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1.
Mol Nutr Food Res ; 63(21): e1900677, 2019 11.
Article in English | MEDLINE | ID: mdl-31483113

ABSTRACT

Nutritional research is currently entering the field of personalized nutrition, to a large extent driven by major technological breakthroughs in analytical sciences and biocomputing. An efficient launching of the personalized approach depends on the ability of researchers to comprehensively monitor and characterize interindividual variability in the activity of the human gastrointestinal tract. This information is currently not available in such a form. This review therefore aims at identifying and discussing published data, providing evidence on interindividual variability in the processing of the major nutrients, i.e., protein, fat, carbohydrates, vitamins, and minerals, along the gastrointestinal tract, including oral processing, intestinal digestion, and absorption. Although interindividual variability is not a primary endpoint of most studies identified, a significant number of publications provides a wealth of information on this topic for each category of nutrients. This knowledge remains fragmented, however, and understanding the clinical relevance of most of the interindividual responses to food ingestion described in this review remains unclear. In that regard, this review has identified a gap and sets the base for future research addressing the issue of the interindividual variability in the response of the human organism to the ingestion of foods.


Subject(s)
Digestion/physiology , Gastrointestinal Tract/physiology , Amino Acids/pharmacokinetics , Biological Variation, Individual , Dietary Carbohydrates/pharmacokinetics , Dietary Fats/pharmacokinetics , Dietary Proteins/pharmacokinetics , Gastrointestinal Microbiome , Humans , Intestinal Absorption , Minerals/pharmacokinetics , Peptide Hydrolases/metabolism , Polymorphism, Genetic , Vitamins/pharmacokinetics
2.
Eur J Nutr ; 58(7): 2657-2667, 2019 Oct.
Article in English | MEDLINE | ID: mdl-30218140

ABSTRACT

PURPOSE: To determine the influence of meal composition on the glycaemic impact of different carbohydrate staples, and the accuracy of "adjusted calculated meal GI" compared with "measured mixed-meal GI". METHODS: In a non-blind randomized crossover trial fasted healthy subjects consumed four dinner-type mixed meals of realistic serving size comprising a carbohydrate staple of either mashed potato, pasta, rice or a glucose drink, combined with fixed portions of boiled carrots, poached salmon and herb sauce. Blood samples collected between 0 and 180 min were analysed for glucose and insulin concentrations. Adjusted calculated meal GI values were determined against a 50 g reference glucose drink, and compared to corresponding measured mixed-meal GIs, supplemented with data from four previous mixed-meal postprandial glycaemic response studies. RESULTS: The common carbohydrate staples, and the glucose drink, ingested as part of the salmon mixed meal induced a significantly lower post-prandial relative glycaemic response (RGR) and concurrent higher relative insulin response than the same amount of staple eaten alone. Adjusted calculated mixed-meal GI closely predicted measured mixed-meal GI in healthy subjects for 15 out of 17 mixed meals examined, showing the need to account for effects of fat and protein when predicting measured mixed-meal GI. Further, we showed the validity of using customarily consumed food amounts in mixed-meal postprandial RGR study design. CONCLUSIONS: Adjusted calculated mixed-meal GI appears a useful model to predict measured mixed-meal GI in healthy subjects and with further development and validation could aid nutrition research and rational design of healthy meals for personalized nutrition and particular consumer groups.


Subject(s)
Diet/methods , Dietary Carbohydrates/administration & dosage , Glucose/administration & dosage , Glycemic Index/physiology , Meals/physiology , Seafood , Blood Glucose/metabolism , Cross-Over Studies , Female , Healthy Volunteers , Humans , Insulin/blood , Male , Middle Aged , Postprandial Period , Reference Values
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