Assessment of Biomarker Profile in Patients Post Carotid Angioplasty and Stenting

М.М. Tanashyan, V. Annushkin, A. Raskurazhev, O. Lagoda, Аlla А. Shabalina, R. Medvedev, V. Shchipakin
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Abstract

Introduction. Cardiovascular diseases are predominantly caused by atherosclerosis as a multifactorial chronic condition. Alterations in the hematological system and the blood vessel wall are considered as highly significant for onset and development of cerebrovascular disorders associated with atherosclerosis. Biomarkers as measurable indicators are to verify abnormal activity. Objective: to assess atherogenesis biomarkers in patients after carotid angioplasty and stenting (CAS) as associated with development of cerebrovascular disease. Materials and methods. We evaluated 50 individuals (50% men, 50% women; average age 65.4 6.4 years) with established cerebrovascular disease associated with brain atherosclerosis. All of them had hemodynamically significant abnormalities in the internal carotid artery (ICA) with both symptomatic (stenosis 60% and more) and asymptomatic (stenosis 70% and more) stenoses confirmed by duplex scanning of the brachiocephalic arteries. All patients underwent CAS as indicated. Before and 1 year after the intervention, we performed clinical and neurological examinations, brain magnetic resonance imaging, and laboratory tests of atherogenesis biomarkers. Results. At baseline, all the individuals demonstrated a pro-atherogenic shift in the assessed indicators, predominantly markers of extracellular matrix degradation, inflammation and atherogenesis (including osteoprotegerin and chromogranin А). Additionally, we established a direct correlation between osteoprotegerin levels and the characteristics of mostly hyperechoic atherosclerotic plaques (r = 0.29; p 0.05). A year later, no signs of restenosis were shown in follow-up ultrasound assessment of stented arteries in any patient. In 1 year post CAS, we found significant changes in the levels of osteoprotegerin (decrease to 1.765 pg/mL [1.592; 1.937]; p 0.05) and chromogranin А (elevation to 31.3 g/L [13.9; 90.7]; p 0.05). Re-assessment demonstrated association between changes in the pattern of the nitrogen oxide system, which tends to improve (NO elevation to 38.23 mol/L [32.95; 43.51]; p 0.001), and atheroprotective shift in the morphology of atherosclerotic plaques and biomarker profile. Conclusion. Prospective, 1-year long observation for patients who underwent CAS for symptomatic/asymptomatic hemodynamically significant ICA stenoses revealed favourable atheroprotective shift in both ultrasound and hematological atherogenesis biomarker ratio. This shift contributed to the absence of cerebral atherosclerosis progression during the follow-up. The process may be mediated by chromogranin А and osteoprotegerin, and their further research is needed from perspective of atherogenesis.
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颈动脉血管成形术和支架植入术后患者生物标志物的评估
介绍。心血管疾病主要由动脉粥样硬化引起,是一种多因素慢性疾病。血液系统和血管壁的改变被认为是与动脉粥样硬化相关的脑血管疾病发生和发展的重要因素。生物标志物作为可测量的指标,用于验证异常活动。目的:评估颈动脉成形术和支架植入术(CAS)后患者动脉粥样硬化生物标志物与脑血管疾病发展的相关性。材料和方法。我们评估了50个人(50%的男性,50%的女性;平均年龄65.4 - 6.4岁,伴有脑血管疾病合并脑动脉粥样硬化。所有患者均有明显的颈内动脉血流动力学异常,经头臂动脉双相扫描证实有症状(狭窄60%及以上)和无症状(狭窄70%及以上)狭窄。所有患者均行CAS治疗。在干预前和干预后1年,我们进行了临床和神经学检查、脑磁共振成像和动脉粥样硬化生物标志物的实验室测试。结果。在基线时,所有个体在评估指标中都表现出促动脉粥样硬化的转变,主要是细胞外基质降解、炎症和动脉粥样硬化的标志物(包括骨保护素和铬粒蛋白А)。此外,我们建立了骨保护素水平与大多数高回声动脉粥样硬化斑块特征之间的直接相关性(r = 0.29;p 0.05)。一年后,在随访的支架动脉超声评估中没有发现再狭窄的迹象。在CAS后1年,我们发现骨保护素水平有显著变化(降至1.765 pg/mL [1.592;1.937);p 0.05)和嗜铬粒蛋白А(升高至31.3 g/L [13.9;90.7);p 0.05)。重新评估表明氮氧化物系统模式的变化之间存在关联,该模式趋于改善(NO升高至38.23 mol/L [32.95;43.51);P 0.001),以及动脉粥样硬化斑块形态和生物标志物特征的动脉粥样硬化保护转变。结论。对因有症状/无症状血流动力学意义显著的ICA狭窄而接受CAS治疗的患者进行为期1年的前瞻性观察显示,超声和血液粥样硬化生物标志物比率均发生了有利的动脉粥样硬化保护转变。这一转变导致随访期间没有脑动脉粥样硬化进展。这一过程可能是由嗜铬粒蛋白А和骨保护素介导的,需要从动脉粥样硬化的角度进一步研究。
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来源期刊
Annals of Clinical and Experimental Neurology
Annals of Clinical and Experimental Neurology Medicine-Neurology (clinical)
CiteScore
0.80
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0.00%
发文量
32
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