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冠心病患者血清vasostatin-2水平降低与冠状动脉病变严重程度相关 被引量:2

Correlation between decrease in vasostatin-2 level and severity of coronary heart disease
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摘要 目的:探讨嗜铬粒蛋白A(CgA)降解片段vasostatin-2(VS-2)与冠心病发生的关系。方法:入选冠状动脉(冠脉)造影证实的冠心病(冠脉腔内径狭窄≥50%)患者554例和对照281例(冠脉造影阴性或冠脉腔内径狭窄<30%)。采用酶联免疫吸附(ELISA)法检测2组患者血清VS-2、高敏C反应蛋白(hs-CRP)、可溶性细胞间黏附分子1(sICAM-1)及可溶性血管细胞黏附分子1(sVCAM-1)水平。运用多元Logistic回归分析冠心病的危险因素。结果:与对照组相比,冠心病患者血清VS-2水平显著降低[(4.45±2.64)μg/L比(5.82±3.22)μg/L,P<0.001],hs-CRP、sICAM-1及sVCAM-1水平升高(均P<0.001)。VS-2水平与冠心病病变支数负相关(r=-0.206,P<0.05)。多元Logistic回归分析显示VS-2水平下降是冠心病的危险因素(P<0.05)。结论:冠心病患者血清VS-2水平显著下降,与冠心病严重程度呈负相关。 Objective To investigate the correlation between vasostatin-2 (VS-2), a peptide fragment derived from chromogranin A, and severity of coronary heart disease (CHD). Methods Five hundred and fifty four patients with CHD (luminal diameter narrowing i〉50% ) were enrolled in this study, and 281 subjects with normal coronary arteries or non- significant CHD (luminal diameter narrowing 〈30%) were served as controls. Enzyme-linked immunosorbent assay (ELISA) was performed to determine serum levels of VS-2, high-sensitivity C-reactive protein (hs-CRP), soluble intercellular adhesion molecule 1 (sIC_AM-I) and soluble vascular cell adhesion molecule 1 (sVCAM-1). Results Compared with control group, serum VS-2 level was significantly lower in CHD patients [(4.45±2.64) μg/L vs (5.82±3.22) μg/L, P〈0.001], hs- CRP, sICAM-1 and sVCAM-1 level was significantly higher in CHD patients (all P〈0.001). VS-2 was negatively correlated with number of diseased coronary arteries (r=-0.206, P〈0.05). Muhivariable logistic regression analysis demonstrated that decreased vasostatin-2 level is an independent risk factor for CHD (P〈0.05). Conclusions Serum VS-2 level is significantly lower in CHD patients and is correlated negatively with the severity of CHD.
出处 《内科理论与实践》 2013年第4期264-267,共4页 Journal of Internal Medicine Concepts & Practice
基金 国家自然科学基金(项目编号:81070240)
关键词 Vasostatin-2 炎症 血管内皮 冠状动脉粥样硬化性心脏病 Vasostatin-2 Inflammation Vascular endothelium Coronary atherosclerotic heart disease
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