Circulating midkine in children with Henoch-Schönlein purpura: Clinical implications

Zhantao Su1, Xin Lv2, Yi Liu2

  • 1Pediatric Research Institute, Qilu Children's Hospital of Shandong University, Ji'nan 250022, China; Department of Pediatric, Shandong Police Hospital, Ji'nan 250002, China.

Abstract

Insights

Midkine (MK) levels are elevated in children with Henoch-Schönlein purpura (HSP), particularly those with kidney involvement (HSPN). MK measurement aids in diagnosing HSP and predicting HSPN.

Area of Science:

  • Pediatric immunology
  • Cytokine research
  • Nephrology

Background:

  • Midkine (MK) is a growth factor and cytokine implicated in inflammatory processes.
  • The role of MK in Henoch-Schönlein purpura (HSP) has not been previously investigated.

Purpose of the Study:

  • To explore the potential involvement of midkine in pediatric Henoch-Schönlein purpura.
  • To assess midkine as a diagnostic marker for HSP and its renal complication (HSPN).

Main Methods:

  • Prospective study of 92 children with HSP and 60 healthy controls.
  • Measurement of serum midkine and various cytokines (IL-2, IL-4, IL-6, IL-10, TNF, IFN-γ, IL-17A).
  • Receiver operating characteristic (ROC) analysis to evaluate diagnostic value.

Main Results:

  • Elevated midkine levels were observed in children with HSP compared to controls.
  • Midkine levels were significantly higher in children with HSP and renal involvement (HSPN).
  • Midkine positively correlated with IL-4, IL-6, IL17A, IgA, and IgE; ROC analysis showed high diagnostic accuracy for HSPN (AUC=0.902).

Conclusions:

  • Midkine plays a role in the pathogenesis of Henoch-Schönlein purpura.
  • Serum midkine levels are valuable for diagnosing HSP and predicting renal involvement (HSPN).