High C-Terminal Fibroblast Growth Factor-23, Intact Parathyroid Hormone, and Interleukin-6 as Determinants of

Yenny Kandarini1, Gede Wira Mahadita1, Sianny Herawati2

  • 1Department of Internal Medicine, Division of Nephrology and Hypertension, Udayana University Sanglah Hospital, Denpasar, Bali, Indonesia.

Insights

High levels of C-terminal fibroblast growth factor-23 (FGF-23), intact parathyroid hormone (iPTH), and interleukin-6 (IL-6) are linked to valvular calcification in chronic kidney disease patients on hemodialysis. These biomarkers can help determine calcification risk.

Area of Science:

  • Nephrology
  • Cardiology
  • Biochemistry

Background:

  • Cardiovascular disease (CVD) is the leading cause of mortality in chronic kidney disease-hemodialysis (CKD-HD) patients.
  • CVD in CKD-HD patients is frequently linked to mineral bone disorders (MBD), particularly vascular and valvular calcification.
  • Biomarkers such as C-terminal fibroblast growth factor-23 (FGF-23), intact parathyroid hormone (iPTH), and interleukin-6 (IL-6) are implicated in CKD-MBD, but their role in valvular calcification requires further investigation.

Purpose of the Study:

  • To investigate the association between elevated C-terminal FGF-23, iPTH, and IL-6 levels and the presence of valvular calcification.
  • To determine if these biomarkers can serve as determinants of valvular calcification in patients with CKD-MBD undergoing regular hemodialysis.

Main Methods:

  • An analytical cross-sectional study was conducted on CKD-HD patients aged 18-60 without prior CVD, malignancy, or diabetes.
  • C-terminal FGF-23, iPTH, and IL-6 were quantified using ELISA, chemiluminescent immunometric assay, and sandwich enzyme immunoassay, respectively.
  • Valvular calcification of the aortic and mitral valves was assessed via echocardiography, with data analyzed using Chi-squared/Fisher's exact tests and multivariate logistic regression.

Main Results:

  • Bivariate analysis revealed significant associations between C-terminal FGF-23 (PR=1.33), iPTH (PR=1.361), and IL-6 (PR=1.2) and valvular calcification.
  • Multivariate logistic regression indicated that high C-terminal FGF-23 (exp(B)=16.44), iPTH (exp(B)=33.312), and IL-6 (exp(B)=21.58) were significant determinants of valvular calcification.

Conclusions:

  • Elevated levels of C-terminal FGF-23, iPTH, and IL-6 are independently associated with valvular calcification in CKD-MBD patients on hemodialysis.
  • These biomarkers may play a crucial role in the development of valvular calcification in this patient population.
  • Further research is warranted to explore the therapeutic implications of targeting these biomarkers for preventing valvular calcification in CKD-HD patients.
Abstract

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