Analysis of vitamin D3 metabolites in survivors of infantile idiopathic hypercalcemia caused by CYP24A1 mutation or SLC34A1 mutation.

Abstract

Infantile hypercalcemia (IH), is a rare disorder caused by CYP24A1 or SLC34A1 variants which lead to disturbed catabolism of 25(OH)D3 and 125(OH)2D3 or increased generation of 125(OH)2D3.

AIM OF STUDY:

To assess the status of 2425(OH)2D3 and other markers of vitamin D in IH survivors, in whom variants of CYP24A1 or SLC34A1 gene were found and to compare these unique biochemical features with those obtained from subjects who were diagnosed in the first year of life with hypercalcemia, elevated 25(OH)D3 and low PTH but in whom neither CYP24A1 nor SLC34A1 variant was found.

PATIENTS AND METHODS:

16 IH survivors in whom CYP24A1 (n = 13) or SLC34A1 (n = 3) variants were found and 41 subjects in whom hypercalcemia was diagnosed in the first year of life but in whom CYP24A1 or SLC34A1 variants were not found were included in the study. 25(OH)D3, 3-epi-25(OH)D3, 25(OH)D2, 2425(OH)2D3 were assessed by liquid chromatography coupled with tandem mass spectrometry. 125(OH)2D3 concentrations were assessed by chemiluminescence.

RESULTS:

Subjects with CYP24A1 variants, despite normal 25(OH)D3 levels, had higher 25(OH)D3/2425(OH)2D3 ratio values (487; 265-1073 ng/mL) when compared to subjects with SLC34A1 variants (16; 16-23 ng/mL) and with subjects in whom CYP24A1 or SLC34A1 were not found (56; 9-56 ng/mL) (p = 0.00003). Separation of interfering metabolite further increased differences between subjects with and without CYP24A1 mutation.

CONCLUSIONS:

Survivors of IH with CYP24A1 variant, despite being normocalcemic, still presented extremely high 25(OH)D3/2425(OH)2D3 ratio values. Separation of interfering compound further increased differences between subjects with CYP24A1 mutation and without this mutation.

• Authors: Ewa Kowalska, Rafał Rola, Marek Wójcik, Natalia Łaszcz, Paweł Płudowski, Aldona Wierzbicka, Agnieszka Janiec, Janusz Książyk, Paulina Halat, Elżbieta Ciara, Łukasz Obrycki, Ewa Pronicka, Mieczysław Litwin
• Journal: The Journal of steroid biochemistry and molecular biology (J Steroid Biochem Mol Biol) Vol. 208 Pg. 105824 (04 2021) ISSN: 1879-1220 [Electronic] England
• PMID: 33516786 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
• Copyright: Copyright © 2021 Elsevier Ltd. All rights reserved.

Chemical References

• SLC34A1 protein, human
• Sodium-Phosphate Cotransporter Proteins, Type IIa
• Vitamin D
• Cholecalciferol
• CYP24A1 protein, human
• Vitamin D3 24-Hydroxylase

Topics

• Cholecalciferol (administration & dosage, genetics, metabolism)
• Chromatography, Liquid
• Female
• Humans
• Hypercalcemia (drug therapy, genetics, metabolism, pathology)
• Infant
• Infant, Newborn
• Male
• Mutation
• Sodium-Phosphate Cotransporter Proteins, Type IIa (genetics)
• Tandem Mass Spectrometry
• Vitamin D (genetics, metabolism)
• Vitamin D3 24-Hydroxylase (blood, genetics)