Relation of osteoprotegerin to coronary calcium and aortic plaque (from The Dallas Heart Study)

被引:184
作者
Abedin, Moeen
Omland, Torbjorn
Ueland, Thor
Khera, Amit
Aukrust, Pal
Murphy, Sabina A.
Jain, Tulika
Gruntmanis, Ugis
McGuire, Darren K.
de Lemos, James A. [1 ]
机构
[1] Univ Texas, SW Med Ctr, Donald W Reynolds Cardiovasc Clin Res Ctr, Dallas, TX 75230 USA
[2] Univ Oslo, Akershus Univ Hosp, Dept Med, Oslo, Norway
[3] Univ Oslo, Rikshosp, Internal Med Res Inst, N-0027 Oslo, Norway
[4] Harvard Univ, Sch Med, Brigham & Womens Hosp, Donald W Reynolds Cardiovasc Clin Res Ctr, Boston, MA 02115 USA
[5] Univ Texas, SW Med Ctr, Div Endocrinol, Dallas, TX 75230 USA
关键词
D O I
10.1016/j.amjcard.2006.08.064
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Circulating osteoprotegerin (OPG) has been shown to be elevated in patients with vascular disease. The role of OPG as a biomarker for atherosclerosis in a large, unselected population is not well known. Plasma OPG levels were measured in 3,386 subjects in the Dallas Heart Study, a multiethnic, population-based probability sample of adults aged 30 to 65 years. Coronary artery calcium (CAC) was measured by electron beam computed tomography. Aortic plaque was assessed by magnetic resonance imaging. Multivariable logistic regression was used to assess associations among OPG, cardiovascular risk factors, CAC, and aortic plaque. Age, female gender, black race, smoking, personal and family history of coronary artery disease (CAD), diabetes mellitus, hyperlipidemia, CAC, and aortic plaque were significantly associated with higher plasma OPG levels (p < 0.01) in univariable analyses. The prevalence of CAC and aortic plaque increased across OPG quartiles (p < 0.001 for each). An OPG level in the fourth quartile was independently associated with CAC (RR 1.39, 95% confidence interval 1.01 to 1.93) and aortic plaque (RR 1.42, 95% confidence interval 1.09 to 1.86) after adjustment for age, gender, smoking, diabetes, hyperlipidemia, and family history of premature CAD. In conclusion, plasma OPG is independently associated with CAC and aortic plaque in an unselected population, suggesting it may be a novel biomarker for atherosclerosis in humans. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:513 / 518
页数:6
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