PCSK9: from biology to clinical applications.


Journal

Pathology
ISSN: 1465-3931
Titre abrégé: Pathology
Pays: England
ID NLM: 0175411

Informations de publication

Date de publication:
Feb 2019
Historique:
received: 11 09 2018
revised: 03 10 2018
accepted: 03 10 2018
pubmed: 14 12 2018
medline: 26 2 2019
entrez: 8 12 2018
Statut: ppublish

Résumé

Proprotein convertase subtilisin/kexin type 9 (PCSK9) is a crucial protein governing the circulating levels of low density lipoprotein-cholesterol (LDL-C), by virtue of its pivotal role in the degradation of the LDL receptor (LDLR). In the last 15 years, in vitro and in vivo studies have allowed our understanding of the physiological role of PCSK9. In the current report, we review the key studies that have established the mode of action of PCSK9, leading to the development of PCSK9 inhibitors for clinical use. Data from clinical trials investigating these therapies clearly and unambiguously demonstrate the safety and efficacy of these new drugs that have the power to dramatically reduce LDL-C and associated cardiovascular diseases.

Identifiants

pubmed: 30522786
pii: S0031-3025(18)30426-4
doi: 10.1016/j.pathol.2018.10.012
pii:
doi:

Substances chimiques

Cholesterol, LDL 0
LDLR protein, human 0
PCSK9 Inhibitors 0
Protease Inhibitors 0
Receptors, LDL 0
PCSK9 protein, human EC 3.4.21.-
Proprotein Convertase 9 EC 3.4.21.-

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

177-183

Informations de copyright

Copyright © 2018 Royal College of Pathologists of Australasia. Published by Elsevier B.V. All rights reserved.

Auteurs

Valentin Blanchard (V)

Laboratoire Inserm UMR 1188 DéTROI, Université de La Réunion, Sainte-Clotilde, France.

Ilya Khantalin (I)

Laboratoire Inserm UMR 1188 DéTROI, Université de La Réunion, Sainte-Clotilde, France; CHU de La Réunion, Service de Chirurgie Vasculaire, Saint-Denis, France.

Stéphane Ramin-Mangata (S)

Laboratoire Inserm UMR 1188 DéTROI, Université de La Réunion, Sainte-Clotilde, France.

Kévin Chémello (K)

Laboratoire Inserm UMR 1188 DéTROI, Université de La Réunion, Sainte-Clotilde, France.

Brice Nativel (B)

Laboratoire Inserm UMR 1188 DéTROI, Université de La Réunion, Sainte-Clotilde, France.

Gilles Lambert (G)

Laboratoire Inserm UMR 1188 DéTROI, Université de La Réunion, Sainte-Clotilde, France. Electronic address: valentin.blanchard@univ-reunion.fr.

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Classifications MeSH