Journal
MOLECULAR NUTRITION & FOOD RESEARCH
Volume 64, Issue 5, Pages -Publisher
WILEY
DOI: 10.1002/mnfr.201900921
Keywords
pi-methyl histidine; amino acid metabolism; chicken; beef consumption; meat biomarkers; trimethylamine-N-oxide
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Funding
- BioNH call under the JPI initiative A Healthy Diet for a Healthy Life (JPI-HDHL)
- German Federal Ministry of Food and Agriculture (BMEL) through the Federal Office for Agriculture and Food (BLE) [2814ERA01E]
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Scope Common methods for food intake assessment are error-prone. Estimating food intake via metabolite biomarkers in blood/urine is challenged by inter-individual variation. Here, meat intake markers based on criteria defined within the FoodBAll consortium, including dose dependency, specificity, kinetics, and their ability to predict meat dose, are evaluated. Methods and results In two randomized human interventions, meat at different doses are consumed. Plasma concentrations of 100 analytes, including previously proposed meat intake markers, are determined at different time points up to 24 h after meat ingestion using targeted liquid chromatography-tandem mass spectrometry. Plasma concentrations of pi-methylhistidine (pi-M-His) correlated best with the chicken meat amount consumed even after 24 h (R-2 = 0.96). Both, anserine and pi-M-His show first-order elimination kinetics, irrespective of meat dose (t(1/2) is 1.4 and 5.9 h, respectively). Surprisingly, pi-M-His best predicted the amount of beef consumed, albeit at lower concentrations. Furthermore, trimethylamine-N-oxide (TMAO) increases only after beef, while dimethylglycine only after chicken consumption. The lack of baseline concentrations for pi-M-His and anserine is likely the strength of these compounds to predict meat dose. Conclusion Quantitative assessment of meat intake within 24 h is most accurate with pi-M-His, whereas TMAO and dimethylglycine best discriminate between chicken and beef.
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