Do we need new lipid-lowering agents in the era of PCSK9 inhibitors? Recent advances.
Anticholesteremic Agents
/ pharmacology
Atherosclerosis
/ complications
Cardiovascular Diseases
/ etiology
Cholesterol, LDL
Ezetimibe
/ therapeutic use
Humans
Hydroxymethylglutaryl-CoA Reductase Inhibitors
/ therapeutic use
Hypolipidemic Agents
/ therapeutic use
PCSK9 Inhibitors
Proprotein Convertase 9
/ metabolism
LDL cholesterol
PCSK9 inhibitors
RNA- -based therapy
atherosclerotic disease
lipid lowering agents
Journal
Kardiologia polska
ISSN: 1897-4279
Titre abrégé: Kardiol Pol
Pays: Poland
ID NLM: 0376352
Informations de publication
Date de publication:
2022
2022
Historique:
received:
02
05
2022
accepted:
02
05
2022
pubmed:
7
5
2022
medline:
9
9
2022
entrez:
6
5
2022
Statut:
ppublish
Résumé
Atherosclerotic disease remains the leading cause of death worldwide. Much of atherosclerotic disease initiation and progression is driven by dyslipidemia. With the advent of statins, ezetimibe, and more recently the proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors, physicians across all specialties have access to an armamentarium to address this major pathophysiological driver. Nevertheless, there is still a large unmet need in terms of optimizing pharmacotherapeutic lipid lowering strategies. This article will review the evidence pertaining to the major lipid-lowering agents that have been introduced lately, or still are under development, after the advent of statins, ezetimibe and PCSK9 inhibitors. There is cumulating evidence suggesting that there soon will be a broad specter of differential therapies across a variety of mechanistic pathways that will enter clinical medicine. Knowledge about these potential recent advances and various upcoming therapeutic options will make choice easier for physicians, and will lead to more personalized selections of available treatments.
Identifiants
pubmed: 35521719
pii: VM/OJS/J/89904
doi: 10.33963/KP.a2022.0117
doi:
Substances chimiques
Anticholesteremic Agents
0
Cholesterol, LDL
0
Hydroxymethylglutaryl-CoA Reductase Inhibitors
0
Hypolipidemic Agents
0
PCSK9 Inhibitors
0
PCSK9 protein, human
EC 3.4.21.-
Proprotein Convertase 9
EC 3.4.21.-
Ezetimibe
EOR26LQQ24
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM