Evidence map›Paper›PMID 40773468›Full record

ArticlePloS one2025

Variability of test parameters from mice of different age groups in published data sets.

Bernhard Aigner

Abstract read
In one paragraph

Article in PloS one, 2025. 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. Article
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

1 author.

Bernhard AignerChair for Molecular Animal Breeding and Biotechnology, LMU Munich, Munich, Germany.ORCID https://orcid.org/0000-0003-1644-2711

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The use of mice as animal models in biomedical research allows the standardization of genetic background, housing conditions as well as experimental protocols, which all affect phenotypic variability. In this study, the phenotypic variability of test parameters was analyzed in genetically identical mice of different age groups, i.e., early adults versus late adults. Therefore, published data sets of genetically identical mice of different age groups collected from the same investigator/ project were retrospectively analyzed. Morphological parameters, blood parameters and behavioral tests were analyzed which are predominantly used in biomedical research. The JaxKOMP project examined C57BL/6NJ mice with an age of 7-20 weeks and 66-81 weeks. Further substrains of C57BL/6N mice with an age of 8-16 weeks and 49-63 weeks were examined as wild-type controls from various investigators of the International Mouse Phenotyping Consortium (IMPC). Additional data sets of young and old groups of genetically identical mice were derived from the Mouse Phenome Database (MPD) and the RIKEN BioResource Research Center (RBRC). The phenotypic variability of the chosen traits and parameters was measured by calculating the coefficient of variation (CV = standard deviation/ mean) of the animals with the same sex of a given mouse strain. Subsequently, the CVs of the young and the old mouse group were compared. The comparison of the phenotypic variability of the late adults versus early adults revealed the appearance of unpredictable interactions between genotype, environment and experiment. Overall, a higher phenotypic variability of the late adults appeared almost consistently for body weight including lean mass and fat mass for females as well as for hematology and immunology parameters, particularly for females. Clinical chemistry often appeared inconspicuous. No noticeable differences were detected for the traits echocardiography and electrocardiogram, whereas late adults also often showed a higher phenotypic variability for behavioral tests.

Indexed as

AgingAge FactorsAnimalsBehavior, AnimalFemaleMaleMiceMice, Inbred C57BLPhenotype

Identifiers

PMID40773468
PMCPMC12331085

What Socratic holds

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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 Socratic graph.