» Articles » PMID: 33163716

Fibroblast Growth Factor 23 and Mortality Among Prevalent Hemodialysis Patients in the Japan Dialysis Outcomes and Practice Patterns Study

Overview
Journal Kidney Int Rep
Publisher Elsevier
Specialty Nephrology
Date 2020 Nov 9
PMID 33163716
Citations 12
Authors
Affiliations
Soon will be listed here.
Abstract

Introduction: Elevated fibroblast growth factor 23 (FGF23) levels have been strongly associated with mortality in the predialysis and incident hemodialysis populations, but few studies have examined this relationship in a large cohort of prevalent hemodialysis patients and in particular among persons with high dialysis vintage. To address this, we analyzed data from the Japan Dialysis Outcomes and Practice Patterns Study (J-DOPPS).

Methods: We included 1122 prevalent hemodialysis patients from the J-DOPPS phase 5 (2012-2015) who had FGF23 measurements. We evaluated the association of FGF23 levels with all-cause mortality and cardiovascular composite outcome using Cox regression adjusted for potential confounders.

Results: At study enrollment, median dialysis vintage was 5.8 years (interquartile range, 2.7-12.4 years) and median FGF23 level was 2113 pg/ml (interquartile range, 583-6880 pg/ml). During 3-year follow-up, 154 of the 1122 participants died. In adjusted analyses, higher FGF23 was associated with a greater hazard of death (hazard ratio per doubling of FGF23, 1.12; 95% confidence interval, 1.03-1.21); however, the association became weaker as the dialysis vintage increased and finally disappeared in the highest tertile (>9.4 years). Similar patterns of effect modification by dialysis vintage were observed for cardiovascular composite outcome and in time-dependent models.

Conclusion: Elevated FGF23 was associated with mortality and cardiovascular events in prevalent hemodialysis patients, but the association was attenuated at longer dialysis vintages. This novel finding suggests that long-term hemodialysis patients may be less susceptible to the detrimental effects of FGF23 or correlated biological processes, and additional studies are needed to gain understanding of these possibilities.

Citing Articles

PTH may predict early mortality in incident patients on hemodialysis: results from a large cohort.

Aquino H, Canziani M, Barra A, Roque-da-Silva A, Strogoff-de-Matos J, Dalboni M Int Urol Nephrol. 2024; 57(2):545-551.

PMID: 39222240 DOI: 10.1007/s11255-024-04188-1.


Roles of Parathyroid Hormone and Fibroblast Growth Factor 23 in Advanced Chronic Kidney Disease.

Nakagawa Y, Komaba H Endocrinol Metab (Seoul). 2024; 39(3):407-415.

PMID: 38752265 PMC: 11220210. DOI: 10.3803/EnM.2024.1978.


Diabetes mellitus modifies the association between chronic kidney disease-mineral and bone disorder biomarkers and aortic stiffness in peritoneal dialysis patients.

Huang H, Hsu B, Wang C, Tsai J, Chen Y, Hung S Sci Rep. 2024; 14(1):4554.

PMID: 38402283 PMC: 10894213. DOI: 10.1038/s41598-024-55364-3.


Fibroblast growth factor-23 and cardiovascular disease among prevalent hemodialysis patients focusing on residual kidney function.

Kee Y, Jeon H, Oh J, Cho A, Lee Y, Yoon J Front Endocrinol (Lausanne). 2023; 14:1099975.

PMID: 37501787 PMC: 10368752. DOI: 10.3389/fendo.2023.1099975.


FGF23 and klotho at the intersection of kidney and cardiovascular disease.

Edmonston D, Grabner A, Wolf M Nat Rev Cardiol. 2023; 21(1):11-24.

PMID: 37443358 DOI: 10.1038/s41569-023-00903-0.


References
1.
Nowak A, Friedrich B, Artunc F, Serra A, Breidthardt T, Twerenbold R . Prognostic value and link to atrial fibrillation of soluble Klotho and FGF23 in hemodialysis patients. PLoS One. 2014; 9(7):e100688. PMC: 4084634. DOI: 10.1371/journal.pone.0100688. View

2.
Pisoni R, Gillespie B, Dickinson D, Chen K, Kutner M, Wolfe R . The Dialysis Outcomes and Practice Patterns Study (DOPPS): design, data elements, and methodology. Am J Kidney Dis. 2004; 44(5 Suppl 2):7-15. DOI: 10.1053/j.ajkd.2004.08.005. View

3.
Fliser D, Kollerits B, Neyer U, Ankerst D, Lhotta K, Lingenhel A . Fibroblast growth factor 23 (FGF23) predicts progression of chronic kidney disease: the Mild to Moderate Kidney Disease (MMKD) Study. J Am Soc Nephrol. 2007; 18(9):2600-8. DOI: 10.1681/ASN.2006080936. View

4.
Souma N, Isakova T, Lipiszko D, Sacco R, Elkind M, DeRosa J . Fibroblast Growth Factor 23 and Cause-Specific Mortality in the General Population: The Northern Manhattan Study. J Clin Endocrinol Metab. 2016; 101(10):3779-3786. PMC: 5052338. DOI: 10.1210/jc.2016-2215. View

5.
Scialla J, Parekh R, Eustace J, Astor B, Plantinga L, Jaar B . Race, Mineral Homeostasis and Mortality in Patients with End-Stage Renal Disease on Dialysis. Am J Nephrol. 2015; 42(1):25-34. PMC: 4562864. DOI: 10.1159/000438999. View