Skip to main content

Advertisement

Log in

Hemodialysis is associated with higher serum FGF23 level when compared with peritoneal dialysis

  • Nephrology - Original Paper
  • Published:
International Urology and Nephrology Aims and scope Submit manuscript

Abstract

Background

Considering the growing relevance of fibroblast growth factor-23 (FGF23) and increased cardiovascular mortality in dialysis population, an analysis was performed to assess the influence of dialysis modality (peritoneal dialysis and hemodialysis) on level of FGF23.

Methods

A cross-sectional study was performed in 80 continuous ambulatory peritoneal dialysis (CAPD) and 65 hemodialysis (HD) patients without residual renal function. Levels of calcium, phosphate, parathyroid hormone and FGF23 were measured, and their correlations were analyzed. Data on demographics, dialysis modality and FGF23 level were also analyzed.

Results

A significant correlation was found between FGF23 and serum calcium, serum phosphate and dialysis vintage in dialysis patients. Level of FGF23 was significantly higher in hemodialysis patients than that in peritoneal dialysis population. Multivariable regression revealed that, compared to CAPD, hemodialysis was found to be a predictor for higher FGF23 level, which was independent of serum calcium and phosphate level (P < 0.05).

Conclusions

These findings demonstrate that FGF23 levels are significantly higher in hemodialysis patients than that in peritoneal dialysis patients. We demonstrate an important association between dialysis modality (HD vs CAPD) and higher FGF23, independent of classical determinants (serum calcium and phosphate level).

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2

Similar content being viewed by others

References

  1. Gutierrez OM, Mannstadt M, Isakova T, Rauh-Hain JA, Tamez H, Shah A, Smith K, Lee H, Thadhani R, Juppner H, Wolf M (2008) Fibroblast growth factor 23 and mortality among patients undergoing hemodialysis. N Engl J Med 359:584–592

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  2. Wolf M, Molnar MZ, Amaral AP, Czira ME, Rudas A, Ujszaszi A, Kiss I, Rosivall L, Kosa J, Lakatos P, Kovesdy CP, Mucsi I (2011) Elevated fibroblast growth factor 23 is a risk factor for kidney transplant loss and mortality. J Am Soc Nephrol 22:956–966

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  3. Parker BD, Schurgers LJ, Brandenburg VM, Christenson RH, Vermeer C, Ketteler M, Shlipak MG, Whooley MA, Ix JH (2010) The associations of fibroblast growth factor 23 and uncarboxylated matrix Gla protein with mortality in coronary artery disease: the Heart and Soul Study. Ann Intern Med 152:640–648

    Article  PubMed  PubMed Central  Google Scholar 

  4. Isakova T, Xie H, Yang W, Xie D, Anderson AH, Scialla J, Wahl P, Gutierrez OM, Steigerwalt S, He J, Schwartz S, Lo J, Ojo A, Sondheimer J, Hsu CY, Lash J, Leonard M, Kusek JW, Feldman HI, Wolf M (2011) Fibroblast growth factor 23 and risks of mortality and end-stage renal disease in patients with chronic kidney disease. JAMA 305:2432–2439

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  5. Isakova T, Xie H, Barchi-Chung A, Vargas G, Sowden N, Houston J, Wahl P, Lundquist A, Epstein M, Smith K, Contreras G, Ortega L, Lenz O, Briones P, Egbert P, Ikizler TA, Jueppner H, Wolf M (2011) Fibroblast growth factor 23 in patients undergoing peritoneal dialysis. Clin J Am Soc Nephrol 6:2688–2695

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  6. Couchoud C, Bolignano D, Nistor I, Jager KJ, Heaf J, Heimburger O, Van Biesen W, European Renal Best Practice (ERBP) Diabetes Guideline Development Group (2015) Dialysis modality choice in diabetic patients with end-stage kidney disease: a systematic review of the available evidence. Nephrol Dial Transplant 30(2):310–320

    Article  PubMed  Google Scholar 

  7. Vanholder R, Van Laecke S, Glorieux G (2008) The middle-molecule hypothesis 30 years after: lost and rediscovered in the universe of uremic toxicity? J Nephrol 21(2):146–160

    CAS  PubMed  Google Scholar 

  8. Moist LM, Port FK, Orzol SM, Yong EW, Ostbye T, Wolfe RA, Hulbert-Shearon T, Jones CA, Bloembergen WE (2000) Predictors of loss of residual renal function among new dialysis patients. J Am Soc Nephrol 11(3):556–564

    CAS  PubMed  Google Scholar 

  9. Suda T, Hiroshige K, Ohta T, Watanabe Y, Iwamoto M, Kanegae K, Ohtani A, Nakashima Y (2000) The contribution of residual renal function to overall nutritional status in chronic haemodialysis patients. Nephrol Dial Transplant 15(3):396–401

