Mikko T Nieminen, Paula Vesterinen, T. Tervahartiala, I. Kormi, J. Sinisalo, P. Pussinen, T. Sorsa
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引用次数: 11
摘要
基质金属蛋白酶(MMPs)在炎症过程中发挥重要作用,因为它们降解细胞外蛋白并改变免疫反应。炎症是动脉粥样硬化发生的驱动因素,而MMPs,特别是MMP-8,与动脉粥样硬化斑块的进展有关。MMP-8被证明与心血管疾病(cvd)及其并发症密切相关,因此提供了识别高危患者的潜在标记物。以前,需要费力和昂贵的免疫荧光测定(IFMA)来可靠地检测血清中MMP-8的水平。在这项研究中,我们比较了一种新的内部elisa测定法,dentoELISA,与标准IFMA测定血清MMP-8浓度。作为一种更便宜、更省力的检测方法,ELISA在诊断上的敏感性和特异性与IFMA一样高。ROC统计显示两种分析的曲线下面积高度相似(0.779对0.781)。此外,ELISA测定的浓度与IFMA测定的浓度显著相关(r = 0.881, P < 0.001)。在我们的研究人群中,急性冠状动脉综合征患者(n = 2071)的MMP-8水平明显高于无显著冠状动脉疾病的参考人群(n = 653)。在此背景下,MMP-8-ELISA可以为新型心血管疾病诊断提供有趣的新方法。
Practical implications of novel serum ELISA-assay for matrix metalloproteinase-8 in acute cardiac diagnostics
Matrix metalloproteinases (MMPs) play a major role in inflammatory processes as they degrade extracellular proteins and modify immune responses. Inflammation is the driving factor in atherogenesis and MMPs, particularly MMP-8, has been linked to atherosclerotic plaque progression. MMP-8 is shown to be strongly associated with cardiovascular diseases (CVDs) and its complications thus providing a potential marker to identify patients at risk. Previously, laborious and expensive immunofluorometric assay (IFMA) was needed to reliably detect MMP-8 levels in serum. In this study, we compared a novel in-house ELISA-assay, dentoELISA, to the standard IFMA in determination of serum MMP-8 concentrations. As a cheaper and non-laborious assay, ELISA proved to be diagnostically as sensitive and specific as the IFMA. ROC statistics showed highly similar areas under the curve for both assays (0.779 versus 0.781). Furthermore, the concentrations measured by ELISA correlated significantly with concentrations determined with IFMA (r = 0.881, P < 0.001). In our study population, MMP-8 levels were significantly higher in the acute coronary syndrome patients (n = 2071) in comparison to reference population without significant coronary artery disease (n = 653). With this background, MMP-8-ELISA could provide interesting new approaches to novel CVD diagnostics.