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抗炎化合物在心肌梗死治疗中的转化失败:大型动物模型的荟萃分析

Translational failure of anti-inflammatory compounds for myocardial infarction: a meta-analysis of large animal models.

作者信息

van Hout Gerardus P J, Jansen of Lorkeers Sanne J, Wever Kimberly E, Sena Emily S, Kouwenberg Lisanne H J A, van Solinge Wouter W, Macleod Malcolm R, Doevendans Pieter A, Pasterkamp Gerard, Chamuleau Steven A J, Hoefer Imo E

机构信息

Experimental Cardiology Laboratory, University Medical Center Utrecht, Heidelberglaan 100, Utrecht 3584CX, The Netherlands

Department of Cardiology, University Medical Center Utrecht, Utrecht, The Netherlands.

出版信息

Cardiovasc Res. 2016 Feb 1;109(2):240-8. doi: 10.1093/cvr/cvv239. Epub 2015 Oct 20.

Abstract

AIMS

Numerous anti-inflammatory drugs have been tested in large animal studies of myocardial infarction (MI). Despite positive results, translation of anti-inflammatory strategies into clinical practice has proved to be difficult. Critical disparities between preclinical and clinical study design that influence efficacy may partly be responsible for this translational failure. The aim of the present systematic review was to better understand which factors underlie the failure of transition towards the clinic.

METHODS AND RESULTS

Meta-analysis and regression of large animal studies were performed to identify sources that influenced effect size of anti-inflammatory compounds in large animal models of MI. We included 183 studies, containing 3331 large animals. Infarct size (IS) as a ratio of the area at risk (12.7%; 95% confidence interval, CI 11.1-14.4%, P < 0.001) and IS as a ratio of the left ventricle (3.9%; 95% CI 3.1-4.7%, P < 0.001) were reduced in treatment compared with control groups. Effect size was higher when outcome was assessed early after MI (P = 0.013) and where studies included only male animals (P < 0.001). Mortality in treated animals was higher in studies that blinded the investigator during the experiment (P = 0.041) and depended on the type of drug used (P < 0.001).

CONCLUSIONS

As expected, treatment with anti-inflammatory drugs leads to smaller infarct size in large animal MI models. Timing of outcome assessment, sex, and study quality are significantly associated with outcome and may explain part of the translational failure in clinical settings. Effect size depends on the type of drug used, enabling identification of compounds for future clinical testing.

摘要

目的

多种抗炎药物已在心肌梗死(MI)的大型动物研究中进行了测试。尽管取得了积极成果,但将抗炎策略转化为临床实践却被证明是困难的。临床前和临床研究设计之间影响疗效的关键差异可能部分导致了这种转化失败。本系统评价的目的是更好地了解导致向临床转化失败的因素。

方法和结果

对大型动物研究进行荟萃分析和回归分析,以确定影响MI大型动物模型中抗炎化合物效应大小的因素。我们纳入了183项研究,涉及3331只大型动物。与对照组相比,治疗组的梗死面积(IS)占危险区域面积的比例(12.7%;95%置信区间,CI 11.1 - 14.4%,P < 0.001)以及IS占左心室面积的比例(3.9%;95%CI 3.1 - 4.7%,P < 0.001)均有所降低。当在MI后早期评估结果时(P = 0.013)以及研究仅纳入雄性动物时(P < 0.001),效应大小更高。在实验过程中对研究者进行盲法处理的研究中,治疗动物的死亡率更高(P = 0.041),且取决于所使用的药物类型(P < 0.001)。

结论

正如预期的那样,在大型动物MI模型中,使用抗炎药物治疗可使梗死面积减小。结果评估的时间、性别和研究质量与结果显著相关,可能解释了临床环境中部分转化失败的原因。效应大小取决于所使用的药物类型,有助于确定未来临床测试的化合物。

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