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FGF21 is an insulin-dependent postprandial hormone in adult humans

Samms, Ricardo J.; Lewis, Jo E.; Norton, Luke; Stephens, Francis B.; Gaffney, Christopher J.; Butterfield, Tony; Smith, Dennis; Cheng, Christine; Perfield, James W.; Adams, Andrew C.; Ebling, Francis J.P.; Tsintzas, Kostas

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Authors

Ricardo J. Samms

Jo E. Lewis

Luke Norton

Francis B. Stephens

Christopher J. Gaffney

Tony Butterfield

Dennis Smith

Christine Cheng

James W. Perfield

Andrew C. Adams

Francis J.P. Ebling

KOSTAS TSINTZAS kostas.tsintzas@nottingham.ac.uk
Professor of Human Physiology



Abstract

Context: Fibroblast growth factor 21 (FGF21) secretion has been shown to respond directly to carbohydrate consumption, with glucose, fructose and sucrose all reported to increase plasma levels of FGF21 in rodents and humans. However, carbohydrate consumption also results in secretion of insulin.
Objective: The aim of this study was to examine the combined and independent effects of hyperglycemia and hyperinsulinemia on total and bioactive FGF21 in the postprandial period in humans, and determine whether this effect is attenuated in conditions of altered insulin secretion and action.
Methods: Circulating glucose, insulin, total and bioactive FGF21 and fibroblast activation protein (FAPα) were measured in adults with and without type 2 diabetes (T2D) following an oral glucose tolerance test (OGTT), and under a series of insulin and glucose clamp conditions and following high fat diet in healthy adults.
Results: Circulating total and bioactive FGF21 levels responded acutely to OGTT, and their ratio was attenuated in T2D patients with reduced postprandial insulin response. The clamp studies revealed that insulin but not glucose accounts for the postprandial rise in FGF21. Finally, there was an attenuated rise in FGF21 in response to a high fat dietary intervention that is known to alter insulin-stimulated substrate utilization in metabolically active tissues.
Conclusions: Insulin rather than glucose per se increases total and bioactive FGF21 in the postprandial period in adult humans. Understanding the impact of T2D on bioactive FGF21 will have a significant effect upon the efficacy of therapeutic agents designed to target the FGF21 pathway.

Citation

Samms, R. J., Lewis, J. E., Norton, L., Stephens, F. B., Gaffney, C. J., Butterfield, T., …Tsintzas, K. (in press). FGF21 is an insulin-dependent postprandial hormone in adult humans. Journal of Clinical Endocrinology and Metabolism, https://doi.org/10.1210/jc.2017-01257

Journal Article Type Article
Acceptance Date Aug 1, 2017
Online Publication Date Aug 4, 2017
Deposit Date Aug 17, 2017
Publicly Available Date Aug 5, 2018
Journal Journal of Clinical Endocrinology & Metabolism
Electronic ISSN 0021-972X
Publisher Oxford University Press
Peer Reviewed Peer Reviewed
DOI https://doi.org/10.1210/jc.2017-01257
Public URL https://nottingham-repository.worktribe.com/output/876341
Publisher URL https://academic.oup.com/jcem/article/doi/10.1210/jc.2017-01257/4064265/FGF21-is-an-insulindependent-postprandial-hormone
Contract Date Aug 17, 2017

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