Serum osteoprotegerin levels and long-term prognosis in patients with stable angina pectoris

被引:36
作者
Pedersen, Eva Ringdal [1 ]
Ueland, Thor [2 ]
Seifert, Reinhard [3 ]
Aukrust, Pal [2 ,4 ,5 ]
Schartum-Hansen, Hall [1 ]
Ebbing, Marta [3 ]
Bleie, Oyvind [3 ]
Igland, Jannicke [6 ]
Svingen, Gard [3 ]
Nordrehaug, Jan Erik [1 ,3 ]
Nygard, Ottar [1 ,3 ]
机构
[1] Univ Bergen, Inst Med, N-5021 Bergen, Norway
[2] Oslo Univ Hosp, Rikshosp, Internal Med Res Inst, N-0027 Oslo, Norway
[3] Haukeland Hosp, Dept Heart Dis, N-5021 Bergen, Norway
[4] Oslo Univ Hosp, Rikshosp, Sect Clin Immunol & Infect Dis, N-0027 Oslo, Norway
[5] Univ Oslo, Fac Med, N-0027 Oslo, Norway
[6] Univ Bergen, Inst Publ Hlth & Primary Hlth Care, N-5021 Bergen, Norway
关键词
Osteoprotegerin; Stable angina pectoris; Mortality; Acute myocardial infarction; SOLUBLE RECEPTOR ACTIVATOR; KAPPA-B LIGAND; VASCULAR CALCIFICATION; PLASMA OSTEOPROTEGERIN; AORTIC CALCIFICATION; RISK; OSTEOPONTIN; ASSOCIATION; SEVERITY; MARKER;
D O I
10.1016/j.atherosclerosis.2010.06.027
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives: Osteoprotegerin (OPG) is a member of the tumor necrosis factor superfamily with pleiotropic effects on bone metabolism, endocrine function and the immune system. Circulating OPG levels are elevated in cardiovascular disease (CVD). We assessed serum OPG as predictor of long-term prognosis in patients with suspected stable angina pectoris (SAP) undergoing elective coronary angiography. Methods: Samples were obtained from 1025 patients (median [25th, 75th percentile] age 62 [ 54, 70] years, 71.9% men). At inclusion, 43.2% of patients had single or double vessel disease, whereas 34.3% had triple vessel disease. Results: During a median follow-up of 73 months, 11.0% of patients died, 5.9% died from CVD and 10.0% experienced an acute myocardial infarction (MI). In univariable analyses, strong associations were observed between OPG concentrations and all-cause mortality, CVD mortality and the incidence of MI (fatal or nonfatal). However, adjustment for conventional risk factors attenuated the risk estimates which were no longer significant, except for the subgroup with levels above the 90th percentile. For decile 10 versus deciles 1-9 of serum OPG, the following multivariable hazard ratios (95% confidence intervals) were observed: All-cause mortality: 1.94 (1.18, 3.18), p = 0.01; CVD mortality: 2.29 (1.16, 4.49), p = 0.02; and MI: 1.76 (1.02, 3.06), p = 0.04. Conclusion: In patients with SAP, elevated serum OPG is associated with increased risk of all-cause mortality, CVD mortality and MI, but independent effects are mainly confined to levels above the 90th percentile. (C) 2010 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:644 / 649
页数:6
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