FGF21 Is a Sugar-Induced Hormone Associated with Sweet Intake and Preference in Humans

Research output: Contribution to journal › Journal article › Research › peer-review

Standard

FGF21 Is a Sugar-Induced Hormone Associated with Sweet Intake and Preference in Humans. / Søberg, Susanna; Sandholt, Camilla Helene; Z. Jespersen, Naja ; Toft, Ulla; L. Madsen, Anja ; von Holstein-Rathlou, Stephanie Ø; Grevengoed, Trisha Jean; Christensen, Karl Bang; Bredie, Wender; Potthoff, Matthew J; P. J. Solomon, Thomas; Schéele, Camilla Charlotte; Linneberg, Allan René; Jørgensen, Torben; Pedersen, Oluf Borbye; Hansen, Torben; Gillum, Matthew Paul; Grarup, Niels.

In: Cell Metabolism, Vol. 25, No. 5, 2017, p. 1045-1053.

Research output: Contribution to journal › Journal article › Research › peer-review

Harvard

Søberg, S, Sandholt, CH, Z. Jespersen, N, Toft, U, L. Madsen, A, von Holstein-Rathlou, SØ, Grevengoed, TJ, Christensen, KB, Bredie, W, Potthoff, MJ, P. J. Solomon, T, Schéele, CC, Linneberg, AR, Jørgensen, T, Pedersen, OB, Hansen, T, Gillum, MP & Grarup, N 2017, 'FGF21 Is a Sugar-Induced Hormone Associated with Sweet Intake and Preference in Humans', Cell Metabolism, vol. 25, no. 5, pp. 1045-1053. https://doi.org/10.1016/j.cmet.2017.04.009

APA

Søberg, S., Sandholt, C. H., Z. Jespersen, N., Toft, U., L. Madsen, A., von Holstein-Rathlou, S. Ø., Grevengoed, T. J., Christensen, K. B., Bredie, W., Potthoff, M. J., P. J. Solomon, T., Schéele, C. C., Linneberg, A. R., Jørgensen, T., Pedersen, O. B., Hansen, T., Gillum, M. P., & Grarup, N. (2017). FGF21 Is a Sugar-Induced Hormone Associated with Sweet Intake and Preference in Humans. Cell Metabolism, 25(5), 1045-1053. https://doi.org/10.1016/j.cmet.2017.04.009

Vancouver

Søberg S, Sandholt CH, Z. Jespersen N, Toft U, L. Madsen A, von Holstein-Rathlou SØ et al. FGF21 Is a Sugar-Induced Hormone Associated with Sweet Intake and Preference in Humans. Cell Metabolism. 2017;25(5):1045-1053. https://doi.org/10.1016/j.cmet.2017.04.009

Author

Søberg, Susanna ; Sandholt, Camilla Helene ; Z. Jespersen, Naja ; Toft, Ulla ; L. Madsen, Anja ; von Holstein-Rathlou, Stephanie Ø ; Grevengoed, Trisha Jean ; Christensen, Karl Bang ; Bredie, Wender ; Potthoff, Matthew J ; P. J. Solomon, Thomas ; Schéele, Camilla Charlotte ; Linneberg, Allan René ; Jørgensen, Torben ; Pedersen, Oluf Borbye ; Hansen, Torben ; Gillum, Matthew Paul ; Grarup, Niels. / FGF21 Is a Sugar-Induced Hormone Associated with Sweet Intake and Preference in Humans. In: Cell Metabolism. 2017 ; Vol. 25, No. 5. pp. 1045-1053.

