The Clinical Significance of Inflammatory Biomarkers of Atherosclerosis in Carotid Disease

O. Dubenko
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Abstract

Atherosclerotic disease of the carotid arteries is a major cause of ischemic stroke. The degree of carotid stenosis is the main marker for assessing the risk of stroke in "carotid disease", however, the degree of stenosis alone cannot accurately predict future stroke. Asymptomatic carotid artery stenosis is a well-recognized risk factor for ischemic stroke. Non-stenotic atherosclerotic carotid artery plaques can also cause atheroembolism in the presence of ulceration and rupture of the plaque. We aimed to summarizes the current available evidence on the association between carotid atherosclerosis and serum inflammatory biomarkers. Atherosclerosis is a dynamic process involving inflammatory and thrombotic mechanisms with progressive degree of stenosis. The ability to predict the progression of atherosclerotic stenosis can be useful for clinical practice in assessing the risk of stroke development and its prevention. To identify subgroup of patients with higher risk for ipsilateral stroke is important aim. Inflammatory activity is an integral indicator of the development of atherosclerosis and its complications and plays a key role in the pathogenesis, progression, rupture of atherosclerotic plaque and the development of clinical manifestations in patients with atherosclerotic carotid stenosis. Several serum inflammatory markers such as C-reactive protein, interleukin-6, pentraxin 3, lipoprotein-associated phospholipase A2, adhesion molecules ICAM-1 and selectins and matrix metalloproteinases proposed as tool for risk assessment in patients with carotid atherosclerosis. Even though there are some cardiovascular biomarkers identified, they have only modest predictive value. Some well-established biomarkers for coronary disease are not relevant to carotid atherosclerosis. Future research may clarify the clinical significance of serum inflammatory biomarker in carotid atherosclerosis.
颈动脉粥样硬化炎症生物标志物的临床意义
颈动脉粥样硬化性疾病是缺血性中风的主要原因。颈动脉狭窄程度是评估“颈动脉疾病”中卒中风险的主要标志,但仅凭狭窄程度并不能准确预测未来卒中的发生。无症状颈动脉狭窄是缺血性脑卒中的一个公认的危险因素。非狭窄性动脉粥样硬化性颈动脉斑块也可引起动脉粥样硬化栓塞,存在溃疡和斑块破裂。我们的目的是总结目前可用的证据颈动脉粥样硬化和血清炎症生物标志物之间的关系。动脉粥样硬化是一个涉及炎症和血栓形成机制的动态过程,并伴有狭窄程度的进行性变化。预测动脉粥样硬化性狭窄进展的能力可用于临床实践中评估卒中发展风险及其预防。确定同侧脑卒中高危患者亚组是研究的重要目的。炎症活动是动脉粥样硬化及其并发症发生发展的重要指标,在动脉粥样硬化性颈动脉狭窄患者的发病、进展、斑块破裂及临床表现的发展中起着关键作用。几种血清炎症标志物,如c反应蛋白、白细胞介素-6、戊烷素3、脂蛋白相关磷脂酶A2、粘附分子ICAM-1、选择素和基质金属蛋白酶被建议作为颈动脉粥样硬化患者风险评估的工具。尽管已经确定了一些心血管生物标志物,但它们只有适度的预测价值。一些公认的冠状动脉疾病的生物标志物与颈动脉粥样硬化无关。未来的研究可能会进一步阐明血清炎症标志物在颈动脉粥样硬化中的临床意义。
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