Evidence map›Paper›PMID 42876836›Full record

ArticleFrontiers in aging neuroscience2026

Coordinated cellular architecture reveals weakened cortical structure-behavior coupling in normal aging.

Xiaoyi Zhan, Pengcheng Tan, Tirzah Tan, Chia-Chien Chen

Abstract read
In one paragraph

Article in Frontiers in aging neuroscience, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Xiaoyi ZhanBehavioral Science Program, Division of Natural and Applied Sciences, Duke Kunshan University, Suzhou, Jiangsu, China.
Pengcheng TanBehavioral Science Program, Division of Natural and Applied Sciences, Duke Kunshan University, Suzhou, Jiangsu, China.
Tirzah TanBehavioral Science Program, Division of Natural and Applied Sciences, Duke Kunshan University, Suzhou, Jiangsu, China.
Chia-Chien ChenBehavioral Science Program, Division of Natural and Applied Sciences, Duke Kunshan University, Suzhou, Jiangsu, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Normal aging compromises behavioral functions supported by cortical circuits, yet how age-related cellular reorganization relates to weakened circuit-behavior correspondence remains poorly defined. Here, we examined layer 4 (L4) of the mouse primary somatosensory barrel cortex, a thalamorecipient lamina in which dendritic organization, microglial process architecture, and whisker-dependent tactile function can be analyzed within the same sensory system. Aged mice showed impaired whisker-dependent texture discrimination. Using high-resolution three-dimensional cellular reconstructions, we quantified the morphology and spatial architecture of L4 pyramidal neurons and microglia in young and aged mice. We then applied within-domain principal component analysis (PCA) to derive architecture scores and tested how these scores mapped onto whisker-dependent behavior. Aging reduced the complexity and spatial extent of L4 pyramidal dendritic arbors, while microglia showed reduced process complexity and territorial occupancy. Across both cell types, these changes converged on a more spatially restricted local cellular architecture. PCA organized high-dimensional morphometric variables into dominant architecture scores that captured coordinated morphometric organization within the neuronal and microglial domains. In young animals, dominant architecture scores were associated with whisker-dependent tactile discrimination; residual scores and same-texture encoding indices did not show significant corresponding association. Within-age permutation analyses and direct Fisher r-to-z comparisons supported an age-dependent weakening of architecture-behavior correspondence. These findings identify parallel neuronal and microglial morphological changes as an anatomical axis of cortical aging, with restricted cellular architecture accompanied by weakened architecture-behavior correspondence in sensory cortex.

Indexed as

barrel cortexcortical agingdendritic architecturemicroglial morphologysensory-guided behaviorstructure–behavior coupling

Identifiers

PMID42876836
PMCPMC13662101

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.