Abstract
The development of robust biomarkers of consumption would improve the classification of participants with regard to their dietary exposure. In addition, validation of them in free-living individuals remains an important challenge. The aim of this study is to assess wine intake biomarkers using an NMR metabolomic approach to measure the utility of these biomarkers in a wine interventional study (WIS, n = 56) and also to evaluate them in a free-living individuals (PREDIMED study, n = 91). Nine metabolites showed a significantly higher presence in urinary excretion in WIS after wine intake: five food metabolome metabolites (tartrate, ethyl glucuronide [EtG], 2,3-butanediol, mannitol, and ethanol); one related to the endogenous response to wine exposure (3-methyl-2-oxovalerate) and three unidentified compounds. Receiver operating characteristic (ROC) curve for each single metabolite were evaluated and exhibited areas under the curves (AUC) between 67.4 and 86.3 % when they were evaluated individually. Then, a logistic regression model was fitted to generate a combined-biomarkers model using these metabolites. The model generated which included tartrate-EtG, showed an AUC of 90.7 % in WIS. Similarly, the AUC in the PREDIMED study was 92.4 %. Results showed that a model combining tartrate-EtG is more useful for evaluating exposure to wine than single biomarkers, both in interventional studies and epidemiological data. To our knowledge, this is the first time that a combined-biomarker model using an NMR platform in wine biomarkers’ research has been generated and reproduced in a free-living population.
This is a preview of subscription content, access via your institution.




Abbreviations
- AUC:
-
Area under the curve
- CI:
-
Confidence interval
- COSY:
-
Correlation spectroscopy
- d:
-
Doublet
- EtG:
-
Ethyl glucuronide
- FFQ:
-
Food frequency questionnaires
- FM:
-
Food metabolome
- IQR:
-
Interquartile range
- J:
-
J-coupling
- m:
-
Multiplet
- ROC:
-
Receiver operating characteristic
- s:
-
Singlet
- t:
-
Triplet
- U:
-
Unassigned compound
- WIS:
-
Wine interventional study
References
Bahado-Singh, R. O., Akolekar, R., Mandal, R., et al. (2012). Metabolomics and first-trimester prediction of early-onset preeclampsia. The journal of maternal-fetal & neonatal medicine, 25, 1840–1847.
Bartolomé, B., Monagas, M., Garrido, I., et al. (2010). Almond (Prunus dulcis (Mill.) D.A. Webb) polyphenols: From chemical characterization to targeted analysis of phenolic metabolites in humans. Archives of Biochemistry and Biophysics, 501, 124–133.
Beck, O., Stephanson, N., Böttcher, M., et al. (2007). Biomarkers to disclose recent intake of alcohol: potential of 5-hydroxytryptophol glucuronide testing using new direct UPLC-tandem MS and ELISA methods. Alcohol and Alcoholism, 42, 321–325.
Bemrah, N., Vin, K., Sirot, V., et al. (2012). Assessment of dietary exposure to annatto (E160b), nitrites (E249-250), sulphites (E220-228) and tartaric acid (E334) in the French population: the second French total diet study. Food additives and contaminants Part A, 29, 875–885.
Chiva-Blanch, G., Urpi-Sarda, M., Llorach, R., et al. (2012). Differential effects of polyphenols and alcohol of red wine on the expression of adhesion molecules and inflammatory cytokines related to atherosclerosis: a randomized clinical trial. American Journal of Clinical Nutrition, 95, 326–334.
Darias-Martín, J. J., Rodríguez, O., Díaz, E., & Lamuela-Raventós, R. M. (2000). Effect of skin contact on the antioxidant phenolics in white wine. Food Chemistry, 71, 483–487.
Donovan, J. L., Kasim-Karakas, S., German, J. B., & Waterhouse, A. L. (2002). Urinary excretion of catechin metabolites by human subjects after red wine consumption. British Journal of Nutrition, 87, 31–37.
Estruch, R. (2000). Wine and cardiovascular disease. Food Research International, 33, 219–226.
Estruch, R., Martínez-González, M. A., Corella, D., et al. (2006). Effects of a Mediterranean-style diet on cardiovascular risk factors: a randomized trial. Annals of Internal Medicine, 145, 1–11.
Estruch, R., Ros, E., Salas-Salvadó, J., et al. (2013). Primary prevention of cardiovascular disease with a Mediterranean diet. New England Journal of Medicine, 368, 1279–1290.
