Interleukin-2 levels are associated with carotid artery intima-media thickness

Atherosclerosis. 2005 May;180(1):181-7. doi: 10.1016/j.atherosclerosis.2004.11.015. Epub 2005 Jan 8.

Abstract

Objective: To show that serum interleukin levels are associated with carotid intima-media thickness (IMT).

Background: Inflammation is hypothesized to play a central role in atherogenesis, and serum markers of inflammation are predictive of cardiovascular disease. Interleukin-2, a pro-inflammatory cytokine produced largely by naive CD4 T cells and Th1 (pro-inflammatory) T cells, has been found in a high proportion of carotid plaques.

Methods: High-resolution ultrasound of the carotid arteries and serum cytokine levels were measured in stroke-free participants. The mean of the maximum IMT in bilateral bifurcation, common and internal carotid artery segments was measured. Serum levels of interleukin (IL)-1beta, IL-2, IL-6, C-reactive protein, tumor necrosis factor (TNF) alpha and TNF receptors were measured using enzyme-linked immunosorbent assay.

Results: IL-2 levels were significantly correlated with IMT (r=0.33, P<0.0001), but other cytokines were not. Each unit increase in IL-2 was significantly associated with a mean increase in IMT of 0.18 mm (P=0.0001). After adjusting for other atherosclerotic risk factors, the association was unchanged (mean increase in IMT per unit increase IL-2=0.18 mm, P<0.0001). Each standard deviation increase in the level of IL-2 was associated with an increased risk (adjusted odds ratio 1.80, 95% CI 1.12-2.89) for an IMT> or =1.0mm (75th percentile for IMT).

Conclusion: Serum levels of IL-2, a pro-inflammatory cytokine, are associated with carotid artery IMT, a predictor of stroke and vascular disease. Serum inflammatory markers may provide a novel marker of atherosclerotic risk, and inflammation may provide a new therapeutic target for stroke prevention.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Aged
  • Biomarkers / blood
  • C-Reactive Protein / metabolism
  • Carotid Arteries / pathology
  • Carotid Artery Diseases / blood*
  • Carotid Artery Diseases / epidemiology*
  • Carotid Artery Diseases / pathology
  • Female
  • Humans
  • Interleukin-1 / blood
  • Interleukin-2 / blood*
  • Interleukin-6 / blood
  • Linear Models
  • Male
  • Middle Aged
  • Receptors, Tumor Necrosis Factor, Type I / metabolism
  • Receptors, Tumor Necrosis Factor, Type II / metabolism
  • Risk Factors
  • Tumor Necrosis Factor-alpha / metabolism
  • Tunica Intima / pathology
  • Tunica Media / pathology

Substances

  • Biomarkers
  • Interleukin-1
  • Interleukin-2
  • Interleukin-6
  • Receptors, Tumor Necrosis Factor, Type I
  • Receptors, Tumor Necrosis Factor, Type II
  • Tumor Necrosis Factor-alpha
  • C-Reactive Protein