Recommendations on the measurement and the clinical use of vitamin D metabolites and vitamin D binding protein - A position paper from the IFCC Committee on bone metabolism.

1α,25-dihydroxyvitamin D 24,25-dihydroxyvitamin D 25-hydroxyvitamin D Immunoassays Liquid chromatography Mass spectrometry Standardization Vitamin D Vitamin D Standardization Program Vitamin D binding protein

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:
Jun 2021
Historique:
received: 26 10 2020
revised: 10 01 2021
accepted: 04 03 2021
pubmed: 14 3 2021
medline: 22 6 2021
entrez: 13 3 2021
Statut: ppublish

Résumé

Vitamin D, an important hormone with a central role in calcium and phosphate homeostasis, is required for bone and muscle development as well as preservation of musculoskeletal function. The most abundant vitamin D metabolite is 25-hydroxyvitamin D [25(OH)D], which is currently considered the best marker to evaluate overall vitamin D status. 25(OH)D is therefore the most commonly measured metabolite in clinical practice. However, several other metabolites, although not broadly measured, are useful in certain clinical situations. Vitamin D and all its metabolites are circulating in blood bound to vitamin D binding protein, (VDBP). This highly polymorphic protein is not only the major transport protein which, along with albumin, binds over 99% of the circulating vitamin D metabolites, but also participates in the transport of the 25(OH)D into the cell via a megalin/cubilin complex. The accurate measurement of 25(OH)D has proved a difficult task. Although a reference method and standardization program are available for 25(OH)D, the other vitamin D metabolites still lack this. Interpretation of results, creation of clinical supplementation, and generation of therapeutic guidelines require not only accurate measurements of vitamin D metabolites, but also the accurate measurements of several other "molecules" related with bone metabolism. IFCC understood this priority and a committee has been established with the task to support and continue the standardization processes of vitamin D metabolites along with other bone-related biomarkers. In this review, we present the position of this IFCC Committee on Bone Metabolism on the latest developments concerning the measurement and standardization of vitamin D metabolites and its binding protein, as well as clinical indications for their measurement and interpretation of the results.

Identifiants

pubmed: 33713690
pii: S0009-8981(21)00078-4
doi: 10.1016/j.cca.2021.03.002
pmc: PMC8080555
mid: NIHMS1688418
pii:
doi:

Substances chimiques

Biomarkers 0
Vitamin D-Binding Protein 0
Vitamin D 1406-16-2
Calcifediol P6YZ13C99Q

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

171-197

Subventions

Organisme : Intramural CDC HHS
ID : CC999999
Pays : United States

Informations de copyright

Copyright © 2021 Elsevier B.V. All rights reserved.

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Auteurs

Konstantinos Makris (K)

Clinical Biochemistry Department, KAT General Hospital, 14561 Athens, Greece; Laboratory for Research of the Musculoskeletal System "Th. Garofalidis", Medical School, University of Athens, Athens, Greece. Electronic address: kostas.makris.km@gmail.com.

Harjit P Bhattoa (HP)

Department of Laboratory Medicine, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.

Etienne Cavalier (E)

Department of Clinical Chemistry, University of Liège, CHU de Liège, Domaine du Sart-Tilman, B-4000 Liège, Belgium.

Karen Phinney (K)

Biomolecular Measurement Division, National Institute of Standards and Technology, Gaithersburg, MD, USA.

Christopher T Sempos (CT)

Coordinator, Vitamin D Standardization Program (VDSP), Havre de Grace, MD 21078, USA.

Candice Z Ulmer (CZ)

Clinical Chemistry Branch, Division of Laboratory Sciences, National Center for Environmental Health, Centers for Disease Control and Prevention, Atlanta, GA, USA.

Samuel D Vasikaran (SD)

PathWest Laboratory Medicine, Fiona Stanley Hospital, Murdoch, WA, Australia.

Hubert Vesper (H)

Clinical Chemistry Branch, Division of Laboratory Sciences, National Center for Environmental Health, Centers for Disease Control and Prevention, Atlanta, GA, USA.

Annemieke C Heijboer (AC)

Department of Clinical Chemistry, Endocrine Laboratory, Amsterdam Gastroenterology Endocrinology & Metabolism, Vrije Universiteit Amsterdam and University of Amsterdam, Amsterdam UMC, Amsterdam, Netherlands.

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Classifications MeSH