Associations of Pentraxin 3 With Cardiovascular Disease and All-Cause Death The Cardiovascular Health Study

被引:145
作者
Jenny, Nancy Swords [1 ]
Arnold, Alice M. [3 ]
Kuller, Lewis H. [7 ]
Tracy, Russell P. [1 ,2 ]
Psaty, Bruce M. [4 ,5 ,6 ,8 ]
机构
[1] Univ Vermont, Dept Pathol, Burlington, VT 05405 USA
[2] Univ Vermont, Dept Biochem, Burlington, VT 05405 USA
[3] Univ Washington, Dept Biostat, Seattle, WA 98195 USA
[4] Univ Washington, Dept Med, Cardiovasc Hlth Res Unit, Seattle, WA 98195 USA
[5] Univ Washington, Dept Epidemiol, Cardiovasc Hlth Res Unit, Seattle, WA 98195 USA
[6] Univ Washington, Dept Hlth Serv, Cardiovasc Hlth Res Unit, Seattle, WA 98195 USA
[7] Univ Pittsburgh, Sch Publ Hlth, Dept Epidemiol, Pittsburgh, PA 15260 USA
[8] Grp Hlth Cooperat Puget Sound, Ctr Hlth Studies, Seattle, WA 98101 USA
关键词
cardiovascular diseases; epidemiology; inflammation; mortality; pentraxin; 3; C-REACTIVE PROTEIN; REGULATES TISSUE FACTOR; SERUM-AMYLOID-P; LONG PENTRAXIN; VASCULAR INFLAMMATION; PTX3; EXPRESSION; INDICATOR; MARKER; LINK;
D O I
10.1161/ATVBAHA.108.178947
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective-We examined associations of pentraxin 3 (PTX3), a vascular inflammation marker, with incident cardiovascular disease (CVD) and all-cause death. Methods and Results-1583 Cardiovascular Health Study participants free of prevalent CVD were included. Nonexclusive case groups were angina (n=476), myocardial infarction (MI; n=237), stroke (n=310), CVD death (n=282), and all-cause death (n=772). 535 participants had no events. PTX3 levels were higher in those with subclinical CVD (1.90 +/- 1.89 ng/mL) than those without (1.71 +/- 1.88 ng/mL; P=0.001). Using Cox regression adjusted for age, sex, and ethnicity, a standard deviation increase in PTX3 (1.89 ng/mL) was associated with CVD death (hazard ratio 1.11; 95% confidence interval 1.02 to 1.21) and all-cause death (1.08; 1.02 to 1.15). PTX3 was not associated with angina (1.09; 0.98 to 1.20), MI (0.96; 0.81 to 1.12), or stroke (1.06; 0.95 to 1.18). Adding C-reactive protein (CRP) or CVD risk factors to the models had no significant effects on associations. Conclusions-In these older adults, PTX3 was associated with CVD and all-cause death independent of CRP and CVD risk factors. PTX3 likely reflects different aspects of inflammation than CRP and may provide insight into vascular health in aging and chronic diseases of aging that lead to death. (Arterioscler Thromb Vasc Biol. 2009; 29: 594-599.)
引用
收藏
页码:594 / 599
页数:6
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