Evidence map›Paper›PMID 37656188›Full record

ReviewActa neuropathologica2023

Microglial contribution to the pathology of neurodevelopmental disorders in humans.

Rugile Matuleviciute, Elizabeth T Akinluyi, Tim A O Muntslag, Jennifer M Dewing, Katherine R Long, Anthony C Vernon, Marie-Eve Tremblay, David A Menassa

Abstract readReview
In one paragraph

Review in Acta neuropathologica, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing 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

29 citing papers in PubMed.

  1. Genes · 2026
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  2. Review
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  4. [Volatile oil fromNan fang yi ke da xue xue bao = Journal of Southern Medical University · 2026
    Article
  5. Review
  6. Review
  7. Article
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  9. Inflammatory mechanisms contribute to long-term cognitive deficits induced by perinatal asphyxia via interleukin-1.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
    Article
  10. Review
  11. Review
  12. Article
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  15. Article
  16. Review
  17. 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

8 authors.

Rugile Matuleviciute *MRC Centre for Neurodevelopmental Disorders, King's College London, London, UK.
Elizabeth T Akinluyi *Division of Medical Sciences, University of Victoria, Victoria, Canada.
Tim A O MuntslagPrincess Maxima Centre for Paediatric Oncology, Utrecht, The Netherlands.
Jennifer M DewingFaculty of Medicine, University of Southampton, Southampton, UK.
Katherine R LongMRC Centre for Neurodevelopmental Disorders, King's College London, London, UK.
Anthony C VernonMRC Centre for Neurodevelopmental Disorders, King's College London, London, UK.
Marie-Eve TremblayDivision of Medical Sciences, University of Victoria, Victoria, Canada.
David A MenassaDepartment of Neuropathology & The Queen's College, University of Oxford, Oxford, UK. david.menassa@clneuro.ox.ac.uk.ORCID http://orcid.org/0000-0002-5984-8407

Funding

Medical Research Council MR/N026063/1Medical Research Council MR/S025065/1Medical Research Council MR/W006251/1
6 · The paper itself

Abstract

Microglia are the brain's resident macrophages, which guide various developmental processes crucial for brain maturation, activity, and plasticity. Microglial progenitors enter the telencephalic wall by the 4th postconceptional week and colonise the fetal brain in a manner that spatiotemporally tracks key neurodevelopmental processes in humans. However, much of what we know about how microglia shape neurodevelopment comes from rodent studies. Multiple differences exist between human and rodent microglia warranting further focus on the human condition, particularly as microglia are emerging as critically involved in the pathological signature of various cognitive and neurodevelopmental disorders. In this article, we review the evidence supporting microglial involvement in basic neurodevelopmental processes by focusing on the human species. We next concur on the neuropathological evidence demonstrating whether and how microglia contribute to the aetiology of two neurodevelopmental disorders: autism spectrum conditions and schizophrenia. Next, we highlight how recent technologies have revolutionised our understanding of microglial biology with a focus on how these tools can help us elucidate at unprecedented resolution the links between microglia and neurodevelopmental disorders. We conclude by reviewing which current treatment approaches have shown most promise towards targeting microglia in neurodevelopmental disorders and suggest novel avenues for future consideration.

Indexed as

Autism Spectrum DisorderNeurodevelopmental DisordersBrainHumansMacrophagesMicrogliaNeuropathologyAutism spectrum conditionsHuman-induced pluripotent stem cellsHuman microgliaNeurodevelopmental disordersNeurodevelopmental modelsSchizophreniaSpatial transcriptomics

Identifiers

PMID37656188
PMCPMC10564830

What OpenQuestion holds

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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.