Lipoprotein-associated phospholipase A2 and risk of incident peripheral arterial disease in a multi-ethnic cohort: The Multi-Ethnic Study of Atherosclerosis

Author:

Garg Parveen K1,Jorgensen Neal W2,McClelland Robyn L2,Jenny Nancy S3,Criqui Michael H4,Allison Matthew A4,Greenland Philip56,Rosenson Robert S7,Siscovick David S8,Cushman Mary39

Affiliation:

1. Division of Cardiovascular Medicine, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA

2. Department of Biostatistics, University of Washington, Seattle, WA, USA

3. Department of Pathology and Laboratory Medicine, University of Vermont College of Medicine, Burlington, VT, USA

4. Department of Family Medicine & Public Health, University of California in San Diego, La Jolla, CA, USA

5. Department of Medicine, Northwestern University, Chicago, IL, USA

6. Department of Preventive Medicine, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA

7. Mount Sinai Heart, Icahn School of Medicine at Mount Sinai, New York, NY, USA

8. New York Academy of Medicine, New York, NY, USA

9. Department of Medicine, University of Vermont College of Medicine, Burlington, VT, USA

Abstract

Prospective studies supporting a relationship between elevated lipoprotein-associated phospholipase A2 (Lp-PLA2) and incident peripheral arterial disease (PAD) are limited. We evaluated the association of Lp-PLA2 with incident PAD in a multi-ethnic cohort without clinical cardiovascular disease. A total of 4622 participants with measurement of Lp-PLA2 mass and Lp-PLA2 activity and an ankle–brachial index (ABI) between 0.9 and 1.4 were followed for the development of PAD (median follow-up = 9.3 years), defined as an ABI ⩽0.9 and decline from baseline ⩾0.15. There were 158 incident PAD events during follow-up. In adjusted logistic regression models, each higher standard deviation of both Lp-PLA2 activity and mass did not confer an increased risk of developing PAD [odds ratios, (95% confidence intervals)]: 0.92 (0.66–1.27) for Lp-PLA2 activity and 1.06 (0.85–1.34) for mass. Additionally, no significant interaction was found according to ethnicity: p=0.43 for Lp-PLA2 activity and p=0.55 for Lp-PLA2 mass. We found no evidence of an association between Lp-PLA2 and incident PAD.

Publisher

SAGE Publications

Subject

Cardiology and Cardiovascular Medicine

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