Improved Screening Test for Idiopathic Infantile Hypercalcemia Confirms Residual Levels of Serum 24,25-(OH)<sub>2</sub> D<sub>3</sub> in Affected Patients.

Kaufmann, Martin; Morse, Nicole; Molloy, Billy Joe; Cooper, Donald P; Schlingmann, Karl Peter; Molin, Arnaud; Kottler, Marie Laure; Gallagher, J Christopher et al. · J Bone Miner Res · 2017

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Abstract

CYP24A1 mutations are now accepted as a cause of idiopathic infantile hypercalcemia (IIH). A rapid liquid-chromatography tandem mass spectrometry (LC-MS/MS)-based blood test enabling measurement of the 25-OH-D<sub>3</sub> :24,25-(OH)<sub>2</sub> D<sub>3</sub> ratio (R) can identify IIH patients on the basis of reduced C24-hydroxylation of 25-OH-D<sub>3</sub> by CYP24A1 in vivo. Although values of this ratio are significantly elevated in IIH, somewhat surprisingly, serum 24,25-(OH)<sub>2</sub> D<sub>3</sub> remains detectable. The current study explores possible explanations for this including: residual CYP24A1 enzyme activity in individuals with certain CYP24A1 genotypes, expression of alternative C24-hydroxylases, and the possibility of isobaric contamination of the 24,25-(OH)<sub>2</sub> D<sub>3</sub> peak on LC-MS/MS. We employed an extended 20-min run time on LC-MS/MS to study serum vitamin D metabolites in patients with IIH due to mutations of CYP24A1 or SLC34A1; in unaffected heterozygotes and dialysis patients; in patients with vitamin D deficiency; as well as in normal subjects exhibiting a broad range of 25-OH-D levels. We identified 25,26-(OH)<sub>2</sub> D<sub>3</sub> as a contaminant of the 24,25-(OH)<sub>2</sub> D<sub>3</sub> peak. In normals, the concentration of 24,25-(OH)<sub>2</sub> D<sub>3</sub> greatly exceeds 25,26-(OH)<sub>2</sub> D<sub>3</sub> ; however, 25,26-(OH)<sub>2</sub> D<sub>3</sub> becomes more significant in IIH with CYP24A1 mutations and in dialysis patients, where 24,25-(OH)<sub>2</sub> D<sub>3</sub> levels are low when CYP24A1 function is compromised. Mean R in 30 IIH-CYP24A1 patients was 700 (range, 166 to 2168; cutoff = 140) as compared with 31 in 163 controls. Furthermore, patients possessing CYP24A1 L409S alleles exhibited higher 24,25-(OH)<sub>2</sub> D<sub>3</sub> levels and lower R (mean R = 268; n = 8) than patients with other mutations. We conclude that a chromatographic approach which resolves 24,25-(OH)<sub>2</sub> D<sub>3</sub> from 25,26-(OH)<sub>2</sub> D<sub>3</sub> produces a more accurate R that can be used to differentiate pathological states where CYP24A1 activity is altered. The origin of the residual serum 24,25-(OH)<sub>2</sub> D<sub>3</sub> in IIH patients appears to be multifactorial. © 2017 American Society for Bone and Mineral Research.

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