Early Warning of Ischemic Stroke Based on Atherosclerosis Index Combined With Serum Markers

医学 缺血性中风 索引(排版) 内科学 心脏病学 缺血 计算机科学 万维网
作者
Wenjie Zhou,Shanze Li,Guijiang Sun,Lili Song,Wenjun Feng,Rui Li,Hui Liu,Yaqian Dong,Siyu Chen,Shenshen Yang,Jing Li,Yubo Li
出处
期刊:The Journal of Clinical Endocrinology and Metabolism [Oxford University Press]
卷期号:107 (7): 1956-1964 被引量:20
标识
DOI:10.1210/clinem/dgac176
摘要

Abstract Context Ischemic stroke (IS) is a serious public health problem worldwide, threatening human life and health. Atherosclerosis is the cause of stroke. At present, there are few selective indexes that can be used to evaluate atherosclerosis in the clinic; providers rely mainly on the atherosclerotic index (AI). Disturbance of lipid metabolism is considered to be a key event leading to IS. Objective The purpose of this study was to discover potential biomarkers in the serum of atherosclerosis-induced IS, combined with the AI to provide early warning for the diagnosis of IS. Methods In this study, we used nontargeted metabolomics based on ultra-high performance liquid chromatography–quadrupole time-of-flight mass spectrometry (UPLC-Q/TOF-MS) to measure the changes in serum metabolites in a group of patients with IS. To verify the reproducibility of candidate biomarkers in the population, we expanded the sample size. Results Five metabolites were identified, including sphingomyelin (18:0/14:0), 1-Methylpyrrolinium, PC (18:0/18:0), LysoPC (18:0/0:0), and PC (18: 2/18:2). The combination of these 5 metabolic markers has good diagnostic and predictive ability, and the change level of these metabolites is significantly related to IS. Our results also indicate that changes in glycerophospholipid metabolism may indicate an early risk of IS development. Conclusion These findings may contribute to the development of new diagnostic methods of potential biomarkers in serum combined with the AI, thereby providing early warning for the diagnosis of atherosclerosis-induced IS, and may provide a new insights for pathogenesis in IS.
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