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Published on: October 12, 2017
Lipoprotein profile, lipoprotein-associated phospholipase A2 and cardiovascular risk in hemodialysis patients
Roberta Rolla1, Andreana De Mauri2, Ambra Valsesia1
1Clinical Chemistry Laboratory, Department of Health Sciences, Amedeo Avogadro University of Eastern Piedmont, Novara, Italy.
Insights
Cardiovascular disease risk is high in hemodialysis patients due to altered lipoproteins. Elevated lipoprotein-associated phospholipase A2 (Lp-PLA2) indicates increased cardiovascular events in these patients.
Area of Science:
- Nephrology
- Cardiology
- Biochemistry
Background:
- Cardiovascular disease (CVD) is a major cause of death in hemodialysis patients.
- Accelerated atherosclerosis, inflammation, and altered lipoprotein metabolism contribute to CVD risk.
- Lipoprotein-associated phospholipase A2 (Lp-PLA2) is implicated in atherosclerosis progression.
Purpose of the Study:
- To evaluate Lp-PLA2 and pro-inflammatory markers in the lipoprotein profile of dialysis patients.
- To assess the relationship between these markers and accelerated atherosclerosis and vascular events.
- To understand the atherogenic phenotype of lipoproteins in hemodialysis patients.
Main Methods:
- Compared lipoprotein profiles, high-sensitivity C-reactive protein (CRP), ceruloplasmin, and serum amyloid A protein (SAA) in 102 dialysis patients and 40 controls.
- Followed patients for 1 year to record acute cardiovascular events.
- Measured Lp-PLA2 levels and their ratio with apolipoprotein A1.
Main Results:
- Dialysis patients had lower total cholesterol, LDL, and HDL than controls.
- Dialysis patients showed significantly higher CRP, SAA, ceruloplasmin, and Lp-PLA2 levels.
- Patients with Lp-PLA2 >194 nmol/min/ml experienced more cardiovascular events.
Conclusions:
- Low-density lipoproteins in dialysis patients exhibit a more atherogenic phenotype.
- High-density lipoproteins in dialysis patients have reduced anti-inflammatory properties.
- Lp-PLA2 may serve as a valuable biomarker for assessing cardiovascular risk in dialysis patients.
Background:
Cardiovascular disease is the leading cause of morbidity and mortality in hemodialysis patients; the increased risk of cardiovascular disease is due to accelerated atherosclerosis, inflammation and impaired lipoprotein metabolism. We aimed to evaluate lipoprotein-associated phospholipase A2 (Lp-PLA2) and some pro-inflammatory aspects of the lipoprotein profile in dialyzed patients in order to evaluate the relationship with the accelerated atherosclerosis and vascular accidents.
Methods:
In 102 dialysis patients and 40 non-uremic controls, we investigated the lipoprotein plasma profile, high sensitivity C-reactive protein (CRP), ceruloplasmin and serum amyloid A protein (SAA), and followed patients for 1 year to analyze the risk of acute cardiovascular events.
Results:
Total cholesterol, low-density lipoprotein and high-density lipoprotein plasma levels were significantly lower in uremic patients than controls, whereas CRP, SAA, ceruloplasmin, Lp-PLA2 and their ratio with apolipoprotein A1 were significantly higher. Patients with Lp-PLA2 levels >194 nmol/min/ml had more acute cardiovascular events than patients with lower values.
Conclusion:
Our results show that in dialysis subjects: (1) low-density lipoproteins show a more atherogenic phenotype than in the general population; (2) high-density lipoproteins are less anti-inflammatory; (3) Lp-PLA2 could potentially be used to evaluate cardiovascular risk.
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