Dang Vi T, Huang Aric, Werstuck Geoff H
Thrombosis and Atherosclerosis Research Institute, McMaster University, Hamilton, Ontario, Canada.
Department of Chemistry and Chemical Biology, McMaster University, Hamilton, Ontario, Canada.
Cardiovasc Hematol Disord Drug Targets. 2018;18(3):166-175. doi: 10.2174/1871529X18666180420170108.
Cardiovascular Disease (CVD) is the leading cause of mortality and morbidity worldwide. Four out of five CVD deaths are due to myocardial infarction or stroke. Despite many initiatives that have been established for CVD prevention and risk management, and new therapies to treat existing CVD, patients continue to die from cardiac events. Clearly, we need to identify new therapeutic targets and strategies. Metabolomics offers a novel solution to this problem, as metabolomics-based biomarkers do not only indicate the presence or absence of a disease, but are also capable of assessing risks of developing the disease and detecting the disease prior to the appearance of overt clinical symptoms.
In this review, we describe the analytical techniques and workflow used in untargeted metabolomics. We also identify several case studies that highlight the use of untargeted metabolomics in cardiovascular research.
Five case studies that employ untargeted metabolomics approaches to identify biomarkers for cardiovascular risk, myocardial ischemia, transient ischemic attack, incident coronary heart disease, and myocardial infarction risk prediction are described. The use of the untargeted metabolomics is still relatively new in cardiovascular research. As such, there remains a need for future advancement in metabolomic technologies.
Early diagnosis of CVDs and identification of patients at high risk of developing adverse events would allow for timely intervention that prevents serious consequences or death. There is a need to establish sensitive and non-invasive CV biomarkers, and novel therapeutic targets for the prevention and treatment of CVDs.
心血管疾病(CVD)是全球死亡和发病的主要原因。五分之四的心血管疾病死亡是由心肌梗死或中风导致的。尽管已经制定了许多心血管疾病预防和风险管理措施,以及治疗现有心血管疾病的新疗法,但患者仍死于心脏事件。显然,我们需要确定新的治疗靶点和策略。代谢组学为这个问题提供了一种新的解决方案,因为基于代谢组学的生物标志物不仅能表明疾病的存在与否,还能够评估患该疾病的风险,并在出现明显临床症状之前检测出疾病。
在本综述中,我们描述了非靶向代谢组学中使用的分析技术和工作流程。我们还列举了几个案例研究,突出了非靶向代谢组学在心血管研究中的应用。
描述了五个采用非靶向代谢组学方法来识别心血管风险、心肌缺血、短暂性脑缺血发作、冠心病发病和心肌梗死风险预测生物标志物的案例研究。非靶向代谢组学在心血管研究中的应用仍然相对较新。因此,代谢组学技术未来仍需进一步发展。
心血管疾病的早期诊断以及识别有发生不良事件高风险的患者,将有助于及时进行干预,预防严重后果或死亡。需要建立敏感且非侵入性的心血管生物标志物,以及用于预防和治疗心血管疾病的新治疗靶点。