Dyslipidemia Management in Adults With Diabetes.

PCSK9 inhibitors acide eicosapentanoïque atherosclerosis athéroslécrose eicosapentanoic acid ezetimibe fibrate inhibiteurs de la PCSK9 statines statins ézétimibe

Journal

Canadian journal of diabetes
ISSN: 2352-3840
Titre abrégé: Can J Diabetes
Pays: Canada
ID NLM: 101148810

Informations de publication

Date de publication:
Feb 2020
Historique:
received: 25 06 2019
revised: 06 07 2019
accepted: 08 07 2019
pubmed: 16 9 2019
medline: 30 9 2020
entrez: 16 9 2019
Statut: ppublish

Résumé

Lipid abnormalities beyond elevated low-density lipoprotein (LDL) cholesterol contribute to increased risk of atherosclerotic cardiovascular disease (ASCVD) in type 2 diabetes. We searched for English language randomized controlled trials of lipid-lowering therapies primarily since 2012 that included patients with diabetes. Diet and lifestyle advice are always a starting point for ASCVD prevention in diabetes. After almost 30 years of widespread clinical use in diabetes, statin treatment to reduce LDL cholesterol remains the cornerstone of drug therapy to prevent ASCVD. Ezetimibe appears to be particularly beneficial for high-risk statin-treated patients with diabetes. Similarly, currently available proprotein convertase subtilisin kexin type 9 inhibitors-alirocumab and evolocumab-both reduce ASCVD risk in statin-treated patients with diabetes. High-dose icosapent ethyl is another worthwhile add-on treatment, especially in statin-treated patients with diabetes in whom triglyceride levels remain elevated. Fibrates might reduce ASCVD risk in patients with diabetes with high triglyceride and low high-density lipoprotein cholesterol; however, fibrates are more strongly recommended for prophylaxis of pancreatitis in patients with severe hypertriglyceridemia and may also slow progression of diabetic retinopathy. Several existing and newer drug treatments reduce ASCVD risk through LDL cholesterol and/or triglyceride reduction in patients with diabetes. Novel approaches using antisense oligonucleotides and monoclonal antibodies may provide potential future therapies for diabetic dyslipidemia.

Identifiants

pubmed: 31521544
pii: S1499-2671(19)30373-9
doi: 10.1016/j.jcjd.2019.07.003
pii:
doi:

Substances chimiques

Anticholesteremic Agents 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

53-60

Informations de copyright

Copyright © 2019 Canadian Diabetes Association. Published by Elsevier Inc. All rights reserved.

Auteurs

Julieta Lazarte (J)

Departments of Medicine and Biochemistry and Robarts Research Institute, Schulich School of Medicine and Dentistry, Western University, London, Ontario, Canada.

Robert A Hegele (RA)

Departments of Medicine and Biochemistry and Robarts Research Institute, Schulich School of Medicine and Dentistry, Western University, London, Ontario, Canada. Electronic address: hegele@robarts.ca.

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