Pharmacological Intervention to Modulate HDL: What Do We Target?
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 tr...
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doaj-4036e3773a8e4d43b39ef36393da9c672020-11-24T22:56:48ZengFrontiers Media S.A.Frontiers in Pharmacology1663-98122018-01-01810.3389/fphar.2017.00989322386Pharmacological Intervention to Modulate HDL: What Do We Target?Nicholas J. Woudberg0Sarah Pedretti1Sarah Pedretti2Sandrine Lecour3Rainer Schulz4Nicolas Vuilleumier5Richard W. James6Miguel A. Frias7Miguel A. Frias8Hatter 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 AfricaHatter 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 AfricaDivision of Endocrinology, Diabetes, Hypertension and Nutrition, Department of Internal Medicine Specialities, Faculty of Medicine, University of Geneva, Geneva, SwitzerlandHatter 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 AfricaInstitute of Physiology, Justus Liebig University Giessen, Giessen, GermanyDivision of Laboratory Medicine, Department of Genetics and Laboratory Medicine, Geneva University Hospitals, Geneva, SwitzerlandDivision of Endocrinology, Diabetes, Hypertension and Nutrition, Department of Internal Medicine Specialities, Faculty of Medicine, University of Geneva, Geneva, SwitzerlandDivision of Endocrinology, Diabetes, Hypertension and Nutrition, Department of Internal Medicine Specialities, Faculty of Medicine, University of Geneva, Geneva, SwitzerlandDivision of Laboratory Medicine, Department of Genetics and Laboratory Medicine, Geneva University Hospitals, Geneva, SwitzerlandThe 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.http://journal.frontiersin.org/article/10.3389/fphar.2017.00989/fullHDLpharmaceutical interventionHDL functionalityHDL subclasscardiovascular disease |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Nicholas J. Woudberg Sarah Pedretti Sarah Pedretti Sandrine Lecour Rainer Schulz Nicolas Vuilleumier Richard W. James Miguel A. Frias Miguel A. Frias |
spellingShingle |
Nicholas J. Woudberg Sarah Pedretti Sarah Pedretti Sandrine Lecour Rainer Schulz Nicolas Vuilleumier Richard W. James Miguel A. Frias Miguel A. Frias Pharmacological Intervention to Modulate HDL: What Do We Target? Frontiers in Pharmacology HDL pharmaceutical intervention HDL functionality HDL subclass cardiovascular disease |
author_facet |
Nicholas J. Woudberg Sarah Pedretti Sarah Pedretti Sandrine Lecour Rainer Schulz Nicolas Vuilleumier Richard W. James Miguel A. Frias Miguel A. Frias |
author_sort |
Nicholas J. Woudberg |
title |
Pharmacological Intervention to Modulate HDL: What Do We Target? |
title_short |
Pharmacological Intervention to Modulate HDL: What Do We Target? |
title_full |
Pharmacological Intervention to Modulate HDL: What Do We Target? |
title_fullStr |
Pharmacological Intervention to Modulate HDL: What Do We Target? |
title_full_unstemmed |
Pharmacological Intervention to Modulate HDL: What Do We Target? |
title_sort |
pharmacological intervention to modulate hdl: what do we target? |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Pharmacology |
issn |
1663-9812 |
publishDate |
2018-01-01 |
description |
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. |
topic |
HDL pharmaceutical intervention HDL functionality HDL subclass cardiovascular disease |
url |
http://journal.frontiersin.org/article/10.3389/fphar.2017.00989/full |
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