Fernández-Ballart, J. D., Piñol, J. L., Zazpe, I., et al. (2010). Relative validity of a semi-quantitative food-frequency questionnaire in an elderly Mediterranean population of Spain. British Journal of Nutrition, 103, 1808–1816.
Garcia-Aloy, M., Llorach, R., Urpi-Sarda, M., et al. (2014). Nutrimetabolomics fingerprinting to identify biomarkers of bread exposure in a free-living population from the PREDIMED study cohort. Metabolomics, 1–11. doi:10.1007/s11306-014-0682-6.
Gonthier, M.-P., Cheynier, V., Donovan, J. L., et al. (2003). Microbial Aromatic Acid Metabolites Formed in the Gut Account for a Major Fraction of the Polyphenols Excreted in Urine of Rats Fed Red Wine Polyphenols. Journal of Nutrition, 133, 461–467.
Heinzmann, S. S., Brown, I. J., Chan, Q., et al. (2010). Metabolic profiling strategy for discovery of nutritional biomarkers: proline betaine as a marker of citrus consumption. American Journal of Clinical Nutrition, 92, 436–443.
Heinzmann, S. S., Merrifield, C. A., Rezzi, S., et al. (2011). Stability and Robustness of Human Metabolic Phenotypes in Response to Sequential Food Challenges. Journal of Proteome Research, 11, 643–655.
Helander, A., Böttcher, M., Fehr, C., Dahmen, N., & Beck, O. (2009). Detection Times for Urinary Ethyl Glucuronide and Ethyl Sulfate in Heavy Drinkers during Alcohol Detoxification. Alcohol and Alcoholism, 44, 55–61.
Høiseth, G., Bernard, J. P., Karinen, R., et al. (2007). A pharmacokinetic study of ethyl glucuronide in blood and urine: Applications to forensic toxicology. Forensic Science International, 172, 119–124.
Hwa, H.-L., Kuo, W.-H., Chang, L.-Y., et al. (2008). Prediction of breast cancer and lymph node metastatic status with tumour markers using logistic regression models. J Eval Clin Pract, 14, 275–280.
Jacobs, D. M., Deltimple, N., van Velzen, E., et al. (2008). (1)H NMR metabolite profiling of feces as a tool to assess the impact of nutrition on the human microbiome. NMR in Biomedicine, 21, 615–626.
Lande, R. G., & Marin, B. (2013). A Comparison of Two Alcohol Biomarkers in Clinical Practice: Ethyl Glucuronide Versus Ethyl Sulfate. Journal of Addictive Diseases, 32, 288–292.
Liu, S. Q. (2002). Malolactic fermentation in wine – beyond deacidification. Journal of Applied Microbiology, 92, 589–601.
Llorach, R., Garcia-Aloy, M., Tulipani, S., Vazquez-Fresno, R., & Andres-Lacueva, C. (2012). Nutrimetabolomic Strategies To Develop New Biomarkers of Intake and Health Effects. Journal of Agriculture and Food Chemistry, 60, 8797–8808.
Lloyd, A. J., Beckmann, M., Haldar, S., et al. (2013). Data-driven strategy for the discovery of potential urinary biomarkers of habitual dietary exposure. American Journal of Clinical Nutrition, 97, 377–389.
López-Tamames, E., Puig-Deu, M. A., Teixeira, E., & Buxaderas, S. (1996). Organic acids, sugars, and glycerol content in white winemaking products determined by HPLC: Relationship to climate and varietal factors. American Journal of Enology and Viticulture, 47, 193–198.
Lord, R. S., Burdette, C. K., & Bralley, J. A. (2005). Significance of Urinary Tartaric Acid. Clinical Chemistry, 51, 672–673.
Mennen, L. I., Sapinho, D., Ito, H., et al. (2006). Urinary flavonoids and phenolic acids as biomarkers of intake for polyphenol-rich foods. British Journal of Nutrition, 96, 191–198.
Menni, C., Zhai, G., Macgregor, A., et al. (2013). Targeted metabolomics profiles are strongly correlated with nutritional patterns in women. Metabolomics, 9, 506–514.
