High-sensitivity C-reactive protein in the prediction of coronary events in patients with premature coronary artery disease

被引:77
作者
Speidl, WS [1 ]
Graf, S [1 ]
Hornykewycz, S [1 ]
Nikfardjam, M [1 ]
Niessner, A [1 ]
Zorn, G [1 ]
Wojta, J [1 ]
Huber, K [1 ]
机构
[1] Univ Vienna, Dept Cardiol, A-1090 Vienna, Austria
关键词
D O I
10.1067/mhj.2002.124353
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background and Methods Inflammation plays an important role in the initiation and progression of atherosclerosis and in the pathogenesis of acute cardiovascular events. Recent studies have indicated a possible association between C-reactive protein (CRP) and the clinical outcome of coronary artery disease (CAD). We studied prospectively in a group of 125 patients with premature CAD whether plasma levels of CRP as measured with a high-sensitivity assay predict risk for future coronary events. All patients had stable CAD at time of blood sampling but had originally been seen with unstable angina or myocardial infarction. The mean follow-up time after blood collection was 54 months, and death, myocardial infarction, need for coronary revascularization, or admission to hospital with angina pectoris were defined as clinical end points. Results Patients in the highest tertile of CRP levels had a >3.8-fold risk (risk ratio 3.82, 95% Cl 1.19-12.17) for death, myocardial infarction, or need for coronary revascularization compared with the patients in the first tertile. The relative risk for patients in the second tertile was 3.5-fold higher (95% Cl 1.04-11.56). CRP levels in the third tertile independently predicted risk after adjustment for lipids and other clinical risk factors. Conclusion in patients with clinically stable conditions who have a positive history for acute coronary syndromes before age 50 years, plasma levels of CRP higher than 1.6 mg/L are predictors of future coronary events and therefore indicate the role of underlying chronic inflammation for the clinical course of CAD. Accordingly, reference limits for prediction of risk in CAD have to be lower in this specific patient group than in middle-aged or elderly patients.
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页码:449 / 455
页数:7
相关论文
共 18 条
[1]  
BERANEK JT, 1997, EUR HEART J, V18, P184
[2]   High sensitivity C-reactive protein for predicting cardiovascular disease: an inflammatory hypothesis [J].
Blake, GJ ;
Ridker, PM .
EUROPEAN HEART JOURNAL, 2001, 22 (05) :349-352
[3]   Immune system activation follows inflammation in unstable angina: Pathogenetic implications [J].
Caligiuri, G ;
Liuzzo, G ;
Biasucci, LM ;
Maseri, A .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1998, 32 (05) :1295-1304
[4]   Mechanisms of disease: Acute-phase proteins and other systemic responses to inflammation [J].
Gabay, C ;
Kushner, I .
NEW ENGLAND JOURNAL OF MEDICINE, 1999, 340 (06) :448-454
[5]   Pathophysiology and clinical significance of atherosclerotic plaque rupture [J].
Gutstein, DE ;
Fuster, V .
CARDIOVASCULAR RESEARCH, 1999, 41 (02) :323-333
[6]  
Haverkate F, 1997, LANCET, V349, P462, DOI 10.1016/S0140-6736(96)07591-5
[7]  
HEINRICH J, 1995, THROMB HAEMOSTASIS, V73, P374
[8]   Symptomatic myocardial ischemia and everyday life: Implications for clinical use of interactive monitoring [J].
Kinne, G ;
Droste, C ;
Fahrenberg, J ;
Roskamm, H .
JOURNAL OF PSYCHOSOMATIC RESEARCH, 1999, 46 (04) :369-377
[9]   C-reactive protein, a sensitive marker of inflammation, predicts future risk of coronary heart disease in initially healthy middle-aged men -: Results from the MONICA (Monitoring Trends and Determinants in Cardiovascular Disease) Augsburg Cohort Study, 1984 to 1992 [J].
Koenig, W ;
Sund, M ;
Fröhlich, M ;
Fischer, HG ;
Löwel, H ;
Döring, A ;
Hutchinson, WL ;
Pepys, MB .
CIRCULATION, 1999, 99 (02) :237-242
[10]  
Kuller LH, 1996, AM J EPIDEMIOL, V144, P537, DOI 10.1093/oxfordjournals.aje.a008963