Leukocyte Extracellular Vesicles Predict Progression of Systolic Dysfunction in Heart Failure with Mildly Reduced

Aleksandra Gąsecka1,2, Aleksander Siniarski3,4, Piotr Duchnowski5

  • 11St Chair and Department of Cardiology, Medical University of Warsaw, Banacha 1a, 02-097, Warsaw, Poland.

Insights

Higher concentrations of leukocyte extracellular vesicles (EVs) predict systolic dysfunction progression in heart failure with mildly-reduced ejection fraction (HFmrEF). This finding aids risk stratification for HFmrEF patients.

Area of Science:

  • Cardiology
  • Biomarkers
  • Heart Failure Research

Background:

  • Risk stratification for heart failure with mildly-reduced ejection fraction (HFmrEF) is complex.
  • Identifying reliable biomarkers for disease progression is crucial for effective management.

Purpose of the Study:

  • To evaluate advanced glycation end products (AGEs) and extracellular vesicles (EVs) as predictors of systolic and diastolic dysfunction progression in HFmrEF.
  • To determine if leukocyte EVs can identify patients at higher risk for HFmrEF progression.

Main Methods:

  • Assessed skin AGE accumulation using AGE Reader.
  • Measured plasma EV concentrations via flow cytometry in 74 HFmrEF patients.
  • Monitored systolic and diastolic dysfunction progression over a 6.5-month follow-up period.

Main Results:

  • Leukocyte EV concentrations were significantly higher in patients with systolic dysfunction progression (p=0.002).
  • Leukocyte EVs predicted systolic dysfunction progression with 75.0% sensitivity and 58.3% specificity.
  • Increased leukocyte EVs were associated with a 4.7-fold higher odds of systolic dysfunction progression, independent of other clinical factors.

Conclusions:

  • Elevated leukocyte EV concentrations are a significant predictor of systolic dysfunction progression in HFmrEF.
  • Skin AGE levels and other EV subtypes did not show a significant association with dysfunction progression.
  • Leukocyte EVs represent a promising biomarker for risk stratification in HFmrEF.