The relationship between pre-procedural elevated arterial lactate and contrast-induced nephropathy following primary

Jun-Qing Yang1,2, Xiao-Sheng Guo3, Peng Ran2

  • 1The Second School of Clinical Medicine, Southern Medical University, Guangzhou, China.

Insights

Elevated arterial lactate levels (≥2.0 mmol/L) predict contrast-induced nephropathy (CIN) in ST-segment elevated myocardial infarction (STEMI) patients undergoing percutaneous coronary intervention (PCI). This finding aids in risk stratification for preventing kidney complications after PCI.

Area of Science:

  • Cardiology
  • Nephrology
  • Biomarkers

Background:

  • Contrast-induced nephropathy (CIN) is a complication of percutaneous coronary intervention (PCI).
  • Risk stratification is crucial for CIN prevention.
  • Elevated arterial lactate indicates severe conditions and potential post-intervention issues, but its link to CIN is unclear.

Purpose of the Study:

  • To investigate the association between elevated arterial lactate levels and CIN in ST-segment elevated myocardial infarction (STEMI) patients undergoing primary PCI.

Main Methods:

  • Prospective enrollment of 227 STEMI patients before primary PCI.
  • Arterial lactate measured within 1 hour pre-PCI; CIN defined as serum creatinine increase ≥0.5 mg/dL or 25% within 72 hours.
  • Multivariate regression analysis incorporating Mehran Risk Score factors.

Main Results:

  • 47 patients (20.7%) developed CIN.
  • Mean lactate level was significantly higher in the CIN group (2.68±2.27 vs. 1.74±1.94, P<0.001).
  • Arterial lactate ≥2.0 mmol/L showed 57.5% sensitivity and 75.6% specificity for predicting CIN, with performance similar to Mehran Risk Score (AUC 0.707 vs. 0.697). Lactate ≥2.0 mmol/L independently predicted CIN (OR=3.77, P=0.001).

Conclusions:

  • Arterial lactate level ≥2.0 mmol/L is significantly associated with CIN in STEMI patients post-primary PCI.
  • Lactate serves as a potential biomarker for CIN risk stratification.
  • This finding may improve prevention strategies for CIN.
Abstract

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