年轻急性椎间盘源性腰骶神经根病患者的细胞因子和新生血管生成参数

Q4 Medicine
M. Maksimova, Y. Kotlyar, A. Shabalina
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The level of C-reactive protein was measured by an automatic biochemical analyzer Konelab 30Iprime (ThermoFisher, Finland). The levels of interleukin-1β (IL-1β), interleukin-6 (IL-6), interleukin-8 (IL-8), tumor necrosis factor alpha (TNF-α), vascular endothelial growth factor A (VEGF-A) in blood were determined by enzyme-linked immunosorbent assay (ELISA) on a plate ELISA analyzer Real-best (Russia) using reagent kits Cloud-Clone Corp. (USA, China).Results. Patients with acute discogenic lumbosacral radiculopathy, compared with the control group, has an increase in the levels of C-reactive protein (11.2 [7.1; 15.3] vs. 4.2 [3.5; 4.9] mg/ml; р = 0.011), TNF-α (23.1 [16.8; 29.5] vs. 9.7 [6.9; 12,5] pg/ml; р = 0.001), IL-1β (4.7 [3.1; 6.3] vs. 3.2 [2.3; 4.1] pg/ml; р = 0.041), IL-6 (11.2 [6.1; 16.3] vs. 4.5 [3.1; 5.9] pg/ml; р = 0.007), IL-8 (30. [21.9; 48.8] vs. 20.5 [8.5; 32.6] pg/ml; р = 0.023) and VEGF-A (318 [260; 570] vs.168 [100; 240] pg/ml; р = 0.002).Conclusion. 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引用次数: 0

摘要

介绍。青年人椎间盘源性腰骶痛的发病机制复杂且多因素。关于急性椎间盘源性腰骶神经根病患者中细胞因子和新生血管生成因子含量的证据是缺乏的,而且经常是相互矛盾的。目的:探讨青年急性盘源性腰骶神经根病患者血液中细胞因子及新生血管生成参数的变化。材料和方法。该研究纳入49例患者,其中男性27例(55.1%),女性22例(44.9%),平均年龄36岁[27;[45]据MRI显示,患者因脊柱退行性改变和脊神经受压而出现急性腰骶痛。对照组17例,男性10例(58.8%),女性7例(41.2%),平均年龄33岁[25;41年。c反应蛋白水平采用全自动生化分析仪Konelab 30Iprime (ThermoFisher, Finland)检测。采用酶联免疫吸附法(ELISA),在Real-best(俄罗斯)平板ELISA分析仪上检测血清中白细胞介素-1β (IL-1β)、白细胞介素-6 (IL-6)、白细胞介素-8 (IL-8)、肿瘤坏死因子α (TNF-α)、血管内皮生长因子A (VEGF-A)水平,试剂盒采用云克隆公司(美国,中国)。急性椎间盘源性腰骶神经根病患者与对照组相比,c反应蛋白水平升高(11.2 [7.1;15.3] vs. 4.2 [3.5;4.9毫克/毫升;tnf -α (23.1 [16.8;29.5] vs. 9.7 [6.9;12、5]pg / ml;il-1β (4.7 [3.1;6.3 vs. 3.2 [2.3;4.1] pg / ml;il-6 (11.2 [6.1;16.3] vs. 4.5 [3.1;5.9] pg / ml;il-8 = 0.007);(21.9;48.8] vs. 20.5 [8.5;32.6] pg / ml;VEGF-A (318 [260;57] [100;240] pg / ml;r = 0.002)。这些结果证实了促炎因子和新生血管生成指标在年轻患者急性椎间盘源性腰骶神经根病发展中的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cytokines and neoangiogenesis parameters in young patients with acute discogenic lumbosacral radiculopathy
Introduction. Discogenic lumbosacral pain in young people has a complex and multicomponent pathogenesis. Evidence of the content of cytokines and neoangiogenesis factors in patients with acute discogenic lumbosacral radiculopathy are deficiency and often contradictory. Objective: to evaluate the cytokine and neoangiogenesis parameters in the blood of young patients with acute discogenic lumbosacral radiculopathy.Materials and methods. The study involved 49 patients (27 (55.1%) men and 22 (44.9%) women) with a mean age of 36 [27; 45] years with acute lumbosacral pain caused by degenerative changes in the spine and signs of compression of the spinal nerves, according to MRI. The control group consisted of 17 healthy individuals (10 (58.8%) men and 7 (41.2%) women) with a mean age of 33 [25; 41] years. The level of C-reactive protein was measured by an automatic biochemical analyzer Konelab 30Iprime (ThermoFisher, Finland). The levels of interleukin-1β (IL-1β), interleukin-6 (IL-6), interleukin-8 (IL-8), tumor necrosis factor alpha (TNF-α), vascular endothelial growth factor A (VEGF-A) in blood were determined by enzyme-linked immunosorbent assay (ELISA) on a plate ELISA analyzer Real-best (Russia) using reagent kits Cloud-Clone Corp. (USA, China).Results. Patients with acute discogenic lumbosacral radiculopathy, compared with the control group, has an increase in the levels of C-reactive protein (11.2 [7.1; 15.3] vs. 4.2 [3.5; 4.9] mg/ml; р = 0.011), TNF-α (23.1 [16.8; 29.5] vs. 9.7 [6.9; 12,5] pg/ml; р = 0.001), IL-1β (4.7 [3.1; 6.3] vs. 3.2 [2.3; 4.1] pg/ml; р = 0.041), IL-6 (11.2 [6.1; 16.3] vs. 4.5 [3.1; 5.9] pg/ml; р = 0.007), IL-8 (30. [21.9; 48.8] vs. 20.5 [8.5; 32.6] pg/ml; р = 0.023) and VEGF-A (318 [260; 570] vs.168 [100; 240] pg/ml; р = 0.002).Conclusion. The obtained results confirm the importance of pro-inflammatory factors and indicators of neoangiogenesis in the development of acute discogenic lumbosacral radiculopathy in young patients.
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来源期刊
Russian Neurological Journal
Russian Neurological Journal Medicine-Neurology (clinical)
CiteScore
0.40
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