The Association of Biomarkers of Inflammation and Extracellular Matrix Degradation With the Risk of Abdominal Aortic Aneurysm: The ARIC Study

Author:

Tang Weihong1ORCID,Yao Lu1,Hoogeveen Ron C.2,Alonso Alvaro3,Couper David J.4,Lutsey Pamela L.1,Steenson Carol C.5,Guan Weihua6,Hunter David W.7,Lederle Frank A.89,Folsom Aaron R.1

Affiliation:

1. Division of Epidemiology and Community Health, School of Public Health, University of Minnesota, Minneapolis, MN, USA

2. Section of Cardiovascular Research, Department of Medicine, Baylor College of Medicine, Houston, Texas, USA

3. Department of Epidemiology, Rollins School of Public Health, Emory University, Atlanta, GA, USA

4. Department of Biostatistics, Gillings School of Global Public Health, University of North Carolina at Chapel Hill, NC, USA

5. Department of Imaging, Minneapolis VA Health Care System, Minneapolis, MN, USA

6. Division of Biostatistics, School of Public Health, University of Minnesota, Minneapolis, MN, USA

7. Department of Medicine, School of Medicine, University of Minnesota, Minneapolis, MN, USA

8. Minneapolis VA Health Care System and Department of Medicine, School of Medicine, University of Minnesota, Minneapolis, MN, USA

9. Frank A. Lederle, Deceased January 2018

Abstract

Animal and human laboratory studies suggest that the pathogenesis of abdominal aortic aneurysms (AAAs) involves inflammation and degradation and remodeling of the extracellular matrix. This study prospectively assessed the association between biomarkers for these mechanisms and the presence of AAA during 24 years of follow-up in the Atherosclerosis Risk in Communities (ARIC) study. The ARIC prospectively identified clinically diagnosed AAAs in 15 792 men and women from baseline in 1987 to 1989 to 2011 using hospital discharge codes and death records. Additional asymptomatic AAAs were detected by an abdominal ultrasound scan in 2011 to 2013. Matrix metalloproteinase (MMP)-3, MMP-9, interleukin 6 (IL-6), N-terminal propeptide of Type III procollagen (PIIINP), and osteopontin were measured in blood samples collected between 1987 and 1992 in participants with AAA (544 clinically diagnosed AAAs and 72 ultrasound-detected AAAs) and a random sample of 723 participants selected from baseline and matched with AAAs by age, race and sex. Higher concentrations of MMP-9 and IL-6 were associated with future risk of clinically diagnosed AAA (hazard ratios [95% confidence intervals]: 1.55 [1.22-1.97] and 1.87 [1.48-2.35], respectively, comparing highest versus lowest tertiles) after multivariable adjustment ( P for trend < .001). Matrix metalloproteinase-9 was also associated with ultrasound-detected AAA. In conclusion, blood concentrations of MMP-9 and IL-6 measured in middle age predicted the risk of AAA during 24 years of follow-up.

Funder

The National Heart, Lung, and Blood Institute

Publisher

SAGE Publications

Subject

Cardiology and Cardiovascular Medicine

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