BDNF/TrkB signaling in stable coronary artery disease

O. V. Atamas, M. Antonyuk, T. Novgorodtseva, T. A. Gvozdenko, O. Kytikova
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Abstract

Aim. To study the serum content of brain-derived neurotrophic factor (BDNF) and tyrosine kinase receptor B (TrkB) in patients with coronary artery disease (CAD) and evaluate the relationship of BDNF/TrkB signaling with the severity of coronary atherosclerosis, systemic inflammation (IL-2, IL-4, IL-6, IL-10, TNF-α) and angiogenesis (VEGF).Material and methods. The study included 99 patients with stable CAD who underwent coronary angiography and 30 healthy volunteers. Coronary atherosclerosis was assessed using the Gensini score (GS). In blood serum, the concentrations of BDNF, TrkB, VEGF, IL-2, IL-4, IL-6, IL-10, TNF-α were determined using the enzyme immunoassay. Cluster, correlation, and regression analyzes were used.Results. In patients with CAD, a wide range of variations in BDNF concentrations was observed. To determine homogeneous groups using the k-means clustering, three clusters with different BDNF/TrkB axis vectors were identified. Patients differed in the severity of coronary atherosclerosis, the manifestation of the inflammatory reaction, and the intensity of angiogenesis. In patients with initial and moderate atherosclerotic changes in the coronary arteries, a normal concentration of BDNF and an increased level of TrkB (22,35/1,18 ng/ml) were noted. In patients with severe coronary atherosclerosis, two different BDNF/TrkB variants have been identified. Decreased BDNF and increased TrkB (6,0/1,52 ng/ml) were associated with low VEGF and increased IL-6. Elevated BDNF and normal TrkB values (26,95/0,96 ng/ml) were characteristic of patients with high VEGF expression, indicating angiogenesis activation and/or vulnerable plaques. A direct relationship between BDNF and VEGF (r=0,536, p<0,001) and an inverse relationship with TrkB (r=-0,301, p=0,019), IL-6 (r=-0,306, p=0,002) was revealed. TrkB levels were correlated with TNF-α (r=0,403, p=0,001). Regression analysis showed that BDNF expression is influenced by TrkB (β=-0,237, p=0,009), VEGF (β=0,490, p<0,001), IL-6 (β=-0,339, p<0,001).Conclusion. In patients with stable CAD, different levels of BDNF/TrkB expression were found, which were associated with coronary atherosclerosis severity. BDNF/TrkB signaling is involved in the regulation of inflammation and angiogenesis in stable CAD.
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稳定型冠状动脉疾病中的 BDNF/TrkB 信号传导
研究目的研究冠状动脉疾病(CAD)患者血清中脑源性神经营养因子(BDNF)和酪氨酸激酶受体B(TrkB)的含量,并评估BDNF/TrkB信号传导与冠状动脉粥样硬化严重程度、全身炎症(IL-2、IL-4、IL-6、IL-10、TNF-α)和血管生成(VEGF)的关系。研究对象包括 99 名接受冠状动脉造影术的稳定型 CAD 患者和 30 名健康志愿者。采用 Gensini 评分(GS)对冠状动脉粥样硬化进行评估。采用酶联免疫法测定血清中 BDNF、TrkB、VEGF、IL-2、IL-4、IL-6、IL-10 和 TNF-α 的浓度。采用聚类、相关和回归分析。在CAD患者中,BDNF浓度的变化范围很大。在使用k-means聚类分析确定同质组时,发现了三个具有不同BDNF/TrkB轴向量的聚类。患者的冠状动脉粥样硬化严重程度、炎症反应表现和血管生成强度各不相同。在冠状动脉发生初期和中度动脉粥样硬化病变的患者中,BDNF 浓度正常,TrkB 水平升高(22,35/1,18 纳克/毫升)。在严重冠状动脉粥样硬化患者中,发现了两种不同的 BDNF/TrkB 变异。BDNF的降低和TrkB的升高(6.0/1.52纳克/毫升)与血管内皮生长因子的降低和IL-6的升高有关。BDNF升高和TrkB值正常(26.95/0.96纳克/毫升)是血管内皮生长因子高表达患者的特征,表明血管生成激活和/或斑块脆弱。BDNF与血管内皮生长因子之间存在直接关系(r=0,536,p<0,001),与TrkB(r=-0,301,p=0,019)和IL-6(r=-0,306,p=0,002)之间存在反向关系。TrkB水平与TNF-α相关(r=0,403,p=0,001)。回归分析显示,BDNF的表达受TrkB(β=-0,237,p=0,009)、VEGF(β=0,490,p<0,001)、IL-6(β=-0,339,p<0,001)的影响。在稳定型冠状动脉粥样硬化患者中,BDNF/TrkB的表达水平不同,这与冠状动脉粥样硬化的严重程度有关。BDNF/TrkB信号传导参与了稳定型CAD患者炎症和血管生成的调控。
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来源期刊
Russian Journal of Cardiology
Russian Journal of Cardiology Medicine-Cardiology and Cardiovascular Medicine
CiteScore
2.20
自引率
0.00%
发文量
185
审稿时长
1 months
期刊介绍: Russian Journal of Cardiology has been issued since 1996. The language of this publication is Russian, with tables of contents and abstracts of all articles presented in English as well. Editor-in-Chief: Prof. Eugene V.Shlyakhto, President of the Russian Society of Cardiology. The aim of the journal is both scientific and practical, also with referring to organizing matters of the Society. The best of all cardiologic research in Russia is submitted to the Journal. Moreover, it contains useful tips and clinical examples for practicing cardiologists. Journal is peer-reviewed, with multi-stage editing. The editorial board is presented by the leading cardiologists from different cities of Russia.
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