Interleukin-6 and High-sensitivity C-reactive Protein for the Prediction of Outcomes in Non-ST-segment Elevation Acute Coronary Syndromes

被引:20
作者
Lopez-Cuenca, Angel [1 ]
Manzano-Fernandez, Sergio [1 ,2 ]
Lip, Gregory Y. H. [3 ]
Casas, Teresa [4 ]
Sanchez-Martinez, Marianela [1 ]
Mateo-Martinez, Alicia [1 ]
Perez-Berbel, Patricio [5 ]
Martinez, Javier [5 ]
Hernandez-Romero, Diana [1 ]
Romero Aniorte, Ana I. [1 ]
Valdes, Mariano [1 ,2 ]
Marin, Francisco [1 ,2 ]
机构
[1] Hosp Univ Virgen de la Arrixaca, Dept Cardiol, Murcia 30120, Spain
[2] Univ Murcia, Murcia, Spain
[3] City Hosp, Univ Dept Med, Haemostasis Thrombosis & Vasc Biol Unit, Birmingham, W Midlands, England
[4] Hosp Univ Virgen de la Arrixaca, Dept Bioquim, Murcia 30120, Spain
[5] Hosp Gen Univ Alicante, Dept Cardiol, Alicante, Spain
来源
REVISTA ESPANOLA DE CARDIOLOGIA | 2013年 / 66卷 / 03期
关键词
High-sensitivity C-reactive protein; Interleukin-6; Non-ST-segment acute coronary syndrome; SYSTEMIC INFLAMMATION EVALUATION; UNSTABLE ANGINA-PECTORIS; LONG-TERM MORTALITY; MYOCARDIAL-INFARCTION; RISK STRATIFICATION; ARTERY-DISEASE; HEART-FAILURE; STABLE ANGINA; TASK-FORCE; EVENTS;
D O I
10.1016/j.rec.2012.07.019
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction and objectives: High baseline levels of interleukin-6 and C-reactive protein confer an increased risk of mortality in non-ST-segment elevation acute coronary syndrome. The aim of the study was to determine whether serial measurements of interleukin-6 and high-sensitivity C-reactive protein provide additional information to baseline measurements for risk stratification of non-ST-segment elevation acute coronary syndrome. Methods: Two hundred and sixteen consecutive patients with non-ST-segment elevation acute coronary syndrome were prospectively included. Blood samples were obtained within 24 h of hospital admission and at 30 days of follow-up. The endpoint was a composite of all-cause death, nonfatal myocardial infarction, or acute decompensated heart failure. Results: Both interleukin-6 and high-sensitivity C-reactive protein levels decreased from day 1 to day 30, regardless of adverse events (both P<.001). Interleukin-6 levels at 2 time points (interleukin-6 day 1, per pg/mL; hazard ratio=1.006, 95% confidence interval, 1.002-1.010; P=.002 and interleukin-6 day 30, per pg/mL, hazard ratio=1.047, 95% confidence interval, 1.021-1.075, P<.001) were independent predictors of adverse events, whereas high-sensitivity C-reactive protein day 1 and high-sensitivity C-reactive protein day 30 levels were not. Patients with interleukin-6 day 1 <= 8.24 pg/mL and interleukin-6 day 30 <= 4.45 pg/mL had the lowest event rates (4.7%), whereas those with both above the median values had the highest event rates (35%). After addition of interleukin-6 day 30 to the multivariate model, C-index increased from 0.71 (95% confidence interval, 0.63-0.78) to 0.80 (95% confidence interval, 0.72-0.86), P=.042, and net reclassification improvement was 0.39 (95% confidence interval, 0.14-0.64; P=.002). Conclusions: In this population, both interleukin-6 and high-sensitivity C-reactive protein concentrations decreased after the acute phase. Serial samples of interleukin-6 concentrations improved the prognostic risk stratification of these patients. (c) 2012 Sociedad Espanola de Cardiologia. Published by Elsevier Espana, S.L. All rights reserved.
引用
收藏
页码:185 / 192
页数:8
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