» Articles » PMID: 26491212

FGF23 in Acute and Chronic Illness

Overview
Journal Dis Markers
Publisher Wiley
Specialty Biochemistry
Date 2015 Oct 23
PMID 26491212
Citations 17
Authors
Affiliations
Soon will be listed here.
Abstract

FGF23 is a bone-derived phosphaturic hormone that may become a useful biomarker for the identification of high-risk patients in chronic but also acute disease. It rises early in chronic kidney disease and is strongly and independently associated with excess morbidity and mortality. Emerging data suggest that FGF23 is also elevated in different scenarios of acute illness. In this review, we give an overview on the role of this interesting disease marker and potential and proven interventional strategies and discuss a blueprint for future research.

Citing Articles

Non-Classical Effects of FGF23: Molecular and Clinical Features.

Martinez-Heredia L, Canelo-Moreno J, Garcia-Fontana B, Munoz-Torres M Int J Mol Sci. 2024; 25(9).

PMID: 38732094 PMC: 11084844. DOI: 10.3390/ijms25094875.


Acute liver injury induces expression of FGF23 in hepatocytes via orphan nuclear receptor ERRγ signaling.

Jung Y, Kim Y, Radhakrishnan K, Noh J, Choi J, Kim H Genes Dis. 2023; 10(3):679-682.

PMID: 37396546 PMC: 10308101. DOI: 10.1016/j.gendis.2022.06.003.


Raised FGF23 Correlates to Increased Mortality in Critical Illness, Independent of Vitamin D.

Thein O, Ali N, Mahida R, Dancer R, Ostermann M, Amrein K Biology (Basel). 2023; 12(2).

PMID: 36829583 PMC: 9953634. DOI: 10.3390/biology12020309.


Critical illness and bone metabolism: where are we now and what is next?.

Cai Y, Kang F, Wang X Eur J Med Res. 2022; 27(1):177.

PMID: 36104724 PMC: 9472372. DOI: 10.1186/s40001-022-00805-w.


Interdisciplinary management of FGF23-related phosphate wasting syndromes: a Consensus Statement on the evaluation, diagnosis and care of patients with X-linked hypophosphataemia.

Trombetti A, Al-Daghri N, Brandi M, Cannata-Andia J, Cavalier E, Chandran M Nat Rev Endocrinol. 2022; 18(6):366-384.

PMID: 35484227 DOI: 10.1038/s41574-022-00662-x.


References
1.
Ferrari S, Bonjour J, Rizzoli R . Fibroblast growth factor-23 relationship to dietary phosphate and renal phosphate handling in healthy young men. J Clin Endocrinol Metab. 2004; 90(3):1519-24. DOI: 10.1210/jc.2004-1039. View

2.
Koizumi M, Komaba H, Nakanishi S, Fujimori A, Fukagawa M . Cinacalcet treatment and serum FGF23 levels in haemodialysis patients with secondary hyperparathyroidism. Nephrol Dial Transplant. 2011; 27(2):784-90. DOI: 10.1093/ndt/gfr384. View

3.
Leaf D, Waikar S, Wolf M, Cremers S, Bhan I, Stern L . Dysregulated mineral metabolism in patients with acute kidney injury and risk of adverse outcomes. Clin Endocrinol (Oxf). 2013; 79(4):491-8. PMC: 3686895. DOI: 10.1111/cen.12172. View

4.
Larsson T, Marsell R, Schipani E, Ohlsson C, Ljunggren O, Tenenhouse H . Transgenic mice expressing fibroblast growth factor 23 under the control of the alpha1(I) collagen promoter exhibit growth retardation, osteomalacia, and disturbed phosphate homeostasis. Endocrinology. 2004; 145(7):3087-94. DOI: 10.1210/en.2003-1768. View

5.
Leaf D, Wolf M, Waikar S, Chase H, Christov M, Cremers S . FGF-23 levels in patients with AKI and risk of adverse outcomes. Clin J Am Soc Nephrol. 2012; 7(8):1217-23. PMC: 3408118. DOI: 10.2215/CJN.00550112. View