Murine "model" monotheism: an iconoclast at the altar of mouse
Open accessAbstract
Many use mice for contemporary cardiovascular research, as we should, given the power of the genetic and other tools developed to permit rigorous mechanistic experimentation in this species. We must remain mindful, nonetheless, of the reasons why the results of mouse experiments may not extrapolate readily to human disease. Large gaps separate our mouse experiments and clinical conditions. The differences arise from the genetic homogeneity of inbred mouse strains used in experimentation, the restricted exposure of mice to many microbes and a more monotonous microbiome in mice than in free-living rodents and humans, lack of comorbidities, focus on youthful mice and exaggerated experimental conditions contrived to speed up studies, and the lack of congruence between many experimental “models” and human cardiovascular conditions. We must and should continue to mine studies on mice for the incredibly valuable mechanistic insight they provide. Yet, we as a community could consider more carefully some of the barriers to glib extrapolation of the results of experiments in mice to human disease.
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Insufficient reproducibility has been openly communicated in oncology and cardiovascular biology.
“The controversial matter of insufficient reproducibility was, in fact, communicated openly in oncology and cardiovascular biology (Begley and Ellis, 2012; Errington et al., 2014; Libby, 2015).”
From In Vitro research Reproducibility: Keeping up High Standards (2019) · cites this paper as Libby, 2015
The available figure passage discusses the interpretation of mouse research in cardiovascular science, not insufficient reproducibility. Searches for “reproducibility” and “irreproducible results” found no passage addressing the claimed open communication of that problem in oncology or cardiovascular biology. (LLM, conf=0.69)
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In Vitro research Reproducibility: Keeping up High Standards
Hirsch, C., & Schildknecht, S. (2019) · Frontiers in Pharmacology · doi:10.3389/fphar.2019.01484 · Cited by 161 · see citing works
- Authors
- Libby, P.
- Affiliations
- Brigham and Women's Hospital (US)
- Corresponding author
- Libby, Peter
- ORCID
- Libby, Peter
- Venue
- Circulation Research
- Published
- 2015-11-06
- Volume
- 117
- Issue
- 11
- Pages
- 921-925
- ISSN
- 0009-7330 (ISSN-L)
- 1524-4571
- OpenAlex
- W2168307852
- Cited by
- 60
- References
- 0
- Citations by year
- 2026: 3 · 2025: 5 · 2024: 4 · 2023: 1 · 2022: 4 · 2021: 4 · 2020: 5 · 2019: 9 · 2018: 6 · 2017: 10 · 2016: 9
- FWCI
- 12.39
- Type
- journal article
- Language
- en
- Open access
- green
- nrs.harvard.edu
- Licence
- cc-by
- Locations
- Circulation Research (publishedVersion)
- PubMed (publishedVersion)
- Digital Access to Scholarship at Harvard (DASH) (Harvard University) (submittedVersion, cc-by)
- Circulation Research
- Topics
- Health Sciences › Veterinary › Small Animals › Animal testing and alternatives
- Health Sciences › Medicine › Physiology › Spaceflight effects on biology
- Social Sciences › Arts and Humanities › History and Philosophy of Science › Philosophy and History of Science
- Keywords
- mouse model, cardiovascular disease, translational research, inbred mouse strains, comorbidities, mechanistic insights
- MeSH terms
- Age Factors, Animals, Cardiology, Cardiovascular Diseases, Disease Models, Animal, Humans, Phenotype, Risk Factors, Species Specificity, Comorbidity, Mice, Congenic, Mice, Translational Research, Biomedical
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