Myocardial protection at a crossroads - The need for translation into clinical therapy

被引:431
作者
Bolli, R [1 ]
Becker, L [1 ]
Gross, G [1 ]
Mentzer, R [1 ]
Balshaw, D [1 ]
Lathrop, DA [1 ]
机构
[1] NHLBI, Sci Res Grp, Heart Res Program,Div Heart & Vasc Dis, NIH,US Dept Hlth & Human Serv, Bethesda, MD 20892 USA
关键词
basic science; myocardial ischemia; reperfusion injury; ischemic heart disease; cardiac surgery; cardioprotection; research translation;
D O I
10.1161/01.RES.0000137171.97172.d7
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Over the past 30 years, hundreds of experimental interventions (both pharmacologic and nonpharmacologic) have been reported to protect the ischemic myocardium in experimental animals; however, with the exception of early reperfusion, none has been translated into clinical practice. The National Heart, Lung, and Blood Institute convened a working group to discuss the reasons for the failure to translate potential therapies for protecting the heart from ischemia and reperfusion and to recommend new approaches to accomplish this goal. The Working Group concluded that cardioprotection in the setting of acute myocardial infarction, cardiac surgery, and cardiac arrest is at a crossroads. Present basic research approaches to identify cardioprotective therapies are inefficient and counterproductive. For 3 decades, significant resources have been invested in single-center studies that have often yielded inconclusive results. A new paradigm is needed to obviate many of the difficulties associated with translation of basic science findings. The Working Group urged a new focus on translational research that emphasizes efficacy and clinically relevant outcomes, and recommended the establishment of a system for rigorous preclinical testing of promising cardioprotective agents with clinical trial-like approaches (ie, blinded, randomized, multicenter, and adequately powered studies using standardized methods). A national preclinical research consortium would enable rational translation of important basic science findings into clinical use. The Working Group recommended that the National Institutes of Health proactively intervene to remedy current problems that impede translation of cardioprotective therapies. Their specific recommendations include the establishment of a preclinical consortium and the performance of 2 clinical studies that are likely to demonstrate effectiveness (phase III clinical trials of adenosine in acute myocardial infarction and cardiac surgery).
引用
收藏
页码:125 / 134
页数:10
相关论文
共 49 条
[1]
Ischemia/reperfusion injury [J].
Anaya-Prado, R ;
Toledo-Pereyra, LH ;
Lentsch, AB ;
Ward, PA .
JOURNAL OF SURGICAL RESEARCH, 2002, 105 (02) :248-258
[2]
Na+/H+ exchange inhibitors for cardioprotective therapy:: Progress, problems and prospects [J].
Avkiran, M ;
Marber, MS .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2002, 39 (05) :747-753
[3]
The PULSE initiative - Scientific priorities and strategic planning for resuscitation research and life saving therapies [J].
Becker, LB ;
Weisfeldt, ML ;
Weil, MH ;
Budinger, T ;
Carrico, J ;
Kern, K ;
Nichol, G ;
Shechter, I ;
Traystman, R ;
Webb, C ;
Wiedemann, H ;
Wise, R ;
Sopko, G .
CIRCULATION, 2002, 105 (21) :2562-2570
[4]
Treatment of comatose survivors of out-of-hospital cardiac arrest with induced hypothermia [J].
Bernard, SA ;
Gray, TW ;
Buist, MD ;
Jones, BM ;
Silvester, W ;
Gutteridge, G ;
Smith, K .
NEW ENGLAND JOURNAL OF MEDICINE, 2002, 346 (08) :557-563
[5]
The late phase of preconditioning [J].
Bolli, R .
CIRCULATION RESEARCH, 2000, 87 (11) :972-983
[6]
OXYGEN-DERIVED FREE-RADICALS AND MYOCARDIAL REPERFUSION INJURY - AN OVERVIEW [J].
BOLLI, R .
CARDIOVASCULAR DRUGS AND THERAPY, 1991, 5 :249-268
[7]
BRAUNWAL.E, 1974, CIRCULATION, V50, P206, DOI 10.1161/01.CIR.50.2.206
[8]
Ischemic preconditioning:: From adenosine receptor to KATP channel [J].
Cohen, MV ;
Baines, CP ;
Downey, JM .
ANNUAL REVIEW OF PHYSIOLOGY, 2000, 62 :79-109
[9]
Prolonging the delayed phase of myocardial protection:: Repetitive adenosine A1 receptor activation maintains rabbit myocardium in a preconditioned state [J].
Dana, A ;
Baxter, GF ;
Walker, JM ;
Yellon, DM .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1998, 31 (05) :1142-1149
[10]
Metabolic modulation of acute myocardial infarction -: The ECLA glucose-insulin-potassium pilot trial [J].
Díaz, R ;
Paolasso, A ;
Piegas, LS ;
Tajer, CD ;
Moreno, MG ;
Corvalán, R ;
Isea, JE ;
Romero, G .
CIRCULATION, 1998, 98 (21) :2227-2234