Plasma lipidomic profiles after a low and high glycemic load dietary pattern in a randomized controlled crossover feeding study

Background Dietary patterns low in glycemic load are associated with reduced risk of cardiometabolic diseases. Improvements in serum lipid concentrations may play a role in these observed associations. Objective We investigated how dietary patterns differing in glycemic load affect clinical lipid pa...

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Veröffentlicht in:Metabolomics 2020-12, Vol.16 (12), p.121-121, Article 121
Hauptverfasser: Dibay Moghadam, Sepideh, Navarro, Sandi L., Shojaie, Ali, Randolph, Timothy W., Bettcher, Lisa F., Le, Cynthia B., Hullar, Meredith A., Kratz, Mario, Neuhouser, Marian L., Lampe, Paul D., Raftery, Daniel, Lampe, Johanna W.
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Sprache:eng
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Zusammenfassung:Background Dietary patterns low in glycemic load are associated with reduced risk of cardiometabolic diseases. Improvements in serum lipid concentrations may play a role in these observed associations. Objective We investigated how dietary patterns differing in glycemic load affect clinical lipid panel measures and plasma lipidomics profiles. Methods In a crossover, controlled feeding study, 80 healthy participants (n = 40 men, n = 40 women), 18–45 y were randomized to receive low-glycemic load (LGL) or high glycemic load (HGL) diets for 28 days each with at least a 28-day washout period between controlled diets. Fasting plasma samples were collected at baseline and end of each diet period. Lipids on a clinical panel including total-, VLDL-, LDL-, and HDL-cholesterol and triglycerides were measured using an auto-analyzer. Lipidomics analysis using mass-spectrometry provided the concentrations of 863 species. Linear mixed models and lipid ontology enrichment analysis were implemented. Results Lipids from the clinical panel were not significantly different between diets. Univariate analysis showed that 67 species on the lipidomics panel, predominantly in the triacylglycerol class, were higher after the LGL diet compared to the HGL (FDR 
ISSN:1573-3882
1573-3890
DOI:10.1007/s11306-020-01746-3