Wever Kimberley E, Hooijmans Carlijn R, Riksen Niels P, Sterenborg Thomas B, Sena Emily S, Ritskes-Hoitinga Merel, Warlé Michiel C
Systematic Review Centre for Laboratory animal Experimentation (SYRCLE), Radboud University Medical Center, Nijmegen, The Netherlands.
Department of Internal Medicine and Dept. of Pharmacology-Toxicology, Radboud University Medical Center, Nijmegen, The Netherlands.
PLoS One. 2015 Nov 18;10(11):e0142021. doi: 10.1371/journal.pone.0142021. eCollection 2015.
Ischemic preconditioning (IPC) of the heart is a protective strategy in which a brief ischemic stimulus immediately before a lethal ischemic episode potently limits infarct size. Although very promising in animal models of myocardial infarction, IPC has not yet been successfully translated to benefit for patients.
To appraise all preclinical evidence on IPC for myocardial infarction and identify factors hampering translation.
Using systematic review and meta-analysis, we identified 503 animal studies reporting infarct size data from 785 comparisons between IPC-treated and control animals. Overall, IPC reduced myocardial infarction by 24.6% [95%CI 23.5, 25.6]. Subgroup analysis showed that IPC efficacy was reduced in comorbid animals and non-rodents. Efficacy was highest in studies using 2-3 IPC cycles applied <45 minutes before myocardial infarction. Local and remote IPC were equally effective. Reporting of study quality indicators was low: randomization, blinding and a sample size calculation were reported in 49%, 11% and 2% of publications, respectively.
Translation of IPC to the clinical setting may be hampered by the observed differences between the animals used in preclinical IPC studies and the patient population, regarding comorbidity, sex and age. Furthermore, the IPC protocols currently used in clinical trials could be optimized in terms of timing and the number of ischemic cycles applied. In order to inform future clinical trials successfully, future preclinical studies on IPC should aim to maximize both internal and external validity, since poor methodological quality may limit the value of the preclinical evidence.
心脏缺血预处理(IPC)是一种保护策略,即在致命性缺血发作前给予短暂的缺血刺激,可有效限制梗死面积。尽管在心肌梗死动物模型中前景十分广阔,但IPC尚未成功转化应用于患者并使其受益。
评估关于心肌梗死IPC的所有临床前证据,并确定阻碍其转化应用的因素。
通过系统评价和荟萃分析,我们纳入了503项动物研究,这些研究报告了785组IPC处理组与对照组动物之间的梗死面积数据。总体而言,IPC使心肌梗死面积减少了24.6%[95%置信区间23.5, 25.6]。亚组分析表明,在合并症动物和非啮齿动物中,IPC的疗效降低。在心肌梗死前<45分钟应用2 - 3个IPC周期的研究中,疗效最高。局部和远程IPC同样有效。研究质量指标的报告率较低:分别有49%、11%和2%的出版物报告了随机化、盲法和样本量计算。
临床前IPC研究中使用的动物与患者群体在合并症、性别和年龄方面存在差异,这可能会阻碍IPC向临床应用的转化。此外,目前临床试验中使用的IPC方案在时间安排和缺血周期数量方面可以进行优化。为了成功指导未来的临床试验,未来关于IPC的临床前研究应旨在最大限度地提高内部和外部效度,因为方法学质量差可能会限制临床前证据的价值。