Rifampin monotherapy for children with idiopathic infantile hypercalcemia
- PMID: 36990163
- PMCID: PMC10441173
- DOI: 10.1016/j.jsbmb.2023.106301
Rifampin monotherapy for children with idiopathic infantile hypercalcemia
Abstract
Idiopathic Infantile Hypercalcemia (IIH) is characterized by hypercalcemia and hypercalciuria owing to PTH-independent increases in circulating concentrations of 1,25(OH)2D. At least 3 forms of IHH can be distinguished genetically and mechanistically: infantile hypercalcemia-1 (Hypercalcemia, Infantile, 1; HCINF1) due to CYP24A1 mutations results in decreased inactivation of 1,25(OH)2D; HCINF2 due to SLC34A1 mutations results in excessive 1,25(OH)2D production; and HCINF3 in which a variety of gene variants of uncertain significance (VUS) have been identified and where the mechanism for increased 1,25 (OH)2D is unclear. Conventional management with dietary calcium and vitamin D restriction has only limited success. Induction of the P450 enzyme CYP3A4 by rifampin can provide an alternate pathway for inactivation of 1,25(OH)2D that is useful in HCINF1 and may be effective in other forms of IIH. We sought to assess the efficacy of rifampin to decrease levels of serum 1,25(OH)2D and calcium, and urinary calcium concentrations in subjects with HCINF3, and to compare the response to a control subject with HCINF1. Four subjects with HCINF3 and the control subject with HCINF1 completed the study using rifampin 5 mg/kg/day and 10 mg/kg/day each for 2 months separated by a 2-month washout period. Patients had age-appropriate intake of dietary calcium plus 200 IU vitamin D/day. Primary outcome was efficacy of rifampin to lower serum concentrations of 1,25(OH)2D. The secondary outcomes included the reduction of serum calcium, urinary calcium excretion (as random urine calcium: creatinine (ca:cr) ratio) and serum 1,25(OH)2D/PTH ratio. Rifampin was well tolerated and induced CYP3A4 at both doses in all subjects. The control subject with HCINF1 showed significant response to both rifampin doses with decreases in the serum concentration of 1,25(OH)2D and the 1,25(OH)2D/PTH ratio while the serum and urine ca:cr levels were unchanged. The four patients with HCINF3 showed reductions in 1,25(OH)2D and urinary ca:cr after 10 mg/kg/d, but hypercalcemia did not improve and there were variable responses in 1,25(OH)2D/PTH ratios. These results support further longer-term studies to clarify the usefulness of rifampin as a medical therapy for IIH.
Keywords: CYP24A1; Idiopathic infantile hypercalcemia; Rifampin; Vitamin D.
Copyright © 2023 The Authors. Published by Elsevier Ltd.. All rights reserved.
Conflict of interest statement
Declaration of competing interest None.
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References
-
- Lightwood R, Stapleton T, Idiopathic hypercalcaemia in infants, Lancet 265 (6779) (1953) 255–256. - PubMed
-
- Creery RD, Neill DW, Idiopathic hypercalcaemia in infants with failure to thrive, Lancet 267 (6829) (1954) 110–114. - PubMed
-
- Huang J, Coman D, McTaggart SJ, Burke JR, Long-term follow-up of patients with idiopathic infantile hypercalcaemia, Pediatr. Nephrol. 21 (11) (2006) 1676–1680. - PubMed
-
- Pronicka E, Rowinska E, Kulczycka H, Lukaszkiewicz J, Lorenc R, Janas R, Persistent hypercalciuria and elevated 25-hydroxyvitamin D3 in children with infantile hypercalcaemia, Pediatr. Nephrol. 11 (1) (1997) 2–6. - PubMed
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