The food metabolome: a window over dietary exposure123

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ABSTRACT

The food metabolome is defined as the part of the human metabolome directly derived from the digestion and biotransformation of foods and their constituents. With >25,000 compounds known in various foods, the food metabolome is extremely complex, with a composition varying widely according to the diet. By its very nature it represents a considerable and still largely unexploited source of novel dietary biomarkers that could be used to measure dietary exposures with a high level of detail and precision. Most dietary biomarkers currently have been identified on the basis of our knowledge of food compositions by using hypothesis-driven approaches. However, the rapid development of metabolomics resulting from the development of highly sensitive modern analytic instruments, the availability of metabolite databases, and progress in (bio)informatics has made agnostic approaches more attractive as shown by the recent identification of novel biomarkers of intakes for fruit, vegetables, beverages, meats, or complex diets. Moreover, examples also show how the scrutiny of the food metabolome can lead to the discovery of bioactive molecules and dietary factors associated with diseases. However, researchers still face hurdles, which slow progress and need to be resolved to bring this emerging field of research to maturity. These limits were discussed during the First International Workshop on the Food Metabolome held in Glasgow. Key recommendations made during the workshop included more coordination of efforts; development of new databases, software tools, and chemical libraries for the food metabolome; and shared repositories of metabolomic data. Once achieved, major progress can be expected toward a better understanding of the complex interactions between diet and human health.

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1

From the International Agency for Research on Cancer, Lyon, France (AS); University College Dublin, Dublin, Ireland (LB); the Institut National de la Recherche Agronomique, Clermont-Ferrand, France (CM); Clermont University, Clermont-Ferrand, France (CM); the University of Barcelona, Barcelona, Spain (CA-L); the University of Copenhagen, Frederiksberg, Denmark (LOD); Aberystwyth University, Aberystwyth, United Kingdom (JD); the University of California, Berkeley, CA (SMR); the University of Glasgow, Glasgow, United Kingdom (JJJvdH); and the University of Alberta, Edmonton, Canada (DSW).

2

Supported by the European Union (NutriTech FP7-KBBE-2011-5 grant 289511, EUROCAN FP7-KBBE-2010.2.4.1-2 grant 260791); the Danish Ministry of Science, Technology, and Innovation (for the UNIK Food, Fitness and Pharma Project); the French National Agency for Research (PhenoMeNEp ANR-10-ALIA-007); the Medical Research Council (MR/J010308/1); and the Spanish Ministerio de Economia y Competitividad (MINECO; project AGL2009-13906-C02-01) and by a Senior Visiting Scientist Award (to SMR) granted by the International Agency for Research on Cancer.

3

Address correspondence to A Scalbert, International Agency for Research on Cancer (IARC), Nutrition and Metabolism Section, Biomarkers Group, 150 Cours Albert Thomas, F-69372 Lyon Cedex 08, France. E-mail: [email protected].

4

Abbreviations used: dbNP, Nutritional Phenotype Database; ECMDB, E-coli Metabolome Database; FDR, false discovery rate; GC-MS, gas chromatography–mass spectrometry; HMDB, Human Metabolome Database; LC-MS, liquid chromatography–mass spectrometry; MS, mass spectrometry; MSI, Metabolomics Standards Initiative; MWAS, metabolome-wide association study; NMR, nuclear magnetic resonance spectroscopy; PCA, principal components analysis; PLS-DA, partial least-squares discriminant analysis; TMAO, trimethylamine oxide-N-oxide; YMDB, Yeast Metabolome Database.