关键词: Acute Aortic Dissection Biomarker LCMS Liquid Chip Technology

Mesh : Humans Chemokine CCL4 Epidermal Growth Factor Interleukin-7 Treatment Outcome Cytokines Biomarkers Aortic Dissection / diagnosis Myocardial Infarction / diagnosis Inosine Kynuramine / analogs & derivatives

来  源:   DOI:10.1016/j.avsg.2023.09.086

Abstract:
BACKGROUND: Aortic dissection (AD) is a serious disease. Previous study, the use of peripheral blood biomarkers to diagnose AD showed strong clinical feasibility, but the possible molecular mechanism is unclear.
METHODS: Sera from 79 healthy subjects, 73 patients with well-established AD, and 74 patients with well-established acute myocardial infarction (AMI) were investigated by Liquid Chromatograph-Mass Spectrometer to detect metabolites (AFMK, Glycerophosphocholine, Inosine, SPH). The cell factor expression in the 3 group were detected by Liquid Chip Technology.
RESULTS: The serum content trends of 4 metabolic indexes in patients with AMI and AD group were used as the diagnostic models, and the effective diagnosis rate was 97.8%. The diagnosis rate is 89.8% in distinguishing patients with AMI from patients with AD. The expression in serum of the 3 groups showed that there were significant differences in the expression of 23 cytokines. By correlation analysis, it was found that miP-1, IL-7, MIP-1β, EGF and other cytokines were significantly correlated with the 4 metabolic molecules.
CONCLUSIONS: AFMK, Glycerophosphocholine, Inosine, Sphingfungin B (SPH) metabolites are potential biomarkers for AD, and the influence of related metabolic process may be related to the expression of miP-1, IL-7, MIP-1β, EGF, and other cytokines.
摘要:
背景:主动脉夹层(AD)是一种严重的疾病。以前的研究,使用外周血生物标志物诊断AD具有很强的临床可行性,但可能的分子机制尚不清楚。
方法:来自79名健康受试者(HC)的血清,73例AD患者,并通过LC-MS检测74例确诊的急性心肌梗死(AMI)患者的代谢物(AFMK,甘油磷酸胆碱,肌苷,SPH)。采用液相芯片技术检测三组细胞因子的表达。
结果:以AMI和AD患者血清4项代谢指标的含量变化趋势作为诊断模型。有效诊断率为97.8%。区分AMI患者和AD患者的诊断率为89.8%。3组血清中23种细胞因子的表达存在显著差异。通过相关性分析,发现miP-1,IL-7,MIP-1β,EGF和其他细胞因子与四种代谢分子显著相关。
结论:AFMK,甘油磷酸胆碱,肌苷,SphingfunginB(SPH)代谢物是AD的潜在生物标志物,相关代谢过程的影响可能与miP-1、IL-7、MIP-1β、EGF等细胞因子。
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