Endothelial dysfunction and systemic inflammation in persons with echolucent carotid plaques
Endothelial dysfunction and systemic inflammation in persons with echolucent carotid plaques
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DOI:
10.1160/th05-11-0772
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发表时间:
2006-07-01
影响因子:
6.7
通讯作者:
Hansen, John-Bjarne
中科院分区:
文献类型:
--
作者:
Noto, Ann-Trude With;Mathiesen, Ellisiv Bogeberg;Hansen, John-Bjarne
Echolucent carotid plaques are associated with high risk for future ischemic cerebrovascular events independent of the degree of stenosis. Elevated levels of markers of systemic inflammation and endothelial dysfunction are predictors for future myocardial infarction and stroke.The present study was undertaken to investigate the relations between plaque morphology, endothelial dysfunction assessed by tissue-plasminogen activator antigen (t-PA ag) and vonWillebrand factor (vWF), and systemic inflammation in persons with carotid stenosis.We conducted a cross-sectional study including 133 persons with carotid stenosis and 138 controls without stenosis recruited from the population-based Troms phi Study. High-resolution B-mode and colour Doppler/pulsed-wave Doppler ultrasonography of both carotid arteries was performed, and plaque morphology in terms of echogenicity was assessed. Persons with carotid stenosis had significantly higher plasma t-PA and vWF concentrations than controls. There was a significant inverse relationship between t-PA ag and plaque echogenicity (p=0.034).The increased plasma t-PA ag in persons with carotid stenosis was not associated with increased plasminogen activator inhibitor-I (PAI-I). Persons with echolucent carotid plaques had higher degree of systemic inflammation, and plasma t-PA and vWF concentration increased significantly across quartiles of WBC, fibrinogen, and hs-CRR Our findings may suggest that plasma t-PA may be superior to vWF as a marker for endothelial dysfunction due to its ability to discriminate between various plaque echogenicity, and that the predictive role of t-PA ag in cardiovascular disease is independent of inhibited fibrinolysis.