4.6 Article

Lipoprotein-associated phospholipase A2 (Lp-PLA2) and risk of cardiovascular disease in older adults: Results from the Cardiovascular Health Study

Journal

ATHEROSCLEROSIS
Volume 209, Issue 2, Pages 528-532

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.atherosclerosis.2009.09.021

Keywords

Epidemiology; Inflammation; Cardiovascular diseases; Lipoprotein-associated phospholipase A(2)

Funding

  1. National Heart, Lung, and Blood Institute [N01-HC-35129, N01-HC-45133, N01-HC-75150, N01-HC-85079, N01-HC-85086, N01 HC-15103, N01 HC-55222, U01 HL080295]
  2. National Institute of Neurological Disorders and Stroke
  3. GlaxoSmithKline

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Objective: To examine associations between lipoprotein-associated phospholipase A(2) (Lp-PLA(2)) antigen level (mass) and enzymatic activity (activity) and cardiovascular disease (CVD) in older adults. Methods: We examined associations of Lp-PLA(2) mass and activity with incident myocardial infarction (MI; n = 508), stroke (n = 565) and CVD death (n = 665) using Cox regressions adjusted for age, sex, ethnicity and CVD risk factors in 3949 older adults, aged = 65 years at baseline, from the Cardiovascular Health Study (CHS). Results: Lp-PLA(2) was associated with incident CVD events in these older adults. Hazard ratios (95% confidence intervals) for highest versus lowest tertiles of Lp-PLA(2) mass were 1.49 (1.19-1.85) for MI, 1.21 (0.98-1.49) for stroke and 1.11 (0.92-1.33) for CVD death. The highest tertile of Lp-PLA(2) activity was associated with MI (1.36; 1.09-1.70) and CVD death (1.23; 1.02-1.50). Combined Lp-PLA(2) tertile 3 and CRP > 3 mg/l, compared to Lp-PLA(2) tertile 1 and CRP < 1 mg/l, was associated with MI (2.29; 1.49-3.52) for Lp-PLA(2) mass and MI (1.66; 1.10-2.51) and CVD death (1.57; 1.08-2.26) for activity. For MI, both mass and activity added excess risk to elevated CRP alone (similar to 20% excess risk) and activity added excess risk for CVD death (similar to 12%). Conclusion: Lp-PLA(2) mass and activity were associated with incident CVD events in older adults in CHS. Lp-PLA(2) and CRP were independent and additive in prediction of events. While associations were modest, these results support further exploration of Lp-PLA(2) to identify older individuals at risk for CVD. (C) 2009 Elsevier Ireland Ltd. All rights reserved.

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