ReviewChronic Inflammatory Diseases and Cardiovascular Risk: A Systematic Review
Section snippets
Methods
Studies were identified via a MEDLINE search using the following key words: “inflammation,” “chronic inflammatory diseases,” “atherosclerosis,” “coronary artery disease,” “coronary heart disease,” “ischemic heart disease,” and “myocardial infarction” (Fig. 1 and Appendix). Assessment for inclusion of studies was performed independently by two authors (I.R. and J.G.). Disagreements between reviewers were resolved by consensus. The last search was conducted in June 2010, and studies were screened
Systemic lupus erythematosus
SLE is a chronic inflammatory multisystem disease of unknown etiology (Table 1). It predominantly affects young women and occurs in ∼1 per 1000 white women and ∼1 per 250 African American women.13, 14, 15 Several studies have examined the relationship between SLE and cardiovascular endpoints. In a retrospective case-control study of 8742 patients with SLE, compared to 43,700 control subjects, Ward16 found significantly higher rates of admission for acute MI among patients with SLE. The effect
Mechanisms of disease: endothelial dysfunction and the inflammatory cascade endothelial dysfunction
The normal endothelium produces a vasodilatory response to ischemia. This response is largely mediated by nitric oxide (NO). Endothelial dysfunction refers to either a blunted vasodilatory response or paradoxical vasoconstriction.32 It is associated with diminished production or activity of NO as well as an imbalance of other relaxing and constricting factors such as angiotensin II, endothelin-1, and reactive oxygen species.32, 33, 34, 35 In addition to its vasomotor effects, endothelial
Disclosures
The authors have no conflicts of interest to disclose.
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