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大规模代谢组学分析揭示了早期冠状动脉粥样硬化的潜在生物标志物。

Large-scale Metabolomic Analysis Reveals Potential Biomarkers for Early Stage Coronary Atherosclerosis.

机构信息

Department of Cardiology, The Second Affiliated Hospital of Harbin Medical University, and The Key Laboratory of Myocardial Ischemia, Chinese Ministry of Education, Harbin, 150081, P. R. China.

Department of Epidemiology and Biostatistics, School of Public Health, Medical College of Soochow University, Suzhou, 215123, China.

出版信息

Sci Rep. 2017 Sep 18;7(1):11817. doi: 10.1038/s41598-017-12254-1.

Abstract

Coronary atherosclerosis (CAS) is the pathogenesis of coronary heart disease, which is a prevalent and chronic life-threatening disease. Initially, this disease is not always detected until a patient presents with seriously vascular occlusion. Therefore, new biomarkers for appropriate and timely diagnosis of early CAS is needed for screening to initiate therapy on time. In this study, we used an untargeted metabolomics approach to identify potential biomarkers that could enable highly sensitive and specific CAS detection. Score plots from partial least-squares discriminant analysis clearly separated early-stage CAS patients from controls. Meanwhile, the levels of 24 metabolites increased greatly and those of 18 metabolites decreased markedly in early CAS patients compared with the controls, which suggested significant metabolic dysfunction in phospholipid, sphingolipid, and fatty acid metabolism in the patients. Furthermore, binary logistic regression showed that nine metabolites could be used as a combinatorial biomarker to distinguish early-stage CAS patients from controls. The panel of nine metabolites was then tested with an independent cohort of samples, which also yielded satisfactory diagnostic accuracy (AUC = 0.890). In conclusion, our findings provide insight into the pathological mechanism of early-stage CAS and also supply a combinatorial biomarker to aid clinical diagnosis of early-stage CAS.

摘要

冠状动脉粥样硬化(CAS)是冠心病的发病机制,是一种普遍且慢性的危及生命的疾病。最初,这种疾病并不总是被发现,直到患者出现严重的血管阻塞。因此,需要新的生物标志物来进行适当和及时的早期 CAS 诊断,以便进行早期筛查并及时开始治疗。在本研究中,我们使用非靶向代谢组学方法来识别潜在的生物标志物,以便能够高度敏感和特异性地检测 CAS。偏最小二乘判别分析的得分图清楚地区分了早期 CAS 患者和对照组。同时,与对照组相比,早期 CAS 患者的 24 种代谢物水平显著升高,18 种代谢物水平显著降低,这表明患者的磷脂、鞘脂和脂肪酸代谢存在明显的代谢功能障碍。此外,二元逻辑回归显示,有 9 种代谢物可以作为组合生物标志物,将早期 CAS 患者与对照组区分开来。然后,用一个独立的样本队列对这 9 种代谢物的组合进行了测试,也得到了令人满意的诊断准确性(AUC=0.890)。总之,我们的研究结果为早期 CAS 的病理机制提供了新的见解,并提供了一种组合生物标志物来辅助早期 CAS 的临床诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6cdd/5603568/0dca237ec6d3/41598_2017_12254_Fig1_HTML.jpg

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