    Article  CAS  PubMed  Google Scholar 

  10. Bergstrom J, Heimburger O, Lindholm B (1998) Calculation of the protein equivalent of total nitrogen appearance from urea appearance: which formulas should be used? Perit Dial Int 18:467–473

    CAS  PubMed  Google Scholar 

  11. Sargent JA, Gotch FA (1979) Mass balance: a quantitative guide to clinical nutritional therapy. J Am Diet Assoc 75:547–555

    CAS  PubMed  Google Scholar 

  12. Jean G, Terrat J-C, Vanel T, Hurot J-M, Lorriaux C, Mayor B, Chazot C (2009) High levels of serum fibroblast growth factor (FGF)-23 are associated with increased mortality in long haemodialysis patients. Nephrol Dial Transplant 24:2792–2796

    Article  CAS  PubMed  Google Scholar 

  13. Larsson TE (2011) FGF23 beyond mineral metabolism. A bridge to cardiovascular disease. Clin J Am Soc Nephrol 6:2735–2737

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  14. Wolf M (2012) Update on fibroblast growth factor 23 in chronic kidney disease. Kidney Int 82(7):737–747

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  15. Larsson TE (2010) The role of FGF23 in CKD-MBD and cardiovascular disease: friend or foe? Nephrol Dial Transplant 25:1376–1381

    Article  CAS  PubMed  Google Scholar 

  16. Shimada T, Yamazaki Y, Takahashi M, Hasegawa H, Urakawa I, Oshima T, Ono K, Kakitani M, Tomizuka K, Fujita T, Fukumoto S, Yamashita T (2005) Vitamin D receptor-independent FGF23 actions in regulating phosphate and vitamin D metabolism. Am J Physiol Renal Physiol 289(5):F1088–F1095

    Article  CAS  PubMed  Google Scholar 

  17. Evenepoel P, Viaene L, Meijers B (2011) PTH, FGF23, and calcium: it takes three to tango? Kidney Int 80:1377

    Article  CAS  PubMed  Google Scholar 

  18. Liu S, Zhou J, Tang W, Jiang X, Rowe DW, Quarles LD (2006) Pathogenic role of Fgf23 in Hyp mice. Am J Physiol Endocrinol Metab 291:E38–E49

    Article  CAS  PubMed  Google Scholar 

  19. Vanholder R, Smet RD, Glorieux G, Dhondt A (2003) Survival of hemodialysis patients and uremic toxin removal. Artif Organs 27(3):218–223

    Article  CAS  PubMed  Google Scholar 

  20. Guo AH, Meng JZ, Li DD, Liu WY, Wang SX, Gao F, Jing Y, Jia FY, Ge YM (2011) Adsorptive dialysis for cleaning uremic middle molecular substances. J Clin Rehabil Tissue Eng Res 15(12):2261–2264

    CAS  Google Scholar 

  21. Yan JY, Zhang MF, Ni ZH, Yin Y, Zhu ML, Mou S, Wang Q, Fang W, Zhang WM, Yan YC, Qian JQ (2012) Association of fibroblast growth factor 23 with coronary artery calcification in patients with moderate and advanced stage chronic kidney diseases. Chin J Nephrol 28(5):355–360

    CAS  Google Scholar 

  22. Clark WR, Winchester JF (2003) Middle molecules and small-molecular-weight proteins in ESRD: properties and strategies for their removal. Adv Ren Replace Ther 10(4):270–278

    Article  PubMed  Google Scholar 

Download references

Acknowledgements

The authors thank all staffs in Peritoneal Dialysis center and Hemodialysis center in Peking University 3rd Hospital for sample collection and all the people (healthy volunteers and patients) who participated in the study. This work was funded by The National Natural Science Funds in China (Project 81100522). An abstract was presented in poster form at the 15th Congress for the International Society for Peritoneal Dialysis (ISPD); September, 2014, Madrid, Spain.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Shuhong Bi.

Ethics declarations

Conflict of interest

The authors have declared that they have no competing interests.

Ethical approval

All procedures performed in studies involving human participants were in accordance with the ethical standards of the Human Clinical Study Committee of Peking University Third Hospital.

Informed consent

Informed consent was obtained from all individual participants included in the study.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Bi, S., Liang, Y., Cheng, L. et al. Hemodialysis is associated with higher serum FGF23 level when compared with peritoneal dialysis. Int Urol Nephrol 49, 1653–1659 (2017). https://doi.org/10.1007/s11255-017-1605-z

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11255-017-1605-z

Keywords

Navigation