期刊论文详细信息
INTERNATIONAL JOURNAL OF CARDIOLOGY 卷:268
Soluble IL-1 receptor 2 is associated with left ventricular remodelling in patients with ST-elevation myocardial infarction
Article
Orrem, Hilde L.1,2,3  Shetelig, Christian3,4,5  Ueland, Thor3,6,7  Limalanathan, Shanmuganathan4,5,8  Nilsson, Per H.9,10  Husebye, Trygve4,11  Aukrust, Pal3,6,9,12  Seljeflot, Ingebjorg3,4,5,11  Hoffmann, Pavel3,13  Eritsland, Jan4,5  Mollnes, Tom E.1,7,9,14,15  Andersen, Geir Oystein4,5,11  Yndestad, Arne3,6,9,11 
[1] Oslo Univ Hosp, Dept Immunol, Rikshosp, Oslo, Norway
[2] Oslo Univ Hosp, Dept Anesthesiol, Rikshosp, Oslo, Norway
[3] Univ Oslo, Inst Clin Med, Oslo, Norway
[4] Oslo Univ Hosp Ulleval, Dept Cardiol, Oslo, Norway
[5] Oslo Univ Hosp Ulleval, Ctr Clin Heart Res, Oslo, Norway
[6] Oslo Univ Hosp, Res Inst Internal Med, Rikshosp, Oslo, Norway
[7] Univ Tromso, KG Jebsen TREC, Tromso, Norway
[8] Feiring Heart Clin, Feiring, Norway
[9] Univ Oslo, KG Jebsen Inflammatory Res Ctr, Oslo, Norway
[10] Linnaeus Univ, Linnaeus Ctr Biomat Chem, Kalmar, Sweden
[11] Univ Oslo, Ctr Heart Failure Res, Oslo, Norway
[12] Oslo Univ Hosp, Sect Clin Immunol & Infect Dis, Rikshosp, Oslo, Norway
[13] Oslo Univ Hosp Ulleval, Sect Intervent Cardiol, Oslo, Norway
[14] Nordland Hosp, Res Lab, Bodo, Norway
[15] Norwegian Univ Sci, Ctr Mol Inflammat Res, Trondheim, Norway
关键词: Inflammation;    Cytokine;    Interleukin-1;    Acute coronary syndromes;    Myocardial infarction;    Ventricular remodelling;   
DOI  :  10.1016/j.ijcard.2018.05.032
来源: Elsevier
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【 摘 要 】

Background: The inflammatory response following myocardial infarction (MI) is prerequisite for proper healing of infarcted tissue, but can also have detrimental effects on cardiac function. Interleukin (IL)-1 alpha and IL-1 beta are potent inflammatory mediators and their bioactivity is tightly regulated by IL-1 receptor antagonist (IL-1ra) and soluble (s) IL-1 receptors (R). We aimed to examine whether levels of soluble regulators of IL-1 signalling are changed during ST-elevation MI (STEMI) and their associations with parameters of cardiac injury and ventricular remodelling. Methods: Plasma levels of IL-1Ra, sIL-1R1, sIL-1R2 and sIL-1R accessory protein (sIL-1RAcP) were measured by immunoassays in repeated samples from patients with STEMI (n = 255) and compared to healthy controls (n=65). Results: IL-1Ra, sIL-1R1 and sIL-1R2 levels were all significantly elevated after STEMI, while levels of sIL-1RAcP were lower compared to controls. sIL-1R2 levels (at different time points) correlated positively with C-reactive protein, myocardial infarct size and change in indexed left ventricular end-diastolic and end-systolic volume (LVEDVi and LVESVi) measured by cardiac MR acutely and after 4 months, and negatively with LV ejection fraction. Patients with >median levels of sIL-1R2 in the acute phase were more likely to have increased change in LVEDVi and LVESVi. Importantly, sIL-1R2 remained significantly associated with change in LVEDVi and LVESVi also after adjustment for clinical covariates. Conclusion: Levels of sIL-1R2 are independently associated with parameters of LV adverse remodelling following STEMI. (C 18 Elsevier B.V. All rights reserved.

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