Galectin-3 and Soluble CD146 Identify Cardiorenal Injuries in Severe Burn Patients: A Biomarker-Based Approach

Louis Boutin1,2,3, Sabri Soussi4,5, Angèle Garcia Lavello1

  • 1Department of Anaesthesiology, Critical Care Medicine and Burn Unit, AP-HP, Saint-Louis Hospital, DMU Parabol, FHU PROMICE, Université de Paris, Paris, France.

Cardiorenal Medicine
|August 12, 2024
PubMed

Insights

Cardiorenal syndrome (CRS) is common in severe burn patients. Galectin-3 (Gal3) and soluble CD146 (sCD146) levels can help identify CRS, with their combined use improving prediction accuracy.

Area of Science:

  • Biomarker discovery
  • Critical care medicine
  • Burn injury research

Background:

  • Severe burn injuries frequently lead to acute kidney injury (AKI) and myocardial injury (MI).
  • The combination of AKI and MI, termed cardiorenal syndrome (CRS), presents a significant clinical challenge.
  • Identifying distinct cardiorenal phenotypes is crucial for effective patient management.

Purpose of the Study:

  • To assess the occurrence and reliability of Galectin-3 (Gal3) and soluble CD146 (sCD146) as biomarkers for recognizing CRS in severe burn patients.
  • To evaluate the predictive performance of these biomarkers in identifying CRS.

Main Methods:

  • A single-center prospective proof-of-concept study.
  • Plasma samples were collected daily for 7 days post-admission.
  • CRS was defined by the presence of AKI (KDIGO stage ≥1) and MI (elevated hsTnT).

Main Results:

  • Thirty-eight out of forty patients (95%) developed CRS.
  • Gal3 levels, alone or combined with sCD146, were significantly associated with CRS (p < 0.001).
  • The combination of Gal3 and sCD146 at admission (D0) showed improved predictive performance for CRS (AUC = 0.81).
  • Gal3 levels predicted AKI without MI and MI without AKI, while sCD146 showed poor association with CRS.

Conclusions:

  • CRS is a frequent and severe complication in patients with severe burn injuries.
  • Gal3 levels during the first week post-admission are associated with CRS.
  • Combining Gal3 and sCD146 enhances the prediction of CRS in this patient population.
  • Further studies are needed to confirm the utility of these biomarkers for CRS identification.
Abstract