Inverse relationship between high-density lipoprotein cholesterol raising and high-sensitivity C-reactive protein

W Virgil Brown1, JoAnne M Foody2, Franklin J Zieve3

  • 1Emory University School of Medicine, Atlanta, GA, USA.

Insights

Inflammation marker high-sensitivity C-reactive protein (hsCRP) showed weak baseline links with lipids in older adults. After statin therapy, correlations strengthened, particularly with high-density lipoprotein cholesterol (HDL-C).

Area of Science:

  • Cardiology
  • Clinical Lipidology
  • Inflammation Biomarkers

Background:

  • Limited understanding of high-sensitivity C-reactive protein (hsCRP) associations with lipoproteins beyond LDL-C.
  • High-density lipoprotein (HDL) is of interest due to its anti-inflammatory and cholesterol-mediating roles.
  • Exploratory analysis in older adults at cardiovascular risk.

Purpose of the Study:

  • Assess relationships between hsCRP and various lipids.
  • Evaluate these associations before and after lipid-lowering therapy.
  • Focus on patients aged over 65 with moderate to high cardiovascular disease risk.

Main Methods:

  • Analysis of a 12-week, multicenter, randomized, double-blind study.
  • Correlations assessed in 1054 patients with baseline and 12-week hsCRP ≤ 10 mg/L.
  • Pooled data from ezetimibe/simvastatin (E/S) and atorvastatin (ATV) treatment groups, with significance set at P < .01.

Main Results:

  • Weak, nonsignificant baseline correlations between hsCRP and LDL-C, non-HDL-C, or apolipoprotein B.
  • Significantly stronger correlations after 12 weeks of treatment for most lipid parameters.
  • Inverse correlation between HDL-C and hsCRP observed at baseline and post-treatment across groups.

Conclusions:

  • Lipid factor associations with hsCRP were weak initially but strengthened post-treatment in older patients.
  • High-density lipoprotein cholesterol (HDL-C) showed consistent inverse correlation with hsCRP.
  • Changes in HDL-C and hsCRP were correlated, particularly in E/S and combined treatment groups.
Abstract

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