Soluble alpha‑klotho and 25‑hydroxivitamin D are not associated with brown adipose tissue metabolism in young healthy adults
Metadata
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Amaro Gahete, Francisco José; Vázquez Lorente, Héctor; Sánchez Delgado, Guillermo; Ruiz Ruiz, JonatanEditorial
Springer Nature
Materia
Klotho protein 25-Hydroxyvitamin D Ageing Brown adipose tissue
Date
2025-03-11Referencia bibliográfica
Amaro-Gahete, F.J., Vázquez-Lorente, H., Sanchez-Delgado, G. et al. Soluble alpha-klotho and 25-hydroxivitamin D are not associated with brown adipose tissue metabolism in young healthy adults. J Physiol Biochem (2025). https://doi.org/10.1007/s13105-025-01072-z
Sponsorship
Spanish Ministry of Economy and Competitiveness Instituto de Salud Carlos III (PI13/01393), PTA-12264, (DEP2016-79512-R); European Regional Development Funds (ERDF); Spanish Ministry of Education (FPU13/04365 and FPU14/04172); Fundación Iberoamericana de Nutrición (FINUT); Redes Temáticas de Investigación Cooperativa RETIC (Red SAMID RD16/0022); AstraZeneca HealthCare Foundation; University of Granada; Junta de Andalucía; Fundación Alfonso Martin Escudero; CIBEROBN, Centro de Investigación Biomédica en Red (CB22/03/00058); Instituto de Salud Carlos III; Ministerio de Ciencia e Innovación; Unión Europea – European Regional Development Fund; Universidad de Granada/CBUAAbstract
Background
Soluble Alpha-Klotho (S-αklotho) protein and 25-Hydroxyvitamin D (25-OH-D) have emerged as potential modulators for activating and recruiting Brown Adipose Tissue (BAT). The present study aimed to investigate whether circulating S-αklotho and 25-OH-D levels are related to BAT volume, 18Fluorine-Fluorodeoxyglucose (18F-FDG) uptake, and BAT radiodensity in young healthy adults.
Methods
A total of 128 participants (68% women) aged 18–25 years old participated in this cross-sectional study. Serum levels of S-αklotho were determined by a solid-phase sandwich enzyme-linked immunosorbent assay kit and 25-OH-D serum levels were analyzed using a competitive chemiluminescence immunoassay, both in blood samples collected after an overnight fast. All participants underwent a personalized cold exposure to determine their BAT volume, 18F-FDG uptake, and radiodensity, using a static positron emission tomography combined with computed tomography scan.
Results
After adjusting for multiple covariates, serum levels of S-αklotho (all R2 ≤ 0.228 and P ≥ 0.364), 25-OH-D as continuous (all R2 ≤ 0.242 and P ≥ 0.088) or by vitamin D status (all R2 ≤ 0.767 and P ≥ 0.061) were not associated with either BAT volume and 18F-FDG uptake, or BAT radiodensity.
Conclusion
Serum S-αklotho and 25-OH-D levels within the physiological range are not related to BAT-related variables in young healthy adults. Further studies are needed to fully understand the underlying mechanisms involved in BAT metabolism in humans. (ACTIBATE; ClinicalTrials.gov identifier: not applicable).