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Updated: Jun 2, 2025

Cell-free Biochemical Fluorometric Enzymatic Assay for High-throughput Measurement of Lipid Peroxidation in High Density Lipoprotein
Published on: October 12, 2017
Reduced antioxidant high-density lipoprotein function in heart failure with preserved ejection fraction.
Benjamin Sasko1,2,3, Theodoros Kelesidis4, Sawa Kostin5
1Ruhr-University of Bochum, Medical Department II, Marien Hospital Herne, Bochum, Germany. b.sasko@uk-brandenburg.de.
Reduced HDL antioxidant function is linked to heart failure with preserved ejection fraction (HFpEF). This finding suggests that improving HDL function may be a potential therapeutic target for early HFpEF treatment.
Area of Science:
- Cardiology
- Biochemistry
- Internal Medicine
Background:
- Heart failure (HF) is a growing global health concern with increasing prevalence in Western populations due to cardiovascular risk factors.
- Oxidative stress and inflammation are key contributors to the pathophysiology of heart failure with preserved ejection fraction (HFpEF).
- Previous research indicates a link between dysfunctional high-density lipoprotein (HDL) and HF, but the specific role of oxidized HDL in HFpEF remains unclear.
Purpose of the Study:
- To investigate the association between reduced HDL antioxidant function and the presence of HFpEF.
- To determine if oxidized HDL levels are an independent predictor of HFpEF in patients with suspected heart failure.
Main Methods:
- A cross-sectional observational study involving 366 patients with suspected heart failure.
- Assessment of HDL antioxidant function using a cell-free biochemical assay measuring HDL-lipid peroxide content (HDLox), normalized by HDL-C levels (nHDLox).
- Statistical analysis included multivariate models to identify independent predictors of HFpEF, adjusting for various clinical and biochemical factors.
Main Results:
- Patients with HFpEF exhibited significantly higher mean relative levels of nHDLox compared to those without heart failure.
- nHDLox was identified as an independent predictor of HFpEF in both basic and full multivariate models (p < 0.05).
- A 1-SD increase in nHDLox was associated with a 67% increased risk of HFpEF (p = 0.02).
Conclusions:
- HDL antioxidant function is demonstrably reduced in patients diagnosed with HFpEF.
- Targeting and improving HDL function presents a promising therapeutic strategy for the early management of heart failure.
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