Evidence map›Paper›PMID 38771530›Full record

ArticleActa neuropathologica2024

Disentangling the heterogeneity of multiple sclerosis through identification of independent neuropathological dimensions.

Alyse de Boer, Aletta M R van den Bosch, Nienke J Mekkes, Nina L Fransen, Ekaterina Dagkesamanskaia, Eric Hoekstra, Jörg Hamann, Joost Smolders, Inge Huitinga, Inge R Holtman

Abstract read
In one paragraph

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 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Article
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  3. Article
  4. Review
  5. Article
  6. Co-occurrence of parkinson disease and multiple sclerosis - a critical note.Journal of neural transmission (Vienna, Austria : 1996) · 2026
    Review
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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

10 authors.

Alyse de BoerSection Molecular Neurobiology, Department of Biomedical Sciences, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.ORCID 0000-0002-7150-2038
Aletta M R van den BoschNeuroimmunology Research Group, Netherlands Institute for Neuroscience, Amsterdam, The Netherlands.ORCID 0000-0001-8886-8928
Nienke J MekkesSection Molecular Neurobiology, Department of Biomedical Sciences, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.ORCID 0000-0002-5454-0235
Nina L FransenNeuroimmunology Research Group, Netherlands Institute for Neuroscience, Amsterdam, The Netherlands.ORCID 0000-0003-0958-7162
Ekaterina DagkesamanskaiaSection Molecular Neurobiology, Department of Biomedical Sciences, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.ORCID 0009-0009-8478-8897
Eric HoekstraSection Molecular Neurobiology, Department of Biomedical Sciences, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Jörg HamannNeuroimmunology Research Group, Netherlands Institute for Neuroscience, Amsterdam, The Netherlands.ORCID 0000-0002-9448-1727
Joost SmoldersNeuroimmunology Research Group, Netherlands Institute for Neuroscience, Amsterdam, The Netherlands.ORCID 0000-0001-9766-8661
Inge HuitingaNeuroimmunology Research Group, Netherlands Institute for Neuroscience, Amsterdam, The Netherlands.ORCID 0000-0002-4878-8920
Inge R HoltmanSection Molecular Neurobiology, Department of Biomedical Sciences, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands. i.r.holtman@umcg.nl.ORCID 0000-0001-9752-4756

Funding

European Research Council 101078437Universitair Medisch Centrum Groningen Rosalind Franklin Fellowship
6 · The paper itself

Abstract

Multiple sclerosis (MS) is a heterogeneous neurological disorder with regards to clinical presentation and pathophysiology. Here, we investigated the heterogeneity of MS by performing an exploratory factor analysis on quantitative and qualitative neuropathology data collected for 226 MS donors in the Netherlands Brain Bank autopsy cohort. Three promising dimensions were identified and subsequently validated with clinical, neuropathological, and genetic data. Dimension 1 ranged from a predominance of remyelinated and inactive lesions to extensive pathological changes, higher proportions of active and mixed lesions, and foamy microglia morphology. This pattern was positively correlated with more severe disease, the presence of B and T cells, and neuroaxonal damage. Scoring high on dimension 2 was associated with active lesions, reactive sites, and the presence of nodules. These donors had less severe disease, a specific pattern of cortical lesions, and MS risk variants in the human leukocyte antigen region, the latter indicating a connection between disease onset and this neuropathological dimension. Donors scoring high on dimension 3 showed increased lesional pathology with relatively more mixed and inactive lesions and ramified microglia morphology. This pattern was associated with longer disease duration, subpial cortical lesions, less involvement of the adaptive immune system, and less axonal damage. Taken together, the three dimensions may represent (1) demyelination and immune cell activity associated with pathological and clinical progression, (2) microglia (re)activity and possibly lesion initiation, and (3) loss of lesion activity and scar formation. Our findings highlight that a thorough understanding of the interplay between multiple pathological characteristics is crucial to understand the heterogeneity of MS pathology, as well as its association with genetic predictors and disease outcomes. The scores of donors on the dimensions can serve as an important starting point for further disentanglement of MS heterogeneity and translation into observations and interventions in living cohorts with MS.

Indexed as

Multiple SclerosisAdultAgedAged, 80 and overAutopsyBrainCohort StudiesFemaleHumansMaleMicrogliaMiddle AgedNetherlandsTissue BanksFactor analysisGeneticsMultiple sclerosisNeuropathology

Identifiers

PMID38771530
PMCPMC11108935

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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.