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

Overview
Journal J Clin Med
Specialty General Medicine
Date 2023 Feb 25
PMID 36836085
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Abstract

(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, -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 ( = 0.387) nor that of the femoral head ( 0.430). However, iFGF23 levels showed a significant negative association with the BMD of the lumbar spine ( 0.015) and that of the femoral neck ( = 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.

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References
1.
Jovanovich A, Buzkova P, Chonchol M, Robbins J, Fink H, de Boer I . Fibroblast growth factor 23, bone mineral density, and risk of hip fracture among older adults: the cardiovascular health study. J Clin Endocrinol Metab. 2013; 98(8):3323-31. PMC: 3733860. DOI: 10.1210/jc.2013-1152. View

2.
Isakova T, Xie H, Yang W, Xie D, Anderson A, Scialla J . Fibroblast growth factor 23 and risks of mortality and end-stage renal disease in patients with chronic kidney disease. JAMA. 2011; 305(23):2432-9. PMC: 3124770. DOI: 10.1001/jama.2011.826. View

3.
Bouma-de Krijger A, Vervloet M . Fibroblast growth factor 23: are we ready to use it in clinical practice?. J Nephrol. 2020; 33(3):509-527. PMC: 7220896. DOI: 10.1007/s40620-020-00715-2. View

4.
Tsai M, Leu J, Fang Y, Liou H . High Fibroblast Growth Factor 23 Levels Associated With Low Hemoglobin Levels in Patients With Chronic Kidney Disease Stages 3 and 4. Medicine (Baltimore). 2016; 95(11):e3049. PMC: 4839908. DOI: 10.1097/MD.0000000000003049. View

5.
Brandenburg V, Verhulst A, Babler A, DHaese P, Evenepoel P, Kaesler N . Sclerostin in chronic kidney disease-mineral bone disorder think first before you block it!. Nephrol Dial Transplant. 2018; 34(3):408-414. DOI: 10.1093/ndt/gfy129. View