Evidence map›Paper›PMID 42434686›Full record

ArticleFrontiers in behavioral neuroscience2026

Behavioral phenotypes in aging: structured exploratory computational analysis of multi-assay behavioral data.

Gaurav Singhal, Bernhard T Baune

Abstract read
In one paragraph

Article in Frontiers in behavioral 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.

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0citing papers in PubMed
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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.

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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

2 authors.

Gaurav SinghalDepartment of Otolaryngology, University of Wisconsin-Madison, Madison, WI, United States.
Bernhard T BauneDepartment of Mental Health, University of Münster, Münster, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Aging is associated with progressive alterations in behavioral function, yet majority of the studies interpret behavioral outcomes on an assay-by-assay basis, limiting understanding of how behavioral domains are organized. Our previously published study used a mouse cohort to report assay-specific behavioral effects. In this study, we examined whether aging-related behavioral signals remain localized to individual assays or can be summarized as coordinated domain-level patterns. Methods: A structured rule-based workflow was implemented for feature engineering, direction harmonization, z-score standardization, and domain-level composite construction across locomotion/exploration, anxiety/avoidance, depression/passive coping, cognition/learning, memory, and sociability domains. Outcomes were analyzed using parametric or non-parametric models following assumption screening, with effect sizes reported. Results: Domain-level composite scores did not show significant age- or sex-related effects, indicating limited broad behavioral separation. In contrast, refined feature-level analysis identified modest locomotor differences (core locomotion distance; Kruskal-Wallis Conclusion: Aging-related behavioral changes in this dataset were concentrated in specific assay-level measures rather than broadly distributed across domains. Domain-level aggregation reduced separation of effects, indicating that the present composites should be interpreted as heuristic summaries rather than validated behavioral dimensions. The main added value of this reanalysis is therefore interpretive, showing that the strongest signals remain most evident in selected measures, particularly Barnes Maze outcomes.

Indexed as

agingbehavioral phenotypingC57BL/6 micecognitioncomputational analysislocomotionmemorymultivariate analysis

Identifiers

PMID42434686
PMCPMC13351101

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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.