Impact of the metabolic syndrome on high-sensitivity C reactive protein levels in patients with acute coronary syndrome

Atherosclerosis. 2009 Dec;207(2):591-6. doi: 10.1016/j.atherosclerosis.2009.05.035. Epub 2009 Jun 11.

Abstract

Objective: Underlying predisposition for a heightened inflammatory response is postulated as one of the mechanisms for elevated high-sensitivity C reactive protein (hs-CRP) levels in patients with acute coronary syndrome (ACS). It is unclear whether metabolic syndrome (MetS) may cause a predisposition for heightened hs-CRP response in patients with ACS. The aim of this study is to investigate the interaction between hs-CRP levels and presence of MetS in patients with and without ACS.

Methods: Two hundred and seventy-three consecutive patients presenting with a first ACS event and 261 MetS patients without any ACS event were included to the study. The study participants were divided into three groups as MetS (+) ACS (-) [n=261], MetS (-) ACS (+) [n=110], and MetS (+) ACS (+) [n=163]. Median levels of hs-CRP were compared between and within the three groups.

Results: Hs-CRP levels were lowest in MetS (+) ACS (-) subjects and highest in MetS (+) ACS (+) patients. Factors associated with hs-CRP levels were troponin elevation, presence of ACS, body mass index (BMI), and presence of MetS (R(2)=0.26, p<0.01). Predictors of elevated hs-CRP levels (>0.3mg/dl) were the presence of ACS (OR=3.6, 95% CI=1.9-6.5, p<0.01), presence of MetS (OR=2.1, 95% CI=1.0-4.0, p=0.02), troponin elevation (OR=5.7, 95% CI=2.8-11.5, p<0.01) and BMI (OR=1.1, 95% CI=1.0-1.1, p<0.01).

Conclusions: The presence of MetS had an impact on the increase in hs-CRP levels observed with an ACS event in the study population. These findings suggested that a heightened baseline inflammatory status of MetS may predispose ACS patients to an augmented hs-CRP response.

MeSH terms

  • Acute Coronary Syndrome / blood
  • Acute Coronary Syndrome / etiology*
  • Aged
  • Biomarkers / blood
  • Body Mass Index
  • C-Reactive Protein / metabolism*
  • Case-Control Studies
  • Cross-Sectional Studies
  • Female
  • Humans
  • Inflammation Mediators / blood*
  • Logistic Models
  • Male
  • Metabolic Syndrome / blood
  • Metabolic Syndrome / complications*
  • Middle Aged
  • Odds Ratio
  • Risk Assessment
  • Risk Factors
  • Troponin / blood
  • Up-Regulation

Substances

  • Biomarkers
  • Inflammation Mediators
  • Troponin
  • C-Reactive Protein