Lipoprotein-associated phospholipase A2 and coronary calcification - The Rotterdam coronary calcification study

被引:25
作者
Kardys, Isabella
Oei, Hok-Hay S.
Hofman, Albert
Oudkerk, Matthijs
Witteman, Jacqueline C. M.
机构
[1] Erasmus MC, Dept Epidemiol & Biostat, NL-3000 DR Rotterdam, Netherlands
[2] Univ Groningen, Univ Med Ctr Groningen, Dept Radiol, Groningen, Netherlands
关键词
coronary calcification; inflammation; lipoprotein-associated phospholipase A2; epidemiology;
D O I
10.1016/j.atherosclerosis.2006.04.004
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives: Although several studies have recently suggested that lipoprotein-associated phospholipase A2 (Lp-PLA2) is an independent predictor of coronary events, only one study has examined the association between Lp-PLA2 and coronary calcification, using young adults. We investigated the association between Lp-PLA2 activity and coronary calcification assessed by electron-beam computed tomography (EBT) in a population of older participants. Methods and results: The Rotterdam Coronary Calcification Study is a population-based study in men and women aged >= 55 years. Coronary calcification assessed by EBT was quantified in a calcium score according to Agatston's method. Lp-PLA2 activity measured in samples collected 7 years before scanning (n = 520) was associated with coronary calcification in men after adjustment for age. The odds ratio per standard deviation of Lp-PLA2 activity of having a total calcium score > 1000 was 1.6 (95% confidence interval: 1.1-2.4), as compared to a total calcium score < 100. After adjustment for non-HDL and HDL-cholesterol, this association disappeared. In women, the association was less consistent. For Lp-PLA2 measured concurrently to scanning (n = 703), no association was found with coronary calcification. Conclusions: Lp-PLA2 activity is moderately associated with coronary calcification after adjustment for age. The effect of Lp-PLA2 on coronary calcification may be exerted through its effect on LDL-cholesterot. (c) 2006 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:377 / 383
页数:7
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