Prevalence of FGF23 elevation in patients with hypophosphatemia.

FGF23 hypophosphatemia prevalence tumor

Journal

Clinica chimica acta; international journal of clinical chemistry
ISSN: 1873-3492
Titre abrégé: Clin Chim Acta
Pays: Netherlands
ID NLM: 1302422

Informations de publication

Date de publication:
13 Jan 2024
Historique:
received: 26 11 2023
revised: 28 12 2023
accepted: 10 01 2024
medline: 16 1 2024
pubmed: 16 1 2024
entrez: 15 1 2024
Statut: aheadofprint

Résumé

To investigate the contribution of FGF23 in explaining the cases of hypophosphatemia observed in clinical practice, we aimed to determine for the first time the prevalence of FGF23 elevation in patients with hypophosphatemia and to describe the different mechanisms of FGF23-related hypophosphatemic disorders. We performed a prospective, observational, multicenter, cohort study of 260 patients with hypophosphatemia. Blood measurements (PTH, 1,25-dihydroxyvitamin D, bone alkaline phosphatase, 25-hydroxyvitamin D, and FGF23) were performed on a Liaison XL® (DiaSorin) analyzer. Primary elevation of FGF23 (> 95.4 pg/mL) was reported in 10.4% (95CI: 7.0-14.7) of patients (n=27) with hypophosphatemia, suggesting that at least 1 in 10 cases of hypophosphatemia was erroneously attributed to an etiology other than FGF23 elevation. Patients with elevated blood FGF23 were grouped according to the etiology of the FGF23 elevation. Thus, 10 patients had a renal pathology, chronic kidney disease or post-renal transplantation condition. The remaining patients (n=17) had the following etiologies: malignancies (n=9), benign pancreatic tumor (n=1), post-cardiac surgery (n=4), cirrhosis (n=2), and chronic obstructive pulmonary disease (n=1). In order to improve patient management, it seems essential to better integrate plasma FGF23 measurement into the routine evaluation of hypophosphatemia.

Sections du résumé

BACKGROUND AND AIMS OBJECTIVE
To investigate the contribution of FGF23 in explaining the cases of hypophosphatemia observed in clinical practice, we aimed to determine for the first time the prevalence of FGF23 elevation in patients with hypophosphatemia and to describe the different mechanisms of FGF23-related hypophosphatemic disorders.
MATERIALS AND METHODS METHODS
We performed a prospective, observational, multicenter, cohort study of 260 patients with hypophosphatemia. Blood measurements (PTH, 1,25-dihydroxyvitamin D, bone alkaline phosphatase, 25-hydroxyvitamin D, and FGF23) were performed on a Liaison XL® (DiaSorin) analyzer.
RESULTS RESULTS
Primary elevation of FGF23 (> 95.4 pg/mL) was reported in 10.4% (95CI: 7.0-14.7) of patients (n=27) with hypophosphatemia, suggesting that at least 1 in 10 cases of hypophosphatemia was erroneously attributed to an etiology other than FGF23 elevation. Patients with elevated blood FGF23 were grouped according to the etiology of the FGF23 elevation. Thus, 10 patients had a renal pathology, chronic kidney disease or post-renal transplantation condition. The remaining patients (n=17) had the following etiologies: malignancies (n=9), benign pancreatic tumor (n=1), post-cardiac surgery (n=4), cirrhosis (n=2), and chronic obstructive pulmonary disease (n=1).
CONCLUSION CONCLUSIONS
In order to improve patient management, it seems essential to better integrate plasma FGF23 measurement into the routine evaluation of hypophosphatemia.

Identifiants

pubmed: 38224930
pii: S0009-8981(24)00023-8
doi: 10.1016/j.cca.2024.117782
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

117782

Informations de copyright

Copyright © 2024 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Charlotte Oris (C)

Biochemistry and Molecular Genetics Department, CHU Clermont-Ferrand, 63000 Clermont-Ferrand, France; Clermont Auvergne University, CNRS, INSERM, iGReD, Clermont-Ferrand, France.

Alexandre Lautrette (A)

Department of Intensive Care Medicine, CHU Clermont-Ferrand, 63000 Clermont-Ferrand, France.

Aurore Dougé (A)

Department of Oncology, CHU Clermont-Ferrand, 63000 Clermont-Ferrand, France.

Farouk Bouraima (F)

Biochemistry and Molecular Genetics Department, CHU Clermont-Ferrand, 63000 Clermont-Ferrand, France.

Samy Kahouadji (S)

Biochemistry and Molecular Genetics Department, CHU Clermont-Ferrand, 63000 Clermont-Ferrand, France; Clermont Auvergne University, CNRS, INSERM, iGReD, Clermont-Ferrand, France.

Marie-Eva Pickering (ME)

Rheumatology Department, CHU Clermont-Ferrand, 63000 Clermont-Ferrand, France.

Cyril Garrouste (C)

Department of Nephrology, CHU Clermont-Ferrand, 63000 Clermont-Ferrand, France.

Johan Gagnière (J)

Department of Digestive and Hepatobiliary Surgery, CHU Clermont-Ferrand, 63000 Clermont-Ferrand, France.

Romain Guièze (R)

Department of Clinical Hematology, CHU Clermont-Ferrand, 63000 Clermont-Ferrand, France.

Nicolas D'Ostrevy (N)

Department of Cardiac Surgery, CHU Clermont-Ferrand, 63000 Clermont-Ferrand, France.

Emmanuel Futier (E)

Department of Perioperative Medicine, Anesthesia & Critical Care, CHU Clermont-Ferrand, 63000 Clermont-Ferrand, France.

Vincent Grobost (V)

Department of Internal Medicine, CHU Clermont-Ferrand, 63000 Clermont-Ferrand, France.

Anthony Buisson (A)

Department of Hepato-Gastroenterology, CHU Clermont-Ferrand, 63000 Clermont-Ferrand, France.

Marie Batisse (M)

Department of Oncology, Centre Jean Perrin, 63000 Clermont-Ferrand, France.

Jean-Baptiste Bouillon-Minois (JB)

Department of Emergency Medicine, CHU Clermont-Ferrand, 63000 Clermont-Ferrand, France.

Bruno Pereira (B)

Biostatistics unit (DRCI) Department, CHU Clermont-Ferrand, 63000 Clermont-Ferrand, France.

Julie Durif (J)

Biochemistry and Molecular Genetics Department, CHU Clermont-Ferrand, 63000 Clermont-Ferrand, France.

Vincent Sapin (V)

Biochemistry and Molecular Genetics Department, CHU Clermont-Ferrand, 63000 Clermont-Ferrand, France; Clermont Auvergne University, CNRS, INSERM, iGReD, Clermont-Ferrand, France.

Damien Bouvier (D)

Biochemistry and Molecular Genetics Department, CHU Clermont-Ferrand, 63000 Clermont-Ferrand, France; Clermont Auvergne University, CNRS, INSERM, iGReD, Clermont-Ferrand, France. Electronic address: dbouvier@chu-clermontferrand.fr.

Classifications MeSH