High lipoprotein-associated phospholipase A2 is a risk factor for recurrent coronary events in postinfarction patients

被引:70
作者
Corsetti, JP
Rainwater, DL
Moss, AJ
Zareba, W
Sparks, CE
机构
[1] Univ Rochester, Sch Med & Dent, Dept Pathol & Lab Med, Rochester, NY USA
[2] Univ Rochester, Sch Med & Dent, Dept Med, Cardiol Unit, Rochester, NY 14642 USA
[3] SW Fdn Biomed Res, Dept Genet, San Antonio, TX USA
关键词
D O I
10.1373/clinchem.2006.066845
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background: Recent studies demonstrate that lipoprotein-associated phospholipase A(2) (Lp-PLA(2)) is a risk factor for cardiovascular disease presumably deriving from generation of proinflammatory and proatherogenic species through its hydrolytic activity on lipoprotein-associated phospholipids. The goal of this study was to assess the relationship of Lp-PLA(2) with a set of thrombogenic, lipid, inflammatory, and metabolic blood markers and to determine whether plasma LpPLA(2) is a risk factor for recurrent coronary events in postinfarction patients. Methods: Factor analysis on the set of blood markers and Lp-PLA(2) was performed for 766 patients of the Thrombogenic Factors and Recurrent Coronary Events (THROMBO) postinfarction study. Recurrent coronary event risk was assessed as a function of blood marker concentrations and Lp-PLA(2) by Cox proportional hazards multivariable regression adjusted for significant clinical covariates. Results: Factor analysis revealed that Lp-PLA(2) was associated with one factor dominated by cholesterol and apolipoprotein B and another factor dominated by HDL-cholesterol and triglycerides, with little association with an inflammatory factor dominated by C-reactive protein. Multivariable analysis demonstrated as significant and independent predictors of risk of secondary coronary events only apolipoprotein B in a model without Lp-PLA(2) (hazard ratio, 1.66; 95% confidence interval, 1.14-2.40) and only Lp-PLA(2) in a model with Lp-PLA(2) included [1.90(1.31-2.75)]. Conclusions: Lp-PLA(2) is a significant and independent predictor of risk for recurrent coronary events in postinfarction patients, and Lp-PLA(2) is related to both hype-cholesterolemia and high triglyceride-low HDL dyslipidemia in this study population.(c) 2006 American Association for Clinical Chemistry.
引用
收藏
页码:1331 / 1338
页数:8
相关论文
共 20 条
[1]   Lipoprotein-associated phospholipase A2, high-sensitivity C-reactive protein, and risk for incident coronary heart disease in middle-aged men and women in the Atherosclerosis Risk in Communities (ARIC) study [J].
Ballantyne, CM ;
Hoogeveen, RC ;
Bang, H ;
Coresh, J ;
Folsom, AR ;
Heiss, G ;
Sharrett, AR .
CIRCULATION, 2004, 109 (07) :837-842
[2]   A prospective evaluation of lipoprotein-associated phospholipase A2 levels and the risk of future cardiovascular events in women [J].
Blake, GJ ;
Dada, N ;
Fox, JC ;
Manson, JE ;
Ridker, PM .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2001, 38 (05) :1302-1306
[3]   Association of lipoprotein-associated phospholipase A2 levels with coronary artery disease risk factors, angiographic coronary artery disease, and major adverse events at follow-up [J].
Brilakis, ES ;
McConnell, JP ;
Lennon, RJ ;
Elesber, AA ;
Meyer, JG ;
Berger, PB .
EUROPEAN HEART JOURNAL, 2005, 26 (02) :137-144
[4]   Lipoprotein-associated phospholipase A2, platelet-activating factor acetylhydrolase:: a potential new risk factor for coronary artery disease [J].
Caslake, MJ ;
Packard, CJ ;
Suckling, KE ;
Holmes, SD ;
Chamberlain, P ;
Macphee, CH .
ATHEROSCLEROSIS, 2000, 150 (02) :413-419
[5]   Lipoprotein-associated phospholipase A2 (platelet-activating factor acetylhydrolase) and cardiovascular disease [J].
Caslake, MJ ;
Packard, CJ .
CURRENT OPINION IN LIPIDOLOGY, 2003, 14 (04) :347-352
[6]   Serum glucose and triglyceride determine high-risk subgroups in non-diabetic postinfarction patients [J].
Corsetti, JP ;
Zareba, W ;
Moss, AJ ;
Sparks, CE .
ATHEROSCLEROSIS, 2005, 183 (02) :293-300
[7]   Apolipoprotein B determines risk for recurrent coronary events in postinfarction patients with metabolic syndrome [J].
Corsetti, JP ;
Zareba, W ;
Moss, AJ ;
Sparks, CE .
ATHEROSCLEROSIS, 2004, 177 (02) :367-373
[8]   Metabolic syndrome best defines the multivariate distribution of blood variables in postinfarction patients [J].
Corsetti, JP ;
Zareba, W ;
Moss, AJ ;
Ridker, PM ;
Marder, VJ ;
Rainwater, DL ;
Sparks, CE .
ATHEROSCLEROSIS, 2003, 171 (02) :351-358
[9]   Phospholipase A2 in vascular disease [J].
Hurt-Camejo, E ;
Camejo, G ;
Peilot, H ;
Öörni, K ;
Kovanen, P .
CIRCULATION RESEARCH, 2001, 89 (04) :298-304
[10]   Biological effects of secretory phospholipase A2 group IIA on lipoproteins and in atherogenesis [J].
Jaross, W ;
Eckey, R ;
Menschikowski, M .
EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 2002, 32 (06) :383-393