Oxidised Low-Density Lipoprotein and Its Receptor-Mediated Endothelial Dysfunction Are Associated with Coronary

Yue-E He1, Hui-Xian Qiu1, Rong-Zhou Wu1

  • 1Children's Heart Centre, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, 325027, Zhejiang, China.

Insights

Oxidised low-density lipoprotein (oxLDL) and its receptor LOX-1 are implicated in Kawasaki disease coronary artery lesions (CALs). Elevated plasma oxLDL levels may help predict CALs in the acute phase of KD.

Area of Science:

  • Cardiovascular Research
  • Pediatric Immunology
  • Biomarker Discovery

Background:

  • Kawasaki disease (KD) is a leading cause of acquired pediatric heart disease.
  • Coronary artery lesions (CALs) are a serious complication of KD.
  • The role of oxidised low-density lipoprotein (oxLDL) and its receptor LOX-1 in KD-associated CALs requires further elucidation.

Purpose of the Study:

  • To investigate the involvement of the oxLDL/LOX-1 pathway in the development of CALs in KD.
  • To assess the potential of plasma oxLDL concentration as an early predictive biomarker for CALs in KD patients.

Main Methods:

  • Prospective study involving 80 KD patients, 20 febrile children, and 20 healthy children.
  • Analysis of plasma oxLDL concentration and LOX-1 mRNA expression in peripheral blood mononuclear cells (PBMCs) during the acute phase.
  • Correlation analysis between oxLDL/LOX-1 markers and coronary Z-scores.

Main Results:

  • Plasma oxLDL concentration and LOX-1 mRNA expression were significantly elevated in KD patients, especially those with CALs.
  • A significant positive correlation was observed between plasma oxLDL concentration, LOX-1 mRNA expression, and coronary Z-scores.
  • Plasma oxLDL concentration demonstrated a sensitivity of 71.4% and specificity of 77.2% for predicting CALs at a threshold of ≥12.38 mU/L.

Conclusions:

  • The oxLDL/LOX-1 axis is likely involved in the pathogenesis of CALs in Kawasaki disease.
  • Plasma oxLDL concentration in the acute phase serves as a promising biomarker for early prediction of CALs in KD.

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