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Serum Intact Fibroblast Growth Factor 23 Levels Are Negatively Associated with Bone Mineral Density in Chronic Hemodialysis Patients.

Wen-Teng LeeYu-Wei FangMing-Chih ChenHung-Hsiang LiouChung-Jen LeeMing-Hsien Tsai
Published in: Journal of clinical medicine (2023)
(1) Background: Fibroblast growth factor 23 (FGF23) is predominantly secreted from bone and plays an important role in mineral balance in chronic kidney disease. However, the relationship between FGF23 and bone mineral density (BMD) in chronic hemodialysis (CHD) patients remains unclear. (2) Methods: This was a cross-sectional observational study that involved 43 stable outpatients on CHD. A linear regression model was used to determine risk factors for BMD. Measurements included serum hemoglobin, intact FGF23 (iFGF23), C-terminal FGF23 (cFGF23), sclerostin, Dickkopf-1, α -klotho, 1,25-hydroxyvitamin D, intact parathyroid hormone levels and dialysis profiles. (3) Results: Study participants had a mean age of 59.4 ± 12.3 years, and 65% were male. In the multivariable analysis, cFGF23 levels showed no significant associations with the BMD of the lumbar spine ( p = 0.387) nor that of the femoral head ( p = 0.430). However, iFGF23 levels showed a significant negative association with the BMD of the lumbar spine ( p = 0.015) and that of the femoral neck ( p = 0.037). (4) Conclusions: Among patients on CHD, higher serum iFGF23 levels, but not serum cFGF23 levels, were associated with lower BMD values of the lumbar spine and femoral neck. However, further research is required to validate our findings.
Keyphrases
  • bone mineral density
  • postmenopausal women
  • end stage renal disease
  • body composition
  • chronic kidney disease
  • ejection fraction
  • african american
  • patient reported outcomes
  • drug induced