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A lipidomic analysis approach to evaluate the response to cholesterol-lowering food intake
Authors:Ewa Szymańska  Ferdinand A. van Dorsten  Jorne Troost  Iryna Paliukhovich  Ewoud J. J. van Velzen  Margriet M. W. B. Hendriks  Elke A. Trautwein  John P. M. van Duynhoven  Rob J. Vreeken  Age K. Smilde
Affiliation:1. Netherlands Metabolomics Centre, Leiden, The Netherlands
2. Biosystems Data Analysis, Swammerdam Institute for Life Sciences, University of Amsterdam, Amsterdam, The Netherlands
3. Unilever R&D, Vlaardingen, The Netherlands
4. LACDR, Leiden University, Leiden, The Netherlands
5. Department of Metabolic and Endocrine Diseases, University Medical Center Utrecht, Utrecht, The Netherlands
6. Laboratory of Biophysics, Wageningen University, Wageningen, The Netherlands
Abstract:Plant sterols (PS) are well known to reduce serum levels of total cholesterol and LDL-cholesterol. Lipidomics potentially provides detailed information on a wide range of individual serum lipid metabolites, which may further add to our understanding of the biological effects of PS. In this study, lipidomics analysis was applied to serum samples from a placebo-controlled, parallel human intervention study (n?=?97) of 4-week consumption of two PS-enriched, yoghurt drinks differing in fat content (based on 0.1% vs. 1.5% dairy fat). A comprehensive data analysis strategy was developed and implemented to assess and compare effects of two different PS-treatments and placebo treatment. The combination of univariate and multivariate data analysis approaches allowed to show significant effects of PS intake on the serum lipidome, and helped to distinguish them from fat content and non-specific effects. The PS-enriched 0.1% dairy fat yoghurt drink had a stronger impact on the lipidome than the 1.5% dairy fat yoghurt drink, despite similar LDL-cholesterol lowering effects. The PS-enriched 0.1% dairy fat yoghurt drink reduced levels of several sphingomyelins which correlated well with the reduction in LDL-cholesterol and can be explained by co-localization of sphingomyelins and cholesterol on the surface of LDL lipoprotein. Statistically significant reductions in serum levels of two lysophosphatidylcholines (LPC(16:1), LPC(20:1)) and cholesteryl arachidonate may suggest reduced inflammation and atherogenic potential.
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