Evidence map›Paper›PMID 39364217›Full record

ArticleNeuroprotection (Chichester, England)2024

Microglial senescence in neurodegeneration: Insights, implications, and therapeutic opportunities.

Tobiloba Samuel Olajide, Toheeb O Oyerinde, Omolabake I Omotosho, Oritoke M Okeowo, Olayemi J Olajide, Omamuyouwi M Ijomone

Abstract read
In one paragraph

Article in Neuroprotection (Chichester, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
–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

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

  1. Pooled it
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  12. Exploiting glial cell functions for neurodegeneration therapy.Neuroprotection (Chichester, England) · 2025
    Article
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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

6 authors.

Tobiloba Samuel OlajideLaboratory for Experimental and Translational Neurobiology, University of Medical Sciences, Ondo, Ondo, Nigeria.ORCID 0000-0001-7234-3748
Toheeb O OyerindeLaboratory for Experimental and Translational Neurobiology, University of Medical Sciences, Ondo, Ondo, Nigeria.ORCID 0000-0002-0116-1485
Omolabake I OmotoshoLaboratory for Experimental and Translational Neurobiology, University of Medical Sciences, Ondo, Ondo, Nigeria.ORCID 0009-0005-9934-881X
Oritoke M OkeowoLaboratory for Experimental and Translational Neurobiology, University of Medical Sciences, Ondo, Ondo, Nigeria.ORCID 0000-0002-6385-8229
Olayemi J OlajideCenter for Studies in Behavioral Neurobiology, Department of Psychology, Concordia University, Montreal, Quebec, Canada.ORCID 0000-0002-9259-2837
Omamuyouwi M IjomoneLaboratory for Experimental and Translational Neurobiology, University of Medical Sciences, Ondo, Ondo, Nigeria.ORCID 0000-0002-0933-8409

Funding

Developmental neurotoxicity and autism spectrum disorderK43TW011920 · FIC · UNIVERSITY OF MEDICAL SCIENCES, ONDO · PI Omamuyovwi Meashack Ijomone · 2022 to 2026
$500k
FIC NIH HHS K43 TW011920
6 · The paper itself

Abstract

The existing literature on neurodegenerative diseases (NDDs) reveals a common pathological feature: the accumulation of misfolded proteins. However, the heterogeneity in disease onset mechanisms and the specific brain regions affected complicates the understanding of the diverse clinical manifestations of individual NDDs. Dementia, a hallmark symptom across various NDDs, serves as a multifaceted denominator, contributing to the clinical manifestations of these disorders. There is a compelling hypothesis that therapeutic strategies capable of mitigating misfolded protein accumulation and disrupting ongoing pathogenic processes may slow or even halt disease progression. Recent research has linked disease-associated microglia to their transition into a senescent state-characterized by irreversible cell cycle arrest-in aging populations and NDDs. Although senescent microglia are consistently observed in NDDs, few studies have utilized animal models to explore their role in disease pathology. Emerging evidence from experimental rat models suggests that disease-associated microglia exhibit characteristics of senescence, indicating that deeper exploration of microglial senescence could enhance our understanding of NDD pathogenesis and reveal novel therapeutic targets. This review underscores the importance of investigating microglial senescence and its potential contributions to the pathophysiology of NDDs, including Alzheimer's disease, Parkinson's disease, Huntington's disease, and amyotrophic lateral sclerosis. Additionally, it highlights the potential of targeting microglial senescence through iron chelation and senolytic therapies as innovative approaches for treating age-related NDDs.

Indexed as

agingferritinmicroglianeurodegenerative diseasessenescence-associated secretory phenotypesenescent

Identifiers

PMID39364217
PMCPMC11449118

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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 Socratic graph.