Journal of the Endocrine Society Journal Article

Defective FGFR1 Signaling Disrupts Glucose Regulation

September 10, 2024

Evidence From Humans With FGFR1 Mutations

 

Maria I Stamou, Crystal J Chiu, Shreya V Jadhav, Vanessa Ferreira Lopes, Kathryn B Salnikov, Lacey Plummer, Margaret F Lippincott, Hang Lee, Stephanie B Seminara, Ravikumar Balasubramanian
Journal of the Endocrine Society, Volume 8, Issue 8, August 2024, bvae118
https://doi.org/10.1210/jendso/bvae118

Abstract

Context

Activation of fibroblast growth factor receptor 1 (FGFR1) signaling improves the metabolic health of animals and humans, while inactivation leads to diabetes in mice. Direct human genetic evidence for the role of FGFR1 signaling in human metabolic health has not been fully established.

Objective

We hypothesized that individuals with naturally occurring FGFR1 variants (“experiments of nature”) will display glucose dysregulation.

Methods

Participants with rare FGFR1 variants and noncarrier controls. Using a recall-by-genotype approach, we examined the β-cell function and insulin sensitivity of 9 individuals with rare FGFR1 deleterious variants compared to 27 noncarrier controls, during a frequently sampled intravenous glucose tolerance test at the Reproductive Endocrine Unit and the Harvard Center for Reproductive Medicine, Massachusetts General Hospital. FGFR1-mutation carriers displayed higher β-cell function in the face of lower insulin sensitivity compared to controls.

Conclusion

These findings suggest that impaired FGFR1 signaling may contribute to an early insulin resistance phase of diabetes pathogenesis and support the candidacy of the FGFR1 signaling pathway as a therapeutic target for improving the human metabolic health.

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