Visceral adipose tissue is associated with changes in leptin, FGF-23 and vitamin D metabolism in chronic kidney disease

J Bone Miner ResPublished Cohort study

Authors' conclusion

Adipose tissue may contribute to altered vitamin D metabolism. This effect appeared primarily related to visceral adipose tissue and the progression towards increased fat in the viscera.

Study context

Population
Adults receiving hemodialysis not taking active vitamin D therapy26 at 1 year
Participants
30 adults
Outcome
Associations of change in VAT with FGF-23, leptin and vitamin D metabolism
Follow-up
1 year
Methodological detailscohort of clinical trial participants, longitudinal, VAT and subcutaneous adipose tissue (SAT) area by MDCT; vitamin D metabolites by mass spectroscopy; FGF-23, leptin, adiponectin by ELISA, Spearman correlation, Wilcoxon rank-sum tests and linear regression
  • Cohort of clinical trial participants
  • Longitudinal
  • VAT and SAT area by MDCT; vitamin D metabolites by mass spectroscopy; FGF-23, leptin, adiponectin by ELISA
  • Spearman correlation, Wilcoxon rank-sum tests and linear regression

Main finding

As reported in the abstract

  • Progression towards increased visceral fat (VSR) associated with increased FGF-23 and leptin and decline in 1,25(OH)2D3 to 25(OH)D3 ratio
  • Relative change in leptin and leptin to adiponectin ratio associated with change in FGF-23, controlling for baseline FGF-23 and PTH

Observational data: associations, not effects.

Original publication

Visceral adipose tissue is associated with changes in leptin, FGF-23 and vitamin D metabolism in chronic kidney disease. J Bone Miner Res. Published 16 March 2026. doi:10.1093/jbmr/zjag051

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