PCSK9 inhibitors and dyslipidemia: The clinical evidence

Elevated plasma LDL cholesterol (LDL-C) levels are associated with cardiovascular diseases and statin therapy was proven to decrease LDL-C and reduce cardiovascular death. However, in patients at high cardiovascular risk, achievement of optimal LDL-C levels is challenging, and therefore additional s...

Full description

Bibliographic Details
Main Author: Norata, Giuseppe
Format: Journal Article
Published: 2014
Online Access:http://hdl.handle.net/20.500.11937/55905
_version_ 1848759737034735616
author Norata, Giuseppe
author_facet Norata, Giuseppe
author_sort Norata, Giuseppe
building Curtin Institutional Repository
collection Online Access
description Elevated plasma LDL cholesterol (LDL-C) levels are associated with cardiovascular diseases and statin therapy was proven to decrease LDL-C and reduce cardiovascular death. However, in patients at high cardiovascular risk, achievement of optimal LDL-C levels is challenging, and therefore additional strategies for further lowering LDL-C levels are under development. Recently, silencing of apolipoprotein B gene and MTP inhibition have been approved for the treatment of patients with familial hypercholesterolemia, and there is great interest in the inhibition of proprotein convertase subtilisin/kexin 9 (PCSK9). PCSK9 promotes the degradation of the LDL receptor. The inhibition of PCSK9 favors LDL catabolism and reduces plasma LDL-C levels. Monoclonal antibodies against PCSK9 represent so far the most advanced approach in clinical development, with alirocumab, evolocumab and bococizumab under advanced clinical development. Recent data from the first phase III studies show LDL-C reduction in monotherapy and on top of statins. Long-term studies on cardiovascular endpoints are ongoing and the results will be crucial to translate the benefit of this promising approach into clinical practice. © 2014 Il Pensiero Scientifico Editore.
first_indexed 2025-11-14T10:04:38Z
format Journal Article
id curtin-20.500.11937-55905
institution Curtin University Malaysia
institution_category Local University
last_indexed 2025-11-14T10:04:38Z
publishDate 2014
recordtype eprints
repository_type Digital Repository
spelling curtin-20.500.11937-559052017-09-13T16:11:11Z PCSK9 inhibitors and dyslipidemia: The clinical evidence Norata, Giuseppe Elevated plasma LDL cholesterol (LDL-C) levels are associated with cardiovascular diseases and statin therapy was proven to decrease LDL-C and reduce cardiovascular death. However, in patients at high cardiovascular risk, achievement of optimal LDL-C levels is challenging, and therefore additional strategies for further lowering LDL-C levels are under development. Recently, silencing of apolipoprotein B gene and MTP inhibition have been approved for the treatment of patients with familial hypercholesterolemia, and there is great interest in the inhibition of proprotein convertase subtilisin/kexin 9 (PCSK9). PCSK9 promotes the degradation of the LDL receptor. The inhibition of PCSK9 favors LDL catabolism and reduces plasma LDL-C levels. Monoclonal antibodies against PCSK9 represent so far the most advanced approach in clinical development, with alirocumab, evolocumab and bococizumab under advanced clinical development. Recent data from the first phase III studies show LDL-C reduction in monotherapy and on top of statins. Long-term studies on cardiovascular endpoints are ongoing and the results will be crucial to translate the benefit of this promising approach into clinical practice. © 2014 Il Pensiero Scientifico Editore. 2014 Journal Article http://hdl.handle.net/20.500.11937/55905 10.1714/1563.17029 restricted
spellingShingle Norata, Giuseppe
PCSK9 inhibitors and dyslipidemia: The clinical evidence
title PCSK9 inhibitors and dyslipidemia: The clinical evidence
title_full PCSK9 inhibitors and dyslipidemia: The clinical evidence
title_fullStr PCSK9 inhibitors and dyslipidemia: The clinical evidence
title_full_unstemmed PCSK9 inhibitors and dyslipidemia: The clinical evidence
title_short PCSK9 inhibitors and dyslipidemia: The clinical evidence
title_sort pcsk9 inhibitors and dyslipidemia: the clinical evidence
url http://hdl.handle.net/20.500.11937/55905