Inclisiran: a small interfering RNA strategy targeting PCSK9 to treat hypercholesterolemia.


Journal

Expert opinion on drug safety
ISSN: 1744-764X
Titre abrégé: Expert Opin Drug Saf
Pays: England
ID NLM: 101163027

Informations de publication

Date de publication:
Jan 2022
Historique:
pubmed: 2 10 2021
medline: 20 1 2022
entrez: 1 10 2021
Statut: ppublish

Résumé

Inclisiran is a novel posttranscriptional gene silencing therapy that inhibits proprotein convertase subtilisin/kexin type 9 (PCSK9) synthesis by RNA interference and has a potent, dose-dependent, durable effect in lowering LDL-C, and therefore is an effective drug to treat dyslipidemia, reducing the risk for acute cardiovascular (CV) events. It is safe and well-tolerated. This paper aims to review the mechanism of action of inclisiran while evaluating its efficacy and safety in the treatment of dyslipidemia from data of the clinical trials in the ORION program. Data from the clinical trials in the ORION program demonstrated efficacy and safety of inclisiran in patients with dyslipidemia. Adverse events were similar in the inclisiran and placebo groups in the clinical trials, although injection-site reactions were more frequent with inclisiran than with placebo. Although the combination of efficacy and safety makes inclisiran a good option for the treatment of dyslipidemia compared to other PCSK9 targeting therapeutic strategies, however, further studies should exclude the possibility that inclisiran, through lower-affinity interactions, may influence other mRNAs in the physiological milieu.

Identifiants

pubmed: 34596005
doi: 10.1080/14740338.2022.1988568
doi:

Substances chimiques

ALN-PCS 0
RNA, Small Interfering 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

9-20

Auteurs

Yajnavalka Banerjee (Y)

Mohammed Bin Rashid University of Medicine and Health Sciences, Dubai, United Arab Emirates and Centre of Medical Education, University of Dundee, UK.

Anca Pantea Stoian (A)

Department of Diabetes, Nutrition and Metabolic Diseases, Carol Davila University of Medicine and Pharmacy, Bucharest, Romania.

Arrigo Francesco Giuseppe Cicero (AFG)

Hypertension and Cardiovascular Risk Factors Research Center, Medical and Surgical Sciences Department, Alma Mater Studiorum University of Bologna, Italy.

Federica Fogacci (F)

Hypertension and Cardiovascular Risk Factors Research Center, Medical and Surgical Sciences Department, Alma Mater Studiorum University of Bologna, Italy.

Dragana Nikolic (D)

Department of Health Promotion Sciences Maternal and Infantile Care, Internal Medicine and Medical Specialties (Promise), University of Palermo, Italy.

Alexandros Sachinidis (A)

Department of Health Promotion Sciences Maternal and Infantile Care, Internal Medicine and Medical Specialties (Promise), University of Palermo, Italy.

Ali A Rizvi (AA)

Division of Endocrinology, Diabetes and Metabolism, Department of Medicine, University of South Carolina, Columbia, SC, USA.
Division of Endocrinology, Metabolism, and Lipids, Department of Medicine, Emory University, Atlanta, GA, USA.

Andrej Janez (A)

Department of Endocrinology, Diabetes and Metabolic Diseases, University Clinical Center Ljubljana, Slovenia.

Manfredi Rizzo (M)

Department of Diabetes, Nutrition and Metabolic Diseases, Carol Davila University of Medicine and Pharmacy, Bucharest, Romania.
Department of Health Promotion Sciences Maternal and Infantile Care, Internal Medicine and Medical Specialties (Promise), University of Palermo, Italy.
Division of Endocrinology, Diabetes and Metabolism, Department of Medicine, University of South Carolina, Columbia, SC, USA.

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Classifications MeSH