Inflammatory/Hemostatic Biomarkers and Coronary Artery Calcium Progression in Women at Midlife (from the Study of Women's Health Across the Nation, Heart Study)

Am J Cardiol. 2016 Aug 1;118(3):311-8. doi: 10.1016/j.amjcard.2016.05.009. Epub 2016 May 14.

Abstract

It is unknown whether inflammatory/hemostatic biomarkers are associated with coronary artery calcium (CAC) progression. Our purpose was to evaluate the associations of baseline levels of C-reactive protein, fibrinogen, plasminogen activator inhibitor-1 (PAI-1), tissue plasminogen activator antigen, and circulating factor VII with CAC progression in healthy midlife women. Inflammatory/hemostatic biomarkers were measured at baseline. CAC was quantified by computed tomography scans at baseline and after 2.3 ± 0.5 years of follow-up. Significant CAC progression was defined as present if (1) follow-up CAC Agatston score was >0 if baseline CAC score = 0; (2) annualized change in CAC score was ≥10 if baseline CAC score >0 to <100; and (3) annualized percent change in CAC score was ≥10% if baseline CAC score ≥100. Extent of CAC progression was defined as [log(CAC(follow-up)+25) - log(CAC(baseline)+25)]/year. Logistic and linear regression models were used as appropriate, and the final models were adjusted for baseline CAC score, age, study site, race/ethnicity, menopausal status, sociodemographics, traditional cardiovascular disease (CVD) risk factors, family history of CVD, and CVD medication use. The study included 252 women (baseline age 51.2 ± 2.6 years; 67.5% white; 56.4% premenopausal or early perimenopausal). In final models, only log(PAI-1) was associated with presence of CAC progression (odds ratio 1.91, 95% CI 1.24 to 2.93; per 1 log unit increase in PAI-1; p = 0.003). In addition, higher log(PAI-1) was marginally associated with greater extent of CAC progression (p = 0.06). In conclusion, PAI-1 is associated with the presence of CAC progression in middle-aged women. Targeting PAI-1 may decrease atherogenesis beyond conventional CVD risk factors.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Adult
  • Antigens / immunology
  • Biomarkers / metabolism
  • C-Reactive Protein / metabolism
  • Calcinosis / diagnostic imaging
  • Calcinosis / immunology
  • Calcinosis / metabolism*
  • Cohort Studies
  • Coronary Artery Disease / diagnostic imaging
  • Coronary Artery Disease / immunology
  • Coronary Artery Disease / metabolism*
  • Coronary Vessels / diagnostic imaging
  • Disease Progression
  • Factor VII / metabolism
  • Female
  • Fibrinogen / metabolism
  • Humans
  • Linear Models
  • Logistic Models
  • Middle Aged
  • Plasminogen Activator Inhibitor 1 / metabolism
  • Prospective Studies
  • Tissue Plasminogen Activator / immunology
  • Tomography, X-Ray Computed

Substances

  • Antigens
  • Biomarkers
  • Plasminogen Activator Inhibitor 1
  • SERPINE1 protein, human
  • Factor VII
  • Fibrinogen
  • C-Reactive Protein
  • Tissue Plasminogen Activator