Interleukin-6 and C-reactive protein and risk for death and cardiovascular events in patients with atrial fibrillation

被引:186
作者
Aulin, Julia [1 ,2 ]
Siegbahn, Agneta [1 ,3 ]
Hijazi, Ziad [1 ,2 ]
Ezekowitz, Michael D. [4 ,5 ]
Andersson, Ulrika [1 ]
Connolly, Stuart J. [6 ]
Huber, Kurt [7 ]
Reilly, Paul A. [8 ]
Wallentin, Lars [1 ,2 ]
Oldgren, Jonas [1 ,2 ]
机构
[1] Uppsala Univ, Uppsala Clin Res Ctr, Uppsala, Sweden
[2] Uppsala Univ, Dept Med Sci, Cardiol, Uppsala, Sweden
[3] Uppsala Univ, Dept Med Sci, Clin Chem, Uppsala, Sweden
[4] Lankenau Inst Med Res, Wynnewood, PA USA
[5] Ctr Heart, Wynnewood, PA USA
[6] Populat Hlth Res Inst, Hamilton, ON, Canada
[7] Dept Internal Med Cardiol & Emergency Med 3, Vienna, Austria
[8] Boehringer Ingelheim Pharmaceut Inc, Ridgefield, CT 06877 USA
关键词
CORONARY-ARTERY-DISEASE; LY RANDOMIZED EVALUATION; ANTICOAGULATION THERAPY TRIAL; INFLAMMATION; DABIGATRAN; MORTALITY; WARFARIN; STROKE; HEART; STRATIFICATION;
D O I
10.1016/j.ahj.2015.09.018
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Background Inflammation has been associated with cardiovascular disease and the burden of atrial fibrillation (AF). In this study we evaluate inflammatory biomarkers and future cardiovascular events in AF patients in the RE-LY study. Methods Interleukin-6 (IL-6), C-reactive protein (CRP) (n = 6,187), and fibrinogen (n = 4,893) were analyzed at randomization; outcomes were evaluated by Cox models and C-statistics. Results Adjusted for clinical risk factors IL-6 was independently associated with stroke or systemic embolism (P =.0041), major bleedings (P =.0001), vascular death (P<.0001), and a composite thromboembolic outcome (ischemic stroke, systemic embolism, myocardial infarction, pulmonary embolism and vascular death) (P<.0001). CRP was independently related to myocardial infarction (P =.0047), vascular death (P =.0004), and the composite thromboembolic outcome (P =.0001). When further adjusted for cardiac (troponin andN-terminal fragment B-type natriuretic peptide [NT-proBNP]) and renal (cystatin-C) biomarkers on top of clinical risk factors IL-6 remained significantly related to vascular death (P<.0001), major bleeding (P<.0170) and the composite thromboembolic outcome (P<.0001), and CRP to myocardial infarction (.0104). Fibrinogen was not associated with any outcome. C-index for stroke or systemic embolism increased from 0.615 to 0.642 (P =.0017) when adding IL-6 to the clinically used CHA(2)DS(2)-VASc risk score with net reclassification improvement of 28%. Conclusion In patients with AF, IL-6 is related to higher risk of stroke and major bleeding, and both markers are related to higher risk of vascular death and the composite of thromboembolic events independent of clinical risk factors. Adjustment for cardiovascular biomarkers attenuated the prognostic value, although IL-6 remained related to mortality, the composite of thromboembolic events, and major bleeding, and CRP to myocardial infarction.
引用
收藏
页码:1151 / 1160
页数:10
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