Relationship between myeloid-related protein 8/14 and survival of Chinese peritoneal dialysis patients

Peter Yam-Kau Poon1, Cheuk-Chun Szeto, Bonnie Ching-Ha Kwan

  • 1Department of Medicine, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong, SAR, China.

Abstract

Insights

High serum myeloid-related protein 8/14 (MRP8/14) levels are linked to reduced survival in Chinese peritoneal dialysis patients. Further research is needed to understand MRP8/14

Area of Science:

  • Cardiovascular Medicine
  • Nephrology
  • Inflammation Research

Background:

  • Myeloid-related protein 8/14 (MRP8/14) is a key inflammatory marker released by myeloid cells.
  • Experimental studies suggest MRP8/14's role in inflammation and cardiovascular disease (CVD) pathogenesis.
  • The association between serum MRP8/14 and CVD in Chinese peritoneal dialysis (PD) patients remains unclear.

Purpose of the Study:

  • To investigate the relationship between baseline serum MRP8/14 levels and cardiovascular disease outcomes in Chinese PD patients.
  • To determine if serum MRP8/14 is an independent predictor of survival in PD patients.

Main Methods:

  • A cohort of 102 new Chinese PD patients was studied.
  • Baseline serum MRP8/14 levels were measured and categorized into quartiles.
  • Patients were followed for an average of 23.9 months to assess cardiovascular events and survival.

Main Results:

  • Higher baseline serum MRP8/14 levels showed a trend towards lower 3-year cardiovascular event-free survival (p=0.064).
  • Significantly lower 3-year actuarial survival rates were observed in higher MRP8/14 quartiles (p=0.003).
  • Cox regression identified serum MRP8/14 level as an independent predictor of actuarial survival, with each 1 µg/ml increase conferring a 25.1% higher risk of death (p=0.037).

Conclusions:

  • Elevated baseline serum MRP8/14 levels are associated with reduced actuarial survival in Chinese PD patients.
  • Serum MRP8/14 may play a pathogenic role in cardiovascular disease among PD patients.
  • Further investigation into the role of MRP8/14 in PD-related cardiovascular complications is warranted.