Association of systemic inflammation with the serum apolipoprotein A-1 level: A cross-sectional pilot study

Shigemasa Tani1, Ken Nagao2, Atsushi Hirayama2

  • 1Department of Health Planning Center, Nihon University Hospital, Tokyo, Japan; Division of Cardiology, Department of Medicine, Nihon University School of Medicine, Tokyo, Japan.

Journal of Cardiology
|September 29, 2015
PubMed

Insights

Apolipoprotein A-1 (apoA-1) levels may predict coronary artery disease (CAD) risk. Lower apoA-1 correlated with higher inflammation markers, suggesting its role in CAD development.

Area of Science:

  • Cardiovascular Medicine
  • Biomarkers
  • Inflammation Research

Background:

  • Coronary artery disease (CAD) risk prediction often relies on HDL-cholesterol, but apolipoprotein A-1 (apoA-1) may be superior.
  • Systemic inflammation is implicated in CAD initiation.
  • This study investigated the link between inflammation and apoA-1 levels in CAD risk.

Purpose of the Study:

  • To examine the association between serum apoA-1 levels and markers of systemic inflammation (hs-CRP, WBC count) in patients with CAD risk factors.
  • To determine if apoA-1 is an independent predictor of inflammation in CAD.
  • To assess the longitudinal relationship between apoA-1 and inflammation markers.

Main Methods:

  • Cross-sectional study of 652 outpatients with CAD risk factors.
  • Measured serum apoA-1, high-sensitivity C-reactive protein (hs-CRP), and white blood cell (WBC) count.
  • Multivariate analysis adjusted for traditional CAD risk factors; follow-up for some patients at 6 months.

Main Results:

  • Reduced apoA-1 was independently associated with higher hs-CRP and WBC counts in the overall population and a subset with LDL-C <100 mg/dL.
  • A longitudinal increase in apoA-1 correlated with a decrease in hs-CRP, but not WBC count.
  • These findings suggest apoA-1 is linked to inflammatory processes in CAD.

Conclusions:

  • Increased serum apoA-1 may correlate with decreased hs-CRP and WBC counts, indicating reduced inflammation.
  • ApoA-1, hs-CRP, and WBC count may serve as predictive inflammatory biomarkers for CAD onset.
  • Decreased apoA-1 and increased hs-CRP are potential indices for CAD risk assessment.
Abstract

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