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Pharmacological Intervention to Modulate HDL: What Do We Target?

作者信息

Woudberg Nicholas J, Pedretti Sarah, Lecour Sandrine, Schulz Rainer, Vuilleumier Nicolas, James Richard W, Frias Miguel A

机构信息

Hatter Institute for Cardiovascular Research in Africa and South African Medical Research Council Inter-University Cape Heart Group, Department of Medicine, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.

Division of Endocrinology, Diabetes, Hypertension and Nutrition, Department of Internal Medicine Specialities, Faculty of Medicine, University of Geneva, Geneva, Switzerland.

出版信息

Front Pharmacol. 2018 Jan 22;8:989. doi: 10.3389/fphar.2017.00989. eCollection 2017.


DOI:10.3389/fphar.2017.00989
PMID:29403378
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5786575/
Abstract

The cholesterol concentrations of low-density lipoprotein (LDL) and high-density lipoprotein (HDL) have traditionally served as risk factors for cardiovascular disease. As such, novel therapeutic interventions aiming to raise HDL cholesterol have been tested in the clinical setting. However, most trials led to a significant increase in HDL cholesterol with no improvement in cardiovascular events. The complexity of the HDL particle, which exerts multiple physiological functions and is comprised of a number of subclasses, has raised the question as to whether there should be more focus on HDL subclass and function rather than cholesterol quantity. We review current data regarding HDL subclasses and subclass-specific functionality and highlight how current lipid modifying drugs such as statins, cholesteryl ester transfer protein inhibitors, fibrates and niacin often increase cholesterol concentrations of specific HDL subclasses. In addition this review sets out arguments suggesting that the HDL3 subclass may provide better protective effects than HDL2.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9ca/5786575/69ad869190fc/fphar-08-00989-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9ca/5786575/be6ad774d2e0/fphar-08-00989-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9ca/5786575/69ad869190fc/fphar-08-00989-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9ca/5786575/be6ad774d2e0/fphar-08-00989-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9ca/5786575/69ad869190fc/fphar-08-00989-g002.jpg

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本文引用的文献

[1]
Effects of Anacetrapib in Patients with Atherosclerotic Vascular Disease.

N Engl J Med. 2017-8-28

[2]
Increased inflammatory effect of electronegative LDL and decreased protection by HDL in type 2 diabetic patients.

Atherosclerosis. 2017-7-13

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Detrimental Effect of Hypercholesterolemia on High-Density Lipoprotein Particle Remodeling in Pigs.

J Am Coll Cardiol. 2017-7-11

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Curr Opin Lipidol. 2017-10

[5]
The inverse association of HDL-cholesterol with future risk of hypertension is not modified by its antioxidant constituent, paraoxonase-1: The PREVEND prospective cohort study.

Atherosclerosis. 2017-6-21

[6]
New perspectives on biological HDL-targeted therapies.

Expert Opin Biol Ther. 2017-7

[7]
Anti-Apolipoprotein A-1 IgG Predict All-Cause Mortality and Are Associated with Fc Receptor-Like 3 Polymorphisms.

Front Immunol. 2017-4-18

[8]
Development of CER-001: Preclinical Dose Selection Through to Phase I Clinical Findings.

Clin Drug Investig. 2017-5

[9]
Anacetrapib, but not evacetrapib, impairs endothelial function in CETP-transgenic mice in spite of marked HDL-C increase.

Atherosclerosis. 2017-1-16

[10]
ATP binding cassette A1 (ABCA1) mediates microparticle formation during high-density lipoprotein (HDL) biogenesis.

Atherosclerosis. 2017-1-17

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