4.6 Article

Discovery of Urinary Biomarkers of Seaweed Intake Using Untargeted LC-MS Metabolomics in a Three-Way Cross-Over Human Study

期刊

METABOLITES
卷 11, 期 1, 页码 -

出版社

MDPI
DOI: 10.3390/metabo11010011

关键词

seaweed; biomarkers of intake; untargeted metabolomics

资金

  1. Joint Programming Initiative, A Healthy Diet for a Healthy Life through the project of the FoodBAll - BioNH call [529051002]
  2. China Scholarship Council [201709210013]
  3. Semper Ardens grant from the Carlsberg Foundation

向作者/读者索取更多资源

This study used an untargeted metabolomics approach to discover novel intake biomarkers for seaweeds, providing crucial information for assessing their health effects. By analyzing urine samples from participants who consumed Laminaria digitate and Undaria pinnatifida, four potential intake biomarkers were identified. Further research and validation are needed to assess the specificity and robustness of these biomarkers.
Seaweeds are a marine source rich in potentially bioactive components, and therefore have attracted attention since the middle of the twentieth century. Accurate and objective assessment of the intake of seaweeds to study their health effects is hampered by a lack of validated intake biomarkers. In this three-armed, randomized, cross-over study, an untargeted metabolomics approach was applied for discovering novel intake biomarkers. Twenty healthy participants (9 men and 11 women) were provided each of three test meals in a randomized order: 5 g of Laminaria digitate (LD), 5 g of Undaria pinnatifida (UP), or a control meal with energy-adjusted pea protein. Four urine samples and a 24 h pooled urine were collected along with blood samples at seven time-points. All samples were profiled by LC-ESI-QTOF-MS and the data were analyzed by univariate analysis and excretion kinetics to select putative intake biomarkers. In total, four intake biomarkers were selected from urine samples. They were identified as hydroxyl-dihydrocoumarin at Level III, loliolid glucuronide at level I, and isololiolid glucuronide at level II, while the last one remains unknown. Further identification and validation of these biomarkers by a cross-sectional study is essential to assess their specificity and robustness.

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