Evidence map›Paper›PMID 41701374›Full record

ArticleBrain structure & function2026

Changes in microglial morphologies during brain aging in common marmosets.

Kimberley A Phillips, Savannah K Boyen, Katelin X Oliveira, Reagan Meredith, Chet C Sherwood

Abstract read
In one paragraph

Article in Brain structure & function, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

5 authors.

Kimberley A PhillipsDepartment of Psychology, Trinity University, San Antonio, TX, USA. Kimberley.phillips@trinity.edu.
Savannah K BoyenDepartment of Psychology, Trinity University, San Antonio, TX, USA.
Katelin X OliveiraDepartment of Anthropology and Center for the Advanced Study of Human Paleobiology, The George Washington University, Washington, DC, USA.
Reagan MeredithSouthwest National Primate Research Center, Texas Biomedical Research Institute, San Antonio, TX, USA.
Chet C SherwoodDepartment of Anthropology and Center for the Advanced Study of Human Paleobiology, The George Washington University, Washington, DC, USA.

Funding

The Southwest National Primate Research Center Supplement- Infrastructure improvements of ABSL2 holding areasP51OD011133 · OD · TEXAS BIOMEDICAL RESEARCH INSTITUTE · PI Larry S. Schlesinger · 2012 to 2026
$129.7M
Marmosets as a Model for Understanding Social, Neuroendocrine, and Vascular Contributions to Cognitive AgingR01AG064091 · NIA · TRINITY UNIVERSITY · PI PHILLIPS, KIMBERLEY ANN · 2019 to 2023
$1.4M
NIA NIH HHS R01 AG064091NIH HHS P51 OD011133
6 · The paper itself

Abstract

Microglia are critical modulators of neuronal activity, regulating brain function through removal of dying neurons, pruning non-functional synapses, and producing ligands that support neuronal survival. Microglial morphologies change with aging, shifting from a homeostatic, surveillant state (ramified morphology) to a more reactive state (intermediate, amoeboid, and dystrophic morphology). Common marmosets (Callithrix jacchus) are a valuable translational nonhuman primate model for aging, and studies of neuroinflammation and neurodegenerative disease. These small, genetically diverse platyrrhine primates are considered aged at 7 years, have a maximum potential lifespan of 12+ years, and display age-related changes in motor, sensorimotor, and cognitive function. Here we quantified microglial morphologies in 24 aged marmosets (7–18 years) in the dorsolateral prefrontal cortex (dlPFC, Brodmann’s area 9), hippocampal regions CA1 and CA3, and the entorhinal cortex (ENT) via immunohistochemistry against Iba1. The proportion of ramified microglia showed a significant negative correlation with age in dlPFC, CA1, and CA3, and the proportion of dystrophic microglia showed a significant positive correlation with age in all four regions examined. Males displayed a significantly higher proportion of dystrophic microglia than females in CA1. Sex did not significantly affect the proportion of microglia morphologies in any other brain region. A significant interaction between age and sex was found for the proportion of intermediate microglia in ENT. Overall, these data suggest brain aging in marmosets from middle-age to older adulthood is characterized by an increase in dystrophic microglia, and age-related changes in microglial morphology manifest differently in male and female marmosets in hippocampal regions.

Indexed as

AgingBrainMicrogliaAnimalsCallithrixFemaleMaleAgingIba1Microglial dysfunctionNeurodegeneration

Identifiers

PMID41701374
PMCPMC12913261

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LicenceCC BY
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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.