[From statin revolution to gene silencing therapy: 50 years of evolution in the treatment of hypercholesterolemia].
Dalla rivoluzione delle statine alla terapia di silenziamento genico: 50 anni di evoluzione nella terapia dell’ipercolesterolemia.
Anticholesteremic Agents
/ therapeutic use
Atherosclerosis
/ drug therapy
Cardiovascular Diseases
/ drug therapy
Cholesterol, LDL
Drug Therapy, Combination
Ezetimibe
/ therapeutic use
Gene Silencing
Humans
Hydroxymethylglutaryl-CoA Reductase Inhibitors
/ therapeutic use
Hypercholesterolemia
/ drug therapy
Hyperlipidemias
/ drug therapy
Proprotein Convertase 9
Journal
Giornale italiano di cardiologia (2006)
ISSN: 1972-6481
Titre abrégé: G Ital Cardiol (Rome)
Pays: Italy
ID NLM: 101263411
Informations de publication
Date de publication:
Jul 2022
Jul 2022
Historique:
entrez:
30
6
2022
pubmed:
1
7
2022
medline:
6
7
2022
Statut:
ppublish
Résumé
The last 50 years have experienced a rapid evolution in the development of lipid-lowering agents to reduce low-density lipoprotein cholesterol levels. This significant advance in medicine has not occurred without debate. Whether lowering blood cholesterol levels was beneficial has remained one of the most controversial issues during the past 50 years. The discovery of statins was the revolution that made it possible to delay and stop the progression of the atherosclerotic process resulting in improved health and longevity for millions of people. To date, statins remain the drugs of choice for the treatment of hypercholesterolemia. Despite their use, the risk of cardiovascular events persists. Therefore, the use of non-statin drugs, such as ezetimibe or PCSK9 inhibitors, in combination with statins has been shown to further reduce the risk of cardiovascular events. This review aims to summarize the advances in the field of lipid-lowering therapies over the past 50 years, focusing on advances in the development of drug therapies up to and including gene silencing or gene editing treatments that are expected in the near future.
Substances chimiques
Anticholesteremic Agents
0
Cholesterol, LDL
0
Hydroxymethylglutaryl-CoA Reductase 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
ita
Sous-ensembles de citation
IM