Association of classical and related inflammatory markers with high-sensitivity C-reactive protein in healthy individuals: results from the Stanislas cohort

Clin Chem Lab Med. 2007;45(10):1339-46. doi: 10.1515/CCLM.2007.279.

Abstract

Background: Although high-sensitivity C-reactive protein (hs-CRP) has emerged as a cardiovascular marker, questions arise regarding the relative information provided by other inflammatory molecules. Therefore, as a first step, we examined interrelationships between serum hs-CRP concentrations and inflammatory, adhesion and growth factors in healthy adults.

Methods: Circulating concentrations of hs-CRP, haptoglobin, orosomucoid, interleukin-6 (IL-6), IL-8, IL-18, tumor necrosis factor-alpha (TNF-alpha), TNF-receptor II (TNF-RII), E-, P-, and L-selectins, intercellular adhesion molecule-1 (ICAM-1), monocyte chemoattractant protein-1, endothelial growth factor (EGF), vascular EGF (VEGF), insulin-like growth factor-1 (IGF-1) and IGF-binding protein (IGFBP-3) were measured in 154 men and 161 women of the Stanislas cohort. Leukocyte and platelet counts were also determined.

Results: Correlations were significant between hs-CRP concentrations and leukocyte and platelet counts, as well as haptoglobin, orosomucoid, IL-6, and ICAM-1 concentrations (p< or =0.001). Correlation coefficients for ICAM-1 were higher in men than in women (p< or =0.05). When stratifying subjects according to hs-CRP levels, the group with high hs-CRP levels had significantly higher haptoglobin and orosomucoid concentrations than the others, in addition to higher leukocyte counts and IL-6 concentrations in women, and platelet counts and ICAM-1 concentrations in men.

Conclusions: Further studies are warranted to explain the association pattern for hs-CRP. Partition of these factors according to their association with hs-CRP concentration opens a new perspective for choice of the best factors in terms of cardiovascular risk in relation to hs-CRP, while non-associated markers could be used to give additional information.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Biomarkers / analysis
  • Blood Cell Count
  • C-Reactive Protein / analysis*
  • Child, Preschool
  • Cohort Studies
  • Epidermal Growth Factor / analysis
  • Female
  • Haptoglobins / analysis
  • Humans
  • Inflammation / diagnosis*
  • Inflammation / pathology
  • Insulin-Like Growth Factor Binding Protein 3 / analysis
  • Insulin-Like Growth Factor I / analysis
  • Intercellular Adhesion Molecule-1 / analysis
  • Interleukins / analysis
  • Male
  • Middle Aged
  • Orosomucoid / analysis
  • Selectins / analysis
  • Tumor Necrosis Factors / analysis
  • Vascular Endothelial Growth Factor A / analysis

Substances

  • Biomarkers
  • Haptoglobins
  • Insulin-Like Growth Factor Binding Protein 3
  • Interleukins
  • Orosomucoid
  • Selectins
  • Tumor Necrosis Factors
  • Vascular Endothelial Growth Factor A
  • Intercellular Adhesion Molecule-1
  • Epidermal Growth Factor
  • Insulin-Like Growth Factor I
  • C-Reactive Protein