Oxidation-Specific Biomarkers, Lipoprotein(a), and Risk of Fatal and Nonfatal Coronary Events

被引:129
作者
Tsimikas, Sotirios [1 ]
Mallat, Ziad [2 ]
Talmud, Philippa J. [3 ]
Kastelein, John J. P. [6 ,7 ]
Wareham, Nicholas J. [4 ]
Sandhu, Manjinder S. [5 ]
Miller, Elizabeth R. [1 ]
Benessiano, Joelle [2 ]
Tedgui, Alain [2 ]
Witztum, Joseph L. [1 ]
Khaw, Kay-Tee [5 ]
Boekholdt, S. Matthijs [6 ,7 ]
机构
[1] Univ Calif San Diego, Vasc Med Program, La Jolla, CA 92993 USA
[2] INSERM, Paris Cardiovasc Res Ctr, U970, Paris, France
[3] UCL, Dept Med, Div Cardiovasc Genet, London, England
[4] MRC, Epidemiol Unit, Cambridge, England
[5] Univ Cambridge, Inst Publ Hlth, Dept Publ Hlth & Primary Care, Cambridge, England
[6] Univ Amsterdam, Acad Med Ctr, Dept Cardiol, NL-1105 AZ Amsterdam, Netherlands
[7] Univ Amsterdam, Acad Med Ctr, Dept Vasc Med, NL-1105 AZ Amsterdam, Netherlands
基金
英国医学研究理事会;
关键词
atherosclerosis; biomarkers; myocardial infarction; oxidation; LOW-DENSITY-LIPOPROTEIN; SECRETORY PHOSPHOLIPASE-A2 ACTIVITY; APOLIPOPROTEIN B-100 PARTICLES; APPARENTLY HEALTHY-MEN; OXIDIZED PHOSPHOLIPIDS; ARTERY-DISEASE; EPIC-NORFOLK; PLASMA-LEVELS; SERUM-LEVELS; ATHEROSCLEROSIS;
D O I
10.1016/j.jacc.2010.04.048
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives This study sought to assess whether oxidation-specific biomarkers are associated with an increased risk of coronary artery disease (CAD) events. Background The relationship of a panel of oxidative biomarkers and lipoprotein(a) [Lp(a)] to CAD risk is not fully determined. Methods A prospective case-control study nested in the EPIC (European Prospective Investigation of Cancer)-Norfolk cohort of 45- to 79-year-old apparently healthy men and women followed for similar to 6 years was designed. Cases consisted of participants in whom fatal or nonfatal CAD developed, matched by sex, age, and enrollment time with controls without CAD. Baseline levels of oxidized phospholipids on apolipoprotein B-100 particles and Lp(a) were measured in 763 cases and 1,397 controls. Their relationship to secretory phospholipase A(2) type IIA mass and activity, myeloperoxidase mass, and lipoprotein-associated phospholipase A(2) activity and association with CAD events were determined. Results After adjusting for age, smoking, diabetes, low-and high-density lipoprotein cholesterol, and systolic blood pressure, the highest tertiles of oxidized phospholipids on apolipoprotein B-100 particles and Lp(a) were associated with a significantly higher risk of CAD events (odds ratios: 1.67 and 1.64, respectively; p < 0.001) compared with the lowest tertiles. The odds ratio of CAD events associated with the highest tertiles of oxidized phospholipids on apolipoprotein B-100 particles or Lp(a) was significantly potentiated (approximately doubled) by the highest tertiles of secretory phospholipase A(2) activity and mass but less so for myeloperoxidase and lipoprotein-associated phospholipase A(2) activity. The odds ratios for fatal CAD were higher than for the combined end point. After taking into account the Framingham Risk Score, c-index values progressively increased when oxidative biomarkers were added to the model. Conclusions This EPIC-Norfolk study links pathophysiologically related oxidation-specific biomarkers and Lp(a) with CAD events. Oxidation-specific biomarkers provide cumulative predictive value when added to traditional cardiovascular risk factors. (J Am Coll Cardiol 2010; 56: 946-55) (C) 2010 by the American College of Cardiology Foundation
引用
收藏
页码:946 / 955
页数:10
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