Johnson B Delia, Kip Kevin E, Marroquin Oscar C, Ridker Paul M, Kelsey Sheryl F, Shaw Leslee J, Pepine Carl J, Sharaf Barry, Bairey Merz C Noel, Sopko George, Olson Marian B, Reis Steven E
Graduate School of Public Health, University of Pittsburgh, Parran 127, 130 DeSoto St, Pittsburgh, PA 15261, USA.
Circulation. 2004 Feb 17;109(6):726-32. doi: 10.1161/01.CIR.0000115516.54550.B1.
BACKGROUND: Serum amyloid-alpha (SAA) is a sensitive marker of an acute inflammatory state. Like high-sensitivity C-reactive protein (hs-CRP), SAA has been linked to atherosclerosis. However, prior studies have yielded inconsistent results, and the independent predictive value of SAA for coronary artery disease (CAD) severity and cardiovascular events remains unclear. METHODS AND RESULTS: A total of 705 women referred for coronary angiography for suspected myocardial ischemia underwent plasma assays for SAA and hs-CRP, quantitative angiographic assessment, and follow-up evaluation. Cardiovascular events were death, myocardial infarction, congestive heart failure, stroke, and other vascular events. The women's mean age was 58 years (range 21 to 86 years), and 18% were nonwhite. SAA and hs-CRP were associated with a broad range of CAD risk factors. After adjustment for these risk factors, SAA levels were independently but moderately associated with angiographic CAD (P=0.004 to 0.04) and highly predictive of 3-year cardiovascular events (P<0.0001). By comparison, hs-CRP was not associated with angiographic CAD (P=0.08 to 0.35) but, like SAA, was strongly and independently predictive of adverse cardiovascular outcome (P<0.0001). CONCLUSIONS: Our results show a strong independent relationship between SAA and future cardiovascular events, similar to that found for hs-CRP. Although SAA was independently but moderately associated with angiographic CAD, this association was not found for hs-CRP. These results are consistent with the hypothesis that systemic inflammation, manifested by high SAA or hs-CRP levels, may promote atherosclerotic plaque destabilization, in addition to exerting a possible direct effect on atherogenesis.
背景:血清淀粉样蛋白α(SAA)是急性炎症状态的敏感标志物。与高敏C反应蛋白(hs-CRP)一样,SAA也与动脉粥样硬化有关。然而,先前的研究结果并不一致,SAA对冠状动脉疾病(CAD)严重程度和心血管事件的独立预测价值仍不明确。 方法和结果:共有705名因疑似心肌缺血而接受冠状动脉造影的女性进行了SAA和hs-CRP的血浆检测、定量血管造影评估及随访评估。心血管事件包括死亡、心肌梗死、充血性心力衰竭、中风和其他血管事件。这些女性的平均年龄为58岁(范围21至86岁),18%为非白人。SAA和hs-CRP与多种CAD危险因素相关。在对这些危险因素进行调整后,SAA水平与血管造影CAD独立但呈中度相关(P=0.004至0.04),并对3年心血管事件具有高度预测性(P<0.0001)。相比之下,hs-CRP与血管造影CAD无关(P=0.08至0.35),但与SAA一样,对不良心血管结局具有强烈且独立的预测性(P<0.0001)。 结论:我们的结果表明SAA与未来心血管事件之间存在很强的独立关系,类似于hs-CRP。虽然SAA与血管造影CAD独立但呈中度相关,但hs-CRP未发现这种关联。这些结果与以下假设一致,即高SAA或hs-CRP水平所表现出的全身炎症,除了可能对动脉粥样硬化发生有直接影响外,还可能促进动脉粥样硬化斑块的不稳定。
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