Evidence map›Paper›PMID 41415305›Full record

ArticleFrontiers in toxicology2025

Retrospective analysis of clinical laboratory parameters in Han Wistar rat controls.

Rupert Kellner, Alexander Amberg, Frank Bringezu, Dragomir Ivanov Draganov, Annika Kreuchwig, Wolfgang Muster, Guillemette Duchateau-Nguyen, Nils Oberhauser, Paolo Piraino, Markus Schaefer and 3 more

Abstract read
In one paragraph

Article in Frontiers in toxicology, 2025. 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

13 authors.

Rupert KellnerFraunhofer Institute for Toxicology and Experimental Medicine ITEM, Chemical Safety and Toxicology, Hannover, Germany.
Alexander AmbergSanofi, Preclinical Safety, Frankfurt, Germany.
Frank BringezuMerck Heathcare KGaA, Darmstadt, Germany.
Dragomir Ivanov DraganovHoffmann-La Roche, Roche Innovation Center, Basel, Switzerland.
Annika KreuchwigBayer Research and Development, Pharmaceuticals, Preclinical Development, Berlin, Germany.
Wolfgang MusterHoffmann-La Roche, Roche Innovation Center, Basel, Switzerland.
Guillemette Duchateau-NguyenHoffmann-La Roche, Roche Innovation Center, Basel, Switzerland.
Nils OberhauserNovartis, Basel, Switzerland.
Paolo PirainoOrganon SRL, Bucharest, Romania.
Markus SchaeferSanofi, Preclinical Safety, Frankfurt, Germany.
Nelly SimetskaFraunhofer Institute for Toxicology and Experimental Medicine ITEM, Chemical Safety and Toxicology, Hannover, Germany.
Thomas Steger-HartmannBayer Research and Development, Pharmaceuticals, Preclinical Development, Berlin, Germany.
Sylvia E EscherFraunhofer Institute for Toxicology and Experimental Medicine ITEM, Chemical Safety and Toxicology, Hannover, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Despite the availability of control animal data sets from toxicological studies, the influence of external factors, such as age of animals, test site and study conditions, on clinical laboratory parameters in rats is only sparsely characterized. Objective: In order to analyze the covariates of study design, we leveraged the largest available curated collection of control animal data from toxicological studies, sourced from five European pharmaceutical companies. We investigated the influence of external factors on commonly measured clinical chemistry, enzyme activity and hematology parameters in Han Wistar rats of both sexes. Materials and Methods: 457,605 control group clinical laboratory data points from 1,288 legacy toxicity studies on Han Wistar rats were curated and analyzed by ANOVA and partial eta squared to discern their effect sizes. Results: Our analysis revealed that bodyweight, used as a surrogate for age in rats, significantly influences some parameters, while demonstrating stability in others. Descriptive statistics and tolerance intervals are provided for 20-g body weight class intervals. The effect size of these body weight classes, as calculated by partial eta squared, is large for parameters that change during development (e.g., phosphate or alkaline phosphatase) but was negligible for more stable parameters (e.g., calcium and alanine aminotransferase). For parameters which are less dependent on body weight class, the relative influence of other factors, namely, the company providing the study data, as well as study year is more prominent. These factors likely act as summary factors for various influences such as changes in analytical protocols, diet or housing conditions. Conclusion: This analysis provides a comprehensive overview of parameter variability and offers critical guidance for parameters which need to be controlled when utilizing historical control data to establish reference intervals or generate virtual control groups.

Indexed as

clinical chemistryenzyme activityHan Wistar rathematologymineralspreclinical datareference intervals

Identifiers

PMID41415305
PMCPMC12708259

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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.