Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2016 Jan;2(1):44-53.
doi: 10.1093/ehjcvp/pvv045. Epub 2015 Nov 29.

From proprotein convertase subtilisin/kexin type 9 to its inhibition: state-of-the-art and clinical implications

Affiliations
Review

From proprotein convertase subtilisin/kexin type 9 to its inhibition: state-of-the-art and clinical implications

Eliano P Navarese et al. Eur Heart J Cardiovasc Pharmacother. 2016 Jan.

Abstract

Statins are recommended as first-line therapy for patients with hypercholesterolaemia. A sizable proportion of patients, however, does not reach therapeutic goals, is statin intolerant, or, despite optimal statin therapy, is at high risk of ischaemic events. Proprotein convertase subtilisin/kexin type 9 (PCSK9) plays a major role in lipid metabolism and several comorbidities. Monoclonal antibodies targeting PCSK9 are a new lipid-lowering approach with the potential to improve clinical outcomes in patients with dyslipidaemia. In this review, we discuss current experimental and clinical evidence of the role of PCSK9 and its inhibition on lipid metabolism and several pathologic conditions with a focus on clinical outcomes. A state-of-the-art analysis of current clinical evidence and future directions on PCSK9 and its inhibition is provided.

Keywords: Clinical perspectives; PCSK9 inhibitors; Proprotein convertase subtilisin/kexin type 9 (PCSK9).

PubMed Disclaimer

Similar articles

Cited by

MeSH terms

LinkOut - more resources