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. 2017 Mar 3;102(5):1440–1446. doi: 10.1210/jc.2016-4048

Table 1.

Baseline Characteristics of Both Patients and Response to Treatment

Reference Range Case 1 Case 2
Sex, age Male, 18 y Female, 8 y
Weight 68.3 kg 22.5 kg
Presentation Hematuria, nephrocalcinosis Polyuria, nephrocalcinosis, hypercalcemia
Rifampin dose 600 mg daily 300 mg daily
Baseline 1 mo 10 mo Baseline 11 mo (on treatment) 13 mo (off treatment × 2 mo)
Albumin adjusted calcium, mg/dL 8.9–10.4 10.5 9.6 9.6 10.7 10 11.5
Phosphorus, mg/dL 2.5–4.5 3.6 3.1 4.1 4.2 3.6 4.5
Alkaline phosphatase, U/L 184–415 (Case 1) 82 114 84 242 467 345
0.2–0.73 (Case 2)
Intact PTH, pg/mL 9–69 2 13 16 3 31 3
Creatinine, mg/dL 0.3–0.8 (Case 1) 1.4 1.2 1.1 0.59 0.54 0.65
0.2–0.73 (Case 2)
25(OH)D3, ng/mL 28 ± 27 102 83 65 23 16 35
1,25-dihydroxyvitamin D3, pg/mL 56 ± 27 99 53 59 55 58 76
24,25-dihydroxyvitamin D3, ng/mL 1.6 ± 1 Undetectablea 0.2 0.1 Undetectable 0.1 0.1
25-hydroxyvitamin D3/24,25-dihydroxyvitamin D3, ng/ng 22 ± 13 N/Ab 415 650 N/A 160 350
4β,25-dihydroxyvitamin D3, pg/mLc 53 ± 34 275 594 528 N/A 82 56.7
4β,25-dihydroxyvitamin D3/25-hydroxyvitamin D3, (10−3)c 2.1 ± 0·7 2.7 7.2 5.4 N/A 3.7 1.3
a

Test was performed, but the concentration was below the detectable limits of the assay.

b

Not tested.

c

4β,25-dihydroxyvitamin D3 and the 4β,25-dihydroxyvitamin D3/25-hydroxyvitamin D3 ratio are biomarkers of CYP3A4 induction.