Przyklenk Karin
Cardiovascular Research Institute and Departments of Physiology and Emergency Medicine, Wayne State University School of Medicine, Detroit, MI, USA.
Br J Pharmacol. 2015 Apr;172(8):1961-73. doi: 10.1111/bph.13064. Epub 2015 Feb 27.
The development of novel adjuvant strategies capable of attenuating myocardial ischaemia-reperfusion injury and reducing infarct size remains a major, unmet clinical need. A wealth of preclinical evidence has established that ischaemic 'conditioning' is profoundly cardioprotective, and has positioned the phenomenon (in particular, the paradigms of postconditioning and remote conditioning) as the most promising and potent candidate for clinical translation identified to date. However, despite this preclinical consensus, current phase II trials have been plagued by heterogeneity, and the outcomes of recent meta-analyses have largely failed to confirm significant benefit. As a result, the path to clinical application has been perceived as 'disappointing' and 'frustrating'. The goal of the current review is to discuss the pitfalls that may be stalling the successful clinical translation of ischaemic conditioning, with an emphasis on concerns regarding: (i) appropriate clinical study design and (ii) the choice of the 'right' preclinical models to facilitate clinical translation.
开发能够减轻心肌缺血再灌注损伤并缩小梗死面积的新型辅助策略,仍然是一项重大的、尚未满足的临床需求。大量临床前证据表明,缺血“预处理”具有显著的心脏保护作用,并将这一现象(特别是后处理和远程预处理模式)定位为迄今为止确定的最有前景、最有效的临床转化候选方案。然而,尽管有这一临床前共识,但目前的II期试验一直受到异质性的困扰,最近的荟萃分析结果在很大程度上未能证实有显著益处。因此,临床应用之路被认为是“令人失望的”和“令人沮丧的”。本综述的目的是讨论可能阻碍缺血预处理成功临床转化的陷阱,重点关注以下问题:(i)适当的临床研究设计,以及(ii)选择“正确的”临床前模型以促进临床转化。