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Randomized Controlled Trial
. 2017 Sep 20;8(9):3209-3218.
doi: 10.1039/c7fo00684e.

Plasma metabolite abundances are associated with urinary enterolactone excretion in healthy participants on controlled diets

Affiliations
Randomized Controlled Trial

Plasma metabolite abundances are associated with urinary enterolactone excretion in healthy participants on controlled diets

Fayth L Miles et al. Food Funct. .

Abstract

Enterolignans, products of gut bacterial metabolism of plant lignans, have been associated with reduced risk of chronic diseases, but their association with other plasma metabolites is unknown. We examined plasma metabolite profiles according to urinary enterolignan excretion in a cross-sectional analysis using data from a randomized crossover, controlled feeding study. Eighty healthy adult males and females completed two 28-day feeding periods differing by glycemic load, refined carbohydrate, and fiber content. Lignan intake was calculated from food records using a polyphenol database. Targeted metabolomics was performed by LC-MS on plasma from fasting blood samples collected at the end of each feeding period. Enterolactone (ENL) and enterodiol, were measured in 24 h urine samples collected on the penultimate day of each study period using GC-MS. Linear mixed models were used to test the association between enterolignan excretion and metabolite abundances. Pathway analyses were conducted using the Global Test. Benjamini-Hochberg false discovery rate (FDR) was used to control for multiple testing. Of the metabolites assayed, 121 were detected in all samples. ENL excretion was associated positively with plasma hippuric acid and melatonin, and inversely with epinephrine, creatine, glycochenodeoxycholate, and glyceraldehyde (P < 0.05). Hippuric acid only satisfied the FDR of q < 0.1. END excretion was associated with myristic acid and glycine (q < 0.5). Two of 57 pathways tested were associated significantly with ENL, ubiquinone and terpenoid-quinone biosynthesis, and inositol phosphate metabolism. These results suggest a potential role for ENL or ENL-metabolizing gut bacteria in regulating plasma metabolites.

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Conflict of interest statement

Conflicts of Interest

The authors have no conflicts of interest to declare.

Figures

Figure 1
Figure 1
Scatter plot of dietary lignan intake and urinary enterolactone (ENL) excretion in 80 participants. Dietary intake (µmol/d) during the final seven days before urine collection was calculated using Phenol Explorer. ENL excretion was measured from 24-h urine samples collected at the end of the RG and WG diet periods. Plot shows the association between lignan intake and ENL during each feeding period (black diamond = refined grain (RG) diet, open circle= whole grain (WG) diet). There was no significant association between ENL excretion and dietary lignan intake when analyzed in a multiple linear regression model.

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