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Fibroblast growth factor 21 and fructose dynamics in humans

OBJECTIVE: Fructose consumption is a risk factor for metabolic disease. We recently demonstrated that fibroblast growth factor 21 (FGF21), a metabolic hormone involved in lipid and glucose metabolism, is acutely stimulated in humans by 75 g oral fructose, with peak levels occurring 2 h after consump...

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Autores principales: Migdal, A., Comte, S., Rodgers, M., Heineman, B., Flier, E. M., Herman, M., Dushay, J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6180711/
https://www.ncbi.nlm.nih.gov/pubmed/30338119
http://dx.doi.org/10.1002/osp4.295
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author Migdal, A.
Comte, S.
Rodgers, M.
Heineman, B.
Flier, E. M.
Herman, M.
Dushay, J.
author_facet Migdal, A.
Comte, S.
Rodgers, M.
Heineman, B.
Flier, E. M.
Herman, M.
Dushay, J.
author_sort Migdal, A.
collection PubMed
description OBJECTIVE: Fructose consumption is a risk factor for metabolic disease. We recently demonstrated that fibroblast growth factor 21 (FGF21), a metabolic hormone involved in lipid and glucose metabolism, is acutely stimulated in humans by 75 g oral fructose, with peak levels occurring 2 h after consumption. This study reports on the dose dependency and reproducibility of the FGF21 response to fructose. METHODS: Lean, healthy adults drank either five different doses of fructose dissolved in water, each separated by 2 weeks, or the same dose on three occasions, each separated by 1 week. RESULTS: Fibroblast growth factor 21 levels peaked at 2 h in a dose‐dependent manner. No significant increase in FGF21 was seen after consumption of 10 g fructose, while robust increases were seen after drinking solutions containing 30, 50 and 75 g. At 2 h, the minimal fold change of FGF21 was highest following a 75 g fructose drink, and all subjects demonstrated at least a doubling of FGF21 levels following consumption of this dose. CONCLUSIONS: The increase in FGF21 following an oral fructose challenge is dose dependent, with levels peaking at 2 h independent of dose. The FGF21 response to 75 g fructose is also highly reproducible within individuals. CLINICAL IMPLICATIONS: By demonstrating that the FGF21 response to fructose is dose dependent and reproducible, this study deepens current understanding of FGF21 fructose dynamics and physiology in humans. This is an important area of clinical interest given associations between fructose intake and a wide variety of metabolic derangements.
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spelling pubmed-61807112018-10-18 Fibroblast growth factor 21 and fructose dynamics in humans Migdal, A. Comte, S. Rodgers, M. Heineman, B. Flier, E. M. Herman, M. Dushay, J. Obes Sci Pract Original Articles OBJECTIVE: Fructose consumption is a risk factor for metabolic disease. We recently demonstrated that fibroblast growth factor 21 (FGF21), a metabolic hormone involved in lipid and glucose metabolism, is acutely stimulated in humans by 75 g oral fructose, with peak levels occurring 2 h after consumption. This study reports on the dose dependency and reproducibility of the FGF21 response to fructose. METHODS: Lean, healthy adults drank either five different doses of fructose dissolved in water, each separated by 2 weeks, or the same dose on three occasions, each separated by 1 week. RESULTS: Fibroblast growth factor 21 levels peaked at 2 h in a dose‐dependent manner. No significant increase in FGF21 was seen after consumption of 10 g fructose, while robust increases were seen after drinking solutions containing 30, 50 and 75 g. At 2 h, the minimal fold change of FGF21 was highest following a 75 g fructose drink, and all subjects demonstrated at least a doubling of FGF21 levels following consumption of this dose. CONCLUSIONS: The increase in FGF21 following an oral fructose challenge is dose dependent, with levels peaking at 2 h independent of dose. The FGF21 response to 75 g fructose is also highly reproducible within individuals. CLINICAL IMPLICATIONS: By demonstrating that the FGF21 response to fructose is dose dependent and reproducible, this study deepens current understanding of FGF21 fructose dynamics and physiology in humans. This is an important area of clinical interest given associations between fructose intake and a wide variety of metabolic derangements. John Wiley and Sons Inc. 2018-09-04 /pmc/articles/PMC6180711/ /pubmed/30338119 http://dx.doi.org/10.1002/osp4.295 Text en © 2018 The Authors. Obesity Science & Practice published by John Wiley & Sons Ltd, World Obesity and The Obesity Society. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Migdal, A.
Comte, S.
Rodgers, M.
Heineman, B.
Flier, E. M.
Herman, M.
Dushay, J.
Fibroblast growth factor 21 and fructose dynamics in humans
title Fibroblast growth factor 21 and fructose dynamics in humans
title_full Fibroblast growth factor 21 and fructose dynamics in humans
title_fullStr Fibroblast growth factor 21 and fructose dynamics in humans
title_full_unstemmed Fibroblast growth factor 21 and fructose dynamics in humans
title_short Fibroblast growth factor 21 and fructose dynamics in humans
title_sort fibroblast growth factor 21 and fructose dynamics in humans
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6180711/
https://www.ncbi.nlm.nih.gov/pubmed/30338119
http://dx.doi.org/10.1002/osp4.295
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