# Enhanced Qualities of High-Density Lipoproteins (HDLs) with Antioxidant Abilities Are Associated with Lower Susceptibility of Hypertension in Middle-Aged Korean Participants: Impaired HDL Quality and Hypertension Risk

**Authors:** Kyung-Hyun Cho, Chae-Eun Yang, Sang Hyuk Lee, Yunki Lee, Ashutosh Bahuguna

PMC · DOI: 10.3390/ijms27021108 · International Journal of Molecular Sciences · 2026-01-22

## TL;DR

Better quality HDL particles with antioxidant abilities are linked to lower hypertension risk in middle-aged Koreans.

## Contribution

This study highlights the importance of HDL quality, not just quantity, in predicting hypertension risk.

## Key findings

- Improved HDL quality, including larger particle size and higher antioxidant activity, is associated with lower blood pressure.
- TG and glucose levels relative to HDL-C are probable predictors of hypertension.
- HDL2 and HDL3 characteristics correlate with LDL oxidation and glycation, impacting hypertension risk.

## Abstract

The quality of high-density lipoproteins (HDLs) is characterized by lipid and protein composition, oxidation and glycation extent, and particle size, while the quantity of HDL-C is just the cholesterol amount in HDL. The inverse association between HDL-C and cardiovascular disease (CVD) and hypertension has been well established; however, the U-shaped mortality risk observed from HDL-C underscores that HDL quality and function are equally important. The present cross-sectional study assessed the correlations of serum lipid and glucose profiles, and low-density lipoprotein (LDL) and HDL characteristics, with blood pressure (BP) distribution in ordinary middle-aged Korean participants (n = 50; mean age 47.0 ± 11.7 years; males: n = 25, 49.2.0 ± 11.7 years; females: n = 25, 44.8 ± 11.5 years), with particular focus on HDL quality and its antioxidant capacity. This study observed that serum elevated triglyceride (TG) and glucose levels were directly proportional to elevated systolic BP (SBP) and diastolic BP (DBP), whereas serum total cholesterol (TC), LDL-C, and HDL-C were not correlated with BP. However, HDL-C/TC (%) was negatively associated with SBP (p = 0.036), while TG/HDL-C and glucose/HDL-C ratios were positively associated with both SBP and DBP, suggesting that TG and glucose proportions relative to HDL-C are probable predictors of hypertension. Elevations of TG, oxidation, and glycation in LDL were positively associated with elevations of BP, whereas LDL particle size was negatively correlated with BP. Similarly, elevations of TG and glycation in HDL2 and HDL3 were positively correlated with elevations of BP, while the particle size of HDL2 was negatively correlated with BP. The heightened HDL2-associated paraoxonase (PON) activity and ferric ion reduction ability (FRA) negatively correlated with LDL oxidation and particle size, whereas elevated HDL3-associated PON and FRA activities were inversely related to LDL glycation. An enhanced glycation in HDL2 was negatively correlated with HDL2-associated PON activity and FRA, while an increase in HDL2 particle size was only dependent on the associated PON activity but not on FRA. In conclusion, observational outcomes demonstrated that improved HDL quality and functionality (characterized by large particle size, reduced glycation, and higher FRA and PON activities) were inversely correlated with LDL oxidation, glycation, particle shrinkage, and the risk of hypertension.

## Linked entities

- **Proteins:** PON1 (paraoxonase 1), FOSL1 (FOS like 1, AP-1 transcription factor subunit)
- **Chemicals:** triglyceride (PubChem CID 5460048), glucose (PubChem CID 5793), cholesterol (PubChem CID 5997)
- **Diseases:** cardiovascular disease (MONDO:0004995)

## Full-text entities

- **Genes:** JPH3 (junctophilin 3) [NCBI Gene 57338] {aka CAGL237, HDL2, JP-3, JP3, TNRC22}, HDL3 (Huntington-like neurodegenerative disorder 2) [NCBI Gene 53369] {aka HLN2}, PON1 (paraoxonase 1) [NCBI Gene 5444] {aka ESA, MVCD5, PON}
- **Diseases:** Hypertension (MESH:D006973), CVD (MESH:D002318)
- **Chemicals:** HDL-C (-), glucose (MESH:D005947), lipid (MESH:D008055), TG (MESH:D014280), cholesterol (MESH:D002784)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

15 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12842381/full.md

## References

53 references — full list in the complete paper: https://tomesphere.com/paper/PMC12842381/full.md

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Source: https://tomesphere.com/paper/PMC12842381