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  5. Inclisiran: A New Pharmacological Approach for Hypercholesterolemia

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Article
en
2022

Inclisiran: A New Pharmacological Approach for Hypercholesterolemia

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en
2022
Vol 23 (11)
Vol. 23
DOI: 10.31083/j.rcm2311375

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Aldo Maggioni
Aldo Maggioni

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Stefania Angela Di Fusco
Aldo Maggioni
Chiara Bernelli
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Abstract

Therapeutic approaches based on gene silencing technologies represent a new opportunity to manage hypercholesterolemia. Inclisiran is a small interfering RNA that targets proprotein convertase subtilisin/kexin type 9 (PCSK9) mRNA. Clinical studies have demonstrated that inclisiran is effective, safe, and well-tolerated in reducing low-density lipoprotein cholesterol (LDL-C) in patients with familial hypercholesterolemia, atherosclerotic cardiovascular disease, and atherosclerotic cardiovascular disease risk equivalents. A meta-analysis of phase 3 trials demonstrated a 51% reduction in LDL-C levels at 18 months as compared with placebo. Adverse event incidence was found to be comparable in individuals treated with inclisiran and those receiving placebo, though the reactions at the site of injection were more common in patients receiving inclisiran as compared with those receiving placebo. The recommended inclisiran dose is 284 mg administered as a subcutaneous injection to be repeated after three months with a subsequent 6-month maintenance regimen. Overall, since the pharmacological efficacy of inclisiran in LDL-C reduction is comparable to that of monoclonal antibodies against PCSK9, the longer effect duration and the favorable safety profile may favor this newer approach for hypercholesterolemia management.

How to cite this publication

Stefania Angela Di Fusco, Aldo Maggioni, Chiara Bernelli, Francesco Perone, Vincenzo De Marzo, Edoardo Conte, Francesca Musella, Giuseppe Uccello, Leonardo De Luca, Domenico Gabrielli, Michele Massimo Gulizia, Fabrizio Oliva, Furio Colivicchi (2022). Inclisiran: A New Pharmacological Approach for Hypercholesterolemia. , 23(11), DOI: https://doi.org/10.31083/j.rcm2311375.

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Publication Details

Type

Article

Year

2022

Authors

13

Datasets

0

Total Files

0

Language

en

DOI

https://doi.org/10.31083/j.rcm2311375

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