Different effects of red wine and gin consumption on inflammatory biomarkers of atherosclerosis: a prospective randomized crossover trial: Effects of wine on inflammatory markers
Background: No intervention studies have explored the anti-inflammatory effects of different alcoholic beverages on markers of atherosclerosis. We embarked on a randomized, crossover, single-blinded trial to evaluate the effects of wine and gin on inflammatory biomarkers of atherosclerosis. Methods...
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Veröffentlicht in: | Atherosclerosis 2004-07, Vol.175 (1), p.117-123 |
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Sprache: | eng |
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Zusammenfassung: | Background: No intervention studies have explored the anti-inflammatory effects of different alcoholic beverages on markers of atherosclerosis. We embarked on a randomized, crossover, single-blinded trial to evaluate the effects of wine and gin on inflammatory biomarkers of atherosclerosis.
Methods and results: Forty healthy men (mean age, 37.6
years) consumed 30
g ethanol per day as either wine or gin for 28
days. Before and after each intervention, we measured the expression of lymphocyte function-associated antigen 1 (LFA-1), Mac-1, very late activation antigen 4 (VLA-4), and monocyte chemoattractant protein (MCP-1) in monocytes, as well as the soluble vascular cell adhesion molecule-1 (VCAM-1), intercellular adhesion molecule-1 (ICAM-1), interleukin-1α (IL-1α), C-reactive protein (hs-CRP) and fibrinogen.
After either gin or wine consumption, plasma fibrinogen decreased by 5 and 9%, respectively, and cytokine IL-1α by 23 and 21%. The expression of LFA-1 (−27%), Mac-1 (−27%), VLA-4 (−32%) and MCP-1 (−46%) decreased significantly after wine, but not after gin. Wine reduced the serum concentrations of hs-CRP (−21%), VCAM-1 (−17%) and ICAM-1 (−9%).
Conclusions: Both wine and gin showed anti-inflammatory effects by reducing plasma fibrinogen and IL-1α levels. However, wine had the additional effect of decreasing hs-CRP, as well as monocyte and endothelial adhesion molecules. |
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ISSN: | 0021-9150 1879-1484 |
DOI: | 10.1016/j.atherosclerosis.2004.03.006 |