Key result
Coronary artery disease was associated with significantly higher plasmatic levels of IL-15 (4.19 vs 2.48 pg/mL) and IL-15Rα compared to non-CAD patients, reflecting visceral adipose tissue distribution.
Why the study?
Are IL-15 and IL-15Rα levels associated with coronary artery disease and epicardial adipose tissue distribution?
Cross-Sectional (n=82)
No
Are IL-15 and IL-15Rα levels associated with coronary artery disease and epicardial adipose tissue distribution?
Absolute Event Rate: 4.19% vs 2.48%
p-value: p=0.01
Circulating levels of IL-15 and IL-15Rα are elevated in CAD patients and appear to reflect visceral adipose tissue distribution, with epicardial adipose tissue acting as a potential source.
Hypothesis-generating for IL-15 pathways in CAD adiposity; leaves open any clinical role pending prospective validation.
Interleukin-15 (IL-15) is a pro-inflammatory cytokine which signals via a specific alpha receptor subunit (IL-15Rα). Increased IL-15 level has been observed in cardiovascular patients and IL-15 immunoreactivity has been detected at vulnerable atherosclerotic plaques. Due to the association between adipose tissue distribution, inflammation and coronary artery disease (CAD), we quantified IL-15 and IL-15Rα in CAD patients with different adiposity and adipose tissue distribution and we evaluated whether epicardial adipose tissue (EAT), a visceral fat depot surrounding and infiltrating myocardium, may be a source of both molecules. IL-15 and IL-15Rα proteins were quantified by enzyme-linked immunosorbent assays. Gene expression of IL-15 and IL-15Rα in EAT depots was evaluated by one colour microarray platform. EAT thickness was measured by echocardiography. Plasmatic IL-15 and IL-15Rα levels were higher in CAD than non-CAD patients. After classification according to adipose tissue distribution, IL-15 was higher in CAD patients with increased abdominal adiposity. Increased level of IL-15Rα was observed both in CAD and non-CAD patients with increased abdominal fat. EAT was a source of IL-15 and IL-15Rα and their expression was higher in CAD patients with increased EAT thickness. In conclusion, our data suggest that circulating levels of IL-15 and IL-15Rα seem to reflect visceral distribution of adipose tissue and that EAT may be a potential source of both IL-15 and IL-15Rα. Future studies on the relationship between IL-15, visceral fat and characteristics of atherosclerotic plaques could help to better understand the complex biology of this cytokine.
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Dozio et al. (2014) conducted a cross-sectional in Coronary Artery Disease (n=82). Coronary Artery Disease vs. Non-CAD patients (undergoing valve replacement) was evaluated on Plasmatic level of IL-15 (pg/mL) (p=0.01). Coronary artery disease was associated with significantly higher plasmatic levels of IL-15 (4.19 vs 2.48 pg/mL) and IL-15Rα compared to non-CAD patients, reflecting visceral adipose tissue distribution.
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