To Örebro University

oru.seÖrebro University Publications
Change search
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf
The Use of Monoclonal Antibody-Based Proprotein Convertase Subtilisin-Kexin Type 9 (PCSK9) Inhibitors in the Treatment of Hypercholesterolemia
School of Pharmacy, Temple University, Philadelphia, USA.
School of Pharmacy, Temple University, Philadelphia, USA.
Örebro University, School of Medical Sciences. Cardiology Research Unit, Department of Medicine, Karolinska Institutet, Stockholm, SWE.
Microbiology, Islamic Azad University, Shahr-e-Qods Branch, Tehran, IRN.
Show others and affiliations
2022 (English)In: Cureus, E-ISSN 2168-8184, Vol. 14, no 6, article id e25641Article, review/survey (Refereed) Published
Abstract [en]

In this review, we evaluated several studies in the literature to analyze the benefits and deleterious effects of the use of monoclonal antibodies (MABs)-based proprotein convertase subtilisin-kexin type 9 (PCSK9) inhibitors in patients with hypercholesterolemia. Increased low-density lipoprotein cholesterol (LDL-C) levels lead to an increase in the risk of cardiovascular (CV) disease. Statins are the cornerstones of hypercholesterolemia treatment, but the patient response may often vary, and additional therapies may be needed to control the increased LDL-C levels. MABs bind to PCSK9 receptors, causing a reduction in LDL-C levels. MAB-based PCSK9 inhibitors such as alirocumab and evolocumab have been approved for use in hypercholesterolemia in combination with statins. Studies have suggested that both alirocumab and evolocumab are effective in lowering LDL-C levels, have favorable side effect profiles, and can be administered at convenient dosing intervals; however, further double-blind, randomized trials evaluating the long-term safety and efficacy of both the agents could assist with clinical decision-making.

Place, publisher, year, edition, pages
Cureus Inc. , 2022. Vol. 14, no 6, article id e25641
Keywords [en]
Alirocumab, ascvd, cardiovascular, cholesterol, evolocumab, ldl, ldl-c, low density lipoprotein cholesterol, monoclonal antibody, pcsk9 inhibitors
National Category
Cardiology and Cardiovascular Disease
Identifiers
URN: urn:nbn:se:oru:diva-100115DOI: 10.7759/cureus.25641ISI: 000812328000021PubMedID: 35795514OAI: oai:DiVA.org:oru-100115DiVA, id: diva2:1682052
Available from: 2022-07-08 Created: 2022-07-08 Last updated: 2025-02-10Bibliographically approved

Open Access in DiVA

No full text in DiVA

Other links

Publisher's full textPubMed

Authority records

Magnusson, Peter

Search in DiVA

By author/editor
Magnusson, Peter
By organisation
School of Medical Sciences
In the same journal
Cureus
Cardiology and Cardiovascular Disease

Search outside of DiVA

GoogleGoogle Scholar

doi
pubmed
urn-nbn

Altmetric score

doi
pubmed
urn-nbn
Total: 17 hits
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf