Soluble urokinase plasminogen activator receptor is associated with cardiovascular calcification in peritoneal

Jichao Guan1, Shuwen Gong1, Qiuli He1

  • 1Shaoxing People's Hospital, Shaoxing, Zhejiang, China.

Insights

High levels of soluble urokinase plasminogen activator receptor (suPAR) are linked to cardiovascular calcification in peritoneal dialysis (PD) patients. This finding is particularly significant in elderly PD patients, highlighting suPAR as a potential biomarker for CVD risk.

Area of Science:

  • Nephrology
  • Cardiology
  • Biomarkers

Background:

  • Cardiovascular disease (CVD) is a leading cause of death in peritoneal dialysis (PD) patients.
  • Cardiovascular calcification (CVC) is common in PD patients and predicts mortality.
  • The role of soluble urokinase plasminogen activator receptor (suPAR) in PD-related CVC is not well understood.

Purpose of the Study:

  • To investigate the association between serum suPAR levels and CVC in PD patients.
  • To determine if suPAR can predict the presence and extent of CVC.

Main Methods:

  • Assessed abdominal aortic calcification (AAC), coronary artery calcification (CAC), and cardiac valvular calcification (ValvC) using radiography, CT, and echocardiography.
  • Compared demographic, clinical, and biochemical variables between patients with and without CVC.
  • Used logistic regression and ROC curve analysis to evaluate the association and predictive value of suPAR for CVC.

Main Results:

  • Nearly half of PD patients had AAC (49.1%), and a majority had CAC (68.6%).
  • Elevated serum suPAR levels were significantly associated with the presence and severity of CVC, particularly in elderly patients.
  • suPAR demonstrated predictive value for CVC (AUC=0.651) and notably for ValvC (AUC=0.828).

Conclusions:

  • Cardiovascular calcification is highly prevalent in the PD population.
  • Serum suPAR is a significant predictor of CVC in PD patients, especially in the elderly.
  • suPAR may serve as a valuable biomarker for assessing cardiovascular risk in PD patients.
Abstract

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