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Cell-free Biochemical Fluorometric Enzymatic Assay for High-throughput Measurement of Lipid Peroxidation in High Density Lipoprotein
Published on: October 12, 2017
Circulating oxidized low-density lipoprotein is increased in hypertension
Johan Frostegård1, Ruihua Wu, Carola Lemne
1Unit of Rheumatology, Department of Medicine, Centre for Molecular Medicine, Karolinska Hospital, 17671 Stockholm, Sweden. johan.frostegard@ks.se
Insights
Oxidized low-density lipoprotein (OxLDL) is elevated in hypertensive men, potentially increasing atherosclerosis risk. However, autoantibodies to OxLDL (aOxLDL) showed no significant change, suggesting their role may vary by disease stage.
Area of Science:
- Cardiovascular Research
- Immunology
- Hypertension Studies
Background:
- Oxidized low-density lipoprotein (OxLDL) and autoantibodies to OxLDL (aOxLDL) are linked to atherosclerosis development.
- Hypertension is a significant risk factor for atherosclerosis, necessitating investigation into related biomarkers.
Purpose of the Study:
- To assess the significance of OxLDL and aOxLDL in men with established hypertension.
- To compare OxLDL and aOxLDL levels between hypertensive and normotensive individuals.
Main Methods:
- Recruited 111 hypertensive men and 75 normotensive controls.
- Measured OxLDL and aOxLDL (IgG, IgM) using monoclonal antibody EO6 and ELISA.
- Assessed carotid atherosclerosis and intima-media thickness via ultrasonography.
Main Results:
- Hypertensive men exhibited significantly higher OxLDL levels compared to normotensives (P=0.002).
- No significant differences were found in aOxLDL levels between the groups.
- No association was observed between OxLDL, aOxLDL, and carotid atherosclerosis or intima-media thickness.
Conclusions:
- Elevated OxLDL in hypertensive men may contribute to atherosclerosis development.
- The role of aOxLDL in hypertension-related atherosclerosis appears unchanged in this cohort and might be stage-dependent.
Abstract:
Oxidized low-density lipoprotein (OxLDL) and autoantibodies to OxLDL (aOxLDL) are implicated in the development of atherosclerosis. The objective of this study was to determine the importance of these factors in hypertension, a major risk factor for atherosclerosis. Samples were obtained from 111 men with established hypertension (diastolic pressure >95 mmHg) from the Swedish component of an ongoing hypertension study (European Lacidipine study on Atherosclerosis, ELSA) and from 75 normotensive control men, who were from a Swedish population-screening programme (diastolic pressure <80 mmHg). The presence of carotid atherosclerosis and the intima-media thicknesses were determined by ultrasonography. A monoclonal antibody to OxLDL, EO6, was used to determine oxidation epitopes in LDL. aOxLDL of IgG and IgM subclass were tested by ELISA against OxLDL. Hypertensive men had increased OxLDL levels compared with normotensives ( P =0.002), whereas autoantibodies tested were largely similar between groups. There was no association between the antibodies tested, or OxLDL and carotid atherosclerosis. Age was not associated with OxLDL or aOxLDL measurements. Taken together, our findings indicate that OxLDL is elevated in hypertensive men, which may predispose to atherosclerosis in hypertension. In contrast, aOxLDL levels were unchanged and the role of aOxLDL may depend on disease stage and/or type.
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