Murabito, J. M., Keyes, M. J., Guo, C.-Y., et al. (2009). Cross-sectional relations of multiple inflammatory biomarkers to peripheral arterial disease: The Framingham Offspring Study. Atherosclerosis, 203, 509–514.
O’Gorman, A., Gibbons, H., & Brennan, L. (2013). Metabolomics in the identification of biomarkers of dietary intake. Computational and Structural Biotechnology Journal, 4, e201301004. doi:10.5936/csbj.201301004.
Odunsi, K., Wollman, R. M., Ambrosone, C. B., et al. (2005). Detection of epithelial ovarian cancer using 1H-NMR-based metabonomics. International Journal of Cancer, 113, 782–788.
O’Sullivan, A., Gibney, M. J., & Brennan, L. (2011). Dietary intake patterns are reflected in metabolomic profiles: potential role in dietary assessment studies. American Journal of Clinical Nutrition, 93, 314–321.
Pérez-Magariño, S., & González-San José, M. L. (2004). Evolution of Flavanols, Anthocyanins, and Their Derivatives during the Aging of Red Wines Elaborated from Grapes Harvested at Different Stages of Ripening. Journal of Agriculture and Food Chemistry, 52, 1181–1189.
Pujos-Guillot, E., Hubert, J., Martin, J.-F., et al. (2013). Mass Spectrometry-based Metabolomics for the Discovery of Biomarkers of Fruit and Vegetable Intake: Citrus Fruit as a Case Study. Journal of Proteome Research, 12, 1645–1659.
Recamales, Á. F., Sayago, A., González-Miret, M. L., & Hernanz, D. (2006). The effect of time and storage conditions on the phenolic composition and colour of white wine. Food Research International, 39, 220–229.
Robin, X., Turck, N., Hainard, A., et al. (2011). pROC: an open-source package for R and S+ to analyze and compare ROC curves. BMC Bioinformatics, 12, 77.
Roowi, S., Stalmach, A., Mullen, W., et al. (2009). Green Tea Flavan-3-ols: Colonic Degradation and Urinary Excretion of Catabolites by Humans. Journal of Agriculture and Food Chemistry, 58, 1296–1304.
Roussis, I. G., Lambropoulos, I., & Papadopoulou, D. (2005). Inhibition of the decline of volatile esters and terpenols during oxidative storage of Muscat-white and Xinomavro-red wine by caffeic acid and N-acetyl-cysteine. Food Chemistry, 93, 485–492.
Salinas, M. R., Garijo, J., Pardo, F., Zalacain, A., & Alonso, G. L. (2005). Influence of prefermentative maceration temperature on the colour and the phenolic and volatile composition of rosé wines. Journal of the Science of Food and Agriculture, 85, 1527–1536.
Scalbert, A., Brennan, L., Manach, C., et al. (2014). The food metabolome: a window over dietary exposure. American Journal of Clinical Nutrition, 99, 1286–1308.
Simonetti, P., Gardana, C., & Pietta, P. (2001). Caffeic acid as biomarker of red wine intake. Methods in Enzymology, 335, 122–130.
Son, H.-S., Hwang, G.-S., Kim, K. M., et al. (2009). Metabolomic Studies on Geographical Grapes and Their Wines Using 1H NMR Analysis Coupled with Multivariate Statistics. Journal of Agriculture and Food Chemistry, 57, 1481–1490.
Son, H. S., Kim, K. M., van den Berg, F., et al. (2008). 1H nuclear magnetic resonance-based metabolomic characterization of wines by grape varieties and production areas. Journal of Agriculture and Food Chemistry, 56, 8007–8016.
Sousa, S. A. A., Magalhães, A., & Ferreira, M. M. C. (2013). Optimized bucketing for NMR spectra: Three case studies. Chemometrics and Intelligent Laborary Systems, 122, 93–102.
Stalmach, A., Edwards, C. A., Wightman, J. D., & Crozier, A. (2013). Colonic catabolism of dietary phenolic and polyphenolic compounds from Concord grape juice. Food & Function, 4, 52–62.
Teissedre, P.-L., & Landrault, N. (2000). Wine phenolics: contribution to dietary intake and bioavailability. Food Research International, 33, 461–467.
Urpi-Sarda, M., Garrido, I., Monagas, M., et al. (2009a). Profile of Plasma and Urine Metabolites after the Intake of Almond [Prunus dulcis (Mill.) D.A. Webb] Polyphenols in Humans. Journal of Agriculture and Food Chemistry, 57, 10134–10142.
