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. 2025 Aug;10 Suppl 1(Suppl 1):S40-S52.
doi: 10.1002/epi4.12642. Epub 2022 Sep 28.

A companion to the preclinical common data elements for rodent genetic epilepsy models. A report of the TASK3-WG1B: Paediatric and genetic models working group of the ILAE/AES joint translational TASK force

Affiliations

A companion to the preclinical common data elements for rodent genetic epilepsy models. A report of the TASK3-WG1B: Paediatric and genetic models working group of the ILAE/AES joint translational TASK force

Massimo Mantegazza et al. Epilepsia Open. 2025 Aug.

Abstract

Rodent models of epilepsy remain the cornerstone of research into the mechanisms underlying genetic epilepsy. Reproducibility of experiments using these rodent models, occurring across a diversity of laboratories and commercial vendors, remains an issue impacting the cost-effectiveness and scientific rigor of the studies performed. Here, we present two case report forms (CRFs) describing common data elements (CDE) for genetic rodent models, developed by the TASK3-WG1B Working Group of the International League Against Epilepsy (ILAE)/American Epilepsy Society (AES) Joint Translational Task Force. The first CRF relates to genetic rodent models that have been engineered based on variants described in epilepsy patients. The second CRF encompasses both spontaneous and inbred rodent models. This companion piece describes the elements and discusses the important factors to consider before documenting each required element. These CRFs provide tools that allow investigators to more uniformly describe core experimental data on different genetic models across laboratories, with the aim of improving experimental reproducibility and thus translational impact of such studies.

Keywords: common data elements; epilepsy; genetics; model; preclinical; rodent.

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Conflict of interest statement

AS Galanopoulou is Editor in Chief of Epilepsia Open and associate editor of Neurobiology of Disease journal and has received royalties for publications from Elsevier, Medlink, and Morgan and Claypool publishers. We confirm that we have read the Journal's position on issues involved in ethical publication and affirm that this report is consistent with those guidelines.

Figures

FIGURE 1
FIGURE 1
Schematic illustrating the envisaged use of the “core” genetic CRF in conjunction with individual “experimental” CRFs.

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