Optimal Medical Therapy for Stable Ischemic Heart Disease in 2024: Focus on Blood Pressure and Lipids.

Hypertension LDL-C Lipids Stable ischemic heart disease Targets Triglycerides

Journal

The Medical clinics of North America
ISSN: 1557-9859
Titre abrégé: Med Clin North Am
Pays: United States
ID NLM: 2985236R

Informations de publication

Date de publication:
May 2024
Historique:
medline: 29 3 2024
pubmed: 29 3 2024
entrez: 28 3 2024
Statut: ppublish

Résumé

Hypertension and dyslipidemia are 2 highly prevalent and modifiable risk factors in patients with stable ischemic heart disease. Multiple lines of evidence demonstrate that lowering blood pressure and low-density lipoprotein cholesterol improves clinical outcomes in patients with ischemic heart disease. Accordingly, clinical guidelines recommend intensive treatment targets for these high-risk patients. This article summarizes the pathophysiology, supporting evidence, and treatment recommendations for management of hypertension and dyslipidemia among patients with manifest ischemic heart disease and points to future research and unmet clinical needs.

Identifiants

pubmed: 38548456
pii: S0025-7125(23)00193-1
doi: 10.1016/j.mcna.2023.12.005
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

441-453

Informations de copyright

Copyright © 2023 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Disclosure T. Abrahams has no disclosures. S.J. Nicholls has received research support from AstraZeneca, United Kingdom, Amgen, United States, Anthera, CSL Behring, United States, Cerenis, Eli Lilly, Esperion, United States, Resverlogix, Novartis, Switzerland, InfraRedx, United States, and Sanofi-Regeneron; and is a consultant for Amgen, Akcea, AstraZeneca, Boehringer Ingelheim, CSL Behring, Eli Lilly, Esperion, Kowa, Merck, Takeda, Pfizer, Sanofi-Regeneron, Novo Nordisk, CSL Sequiris, and Vaxxinity. A.J. Nelson has received research support from Amgen, Eli Lilly, Novartis and Boehringer Ingelheim; and is a consultant for Amgen, AstraZeneca, Boehringer Ingelheim, Eli Lilly, Merck, Sanofi, Novo Nordisk, CSL Sequiris, and Vaxxinity.

Auteurs

Timothy Abrahams (T)

Victorian Heart Institute, Monash University, Melbourne, Victoria, Australia.

Stephen J Nicholls (SJ)

Victorian Heart Institute, Monash University, Melbourne, Victoria, Australia.

Adam J Nelson (AJ)

Victorian Heart Institute, Monash University, Melbourne, Victoria, Australia; Adelaide Medical School, University of Adelaide, Adelaide, South Australia. Electronic address: adam.nelson@monash.edu.

Classifications MeSH