Key result
Pitavastatin treatment for 6 months significantly increased plasma adiponectin and, in responders, decreased PAI-1, PDMP, and sCD40L levels in hyperlipidemic patients.
Why the study?
Does pitavastatin 2 mg daily improve plasma levels of PAI-1 and adiponectin in patients with hyperlipidemia?
Observational (n=68)
Does pitavastatin 2 mg daily improve plasma levels of PAI-1 and adiponectin in patients with hyperlipidemia?
Pitavastatin may exert an adiponectin-dependent anti-atherothrombotic effect in hyperlipidemic patients by reducing PAI-1, PDMP, and sCD40L in adiponectin responders.
Hypothesis-generating for pitavastatin effects on platelet markers in hyperlipidemia; randomized trials needed before clinical adoption.
The effects of statins on two platelet activation markers, plasiminogen activator inhibitor (PAI)-1 and adiponectin, were investigated in 68 patients with hyperlipidemia. The patients were treated with pitavastatin with a dosage of 2 mg daily. The plasma levels of platelet-derived microparticles (PDMP), soluble CD40 ligand (sCD40L), sP-selectin, PAI-1, and adiponectin were measured at baseline and after 6 months of treatment in both groups. In hyperlipidemic patients, the plasma levels were higher in PDMP, sCD40L, sP-selectin, and PAI-1, and lower in adiponectin, compared to the normolipidemic controls. Plasma PDMP and sCD40L were positively correlated, while plasma adiponectin was negatively correlated with the plasma levels of PAI-1. No significant differences were observed in the plasma levels of PDMP, sCD40L, sP-selectin, and PAI-1 before and after treatment. A significant increase in plasma adiponectin levels was observed after 6 months of treatment with pitavastatin. When the patients treated with pitavastatin were divided into two groups according to the adiponectin response to pitavastatin treatment, significant decreases in plasma PAI-1, PDMP, and sCD40L levels were observed after pitavastatin treatment in the responder group. These findings suggest that PDMP, sCD40L, and PAI-1 may participate in the development of atherothrombosis in patients with hyperlipidemia, and that pitavastatin may exert an adiponectin-dependent anti-atherothrombotic effect in hyperlipidemic patients.
No takes yet. Share an insight, caveat, or question.
Nomura et al. (2012) conducted an observational in Hyperlipidemia (n=68). Pitavastatin vs. Baseline / Normolipidemic controls was evaluated on Plasma levels of PDMP, sCD40L, sP-selectin, PAI-1, and adiponectin. Pitavastatin treatment for 6 months significantly increased plasma adiponectin and, in responders, decreased PAI-1, PDMP, and sCD40L levels in hyperlipidemic patients.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: