Non-ischaemic titrated cardiac injury caused by radiofrequency catheter ablation of atrial fibrillation mobilizes CD34-positive mononuclear cells by non-stromal cell-derived factor-1alpha mechanism

Europace. 2009 Aug;11(8):1024-31. doi: 10.1093/europace/eup185. Epub 2009 Jul 9.

Abstract

Aims: It has been known that myocardial ischaemia mobilizes CD34+ bone marrow-derived cells by the stromal cell-derived factor (SDF)-1alpha pathway. We hypothesized that non-ischaemic titrated cardiac injury caused by radiofrequency catheter ablation (RFCA) of atrial fibrillation (AF) recruits CD34+ cells by an alternative mechanism.

Methods and results: Fifty-six patients (39 males, 53.0 +/- 13.5 years old) who underwent electrophysiology study (EPS; n = 10) or RFCA of AF (n = 46) were included. Peripheral blood CD34+ cell count and multiple serologic markers were evaluated before, immediately after, at 24 h, and 10 days after the procedure. The results are as follows: (i) the per cent increase in CD34+ cells (%DeltaCD34+) was significant after RFCA compared with after EPS (P < 0.01), and correlated with RF duration and troponin I, respectively. (ii) In contrast, SDF-1alpha decreased after RFCA and had no correlation with %DeltaCD34+ cells while matrix metalloproteinase (MMP)-9 (P < 0.0001) and GRObeta (P < 0.001) increased after RFCA and had correlations with 24 h %DeltaCD34+ cells.

Conclusion: Non-ischaemic titrated cardiac injury caused by AF ablation mobilizes CD34+ cells to the peripheral blood through a non-SDF-1alpha pathway associated with MMP-9 and GRObeta.

Publication types

  • Controlled Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigens, CD34 / immunology*
  • Atrial Fibrillation / immunology*
  • Atrial Fibrillation / surgery*
  • Catheter Ablation / adverse effects*
  • Cells, Cultured
  • Chemokine CXCL12 / immunology
  • Chemokine CXCL2 / immunology
  • Female
  • Heart Injuries / etiology*
  • Heart Injuries / immunology*
  • Humans
  • Male
  • Matrix Metalloproteinase 9 / immunology
  • Middle Aged
  • Myocardial Ischemia / etiology
  • Myocardial Ischemia / immunology
  • T-Lymphocytes / immunology*

Substances

  • Antigens, CD34
  • CXCL2 protein, human
  • Chemokine CXCL12
  • Chemokine CXCL2
  • Matrix Metalloproteinase 9