Skoči na glavni sadržaj

Ostalo

https://doi.org/10.15836/ccar2022.279

New prospects in treatment of dyslipidaemia – putting patient compliance first

Dominik Strikić orcid id orcid.org/0000-0003-3977-9712 ; University Hospital Centre Zagreb, Zagreb, Croatia
Ana Marija Slišković orcid id orcid.org/0000-0001-6622-7572 ; University Hospital Centre Zagreb, Zagreb, Croatia
Andro Vujević orcid id orcid.org/0000-0003-2123-5979 ; University Hospital Centre Zagreb, Zagreb, Croatia
Ivana Sopek-Merkaš orcid id orcid.org/0000-0002-0888-5005 ; Special Hospital for Medical Rehabilitation Krapinske Toplice, Krapinske Toplice, Croatia
Iveta Merćep orcid id orcid.org/0000-0003-2824-9222 ; University Hospital Centre Zagreb, Zagreb, Croatia


Puni tekst: engleski pdf 145 Kb

str. 279-279

preuzimanja: 96

citiraj

Preuzmi JATS datoteku


Sažetak

Ključne riječi

dyslipidaemia; statins; inclisiran; PCSK9 inhibitors; patient compliance

Hrčak ID:

289787

URI

https://hrcak.srce.hr/289787

Datum izdavanja:

8.12.2022.

Posjeta: 249 *



Introduction: Dyslipidaemia is one of the leading cardiovascular risk factors. For a long time, successful treatment options were used, with statin therapy being the cornerstone. Nowadays, more and more new agents are being discovered and approved for the treatment of dyslipidaemia. This summary provides a brief overview of newly approved drugs and those still in development. Methods: For this review, online databases were searched using the keywords “dyslipidaemia”, “statins”, “PCSK9 inhibitors”, “inclisiran” and “new agents”.

Discussion: Statins have been used to treat dyslipidaemia for over 30 years. Studies have shown excellent results in lowering LDL cholesterol levels and reducing cardiovascular risk (1). Therefore, statins have become the most important preventive therapeutics for high-risk patients. However, changes in people’s lifestyles and the fast pace of life have presented us with new challenges and shown us that statins are not enough in some cases. The first monoclonal antibodies approved for the treatment of dyslipidaemia were the PCSK9 inhibitors evolocumab and alirocumab (1,2). Studies have shown very good results in lowering blood LDL cholesterol levels, so PCSK9 inhibitors, given once weekly, have gradually become a second-line treatment option (2). Recently, the EMA approved a new siRNA molecule called inclisiran that interferes with PCSK9 mRNA translation, thereby lowering LDL cholesterol levels. The main advantage of inclisiran is its dosing scheme of once every three months3. Volanesorsen is the first drug to target chylomicrons and lower triglyceride levels. The latest agent in the pipeline is evinacumab, an ANGPLT-3 inhibitor that has shown excellent potential in clinical trials (3).

Conclusion: The reduction in cardiovascular risk with PCSK9 inhibition and inclisiran therapy is not yet known, but its effect on lowering LDL cholesterol is evident. Conventional statin treatment requires everyday oral administration and highly motivated patients, whereas novel agents administered weekly or even monthly are putting patient compliance first.

LITERATURE

1 

Tokgozoglu L, Orringer C, Ginsberg HN, Catapano AL. The year in cardiovascular medicine 2021: dyslipidaemia. Eur Heart J. 2022 February 22;43(8):807–17. https://doi.org/10.1093/eurheartj/ehab875 PubMed: http://www.ncbi.nlm.nih.gov/pubmed/34974612

2 

dos Santos Pereira de Moura JM, Afonso Pais Pacheco Mendes PF, Peliz Reigota C, Valente Gemas VJ. New drugs coming up in the field of lipid control. E-Journal of Cardiology Practice. 2020;19(8). Avaiable from:https://www.escardio.org/Journals/E-Journal-of-Cardiology-Practice/Volume-19/new-drugs-coming-up-in-the-field-of-lipid-control

3 

Bardolia C, Amin NS, Turgeon J. Emerging Non-statin Treatment Options for Lowering Low-Density Lipoprotein Cholesterol. Front Cardiovasc Med. 2021 November 17;8:789931. https://doi.org/10.3389/fcvm.2021.789931 PubMed: http://www.ncbi.nlm.nih.gov/pubmed/34869702


This display is generated from NISO JATS XML with jats-html.xsl. The XSLT engine is libxslt.