Abstract

Atherosclerosis, formerly considered a bland lipid storage disease, actually involves an ongoing inflammatory response. Recent advances in basic science have established a fundamental role for inflammation in mediating all stages of this disease from initiation through progression and, ultimately, the thrombotic complications of atherosclerosis. These new findings provide important links between risk factors and the mechanisms of atherogenesis. Clinical studies have shown that this emerging biology of inflammation in atherosclerosis applies directly to human patients. Elevation in markers of inflammation predicts outcomes of patients with acute coronary syndromes, independently of myocardial damage. In addition, low-grade chronic inflammation, as indicated by levels of the inflammatory marker C-reactive protein, prospectively defines risk of atherosclerotic complications, thus adding to prognostic information provided by traditional risk factors. Moreover, certain treatments that reduce coronary risk also limit inflammation. In the case of lipid lowering with statins, this anti-inflammatory effect does not appear to correlate with reduction in low-density lipoprotein levels. These new insights into inflammation in atherosclerosis not only increase our understanding of this disease, but also have practical clinical applications in risk stratification and targeting of therapy for this scourge of growing worldwide importance.

Keywords

InflammationMedicineDiseaseCoronary atherosclerosisCoronary artery diseaseSystemic inflammationRisk stratificationImmunologyC-reactive proteinRisk factorBioinformaticsCardiologyInternal medicine

MeSH Terms

AgedArteriosclerosisBiomarkersDisease ProgressionFemaleHumansInflammationInflammation MediatorsMaleMiddle AgedMyocardial IschemiaRisk Factors

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Publication Info

Year
2002
Type
review
Volume
105
Issue
9
Pages
1135-1143
Citations
7564
Access
Closed

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Cite This

Peter Libby, Paul M. Ridker, Attilio Maseri (2002). Inflammation and Atherosclerosis. Circulation , 105 (9) , 1135-1143. https://doi.org/10.1161/hc0902.104353

Identifiers

DOI
10.1161/hc0902.104353
PMID
11877368

Data Quality

Data completeness: 90%