Key result
Elevated Lp-PLA2 linked to more acute cardiovascular events in hemodialysis patients.
Cohort (n=142)
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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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Rolla et al. (2015) conducted a cohort in End-stage renal disease on hemodialysis (n=142). Lipoprotein-associated phospholipase A2 (Lp-PLA2) >194 nmol/min/ml and uremic status vs. Lp-PLA2 ≤194 nmol/min/ml and non-uremic controls was evaluated on Acute cardiovascular events. Lp-PLA2 levels >194 nmol/min/ml in hemodialysis patients were associated with more acute cardiovascular events over 1 year compared to lower levels.
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