Identifying the anti-inflammatory response to lipid lowering therapy: a position paper from the working group on atherosclerosis and vascular biology of the European Society of Cardiology.
Animals
Anti-Inflammatory Agents
/ therapeutic use
Atherosclerosis
/ blood
Biomarkers
/ blood
Dyslipidemias
/ blood
Humans
Hypolipidemic Agents
/ therapeutic use
Inflammation
/ blood
Inflammation Mediators
/ blood
Lipids
/ blood
PCSK9 Inhibitors
Proprotein Convertase 9
/ metabolism
Risk Factors
Serine Proteinase Inhibitors
/ therapeutic use
Treatment Outcome
Journal
Cardiovascular research
ISSN: 1755-3245
Titre abrégé: Cardiovasc Res
Pays: England
ID NLM: 0077427
Informations de publication
Date de publication:
01 01 2019
01 01 2019
Historique:
received:
09
08
2018
accepted:
04
12
2018
pubmed:
12
12
2018
medline:
30
1
2020
entrez:
12
12
2018
Statut:
ppublish
Résumé
Dysregulated lipid metabolism induces an inflammatory and immune response leading to atherosclerosis. Conversely, inflammation may alter lipid metabolism. Recent treatment strategies in secondary prevention of atherosclerosis support beneficial effects of both anti-inflammatory and lipid-lowering therapies beyond current targets. There is a controversy about the possibility that anti-inflammatory effects of lipid-lowering therapy may be either independent or not of a decrease in low-density lipoprotein cholesterol. In this Position Paper, we critically interpret and integrate the results obtained in both experimental and clinical studies on anti-inflammatory actions of lipid-lowering therapy and the mechanisms involved. We highlight that: (i) besides decreasing cholesterol through different mechanisms, most lipid-lowering therapies share anti-inflammatory and immunomodulatory properties, and the anti-inflammatory response to lipid-lowering may be relevant to predict the effect of treatment, (ii) using surrogates for both lipid metabolism and inflammation as biomarkers or vascular inflammation imaging in future studies may contribute to a better understanding of the relative importance of different mechanisms of action, and (iii) comparative studies of further lipid lowering, anti-inflammation and a combination of both are crucial to identify effects that are specific or shared for each treatment strategy.
Identifiants
pubmed: 30534957
pii: 5232523
doi: 10.1093/cvr/cvy293
pmc: PMC6302260
doi:
Substances chimiques
Anti-Inflammatory Agents
0
Biomarkers
0
Hypolipidemic Agents
0
Inflammation Mediators
0
Lipids
0
PCSK9 Inhibitors
0
Serine Proteinase Inhibitors
0
PCSK9 protein, human
EC 3.4.21.-
Proprotein Convertase 9
EC 3.4.21.-
Types de publication
Journal Article
Practice Guideline
Research Support, Non-U.S. Gov't
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
10-19Subventions
Organisme : British Heart Foundation
ID : PG/11/46/28979
Pays : United Kingdom
Organisme : British Heart Foundation
ID : PG/18/1/33430
Pays : United Kingdom
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