Biomarker study of symptomatic intracranial atherosclerotic stenosis in patients with acute ischemic stroke

IF 2.8 3区 医学 Q2 CLINICAL NEUROLOGY Frontiers in Neurology Pub Date : 2023-12-06 DOI:10.3389/fneur.2023.1291929
Yingyue Ding, Jinjian Li, Huiyu Shan, Song Yang, Xiyuan Wang, Dexi Zhao
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Abstract

ObjectiveAcute ischemic stroke (AIS) is characterized by high rates of morbidity, disability, mortality, and recurrence, often leaving patients with varying degrees of sequelae. Symptomatic intracranial atherosclerotic stenosis (sICAS) is a significant contributor to AIS pathogenesis and recurrence. The formation and progression of sICAS are influenced by pathways such as lipid metabolism and inflammatory response. Given its high risk of clinical recurrence, timely assessment of intracranial vascular stenosis in AIS is crucial for diagnosing sICAS, treating stroke, and preventing stroke recurrence.MethodsFourteen AIS patients were divided into stenosis and control groups based on the presence or absence of intracranial vessel stenosis. Initially, 4D Label-free proteome quantification technology was employed for mass spectrometry analysis to identify differential proteins between the groups. Subsequently, functional enrichment analysis, including GO classification, KEGG pathway, and Domain, revealed trends related to differential proteins. The STRING (v.11.5) protein interaction network database was used to identify differential protein interactions and target proteins. Finally, parallel reaction monitoring (PRM) validated the selected target proteins.ResultsMass spectrometry identified 1,096 proteins, with 991 being quantitatively comparable. Using a p-value &lt;0.05 and differential expression change thresholds of &gt;1.3 for significant up-regulation and &lt; 1/1.3 for significant down-regulation, 46 differential proteins were identified: 24 significantly up-regulated and 22 significantly down-regulated. PRM experiments validated five proteins related to lipid metabolism and inflammatory response: namely alpha-2-macroglobulin (A2M), lipopolysaccharide-binding protein (LBP), cathepsin G (CTSG), cystatin (CST)3, and fatty acid-binding protein (FABP)1.ConclusionThe detection of changes in these five proteins in AIS patients can aid in the diagnosis of sICAS, inform stroke treatment, and assist in preventing stroke recurrence. Moreover, it can contribute to the development of drugs for preventing AIS recurrence by integrating traditional Chinese and Western medicine.
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急性缺血性脑卒中患者颅内无症状动脉粥样硬化性狭窄的生物标志物研究
目的急性缺血性卒中(AIS)的特点是发病率高、致残率高、死亡率高、复发率高,通常会给患者留下不同程度的后遗症。无症状性颅内动脉粥样硬化性狭窄(sICAS)是 AIS 发病和复发的一个重要因素。sICAS 的形成和发展受脂质代谢和炎症反应等途径的影响。鉴于其临床复发的高风险,及时评估 AIS 颅内血管狭窄对诊断 sICAS、治疗卒中和预防卒中复发至关重要。首先,采用 4D 无标记蛋白质组定量技术进行质谱分析,以确定各组之间的差异蛋白质。随后,功能富集分析(包括 GO 分类、KEGG 通路和域)揭示了与差异蛋白质相关的趋势。STRING(v.11.5)蛋白质相互作用网络数据库用于识别差异蛋白质相互作用和目标蛋白质。最后,平行反应监测(PRM)对选定的目标蛋白质进行了验证。使用 p 值 &lt;0.05 和差异表达变化阈值(&gt;1.3 表示显著上调,&lt; 1/1.3 表示显著下调),确定了 46 个差异蛋白质:其中 24 个明显上调,22 个明显下调。PRM 实验验证了五个与脂质代谢和炎症反应相关的蛋白质:即α-2-巨球蛋白(A2M)、脂多糖结合蛋白(LBP)、酪蛋白G(CTSG)、胱抑素(CST)3 和脂肪酸结合蛋白(FABP)1。此外,还有助于开发中西医结合预防 AIS 复发的药物。
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来源期刊
Frontiers in Neurology
Frontiers in Neurology CLINICAL NEUROLOGYNEUROSCIENCES -NEUROSCIENCES
CiteScore
4.90
自引率
8.80%
发文量
2792
审稿时长
14 weeks
期刊介绍: The section Stroke aims to quickly and accurately publish important experimental, translational and clinical studies, and reviews that contribute to the knowledge of stroke, its causes, manifestations, diagnosis, and management.
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