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Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
Profiling endothelial function, oxidative stress and inflammatory biomarkers in individuals with various
Adriaan Jacobs1,2, Ruan Kruger3,4, Wayne Smith3,4
1Hypertension in Africa Research Team (HART), North-West University, Potchefstroom, South Africa. adriaan.jacobs@nwu.ac.za.
Insights
Young adults with cardiovascular risk factors show early signs of endothelial dysfunction, oxidative stress, and inflammation. Biomarkers link specific risks like adiposity and high cholesterol to these pathways, revealing early cardiovascular disease mechanisms.
Area of Science:
- Cardiovascular Science
- Biomarker Research
- Preventive Cardiology
Background:
- Cardiovascular disease (CVD) stems from endothelial activation, oxidative stress, and inflammation.
- Early interactions between cardiovascular (CV) risk factors and these pathways are not well understood.
- Understanding these early mechanisms is crucial for preventing CVD in young adults.
Purpose of the Study:
- To profile biomarkers of endothelial function, oxidative stress, and inflammation.
- To explore associations between these biomarkers and individual CV risk factors in young adults.
- To elucidate early CVD development mechanisms linked to CV risk factors.
Main Methods:
- Circulating biomarkers were profiled in 1196 young adults (20-30 years) without chronic conditions.
- Participants were stratified by CV risk factors (blood pressure, anthropometry, biochemistry, questionnaires).
- Statistical analyses identified associations between biomarkers and individual CV risk factors (p < 0.05).
Main Results:
- Central adiposity linked to inflammation, endothelial activation, and oxidative stress.
- High LDL cholesterol and alcohol use associated with endothelial activation (P-selectin).
- Smoking, low HDL cholesterol, and alcohol use related to inflammation markers (GDF-15, MCP-1).
- Glycated hemoglobin and blood pressure associated with glutathione reductase activity.
- Blood pressure also linked to interleukin-10 levels.
Conclusions:
- Specific CV risk factors are independently associated with distinct biomarker profiles in young adults.
- These findings provide insights into the initial pathophysiological mechanisms of early CVD development.
- Early identification of these biomarker alterations can inform preventive strategies against CVD.
Abstract:
Cardiovascular risk factors are known to contribute to cardiovascular disease (CVD) development by inducing endothelial activation, increasing oxidative stress and pro-inflammation. The early interaction between these pathways and individual cardiovascular (CV) risk factors is poorly understood. We profiled a range of circulating endothelial function, oxidative stress and inflammatory biomarkers and explored their associations with individual CV risk factors in young (20-30 years, n = 1196) adults without self-reported chronic conditions or medication use. Participants were stratified into CV risk factor groups based on blood pressure, anthropometrical measurements, biochemical analyses and questionnaire data. We identified several differences in biomarker levels between control (without any CV risk factors) and individual CV risk factor groups and confirmed independent associations of these biomarkers with individual risk factors (all p < 0.05). Greater central adiposity was mainly associated with a pro-inflammatory profile (interleukin-6, C-reactive protein and fibrinogen), but also with endothelial activation and oxidative stress (plasminogen activator inhibitor-1 and reactive oxygen species). High low-density lipoprotein cholesterol levels and alcohol use were associated with endothelial activation (P-selectin), while smoking, low high-density lipoprotein cholesterol levels and alcohol use were related to markers of inflammation (growth differentiation factor-15 and monocyte chemoattractant protein-1). Glycated hemoglobin levels and blood pressure were positively associated with glutathione reductase activity, while blood pressure also associated positively with interleukin-10 levels. Our data provides insight into the initial underlying mechanisms associated with early CVD development in young individuals exposed to different cardiovascular risk factors.
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