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症状性与无症状性患者颈动脉粥样硬化斑块微血管密度和血管生成生长因子表达的对比研究。

A comparative study of carotid atherosclerotic plaque microvessel density and angiogenic growth factor expression in symptomatic versus asymptomatic patients.

机构信息

Department of Vascular & Endovascular Surgery, Manchester Royal Infirmary, Manchester, UK.

出版信息

Eur J Vasc Endovasc Surg. 2010 Apr;39(4):388-95. doi: 10.1016/j.ejvs.2009.12.012. Epub 2010 Feb 1.

DOI:10.1016/j.ejvs.2009.12.012
PMID:20122857
Abstract

OBJECTIVE

A challenge facing clinicians is identifying patients with asymptomatic carotid disease at risk of plaque instability. We hypothesise that locally released angiogenic growth factors contribute to plaque instability.

METHODS

Carotid endarterectomy specimens from eight symptomatic and eight asymptomatic patients were interrogated for microvessel density and angiogenic growth factor expression histologically using immunofluorescence, and biochemically using quantitative real-time polymerase chain reaction (q-RT-PCR). Bio-Plex suspension array was used to assess circulating biomarkers in venous blood from the same patients and six healthy age-matched controls.

RESULTS

Immunofluorescence demonstrated significantly greater neovessel density in symptomatic plaques (P=0.010) with elevated expression of hepatocyte growth factor (HGF) (P=0.001) and its receptor MET (P=0.011) than in asymptomatic plaques. The q-RT-PCR demonstrated up-regulation of Endoglin (CD105), HGF (P=0.001) and MET (P=0.011) in the plaques of symptomatic versus asymptomatic patients. Bio-Plex suspension array demonstrated elevated HGF (P=0.002) serum levels in symptomatic versus asymptomatic patients and healthy controls, and decreased platelet-derived growth factor (PDGF) (P=0.036) serum levels in symptomatic versus asymptomatic patients.

CONCLUSION

Plaque instability may be mediated by HGF-induced formation of new microvessels, and decreased vessel stability resulting from decreased PDGF. Suspension array technology has the potential to identify circulating biomarkers that correlate with plaque rupture risk.

摘要

目的

临床医生面临的挑战是识别无症状颈动脉疾病患者中斑块不稳定的风险。我们假设局部释放的血管生成生长因子有助于斑块不稳定。

方法

通过免疫荧光法对 8 例有症状和 8 例无症状患者的颈动脉内膜切除术标本进行微血管密度和血管生成生长因子表达的组织学检测,并通过定量实时聚合酶链反应(q-RT-PCR)进行生化检测。生物 -plex 悬浮阵列用于评估来自同一患者和 6 名年龄匹配的健康对照者的静脉血中的循环生物标志物。

结果

免疫荧光显示有症状斑块的新生血管密度明显更高(P=0.010),且肝细胞生长因子(HGF)(P=0.001)及其受体 MET(P=0.011)的表达升高。q-RT-PCR 显示有症状斑块中 Endoglin(CD105)、HGF(P=0.001)和 MET(P=0.011)的表达上调。生物 -plex 悬浮阵列显示有症状患者血清中 HGF(P=0.002)水平升高,而无症状患者和健康对照组则降低,有症状患者血清中血小板衍生生长因子(PDGF)(P=0.036)水平降低。

结论

斑块不稳定可能是由 HGF 诱导的新微血管形成和 PDGF 减少导致的血管稳定性降低介导的。悬浮阵列技术有可能识别与斑块破裂风险相关的循环生物标志物。

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