Abstract

Background and Aims: Several epidemiological studies have shown that lipoprotein-associated phospholipase A2 (Lp-PLA2) is an independent risk factor for coronary artery disease. Lp-PLA2 is secreted by proinflammatory cells and is highly expressed in the atherosclerotically changed arterial wall. Recently, lower activity of Lp-PLA2 has been observed in plasmas from everolimus-treated patients. In vitro studies revealed reduced Lp-PLA2 expression in hepatocytes and macrophages pre-exposed to everolimus, while antiatherosclerotic activity of everolimus has been shown in animal models of disease.

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