An IL-6-IL-8 score derived from principal component analysis is predictive of adverse outcome in acute myocardial

Gisela A Kristono1,2, Ana S Holley1,2, Kathryn E Hally1,2,3

  • 1Department of Surgery and Anaesthesia, University of Otago Wellington, New Zealand.

Cytokine: X
|February 19, 2021
PubMed

Insights

Principal component analysis (PCA) identified an IL-6-IL-8 score that predicts major adverse cardiovascular events (MACE) after acute myocardial infarction (AMI). This combined score is a stronger predictor of MACE than individual cytokines.

Area of Science:

  • Cardiology
  • Biomarkers
  • Inflammation

Background:

  • Elevated inflammation biomarkers post-acute myocardial infarction (AMI) correlate with major adverse cardiovascular events (MACE).
  • Optimal methods for quantifying the post-AMI inflammatory response remain undetermined.

Purpose of the Study:

  • To explore the utility of principal component analysis (PCA) in creating a combined cytokine score for predicting MACE post-AMI.
  • To identify key inflammatory biomarkers for assessing cardiovascular risk after myocardial infarction.

Main Methods:

  • Plasma samples from 317 AMI patients were analyzed for 13 inflammatory cytokines 48-72 hours post-symptom onset.
  • Principal component analysis (PCA) was used to derive a combined cytokine score from detectable cytokines.
  • Multivariate models assessed independent predictors of MACE over a one-year follow-up period.

Main Results:

  • Interleukin-6 (IL-6) and Interleukin-8 (IL-8) were significantly associated with MACE.
  • A PCA-derived IL-6-IL-8 score independently predicted MACE at one year.
  • The IL-6-IL-8 score demonstrated a stronger predictive capability for MACE compared to individual cytokine levels.

Conclusions:

  • A PCA-derived IL-6-IL-8 score effectively quantifies inflammation and independently predicts MACE post-AMI.
  • This scoring strategy may offer an improved approach to assessing cardiovascular risk after myocardial infarction.
  • Further research is needed to optimize the selection of cytokines for this predictive model.
Abstract