Role of Lipid-Lowering and Anti-Inflammatory Therapies on Plaque Stabilization

Atherosclerosis is the predominant underlying etiopathology of coronary artery disease. Changes in plaque phenotype from stable to high risk may spur future major adverse cardiac events (MACE). Different pharmacological therapies have been implemented to mitigate this risk. Over the last two decades...

Full description

Saved in:
Bibliographic Details
Published inJournal of clinical medicine Vol. 13; no. 11; p. 3096
Main Authors Bryniarski, Krzysztof L, den Dekker, Wijnand, Legutko, Jacek, Gasior, Pawel, Tahon, Jeroen, Diletti, Roberto, Wilschut, Jeroen M, Nuis, Rutger-Jan, Daemen, Joost, Kleczynski, Pawel, Van Mieghem, Nicolas M, Jang, Ik-Kyung
Format Journal Article
LanguageEnglish
Published Basel MDPI AG 01.06.2024
MDPI
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Atherosclerosis is the predominant underlying etiopathology of coronary artery disease. Changes in plaque phenotype from stable to high risk may spur future major adverse cardiac events (MACE). Different pharmacological therapies have been implemented to mitigate this risk. Over the last two decades, intravascular imaging modalities have emerged in clinical studies to clarify how these therapies may affect the composition and burden of coronary plaques. Lipid-lowering agents, such as statins, ezetimibe, and proprotein convertase subtilisin/kexin type 9 inhibitors, were shown not only to reduce low-density lipoprotein levels and MACE but also to directly affect features of coronary plaque vulnerability. Studies have demonstrated that lipid-lowering therapy reduces the percentage of atheroma volume and number of macrophages and increases fibrous cap thickness. Future studies should answer the question of whether pharmacological plaque stabilization may be sufficient to mitigate the risk of MACE for selected groups of patients with atherosclerotic coronary disease.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
ObjectType-Review-3
content type line 23
ISSN:2077-0383
2077-0383
DOI:10.3390/jcm13113096