Role of Soluble ST2 Biomarker in Predicting Recurrence of Atrial Fibrillation after Electrical Cardioversion or Pulmonary Vein Isolation

Int J Mol Sci. 2023 Sep 13;24(18):14045. doi: 10.3390/ijms241814045.

Abstract

This study aims to determine the predictive value of the soluble suppression of tumorigenicity 2 (sST2) biomarker in atrial fibrillation (AF) recurrence. This prospective, observational study included patients with AF referred for electrical cardioversion (ECV) or pulmonary vein isolation (PVI) procedures. Baseline characteristics were collected, and sST2 was determined at baseline and at 3 and 6 months of follow-up. sST2 was determined at baseline in a matched control group. Left atrial voltage mapping was performed in patients undergoing PVI. The sST2 maximal predictive capacity of AF recurrence was at the 3-month FU in the cohort of patients undergoing ECV with respect to 6-month AF recurrence with an AUC of 0.669, a cut-off point of 15,511 pg/mL, a sensitivity of 60.97%, and a specificity of 69.81%. The ROC curve of the sST2 biomarker at baseline and 3 months in the cohort of patients undergoing PVI showed AUCs of 0.539 and 0.490, respectively. The logistic regression model identified the rhythm (AF) and the sST2 biomarker at 3 months as independent factors for recurrence at 6 months in the ECV cohort. In the logistic regression model, sST2 was not an independent factor for recurrence at 6 months of follow-up in the PVI cohort. In patients who underwent ECV, sST2 values at 3 months may provide utility to predict AF recurrence at 6 months of follow-up. In patients who underwent PVI, sST2 had no value in predicting AF recurrence at 6 months of follow-up.

Keywords: atrial fibrillation; electrical cardioversion; pulmonary vein ablation; soluble suppression of tumorigenicity 2 (sST2).

Publication types

  • Observational Study

MeSH terms

  • Atrial Fibrillation* / diagnosis
  • Atrial Fibrillation* / therapy
  • Biomarkers
  • Electric Countershock
  • Humans
  • Interleukin-1 Receptor-Like 1 Protein
  • Prospective Studies
  • Pulmonary Veins* / surgery

Substances

  • Interleukin-1 Receptor-Like 1 Protein
  • Biomarkers

Grants and funding

The authors declare that no funds, grants, or other support were received during the preparation of this manuscript.