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急性疼痛和亚急性疼痛患者血清血管生成因子的变化。

Changes in serum angiogenic factors among patients with acute pain and subacute pain.

作者信息

Yang Xuewei, Yuan Chunmei, Wang Huanling, Wang Yunxia, Liu Mei, Li Zongjin, Zhang Jun

机构信息

Department of Anesthesiology and Pain Medical Center, Tianjin Union Medical Center, Nankai University, Tianjin, China.

School of Medicine, Nankai University, Tianjin, China.

出版信息

Front Mol Neurosci. 2022 Jul 15;15:960460. doi: 10.3389/fnmol.2022.960460. eCollection 2022.

Abstract

Screening serum biomarkers for acute and subacute pain is important for precise pain management. This study aimed to examine serum levels of angiogenic factors in patients with acute and subacute pain as potential biomarkers. Serum samples were collected from 12 healthy controls, 20 patients with postherpetic neuralgia (PHN), 4 with low back pain (LBP), and 1 with trigeminal neuralgia (TN). Pain intensity in these patients was evaluated using the visual analog scale (VAS). The serum concentrations of 11 angiogenic biomarkers were examined by Milliplex Map Human Angiogenesis Magnetic Bead Panel 2. The pain assessment from VAS showed that all patients showed moderate and severe pain. Among 11 angiogenic factors, osteopontin (OPN), thrombospondin-2 (TSP-2), soluble platelet endothelial cell adhesion molecule-1 (sPECAM-1), soluble urokinase-type plasminogen activator receptor (suPAR), and soluble epidermal growth factor receptors (sErbB2) were up-regulated and soluble interleukin-6 receptor α (sIL-6Rα) were down-regulated in patients with pain compared to the healthy participants (all -values were < 0.005). Moreover, a linear regression model showed that the serum OPN concentration was correlated with pain intensity in patients with PHN ( = 0.03). There was no significant difference between the serum concentration of soluble epidermal growth factor receptors, sErbB3, soluble AXL, tenascin, and soluble neuropilin-1 in patients with acute and subacute pain and that of healthy controls. The results of this study provided new valuable insights into our understanding of angiogenic factors that may contribute to as mechanistic biomarkers of pain, and reveal the pathophysiological mechanism of pain. www.chictr.org.cn, identifier ChiCTR2200061775.

摘要

筛查用于急性和亚急性疼痛的血清生物标志物对于精确的疼痛管理很重要。本研究旨在检测急性和亚急性疼痛患者血清中血管生成因子的水平,以确定其作为潜在生物标志物的可能性。收集了12名健康对照者、20名带状疱疹后神经痛(PHN)患者、4名腰痛(LBP)患者和1名三叉神经痛(TN)患者的血清样本。使用视觉模拟量表(VAS)评估这些患者的疼痛强度。通过Milliplex Map Human Angiogenesis Magnetic Bead Panel 2检测11种血管生成生物标志物的血清浓度。VAS疼痛评估显示,所有患者均表现为中度和重度疼痛。在11种血管生成因子中,与健康参与者相比,骨桥蛋白(OPN)、血小板反应蛋白-2(TSP-2)、可溶性血小板内皮细胞黏附分子-1(sPECAM-1)、可溶性尿激酶型纤溶酶原激活物受体(suPAR)和可溶性表皮生长因子受体(sErbB2)在疼痛患者中上调,可溶性白细胞介素-6受体α(sIL-6Rα)下调(所有P值均<0.005)。此外,线性回归模型显示,PHN患者血清OPN浓度与疼痛强度相关(P = 0.03)。急性和亚急性疼痛患者与健康对照者血清中可溶性表皮生长因子受体、sErbB3、可溶性AXL、腱生蛋白和可溶性神经纤毛蛋白-1的浓度无显著差异。本研究结果为我们理解可能作为疼痛机制生物标志物的血管生成因子提供了新的有价值的见解,并揭示了疼痛的病理生理机制。 www.chictr.org.cn,标识符ChiCTR2200061775

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e58/9335149/3f453f5be99c/fnmol-15-960460-g001.jpg

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