Urpi-Sarda, M., Monagas, M., Khan, N., et al. (2009b). Epicatechin, procyanidins, and phenolic microbial metabolites after cocoa intake in humans and rats. Analytical and Bioanalytical Chemistry, 394, 1545–1556.
van Dorsten, F. A., Grün, C. H., van Velzen, E. J., et al. (2010). The metabolic fate of red wine and grape juice polyphenols in humans assessed by metabolomics. Molecular Nutrition & Food Research, 54, 897–908.
Vázquez-Fresno, R., Llorach, R., Alcaro, F., et al. (2012). (1) H-NMR-based metabolomic analysis of the effect of moderate wine consumption on subjects with cardiovascular risk factors. Electrophoresis, 33, 2345–2354.
Weinmann, W., Schaefer, P., Thierauf, A., Schreiber, A., & Wurst, F. M. (2004). Confirmatory analysis of ethylglucuronide in urine by liquid-chromatography/electrospray ionization/tandem mass spectrometry according to forensic guidelines. Journal of the American Society for Mass Spectrometry, 15, 188–193.
Wojcik, M. H., & Hawthorne, J. S. (2007). Sensitivity of commercial ethyl glucuronide (ETG) testing in screening for alcohol abstinence. Alcohol and Alcoholism, 42, 317–320.
Wurst, F. M., Dresen, S., Allen, J. P., et al. (2006). Ethyl sulphate: a direct ethanol metabolite reflecting recent alcohol consumption. Addiction, 101, 204–211.
Xia, J., Broadhurst, D., Wilson, M., & Wishart, D. (2013). Translational biomarker discovery in clinical metabolomics: an introductory tutorial. Metabolomics, 9, 280–299.
Xia, J., & Wishart, D. S. (2011). Web-based inference of biological patterns, functions and pathways from metabolomic data using MetaboAnalyst. Nature Protocols, 6, 743–760.
Zamora-Ros, R., Urpí-Sardà, M., Lamuela-Raventós, R. M., et al. (2009). Resveratrol metabolites in urine as a biomarker of wine intake in free-living subjects: The PREDIMED Study. Free Radical Biology and Medicine, 46, 1562–1566.
Acknowledgments
Supported by the Spanish National Grants from Ministry of Economy and Competitiveness (MINECO) and cofounded by FEDER (Fondo Europeo de Desarrollo Regional): AGL2006-14228-C03-02/ALI, AGL2009-13906-C02-01, AGL2010-10084-E, the CONSOLIDER INGENIO 2010 Programme, FUN-C-FOOD (CSD2007-063), CIberOBN, as well as PI13/01172 Project, (Plan N de I+D+i 2013-2016) by ISCII-Subdirección General de Evaluación y Fomento de la Investigación. We also thank the award of 2014SGR1566 from the Generalitat de Catalunya’s Agency AGAUR. R.V.-F, O.K, M.U.-S and R. Ll. would like to thank the FPI fellowship, the “Juan de la Cierva” and the “Ramon y Cajal” programmes of the Spanish Government and the Fondo Social Europeo. We thank the participants for their collaboration in the study.
Conflict of interest
All the authors declare no competing financial interest.
Compliance with ethical requirements
WIS study. The study received the ethical approval Institutional Review Board of the Hospital Clinic of Barcelona. All participants had signed an informed consent. This trial has been registered in the Current Controlled Trials in London, International Standard Randomized Controlled Trial Number (ISRCTN88720134).
PREDIMED study. The trial protocol was conducted according to the Declaration of Helsinki and was approved by the institutional review boards of all the centres involved. All participants had signed an informed consent. This trial has been registered in the Current Controlled Trials in London, International Standard Randomized Controlled Trial Number (ISRCTN35739639).
Author information
Authors and Affiliations
Corresponding authors
Electronic supplementary material
Below is the link to the electronic supplementary material.
Rights and permissions
About this article
Cite this article
Vázquez-Fresno, R., Llorach, R., Urpi-Sarda, M. et al. An NMR metabolomics approach reveals a combined-biomarkers model in a wine interventional trial with validation in free-living individuals of the PREDIMED study. Metabolomics 11, 797–806 (2015). https://doi.org/10.1007/s11306-014-0735-x
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s11306-014-0735-x