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| Item Type: | Article |
|---|---|
| Title: | Rethinking animal attrition in preclinical research: expressing causal mechanisms of selection bias using directed acyclic graphs |
| Creators Name: | Collazo, A., Kuhn, H.G., Kurth, T., Piccininni, M. and Rohmann, J.L. |
| Abstract: | Animal attrition in preclinical experiments can introduce bias in the estimation of causal treatment effects, as the treatment-outcome association in surviving animals may not represent the causal effect of interest. This can compromise the internal validity of the study despite randomization at the outset. Directed Acyclic Graphs (DAGs) are useful tools to transparently visualize assumptions about the causal structure underlying observed data. By illustrating relationships between relevant variables, DAGs enable the detection of even less intuitive biases, and can thereby inform strategies for their mitigation. In this study, we present an illustrative causal model for preclinical stroke research, in which animal attrition induces a specific type of selection bias (i.e., collider stratification bias) due to the interplay of animal welfare, initial disease severity and negative side effects of treatment. Even when the treatment had no causal effect, our simulations revealed substantial bias across different scenarios. We show how researchers can detect and potentially mitigate this bias in the analysis phase, even when only data from surviving animals are available, if knowledge of the underlying causal process that gave rise to the data is available. Collider stratification bias should be a concern in preclinical animal studies with severe side effects and high post-randomization attrition. |
| Keywords: | Animal Attrition, Collider Stratification Bias, Internal Validity, Preclinical Research, Selection Bias |
| Source: | Journal of Cerebral Blood Flow and Metabolism |
| ISSN: | 0271-678X |
| Publisher: | Sage Publications |
| Page Range: | 271678X241275760 |
| Date: | 20 August 2024 |
| Official Publication: | https://doi.org/10.1177/0271678X241275760 |
| PubMed: | View item in PubMed |
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