Animal models and animal-free innovations for cardiovascular research: current status and routes to be explored. Consensus document of the ESC Working Group on Myocardial Function and the ESC Working Group on Cellular Biology of the Heart. Issue 15 (6th January 2022)

• Record Type: Journal Article
• Authors: van der Velden, Jolanda; Asselbergs, Folkert W; Bakkers, Jeroen; Batkai, Sandor; Bertrand, Luc; Bezzina, Connie R; Bot, Ilze; Brundel, Bianca J J M; Carrier, Lucie; Chamuleau, Steven; Ciccarelli, Michele; Dawson, Dana; Davidson, Sean M; Dendorfer, Andreas; Duncker, Dirk J; Eschenhagen, Thomas; Fabritz, Larissa; Falcão-Pires, Ines; Ferdinandy, Péter; Giacca, Mauro; Girao, Henrique; Gollmann-Tepeköylü, Can; Gyongyosi, Mariann; Guzik, Tomasz J; Hamdani, Nazha; Heymans, Stephane; Hilfiker, Andres; Hilfiker-Kleiner, Denise; Hoekstra, Alfons G; Hulot, Jean-Sébastien; Kuster, Diederik W D; van Laake, Linda W; Lecour, Sandrine; Leiner, Tim; Linke, Wolfgang A; Lumens, Joost; Lutgens, Esther; Madonna, Rosalinda; Maegdefessel, Lars; Mayr, Manuel; van der Meer, Peter; Passier, Robert; Perbellini, Filippo; Perrino, Cinzia; Pesce, Maurizio; Priori, Silvia; Remme, Carol Ann; Rosenhahn, Bodo; Schotten, Ulrich; Schulz, Rainer; Sipido, Karin R; Sluijter, Joost P G; van Steenbeek, Frank; Steffens, Sabine; Terracciano, Cesare M; Tocchetti, Carlo Gabriele; Vlasman, Patricia; Yeung, Kak Khee; Zacchigna, Serena; Zwaagman, Dayenne; Thum, Thomas;
• Is Part Of: Cardiovascular research. Volume 118:Issue 15(2022)
• Page Start: 3016
• Page End: 3051
• Publication Date: 2022-01-06
• Subjects: iPSC -- Tissue engineering -- Multiomics -- Network medicine -- Bioinformatics -- Big data -- Comorbidities -- Cardiovascular disease; Cardiovascular system -- Diseases -- Periodicals; Cardiovascular system -- Periodicals; 616.1
• DOI: 10.1093/cvr/cvab370
• Languages: English
• ISSNs: 0008-6363

Abstract

Abstract: Cardiovascular diseases represent a major cause of morbidity and mortality, necessitating research to improve diagnostics, and to discover and test novel preventive and curative therapies, all of which warrant experimental models that recapitulate human disease. The translation of basic science results to clinical practice is a challenging task, in particular for complex conditions such as cardiovascular diseases, which often result from multiple risk factors and comorbidities. This difficulty might lead some individuals to question the value of animal research, citing the translational 'valley of death', which largely reflects the fact that studies in rodents are difficult to translate to humans. This is also influenced by the fact that new, human-derived in vitro models can recapitulate aspects of disease processes. However, it would be a mistake to think that animal models do not represent a vital step in the translational pathway as they do provide important pathophysiological insights into disease mechanisms particularly on an organ and systemic level. While stem cell-derived human models have the potential to become key in testing toxicity and effectiveness of new drugs, we need to be realistic, and carefully validate all new human-like disease models. In this position paper, we highlight recent advances in trying to reduce the number of animals for cardiovascular research ranging from stem cell-derived models to in situ modelling of heart properties, bioinformatic models based on large datasets, and state-of-the-art animal models, which show clinically relevant characteristics observed in patients with a cardiovascular disease. We aim to provide a guide to help researchers in their experimental design to translate bench findings to clinical routine taking the replacement, reduction, and refinement (3R) as a guiding concept.