A comprehensive review on the lipid and pleiotropic effects of pitavastatin.

Prog Lipid Res

Department of Preventive Cardiology and Lipidology, Medical University of Lodz (MUL), Lodz, Poland; Cardiovascular Research Centre, University of Zielona Gora, Zielona-Gora, Poland. Electronic address:

Published: November 2021

AI Article Synopsis

  • Statins, particularly HMG-CoA reductase inhibitors, are the primary treatment for high cholesterol, offering both primary and secondary prevention benefits.
  • Pitavastatin, a unique lipophilic statin, not only effectively lowers cholesterol and triglycerides but also exhibits additional benefits like reducing inflammation and improving blood vessel function.
  • This review focuses on the lipid-lowering effects of pitavastatin, while also exploring its various non-lipid-related advantages, making it a compelling option for managing different diseases.

Article Abstract

The 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase inhibitors, or statins, are administered as first line therapy for hypercholesterolemia, both in primary and secondary prevention. There is a growing body of evidence showing that beyond their lipid-lowering effect, statins have a number of additional beneficial properties. Pitavastatin is a unique lipophilic statin with a strong effect on lowering plasma total cholesterol and triacylglycerol. It has been reported to have pleiotropic effects such as decreasing inflammation and oxidative stress, regulating angiogenesis and osteogenesis, improving endothelial function and arterial stiffness, and reducing tumor progression. Based on the available studies considering the risk of statin-associated muscle symptoms it seems to be also the safest statin. The unique lipid and non-lipid effects of pitavastatin make this molecule a particularly interesting option for the management of different human diseases. In this review, we first summarized the lipid effects of pitavastatin and then strive to unravel the diverse pleiotropic effects of this molecule.

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Source
http://dx.doi.org/10.1016/j.plipres.2021.101127DOI Listing

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