E-selectin and P-selectin are the major cell adhesion molecules expressed by endothelium cells. Higher circulating concentrations of E-selectin and P-selectin have been associated with the development of atherosclerotic plaque and an increase in cardiovascular disease (CVD) risk(Reference Galkina and Ley1). Reductions in E-selectin has previously been demonstrated after dietary substitution of saturated fatty acids (SFA) with monounsaturated fatty acids(Reference Vafeiadou, Weech and Altowaijri2). In vitro, replacement of SFA with unsaturated fatty acids (UFA) was found to decrease platelet sensitivity to a collagen receptor (Glycoprotein VI) selective agonist in the RISSCI-1 (Reading, Imperial, Surrey Saturated Fat Cholesterol Intervention) study(Reference Wong, Kriek and Koutsos3). The aim of this study was to determine whether the replacement of dietary SFA with UFA was also associated with differences in circulating cell adhesion molecule concentrations (intercellular adhesion molecule-1 (ICAM-1), vascular adhesion molecule-1 (VCAM-1), E-selectin and P-selectin) in men from the RISSCI-1 study.
Healthy men (n = 107), aged 30–65 y who participated in the RISSCI-1 study (ClinicalTrials.gov Identifier NCT03270527), consumed a high-SFA diet (33% total energy (TE) of total fat: SFA 18% TE and UFA 15% TE) for 4 weeks followed by a low-SFA diet (34% TE of total fat: SFA ≤10% TE and UFA 24% TE) for 4 weeks by the exchange of cooking oil, dairy, spreads and snacks high in SFA with those high in UFA. Concentrations of ICAM-1, VCAM-1, E-selectin and P-selectin were measured with the R&D Systems Human Adhesion Molecule Multiplex kit at baseline (week 0), at the end of a high-SFA diet (week 4) and at the end of a low-SFA diet (week 8). Wilcoxon signed-rank test was performed to determine differences in cell adhesion molecule concentrations from baseline to a high-SFA diet and then a low-SFA diet.
Relative to baseline, there was a 0.4% increase in plasma E-selectin during the high-SFA diet which decreased by 5.3% following the low-SFA diet (P = 0.008). Similarly, the changes in plasma P-selectin from baseline was 2.6% greater in response to the high-SFA diet which was found to be reduced by 4.3% following the low-SFA diet (P = 0.001). No significant changes were found in ICAM-1 and VCAM-1 concentrations following the high and low-SFA diets.
These findings provide evidence to suggest that the replacement of dietary SFA with UFA, in line with UK public health recommendations, may have a favourable effect on CVD risk by reducing the concentration of E-selectin and P-selectin.
Acknowledgements
RISSCI Study was funded by the BBSRC UK (reference: BB/P010245/1).