Lindner Thomas W, Deakin Charles D, Aarsetøy Hildegunn, Rubertsson Sten, Heltne Jon-Kenneth, Søreide Eldar
Department of Anaesthesiology and Intensive Care , Stavanger University Hospital , Stavanger , Norway.
South Central Ambulance Service NHS Foundation Trust , Otterbourne , UK ; NIHR Southampton Respiratory Biomedical Research Unit , Southampton University Hospital NHS Foundation Trust , Southampton , UK ; School of Health Sciences , University of Surrey , UK.
Open Heart. 2014 Aug 14;1(1):e000138. doi: 10.1136/openhrt-2014-000138. eCollection 2014.
In the last few years the genetic influence on health and disease outcome has become more apparent. The ACE genotype appears to play a significant role in the pathophysiology of several disease processes. This pilot study aims at showing the feasibility to examine the genetic influence of the ACE genotype on return of spontaneous circulation (ROSC) in out-of-hospital cardiac arrest (OHCA).
We performed a prospective observational study of all OHCAs of presumed cardiac origin in a well-defined population. We collected prehospital blood samples for the determination of ACE genotype and used this information together with Utstein template parameters in a multivariable analysis to examine the relationship between ROSC and ACE genotype.
We collect blood samples in 156 of 361 patients with OHCA of presumed cardiac origin, 127 samples were analysed (mean age 67 years, 86% male, 79% witnessed OHCA, 80% bystander CPR, 62% had a shockable rhythm, ROSC 77%). Distribution of the ACE gene polymorphisms: insertion polymorphism (II) n=22, 17%, insertion/deletion polymorphism (ID) n=66, 52% and deletion polymorphism (DD) n=39, 31%. We found no significant association between ACE II vs ACE DD/DI and ROSC (OR 1.72; CI 0.52 to 5.73; p=0.38). Other ACE genotype groupings (II/ID vs DD or II vs DD) did not change the overall finding of lack of impact of ACE genotype on ROSC.
This pilot study did not indicate a significant association between ACE gene polymorphism and ROSC. However, it has demonstrated that prehospital genetic studies including blood sampling are feasible and ethically acceptable.
在过去几年中,基因对健康和疾病结局的影响已变得更加明显。血管紧张素转换酶(ACE)基因型似乎在几种疾病过程的病理生理学中发挥重要作用。这项初步研究旨在表明,在院外心脏骤停(OHCA)中,研究ACE基因型对自主循环恢复(ROSC)的基因影响是可行的。
我们对一个明确界定人群中所有推测为心脏源性的OHCA进行了前瞻性观察研究。我们收集院前血样以确定ACE基因型,并在多变量分析中使用此信息以及乌斯坦模板参数来研究ROSC与ACE基因型之间的关系。
在361例推测为心脏源性的OHCA患者中,我们采集了156例的血样,分析了127份样本(平均年龄67岁,86%为男性,79%的OHCA有目击者,80%由旁观者进行心肺复苏,62%有可电击心律,ROSC为77%)。ACE基因多态性的分布:插入多态性(II)n = 22,占17%;插入/缺失多态性(ID)n = 66,占52%;缺失多态性(DD)n = 39,占31%。我们发现ACE II与ACE DD/DI和ROSC之间无显著关联(比值比1.72;可信区间0.52至5.73;p = 0.38)。其他ACE基因型分组(II/ID与DD或II与DD)并未改变ACE基因型对ROSC缺乏影响这一总体结果。
这项初步研究未表明ACE基因多态性与ROSC之间存在显著关联。然而,它已证明包括血样采集在内的院前基因研究是可行的且在伦理上是可接受的。