sST2 as a value-added biomarker in heart failure

Clin Chim Acta. 2020 Feb:501:120-130. doi: 10.1016/j.cca.2019.10.029. Epub 2019 Oct 31.

Abstract

Soluble suppression of tumorigenicity-2 (sST2) is a biomarker widely investigated during the last few years. Its role has become clear in pathological conditions such as fibrosis and inflammation. From translational research to laboratory medicine, considerable efforts have been made to elucidate the features of sST2 biomarker and to consider its contribution to HF management. In this review, we summarized the results from recent works concerning sST2, and particularly we focused on the interest of sST2 in conditions for which classical biomarkers value interpretation is misleading. Indeed, despite other HF biomarkers, sST2 was proved to be independent from common comorbidities such as renal dysfunction and hypertension. Thus, sST2 showed promise for a combined strategy with natriuretic peptides, mainly for specific categories of patients. Particular attention was paid to findings on sST2 in HF with preserved ejection fraction (HFpEF), a form of HF for which reliable and specific biomarkers are awaited. Finally, a place is reserved to sST2 kinetics from basal to follow up values in order to improve clinical decision making and to customize patient treatments.

Keywords: Comorbidities; Heart failure with preserved ejection fraction; Multimarker approach; Personalized medicine; sST2.

Publication types

  • Review

MeSH terms

  • Biomarkers / analysis
  • Heart Failure / diagnosis*
  • Heart Failure / metabolism
  • Humans
  • Interleukin-1 Receptor-Like 1 Protein / analysis*
  • Interleukin-1 Receptor-Like 1 Protein / metabolism
  • Kinetics

Substances

  • Biomarkers
  • IL1RL1 protein, human
  • Interleukin-1 Receptor-Like 1 Protein