Interaction between serum endotoxemia and proprotein convertase subtilisin/kexin 9 (PCSK9) in patients with atrial fibrillation. a post-hoc analysis from the ATHERO-AF cohort

Abstract Background and aims Lipopolysaccharides (LPS) are emerging as a novel risk factor for cardiovascular events (CVEs). Furthermore, in vitro evidence suggested that LPS may elicit proprotein convertase subtilisin/kexin 9 (PCSK9) expression, but their relationship in vivo has not been investigated. Methods We conducted a post-hoc analysis of a prospective, single centre cohort study of 907 patients with non-valvular atrial fibrillation (AF). At baseline, PCSK9, LPS and NADPH oxidase (sNox2-dp) were measured. PCSK9 and LPS were correlated with incidence of CVEs. Results Median PCSK9 and LPS were 1200 [900–1970] and 49.9 [15.0–108.2] pg/ml, respectively. LPS and PCSK9 were significantly correlated (rS 0.378, p p =  0.009). Other factors independently associated with PCSK9 above the median were sNox2-dp (OR 1.759 C.I. 95% 1.167–2.650, p =  0.007), use of antiplatelet drugs (OR 0.437 95%CI 0.219–0.871 p =  0.017) and high adherence to Mediterranean diet (OR 0.737 95%CI 0.643–0.845 p =  0.001). Olive oil (OR 0.376 95%CI 0.185–0.763, p =  0.001) and wine (OR 0.460 95%CI 0.289–0.733 p =  0.007) were negatively associated with PCSK9. Patients with concomitant high PCSK9 and LPS (LPS ≥88 pg/ml and PCSK9 ≥1570 pg/ml) had an increased risk of CVEs compared to those with low levels (LPS p =  0.022). Conclusions This study demonstrated, for the first time in vivo, that circulating levels of PCSK9 and LPS are associated with a mechanism possibly involving NADPH oxidase activation. Patients with concomitant increase of PCSK9 and LPS showed a higher risk of CVEs.