Bibtex

@article{6a2b27d85d224f28ae945a57d6e27ea3,
title = "FGF21 Is a Sugar-Induced Hormone Associated with Sweet Intake and Preference in Humans",
abstract = "The liking and selective ingestion of palatablefoods—including sweets—is biologically controlled,and dysfunction of this regulation may promote unhealthyeating, obesity, and disease. The hepatokinefibroblast growth factor 21 (FGF21) reduces sweetconsumption in rodents and primates, whereasknockout of Fgf21 increases sugar consumption inmice. To investigate the relevance of these findingsin humans, we genotyped variants in the FGF21 locusin participants from the Danish Inter99 cohort(n = 6,514) and examined their relationship with adetailed range of food and ingestive behaviors. Thisrevealed statistically significant associations betweenFGF21 rs838133 and increased consumptionof candy, as well as nominal associations withincreased alcohol intake and daily smoking. Moreover,in a separate clinical study, plasma FGF21levels increased acutely after oral sucrose ingestionand were elevated in fasted sweet-disliking individuals.These data suggest the liver may secretehormones that influence eating behavior.",
author = "Susanna S{\o}berg and Sandholt, {Camilla Helene} and {Z. Jespersen}, Naja and Ulla Toft and {L. Madsen}, Anja and {von Holstein-Rathlou}, {Stephanie {\O}} and Grevengoed, {Trisha Jean} and Christensen, {Karl Bang} and Wender Bredie and Potthoff, {Matthew J} and {P. J. Solomon}, Thomas and Sch{\'e}ele, {Camilla Charlotte} and Linneberg, {Allan Ren{\'e}} and Torben J{\o}rgensen and Pedersen, {Oluf Borbye} and Torben Hansen and Gillum, {Matthew Paul} and Niels Grarup",
year = "2017",
doi = "10.1016/j.cmet.2017.04.009",
language = "English",
volume = "25",
pages = "1045--1053",
journal = "Cell Metabolism",
issn = "1550-4131",
publisher = "Cell Press",
number = "5",

}

RIS

TY - JOUR

T1 - FGF21 Is a Sugar-Induced Hormone Associated with Sweet Intake and Preference in Humans

AU - Søberg, Susanna

AU - Sandholt, Camilla Helene

AU - Z. Jespersen, Naja

AU - Toft, Ulla

AU - L. Madsen, Anja

AU - von Holstein-Rathlou, Stephanie Ø

AU - Grevengoed, Trisha Jean

AU - Christensen, Karl Bang

AU - Bredie, Wender

AU - Potthoff, Matthew J

AU - P. J. Solomon, Thomas

AU - Schéele, Camilla Charlotte

AU - Linneberg, Allan René

AU - Jørgensen, Torben

AU - Pedersen, Oluf Borbye

AU - Hansen, Torben

AU - Gillum, Matthew Paul

AU - Grarup, Niels

PY - 2017

Y1 - 2017

N2 - The liking and selective ingestion of palatablefoods—including sweets—is biologically controlled,and dysfunction of this regulation may promote unhealthyeating, obesity, and disease. The hepatokinefibroblast growth factor 21 (FGF21) reduces sweetconsumption in rodents and primates, whereasknockout of Fgf21 increases sugar consumption inmice. To investigate the relevance of these findingsin humans, we genotyped variants in the FGF21 locusin participants from the Danish Inter99 cohort(n = 6,514) and examined their relationship with adetailed range of food and ingestive behaviors. Thisrevealed statistically significant associations betweenFGF21 rs838133 and increased consumptionof candy, as well as nominal associations withincreased alcohol intake and daily smoking. Moreover,in a separate clinical study, plasma FGF21levels increased acutely after oral sucrose ingestionand were elevated in fasted sweet-disliking individuals.These data suggest the liver may secretehormones that influence eating behavior.

AB - The liking and selective ingestion of palatablefoods—including sweets—is biologically controlled,and dysfunction of this regulation may promote unhealthyeating, obesity, and disease. The hepatokinefibroblast growth factor 21 (FGF21) reduces sweetconsumption in rodents and primates, whereasknockout of Fgf21 increases sugar consumption inmice. To investigate the relevance of these findingsin humans, we genotyped variants in the FGF21 locusin participants from the Danish Inter99 cohort(n = 6,514) and examined their relationship with adetailed range of food and ingestive behaviors. Thisrevealed statistically significant associations betweenFGF21 rs838133 and increased consumptionof candy, as well as nominal associations withincreased alcohol intake and daily smoking. Moreover,in a separate clinical study, plasma FGF21levels increased acutely after oral sucrose ingestionand were elevated in fasted sweet-disliking individuals.These data suggest the liver may secretehormones that influence eating behavior.

U2 - 10.1016/j.cmet.2017.04.009

DO - 10.1016/j.cmet.2017.04.009

M3 - Journal article

C2 - 28467924

VL - 25

SP - 1045

EP - 1053

JO - Cell Metabolism

JF - Cell Metabolism

SN - 1550-4131

IS - 5

ER -

ID: 177184338