FASTTRACK -: Myeloid-related protein 8/14 complex is released by monocytes and granulocytes at the site of coronary occlusion:: a novel, early, and sensitive marker of acute coronary syndromes

被引:171
作者
Altwegg, Lukas A.
Neidhart, Michel
Hersberger, Martin
Mueller, Simone
Eberli, Franz R.
Corti, Roberto
Roffi, Marco
Suetsch, Gabor
Gay, Steffen
von Eckardstein, Arnold
Wischnewsky, Manfred B.
Luescher, Thomas F.
Maier, Willibald
机构
[1] Univ Zurich Hosp, Cardiovasc Ctr, CH-8091 Zurich, Switzerland
[2] Univ Zurich Hosp, Inst Clin Chem, CH-8091 Zurich, Switzerland
[3] Univ Zurich Hosp, Div Expt Rheumatol, CH-8091 Zurich, Switzerland
[4] Univ Bremen, Ctr Appl Informat Technol, D-2800 Bremen 33, Germany
关键词
myeloid-related protein 8/14 complex; acute coronary syndrome; inflammation; thrombus; plaque;
D O I
10.1093/eurheartj/ehm078
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims We investigated whether myeloid-related protein 8/14 complex (MRP8/14) expressed by infiltrating monocytes and granulocytes may represent a mediator and early biomarker of acute coronary syndromes (ACS). Methods and results Immunohistochemistry of coronary thrombi was done in 41 ACS patients. Subsequently, levels of MRP8/14 were assessed systemically in 75 patients with ACS and culprit lesions, with stable coronary artery disease (CAD), or with normal coronary arteries. In a subset of patients, MRP8/14 was measured systemically and at the site of coronary occlusion. Macrophages and granulocytes, but not platelets stained positive for MRP8/14 in 76% of 41 thrombi patients. In ACS, local MRP8/14 levels [22.0 (16.2-41.5) mg/L] were increased when compared with systemic levels [13.4 (8.1-14.7) mg/L, P= 0.03]. Systemic levels of MRP8/14 were markedly elevated [15.1 (12.1-21.8) mg/L, P=0.001] in ACS when compared with stable CAD [4.6 (3.5-7.1) mg/L] or normals [4.8 (4.0-6.3) mg/L]. Using a cut-off level of 8 mg/L, MRP8/14 but not myoglobin or troponin, identified ACS presenting within 3 h from symptom onset. Conclusion In ACS, MRP8/14 is markedly expressed at the site of coronary occlusion by invading phagocytes. The occurrence of elevated MRP8/14 in the systemic circulation prior to markers of myocardial necrosis makes it a prime candidate for the detection of unstable plaques and management of ACS.
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页码:941 / 948
页数:8
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