Intra-cardiac and peripheral levels of biochemical markers of fibrosis in patients undergoing catheter ablation for atrial fibrillation

Europace. 2017 Dec 1;19(12):1944-1950. doi: 10.1093/europace/euw315.

Abstract

Aims: Measurement of circulating biomarkers of fibrosis may have a role in selecting patients and treatment strategy for catheter ablation. Pro-collagen type III N-terminal pro-peptide (PIIINP), C-telopeptide of type I collagen (ICTP), fibroblast growth factor 23 (FGF-23), and galectin 3 (gal-3) have all been suggested as possible biomarkers for this indication, but studies assessing whether peripheral levels reflect intra-cardiac levels are scarce.

Methods and results: We studied 93 patients undergoing ablation for paroxysmal atrial fibrillation (AF) (n = 63) or non-paroxysmal AF (n = 30). Femoral venous, left and right atrial, and coronary sinus blood were analysed using ELISA to determine biomarker levels. Levels were compared with control patients (n = 36) and baseline characteristics, including left atrial voltage mapping data. C-telopeptide of type I collagen levels were higher in AF than in non-AF patients (P = 0.007). Peripheral ICTP levels were higher than all intra-cardiac levels (P < 0.001). Peripheral gal-3 levels were higher than left atrial levels (P = 0.001). Peripheral levels of FGF-23 and PIIINP were not significantly different from intra-cardiac levels. CS levels of ICTP were higher than right and left atrial levels (P < 0.001). gal-3 was higher in women vs. men (P ≤ 0.001) and with higher body mass index (P ≤ 0.001). ICTP levels increased with reducing ejection fraction (P ≤ 0.012).

Conclusions: Atrial fibrillation patients have higher levels of circulating ICTP than matched non-AF controls. In AF ablation patients, intra-cardiac sampling of FGF-23 or PIIINP gives no further information over peripheral sampling. For gal-3 and ICTP, intra-cardiac sampling may be necessary to assess their association with intra-cardiac processes. None of the biomarkers is related to fibrosis assessed by left atrial voltage.

Keywords: Ablation; Atrial fibrillation; Biomarker; Fibrosis.

Publication types

  • Comparative Study

MeSH terms

  • Aged
  • Atrial Fibrillation / blood*
  • Atrial Fibrillation / diagnosis
  • Atrial Fibrillation / physiopathology
  • Atrial Fibrillation / surgery*
  • Atrial Remodeling*
  • Biomarkers / blood
  • Blood Proteins
  • Case-Control Studies
  • Catheter Ablation*
  • Clinical Decision-Making
  • Collagen Type I / blood*
  • Electrophysiologic Techniques, Cardiac
  • Enzyme-Linked Immunosorbent Assay
  • Female
  • Fibroblast Growth Factor-23
  • Fibroblast Growth Factors / blood*
  • Fibrosis
  • Galectin 3 / blood*
  • Galectins
  • Heart Atria / metabolism*
  • Heart Atria / pathology
  • Heart Atria / physiopathology
  • Humans
  • Male
  • Middle Aged
  • Patient Selection
  • Peptide Fragments / blood*
  • Peptides / blood*
  • Predictive Value of Tests
  • Procollagen / blood*
  • Treatment Outcome
  • Ventricular Function, Left

Substances

  • Biomarkers
  • Blood Proteins
  • Collagen Type I
  • FGF23 protein, human
  • Galectin 3
  • Galectins
  • LGALS3 protein, human
  • Peptide Fragments
  • Peptides
  • Procollagen
  • collagen type I trimeric cross-linked peptide
  • procollagen Type III-N-terminal peptide
  • Fibroblast Growth Factors
  • Fibroblast Growth Factor-23