz Centre for Research in Neurodegenerative Disease, University of Toronto, Toronto, ON, Canada.
Jan LewerenzDepartment of Neurology, Ulm University Hospital, Ulm, Germany.
Josep DalmauDepartment of Neurology, University of Pennsylvania, Philadelphia, PA, USA.
Francesc GrausInstitut d'Investigacions Biomèdiques August Pi i Sunyer (FCRB-IDIBAPS), Neuroimmunology Program, Barcelona, Spain.
Inga Koneczny *Division of Neuropathology and Neurochemistry, Department of Neurology, Medical University of Vienna, Waehringer Guertel 18-20, 1090, Vienna, Austria. inga.koneczny@meduniwien.ac.at.
Romana Höftberger *Division of Neuropathology and Neurochemistry, Department of Neurology, Medical University of Vienna, Waehringer Guertel 18-20, 1090, Vienna, Austria. romana.hoeftberger@meduniwien.ac.at.

Funding

Austrian Science Fund I6565-BAustrian Science Fund SYNABSAustrian Science Fund T996-B30Bundesministerium für Bildung und Forschung 01GM2208ABundesministerium für Bildung und Forschung 01GM2208BHelsingin Yliopisto TYH2022316Horizon 2020 Framework Programme N° 825575Instituto de Salud Carlos III PI21/00165Tekniikan Akatemia 341007
6 · The paper itself

Abstract

Anti-IgLON5 disease is a unique condition that bridges autoimmunity and neurodegeneration. Since its initial description 10 years ago, an increasing number of autopsies has led to the observation of a broader spectrum of neuropathologies underlying a particular constellation of clinical symptoms. In this study, we describe the neuropathological findings in 22 patients with anti-IgLON5 disease from 9 different European centers. In 15 patients (68%), we observed a hypothalamic and brainstem-predominant tauopathy of varying severity in which the original research neuropathological criteria were readily applicable. This pathology was observed in younger patients (median age at onset 61 years) with a long disease duration (median 9 years). In contrast, in 7 (32%) patients, the originally described brainstem tauopathy was nearly absent or only minimal in the form of delicate threads, despite mild-to-moderate neurodegenerative features, consistent clinical symptoms and the presence of anti-IgLON5 antibodies in CSF and serum. These patients were older at onset (median 79 years) and had shorter disease duration (median < 1 year). Overall, about one-third of the patients showed concomitant TDP-43 pathology within the regions affected by tau pathology and/or neurodegeneration. Based on these observations and in view of the spectrum of the tau burden in the core regions involved in the disease, we propose a simple staging system: stage 1 mild neurodegeneration without overt or only minimal tau pathology, stage 2 moderate neurodegeneration and mild/ moderate tauopathy and stage 3 prominent neurodegeneration and tau pathology. This staging intends to reflect a potential (age- and time-dependent) progression of tau pathology, supporting the current notion that tau accumulation is a secondary phenomenon related to the presence of anti-IgLON5 antibodies in the CNS. Finally, we adapt the original research criteria of the anti-IgLON5 disease-related tauopathy to include the spectrum of pathologies observed in this larger postmortem series.

Indexed as

Brain StemCell Adhesion Molecules, NeuronalTauopathiestau ProteinsAdultAgedAged, 80 and overAutoantibodiesDNA-Binding ProteinsFemaleHumansMaleMiddle AgedAutoantibodiesCell Adhesion Molecules, NeuronalDNA-Binding ProteinsIgLON5 protein, humanTARDBP protein, humantau Proteins3R4R tauALSAnti-IgLON5 diseaseAnti-IgLON5 tauopathyAtypicalBrainstem tauopathyDementiaIgLON5Motor neuron diseaseNeuropathologyPSPStagesTDP-43

Identifiers

PMID39400557
PMCPMC11473580

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