TY - JOUR
T1 - Translating cardioprotection for patient benefit
T2 - position paper from the Working Group of Cellular Biology of the Heart of the European Society of Cardiology
AU - Hausenloy, Derek J.
AU - Botker, Hans Erik
AU - Condorelli, Gianluigi
AU - Ferdinandy, Peter
AU - Garcia-Dorado, David
AU - Heusch, Gerd
AU - Lecour, Sandrine
AU - van Laake, Linda W.
AU - Madonna, Rosalinda
AU - Ruiz-Meana, Marisol
AU - Schulz, Rainer
AU - Sluijter, Joost P. G.
AU - Yellon, Derek M.
AU - Ovize, Michel
PY - 2013/4/1
Y1 - 2013/4/1
N2 - Coronary heart disease (CHD) is the leading cause of death and disability worldwide. Despite current therapy, the morbidity and mortality for patients with CHD remains significant. The most important manifestations of CHD arise from acute myocardial ischaemiareperfusion injury (IRI) in terms of cardiomyocyte death and its long-term consequences. As such, new therapeutic interventions are required to protect the heart against the detrimental effects of acute IRI and improve clinical outcomes. Although a large number of cardioprotective therapies discovered in pre-clinical studies have been investigated in CHD patients, few have been translated into the clinical setting, and a significant number of these have failed to show any benefit in terms of reduced myocardial infarction and improved clinical outcomes. Because of this, there is currently no effective therapy for protecting the heart against the detrimental effects of acute IRI in patients with CHD. One major factor for this lack of success in translating cardioprotective therapies into the clinical setting can be attributed to problems with the clinical study design. Many of these clinical studies have not taken into consideration the important data provided from previously published pre-clinical and clinical studies. The overall aim of this ESC Working Group Cellular Biology of the Heart Position Paper is to provide recommendations for optimizing the design of clinical cardioprotection studies, which should hopefully result in new and effective therapeutic interventions for the future benefit of CHD patients.
AB - Coronary heart disease (CHD) is the leading cause of death and disability worldwide. Despite current therapy, the morbidity and mortality for patients with CHD remains significant. The most important manifestations of CHD arise from acute myocardial ischaemiareperfusion injury (IRI) in terms of cardiomyocyte death and its long-term consequences. As such, new therapeutic interventions are required to protect the heart against the detrimental effects of acute IRI and improve clinical outcomes. Although a large number of cardioprotective therapies discovered in pre-clinical studies have been investigated in CHD patients, few have been translated into the clinical setting, and a significant number of these have failed to show any benefit in terms of reduced myocardial infarction and improved clinical outcomes. Because of this, there is currently no effective therapy for protecting the heart against the detrimental effects of acute IRI in patients with CHD. One major factor for this lack of success in translating cardioprotective therapies into the clinical setting can be attributed to problems with the clinical study design. Many of these clinical studies have not taken into consideration the important data provided from previously published pre-clinical and clinical studies. The overall aim of this ESC Working Group Cellular Biology of the Heart Position Paper is to provide recommendations for optimizing the design of clinical cardioprotection studies, which should hopefully result in new and effective therapeutic interventions for the future benefit of CHD patients.
KW - Cardioprotection: Ischaemia
KW - Reperfusion
KW - Acute myocardial infarction
KW - Cardiac surgery
KW - ELEVATION-MYOCARDIAL-INFARCTION
KW - RANDOMIZED CONTROLLED-TRIAL
KW - PERCUTANEOUS CORONARY INTERVENTION
KW - BYPASS GRAFT-SURGERY
KW - MITOCHONDRIAL PERMEABILITY TRANSITION
KW - GLUCOSE-INSULIN-POTASSIUM
KW - INJURY SALVAGE KINASE
KW - HYDROGEN EXCHANGE INHIBITION
KW - CONTROLLED CLINICAL-TRIAL
KW - DIABETIC HUMAN MYOCARDIUM
U2 - 10.1093/cvr/cvt004
DO - 10.1093/cvr/cvt004
M3 - Literature review
C2 - 23334258
SN - 0008-6363
VL - 98
SP - 7
EP - 27
JO - Cardiovascular Research
JF - Cardiovascular Research
IS - 1
ER -