HDL-C levels modify the association between C-reactive protein and coronary artery calcium score

K-C Sung1, E-J Cho2, Y-H Lim3

  • 1Division of Cardiology, Department of Internal Medicine, Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.

Insights

High-sensitivity C-reactive protein (hs-CRP) predicts cardiovascular events. This study found hs-CRP is associated with coronary artery calcification, but only in individuals with low high-density lipoprotein cholesterol (HDL-C) levels.

Area of Science:

  • Cardiovascular Medicine
  • Biomarkers
  • Epidemiology

Background:

  • C-reactive protein (CRP) is a marker for cardiovascular disease (CVD) risk.
  • The relationship between CRP and preclinical atherosclerosis is not fully understood.
  • High-density lipoprotein cholesterol (HDL-C) is known to be inversely associated with CVD risk.

Purpose of the Study:

  • To investigate if HDL-C modifies the association between CRP concentration and preclinical atherosclerosis.
  • To examine the link between CRP levels and coronary artery calcification (CAC) scores.
  • To determine if HDL-C levels influence the predictive value of CRP for atherosclerosis.

Main Methods:

  • Analysis of data from 12,030 Korean male subjects.
  • Cardiac computed tomography (CT) for coronary artery calcification (CAC) scoring.
  • Logistic regression to assess associations between CRP and CAC scores >0, stratified by HDL-C quartiles.

Main Results:

  • A positive association was observed between CRP and CAC score >0 in the lowest HDL-C quartile (OR 1.41, p=0.027).
  • This association was not significant in the highest HDL-C quartile (OR 0.80, p=0.425).
  • Higher CRP levels were associated with increased prevalence of CAC scores >0 (p < 0.0001).

Conclusions:

  • The association between CRP concentration and coronary artery calcification is dependent on HDL-C levels.
  • CRP may be a more significant predictor of subclinical atherosclerosis in individuals with low HDL-C.
  • Findings highlight the complex interplay between CRP, HDL-C, and atherosclerosis.
Abstract

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