Department of Clinical Medicine, The Arctic University of Norway, Tromsø, Norway; Department of Neurology, University Hospital of North Norway, Tromsø, Norway.
Department of Clinical Medicine, The Arctic University of Norway, Tromsø, Norway; Department of Neurology, University Hospital of North Norway, Tromsø, Norway.
Atherosclerosis. 2018 Apr;271:1-8. doi: 10.1016/j.atherosclerosis.2018.02.005. Epub 2018 Feb 7.
Novel biomarkers are linked to cardiovascular disease (CVD). The aim of the present study was to investigate the association between 28 blood biomarkers and the formation and progression of carotid plaque.
In a nested case control study with 703 participants from the population based Tromsø Study, a large biomarker panel was measured in blood obtained at baseline. Carotid ultrasound was assessed both at baseline and at 6 years of follow-up. Four groups were defined: Group 1: no plaque at baseline or at follow-up (reference group); Group 2: novel plaque at follow-up; Group 3: stable plaque at follow-up; Group 4: progression of plaque at follow-up. By multinomial logistic regression analyses, we assessed the risk of being in the different plaque groups with regard to traditional cardiovascular risk factors and levels of biomarkers at baseline.
Adjusted for traditional risk factors, interleukin-6 (IL-6) was an independent predictor of plaque progression (OR 1.44, 95% CI 1.12-1.85 per SD increase in IL-6 level). This result remained significant after inclusion of other novel biomarkers to the model, and when subjects with former CVD were excluded. Neopterin was protective of novel plaque formation (OR 0.73, 95% CI 0.57-0.93). Myeloperoxidase and Caspase-1 were independent predictors of plaque progression, but this effect disappeared when excluding subjects with former CVD.
IL-6 is an independent predictor of plaque progression, suggesting that it may be a marker of progressive atherosclerosis in the general population and that its central role in CVD may be related to promotion of plaque growth.
新的生物标志物与心血管疾病(CVD)有关。本研究的目的是探讨 28 种血液生物标志物与颈动脉斑块的形成和进展之间的关系。
在一项基于人群的特罗姆瑟研究中,对 703 名参与者进行了嵌套病例对照研究,在基线时测量了大量的生物标志物。在基线和 6 年随访时进行颈动脉超声检查。定义了四个组:组 1:基线或随访时无斑块(参照组);组 2:随访时出现新斑块;组 3:随访时斑块稳定;组 4:随访时斑块进展。通过多项逻辑回归分析,我们评估了与传统心血管危险因素和基线生物标志物水平相比,不同斑块组的风险。
调整传统危险因素后,白细胞介素-6(IL-6)是斑块进展的独立预测因子(IL-6 水平每增加 1 个标准差,OR 为 1.44,95%CI 为 1.12-1.85)。当将其他新的生物标志物纳入模型并排除有既往 CVD 的患者时,这一结果仍然具有统计学意义。新蝶呤对新斑块形成具有保护作用(OR 0.73,95%CI 0.57-0.93)。髓过氧化物酶和 Caspase-1 是斑块进展的独立预测因子,但排除有既往 CVD 的患者后,这种影响消失。
IL-6 是斑块进展的独立预测因子,表明其可能是一般人群中进行性动脉粥样硬化的标志物,其在 CVD 中的核心作用可能与促进斑块生长有关。