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
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
117782Informations 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.