Serum Fetuin-A, Cardiovascular Risk Factors, and Six-Year Follow-up Outcome in Patients With Coronary Heart Disease

被引:32
|
作者
Roos, Marcel [1 ]
von Eynatten, Maximilian [1 ]
Heemann, Uwe [1 ]
Rothenbacher, Dietrich [2 ]
Brenner, Hermann [2 ]
Breitling, Lutz P. [2 ]
机构
[1] Tech Univ Munich, Klinikum Rechts Isar, Dept Nephrol, D-8000 Munich, Germany
[2] German Canc Res Ctr, Div Clin Epidemiol & Aging Res, D-6900 Heidelberg, Germany
来源
AMERICAN JOURNAL OF CARDIOLOGY | 2010年 / 105卷 / 12期
关键词
C-REACTIVE PROTEIN; MYOCARDIAL-INFARCTION; INSULIN-RESISTANCE; METABOLIC SYNDROME; ASSOCIATION; CALCIFICATION; LIVER;
D O I
10.1016/j.amjcard.2010.01.342
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
High circulating fetuin-A has recently been linked to risk of primary cardiovascular disease (CVD). The clinical importance of fetuin-A in patients at markedly increased cardiovascular risk, however, has not been fully elucidated. We studied the association between serum fetuin-A and future cardiovascular outcome in patients with prevalent coronary heart disease (CHD). Fetuin-A levels were measured in 1,049 patients with CHD. Associations with traditional cardiovascular risk factors and with secondary CVD events during 6 years of follow-up (median 73.4 months, interquartile range 57.4 to 74.3) were analyzed. Serum fetuin-A levels were significantly increased in patients with prevalent hypertriglyceridemia (0.71 vs 0.69 g/L, p = 0.013). No association with baseline metabolic syndrome was found (odds ratio 0.95 for highest vs lowest fetuin-A quintile, 95% confidence interval 0.59 to 1.53, p = 0.82). In Cox proportional hazards analyses, serum fetuin-A levels were not significantly associated with secondary CVD events (hazard ratio 0.67 for highest vs lowest fetuin-A quintile, 95% confidence interval 0.37 to 1.21, p = 0.18). In conclusion, fetuin-A is significantly associated hypertriglyceridemia but not with other traditional cardiovascular risk factors or metabolic syndrome in patients with manifest CHD. Measurement of serum fetuin-A levels may not emerge as a valuable tool for evaluating future CVD risk in patients aggressively treated for advanced atherosclerosis. (C) 2010 Elsevier Inc. All rights reserved. (Am J Cardiol 2010;105:1666-1672)
引用
收藏
页码:1666 / 1672
页数:7
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