通过代谢组学定义急性冠状动脉综合征
Defining Acute Coronary Syndrome through Metabolomics.
作者信息
Surendran Arun, Atefi Negar, Zhang Hannah, Aliani Michel, Ravandi Amir
机构信息
Cardiovascular Lipidomics Laboratory, St. Boniface Hospital, Albrechtsen Research Centre, Winnipeg, MB R2H 2A6, Canada.
Mass Spectrometry and Proteomics Core Facility, Rajiv Gandhi Centre for Biotechnology, Thiruvananthapuram 695014, Kerala, India.
出版信息
Metabolites. 2021 Oct 6;11(10):685. doi: 10.3390/metabo11100685.
As an emerging platform technology, metabolomics offers new insights into the pathomechanisms associated with complex disease conditions, including cardiovascular diseases. It also facilitates assessing the risk of developing the disease before its clinical manifestation. For this reason, metabolomics is of growing interest for understanding the pathogenesis of acute coronary syndromes (ACS), finding new biomarkers of ACS, and its associated risk management. Metabolomics-based studies in ACS have already demonstrated immense potential for biomarker discovery and mechanistic insights by identifying metabolomic signatures (e.g., branched-chain amino acids, acylcarnitines, lysophosphatidylcholines) associated with disease progression. Herein, we discuss the various metabolomics approaches and the challenges involved in metabolic profiling, focusing on ACS. Special attention has been paid to the clinical studies of metabolomics and lipidomics in ACS, with an emphasis on ischemia/reperfusion injury.
作为一种新兴的平台技术,代谢组学为与包括心血管疾病在内的复杂疾病状况相关的病理机制提供了新的见解。它还有助于在疾病临床表现之前评估发病风险。因此,代谢组学对于理解急性冠脉综合征(ACS)的发病机制、寻找ACS的新生物标志物及其相关风险管理越来越受到关注。基于代谢组学的ACS研究已经通过识别与疾病进展相关的代谢组学特征(如支链氨基酸、酰基肉碱、溶血磷脂酰胆碱),在生物标志物发现和机制洞察方面展现出巨大潜力。在此,我们讨论各种代谢组学方法以及代谢谱分析中涉及的挑战,重点关注ACS。特别关注了ACS中代谢组学和脂质组学的临床研究,重点是缺血/再灌注损伤。