Novel targets and future strategies for acute cardioprotection: Position Paper of the European Society of Cardiology Working Group on Cellular Biology of the Heart
J. Hausenloy, Derek; Garcia-Dorado, David; Bøtker, Hans Erik; M. Davidson, Sean; Downey, James; B. Engel, Felix; Jennings, Robert; Lecour, Sandrine; Leor, Jonathan; Madonna, Rosalinda; Ovize, Michel; Perrino, Cinzia; Prunier, Fabrice; Schulz, Rainer; Sluijter, Joost P.G.; Van Laake, Linda W.; Vinten-Johansen, Jakob; M. Yellon, Derek; Ytrehus, Kirsti; Heusch, Gerd; Ferdinandy, Péter
(2017) Cardiovascular Research, volume 113, issue 6, pp. 564 - 585
(Article)
Abstract
Ischaemic heart disease and the heart failure that often results, remain the leading causes of death and disability in Europe and worldwide. As such, in order to prevent heart failure and improve clinical outcomes in patients presenting with an acute ST-segment elevation myocardial infarction and patients undergoing coronary artery bypass
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graft surgery, novel therapies are required to protect the heart against the detrimental effects of acute ischaemia/reperfusion injury (IRI). During the last three decades, a wide variety of ischaemic conditioning strategies and pharmacological treatments have been tested in the clinic - however, their translation from experimental to clinical studies for improving patient outcomes has been both challenging and disappointing. Therefore, in this Position Paper of the European Society of Cardiology Working Group on Cellular Biology of the Heart, we critically analyse the current state of ischaemic conditioning in both the experimental and clinical settings, provide recommendations for improving its translation into the clinical setting, and highlight novel therapeutic targets and new treatment strategies for reducing acute myocardial IRI.
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Keywords: Cardioprotection, Ischaemia, Ischaemic conditioning, Myocardial Infarction, Reperfusion, Physiology, Cardiology and Cardiovascular Medicine, Physiology (medical), Journal Article
ISSN: 0008-6363
Publisher: Oxford University Press
Note: Funding Information: D.J.H. was funded by the British Heart Foundation (grant number FS/10/039/28270), the Rosetrees Trust, and is supported by the National Institute for Health Research University College London Hospitals Biomedical Research Centre. D.G.-D. is supported by the Spanish Institute of Health, Instituto de Salud Carlos III (grants PIE 13/00027, RETICS-RIC,RD12/0042/0021, and PI14/01431). C.P. was funded by the Italian Ministry of Health (grant number: GR-2009-1596220) and by the Italian Ministry of University (grant number: RBFR124FEN). L.V.L. was supported by the Netherlands Heart Foundation (Dekker 2013T056) and European Society of Cardiology Research Grant 2016. K.Y. has been supported by the Norwegian Council on Cardiovascular Diseases, Norway. G.H. was supported by the German Research Foundation (He 1320/18-3 and SFB 1116/B8). P.F. and R.S. were funded by the European Foundation for the Study of Diabetes (EFSD) New Horizons Collaborative Research Initiative from the European Association for the Study of Diabetes (EASD) and by the European Cooperation in Science and Technology (COST EU-ROS). P.F. was funded by the National Research Development and Innovation Office of Hungary (OTKA K 109737, OTKA ANN 107803, NVKP 16-1-2016-0017). Publisher Copyright: © 2017 The Author.
(Peer reviewed)