Abstract | OBJECTIVE: 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 > or =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>3mg/l, compared to Lp-PLA(2) tertile 1 and CRP<1mg/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 ( approximately 20% excess risk) and activity added excess risk for CVD death ( approximately 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.
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Authors | Nancy Swords Jenny, Cam Solomon, Mary Cushman, Russell P Tracy, Jeanenne J Nelson, Bruce M Psaty, Curt D Furberg |
Journal | Atherosclerosis
(Atherosclerosis)
Vol. 209
Issue 2
Pg. 528-32
(Apr 2010)
ISSN: 1879-1484 [Electronic] Ireland |
PMID | 19804884
(Publication Type: Journal Article, Research Support, N.I.H., Extramural)
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Copyright | Copyright 2009 Elsevier Ireland Ltd. All rights reserved. |
Chemical References |
- C-Reactive Protein
- 1-Alkyl-2-acetylglycerophosphocholine Esterase
|
Topics |
- 1-Alkyl-2-acetylglycerophosphocholine Esterase
(blood)
- Aged
- C-Reactive Protein
(metabolism)
- Cardiovascular Diseases
(blood, etiology)
- Female
- Humans
- Myocardial Infarction
(etiology)
- Population Surveillance
- Prospective Studies
- Risk
- Stroke
(etiology)
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