Platelet to Lymphocyte Ratio Predicts Contrast-Induced Nephropathy in Patients With ST-Segment Elevation Myocardial

Xi-Peng Sun1, Jing Li1, Wei-Wei Zhu1

  • 11 Department of Cardiology, Xuanwu Hospital, Capital Medical University, Beijing, China.

Angiology
|May 4, 2017
PubMed

Insights

A higher platelet-to-lymphocyte ratio (PLR) is linked to contrast-induced nephropathy (CIN) in ST-segment elevation myocardial infarction (STEMI) patients. This finding suggests PLR may predict CIN risk following primary percutaneous coronary intervention (pPCI).

Area of Science:

  • Cardiology
  • Nephrology
  • Hematology

Background:

  • Contrast-induced nephropathy (CIN) is a complication in patients undergoing procedures with contrast media.
  • ST-segment elevation myocardial infarction (STEMI) patients undergoing primary percutaneous coronary intervention (pPCI) are at risk for CIN.
  • The platelet-to-lymphocyte ratio (PLR) is a marker of inflammation and has been explored as a predictor for various conditions.

Purpose of the Study:

  • To investigate the association between the platelet-to-lymphocyte ratio (PLR) and the incidence of contrast-induced nephropathy (CIN).
  • To determine if PLR is an independent predictor of CIN in patients with STEMI undergoing pPCI.

Main Methods:

  • A cohort of 5719 patients with STEMI undergoing pPCI was retrospectively analyzed.
  • PLR was calculated from admission blood counts.
  • CIN was defined as an increase in serum creatinine within 72 hours post-contrast administration.

Main Results:

  • Contrast-induced nephropathy (CIN) occurred in 4.4% of patients (252/5719).
  • Patients who developed CIN had a significantly higher PLR compared to those without CIN (173.8 vs. 116.2, P < .001).
  • Logistic regression identified PLR as an independent predictor of CIN (OR: 1.432, 95% CI: 1.205-1.816, P = .031), alongside other clinical factors.

Conclusions:

  • Elevated PLR is an independent risk factor for developing CIN in STEMI patients undergoing pPCI.
  • PLR may serve as a useful predictive biomarker for CIN in this patient population.
  • Further research could explore the mechanisms linking PLR to CIN and its clinical implications.