Literature DB >> 21596380

Clinical aspects of PCSK9.

Bertrand Cariou1, Cédric Le May, Philippe Costet.   

Abstract

Proprotein convertase subtilisin kexin type 9 (PCSK9) is a circulating protein that impairs LDL clearance by promoting the LDL receptor (LDLR) degradation. PCSK9 has emerged as a new pharmacological target for hypercholesterolemia, and different PCSK9 inhibitors are now evaluated in clinical trials. Here, we propose an overview of the clinical perspectives of PCSK9. First, we describe the clinical features of patients with PCSK9 mutations, and how these variations impact the cardiovascular risk. Then, we extensively discuss the potential role of circulating PCSK9 as a new biomarker of lipid metabolism. Indeed, many studies conducted in healthy and type 2 diabetic patients have tested the association of circulating PCSK9 with LDL-cholesterol as well as with multiple metabolic parameters. The overall picture of the clinical relevance of circulating PCSK9 is complicated by the effect of nutritional status and hypolipidemic drugs such as statins, fibrates, ezetimibe on plasma PCSK9 concentrations. Finally, we present a brief overview of the available therapeutic strategies to inhibit PCSK9.
Copyright © 2011 Elsevier Ireland Ltd. All rights reserved.

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Year:  2011        PMID: 21596380     DOI: 10.1016/j.atherosclerosis.2011.04.018

Source DB:  PubMed          Journal:  Atherosclerosis        ISSN: 0021-9150            Impact factor:   5.162


  40 in total

Review 1.  Lipid lowering with PCSK9 inhibitors.

Authors:  Razvan T Dadu; Christie M Ballantyne
Journal:  Nat Rev Cardiol       Date:  2014-06-24       Impact factor: 32.419

2.  Relation of resistin to proprotein convertase subtilisin-kexin type 9 levels in coronary artery disease patients with different nutritional status.

Authors:  S Li; R X Xu; Y Zhang; Y L Guo; C G Zhu; G Liu; Q Dong; J J Li
Journal:  J Endocrinol Invest       Date:  2015-05-24       Impact factor: 4.256

3.  Short-term impact of low-dose atorvastatin on serum proprotein convertase subtilisin/kexin type 9.

Authors:  Yuan-Lin Guo; Jun Liu; Rui-Xia Xu; Cheng-Gang Zhu; Na-Qiong Wu; Li-Xin Jiang; Jian-Jun Li
Journal:  Clin Drug Investig       Date:  2013-12       Impact factor: 2.859

4.  Lipid nanoparticle delivery systems for siRNA-based therapeutics.

Authors:  C Wan; T M Allen; P R Cullis
Journal:  Drug Deliv Transl Res       Date:  2014-02       Impact factor: 4.617

5.  PCSK9 LNA antisense oligonucleotides induce sustained reduction of LDL cholesterol in nonhuman primates.

Authors:  Marie W Lindholm; Joacim Elmén; Niels Fisker; Henrik F Hansen; Robert Persson; Marianne R Møller; Christoph Rosenbohm; Henrik Ørum; Ellen M Straarup; Troels Koch
Journal:  Mol Ther       Date:  2011-11-22       Impact factor: 11.454

6.  Docosahexaenoic Acid Attenuates Cardiovascular Risk Factors via a Decline in Proprotein Convertase Subtilisin/Kexin Type 9 (PCSK9) Plasma Levels.

Authors:  Celia Rodríguez-Pérez; Vanu Ramkumar Ramprasath; Shuaihua Pu; Ali Sabra; Rosa Quirantes-Piné; Antonio Segura-Carretero; Peter J H Jones
Journal:  Lipids       Date:  2015-11-30       Impact factor: 1.880

7.  Relation between proprotein convertase subtilisin/kexin type 9 and directly measured low-density lipoprotein cholesterol.

Authors:  Kristen M Tecson; Katherine S Panettiere-Kennedy; Jane I Won; Puja Garg; Oluseun Olugbode; Peter A McCullough
Journal:  Proc (Bayl Univ Med Cent)       Date:  2017-01

8.  Xanthohumol improves dysfunctional glucose and lipid metabolism in diet-induced obese C57BL/6J mice.

Authors:  Cristobal L Miranda; Valerie D Elias; Joshua J Hay; Jaewoo Choi; Ralph L Reed; Jan F Stevens
Journal:  Arch Biochem Biophys       Date:  2016-03-11       Impact factor: 4.013

9.  The M2 module of the Cys-His-rich domain (CHRD) of PCSK9 protein is needed for the extracellular low-density lipoprotein receptor (LDLR) degradation pathway.

Authors:  Yascara Grisel Luna Saavedra; Robert Day; Nabil G Seidah
Journal:  J Biol Chem       Date:  2012-10-26       Impact factor: 5.157

Review 10.  [PCSK9 as new target in hyperlipidemia treatment].

Authors:  P Stawowy; S Kelle; E Fleck
Journal:  Herz       Date:  2013-08-08       Impact factor: 1.443

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