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为患者谋福利的心脏保护:来自欧洲心脏病学会心脏细胞生物学工作组的立场文件。

Translating cardioprotection for patient benefit: position paper from the Working Group of Cellular Biology of the Heart of the European Society of Cardiology.

机构信息

The Hatter Cardiovascular Institute, University College London, 67 Chenies Mews, London WC1E 6HX, UK.

出版信息

Cardiovasc Res. 2013 Apr 1;98(1):7-27. doi: 10.1093/cvr/cvt004. Epub 2013 Jan 19.

DOI:10.1093/cvr/cvt004
PMID:23334258
Abstract

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 ischaemia-reperfusion 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.

摘要

冠心病(CHD)是全球范围内导致死亡和残疾的主要原因。尽管目前有治疗方法,但 CHD 患者的发病率和死亡率仍然很高。CHD 最重要的表现是心肌缺血再灌注损伤(IRI)导致的心肌细胞死亡及其长期后果。因此,需要新的治疗干预措施来保护心脏免受急性 IRI 的有害影响,改善临床结局。尽管在临床前研究中发现了大量的心脏保护疗法,但只有少数几种被应用于 CHD 患者,其中许多在减少心肌梗死和改善临床结局方面并没有显示出任何益处。由于这一原因,目前尚无有效的疗法可以保护 CHD 患者免受急性 IRI 的有害影响。将心脏保护疗法转化为临床应用的失败,一个主要原因可以归因于临床研究设计存在问题。许多这些临床研究没有考虑到之前发表的临床前和临床研究提供的重要数据。本 ESC 工作组《心脏细胞生物学立场文件》的总体目标是为优化临床心脏保护研究的设计提供建议,希望这将为 CHD 患者的未来带来新的、有效的治疗干预措施。

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