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Expression of Hypoxia-Inducible Factor-1α (HIF1A) and Lp-PLA2 in Low, Intermediate, and High Cardiovascular Disease
Teuku Heriansyah1, Indah Nur Chomsy2, Kumboyono Kumboyono3
1Department of Cardiology and Vascular Medicine, Syiah Kuala University, Banda Aceh 23111, Indonesia.
Insights
This study reveals a strong correlation between hypoxia-inducible factor-1α (HIF1A) and lipoprotein-associated phospholipase A2 (Lp-PLA2) in cardiovascular disease (CVD) risk populations. HIF1A expression rises with CVD risk, while Lp-PLA2 levels decrease, despite their strong association.
Area of Science:
- Cardiovascular Research
- Molecular Biology
- Biochemistry
Background:
- Cardiovascular disease (CVD) pathogenesis involves complex, multifactorial processes, primarily atherosclerosis.
- Inflammation during atherogenesis can lead to hypoxia, activating hypoxia-inducible factor-1α (HIF1A).
- Lipoprotein-associated phospholipase A2 (Lp-PLA2) is an inflammatory mediator implicated in atherogenesis.
Purpose of the Study:
- To quantify hypoxia-inducible factor-1α (HIF1A) expression.
- To assess the correlation between HIF1A and Lp-PLA2 expression.
- To analyze these markers across low-risk, intermediate, and high-risk cardiovascular disease (CVD) populations.
Main Methods:
- Correlational analysis of 160 individuals categorized by Framingham Risk Score (FRS).
- Measurement of Lp-PLA2 and HIF-1α concentrations in venous blood samples using ELISA.
- Statistical analysis including normality, homogeneity, ANOVA, post hoc-Tukey HSD, and Pearson correlation.
Main Results:
- A very strong positive correlation was observed between HIF1A and Lp-PLA2 expression across all risk groups (low-risk r=0.512, intermediate r=0.512, high-risk r=0.715, P<0.05).
- HIF1A concentration increased significantly with higher CVD risk.
- Lp-PLA2 concentrations did not consistently align with the Framingham Risk Score.
Conclusions:
- HIF1A expression demonstrates an upward trend with increasing atherosclerosis risk.
- Lp-PLA2 expression shows a decreasing trend as atherosclerosis risk, based on FRS, increases.
- A significant correlation exists between HIF1A and Lp-PLA2 expression, irrespective of the FRS category.
Background:
The pathomechanism of CVD is a complex and multifactorial process. The primary mechanism of CVD is atherosclerosis. Inflammation in atherogenesis raises the risk of hypoxia, which will activate hypoxia-inducible factor-1α (HIF1A). Also, together with lipoprotein-associated phospholipase A2 (Lp-PLA2), an inflammatory mediator for atherogenesis.
Purpose:
This study aims to measure the hypoxia-inducible factor-1α (HIF1A) expression and its correlation to Lp-PLA2 expression at low-risk, intermediate, and high-risk CVD populations.
Patients And Methods:
The study used a correlational analysis method with a total sampling technique in 160 individuals in the risk population. The atherosclerosis risk group was analyzed using the Framingham Risk Score and categorized into low, intermediate, and high-risk groups. Venous blood samples taken from respondents were measured using the ELISA method with Lp-PLA2 and HIF-1α as parameters. Data were analyzed using normality test, homogeneity test, one-way ANOVA, post hoc-Tukey HSD, and Pearson correlation.
Results:
The concentration of HIF1A had a very strong correlation with Lp-PLA2 expression, both in the low-risk group (r = 0.512), intermediate (r = 0.512), and high (r = 0.715) (P <0.05). However, the concentrations of Lp-PLA2 did not match the FRS.
Conclusion:
HIF1A expression increased with increasing risk, while Lp-PLA2 expression decreased with increasing risk of atherosclerosis based on the FRS category. There is a significant correlation between HIF1A expression and Lp-PLA2 expression based on FRS.
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