Association of CXCR4 expression with coronary collateralization in patients with chronic total coronary occlusion: A nested case-control study

Int J Cardiol. 2017 Feb 1:228:501-506. doi: 10.1016/j.ijcard.2016.11.068. Epub 2016 Nov 9.

Abstract

Objective: CXCR4 signaling contributes to the development and progression of neovascularization. The objective of this study was to investigate whether CXCR4 expression in peripheral CD34+ cells associated with the coronary collateralization (CC) in patients with chronic total coronary occlusion (CTO).

Methods and results: We measured CXCR4 expression in peripheral CD34+ cells and assessed its relation with CC in a nested case-control study including 78 cases and 78 matched controls aged 38-69years, assessed in January 2011 to December 2012 and with at least 1year of follow-up before the index date. Cases were defined as good coronary collateralization (GCC) according to the Rentrop scoring system (Rentrop score of 2 or 3); for each case, one age-matched control with poor coronary collateralization (PCC) (Rentrop score 0 or 1) was randomly selected from the study participants. Demographic, biochemical, and angiographic variables were collected. In multivariate analysis, the OR (95% CI) of CXCR4 expression was 0.018 (0.017 to 0.020) in patients with GCC versus PCC. Independent effect of CXCR4 expression on CC was (OR 0.012, 95% CI 0.010-0.014) when adjusted for other variables. A nonlinear relationship between CXCR4 expression and CC was observed. The CC degree increased when CXCR4 expression exceeded the turning point (30%) (OR 0.025, 95% CI 0.022-0.028; p<0.001). When the CXCR4 expression exceeded 75%, increased CXCR4 level could not promoted CC (OR 0.000, 95% CI 0.008-0.007; p=0.974).

Conclusion: Increased CXCR4 level in peripheral CD34+ cells was associated with GCC in patients with CTO.

Keywords: CXCR4; Chronic total coronary occlusion; Coronary collateralization; Nested case–control study.

MeSH terms

  • Adult
  • Aged
  • Case-Control Studies
  • Chronic Disease
  • Collateral Circulation*
  • Coronary Angiography
  • Coronary Circulation / physiology*
  • Coronary Occlusion / diagnosis
  • Coronary Occlusion / metabolism*
  • Coronary Occlusion / physiopathology
  • Disease Progression
  • Female
  • Follow-Up Studies
  • Humans
  • Male
  • Middle Aged
  • Receptors, CXCR4 / biosynthesis*
  • Risk Factors
  • Ventricular Function, Left / physiology

Substances

  • CXCR4 protein, human
  • Receptors, CXCR4