Skip to main content

Table 1 Characteristics of children with X-liked hypophosphatemia included in the study

From: Growth hormone treatment improves final height in children with X-linked hypophosphatemia

Parameters

Patients treated with rhGH

Patients not treated with rhGH

p

Mean ± SD [min–max] or n (%)

Mean ± SD [min–max] or n (%)

Number of patients

34

29

Boys/girls, n (%)

13 (38%)/21 (62%)

10 (34%)/19 (66%)

0.49

Birth weight, SDS

− 0.5 ± 2.0

0.4 ± 1.2

0.11

[− 5.0  to 3.5]

[− 1.5 to 2.0]

Birth length, SDS

− 0.5 ± 1.9

0.5 ± 1.2

0.09

[− 5.0 to 3.0]

[− 1.7 to 1.9]

Patients carrying a PHEX mutation, n (%)

32 (94%)

24 (86%)

0.29

Age at XLH diagnosis, years

3.4 ± 3.4

2.6 ± 2.6

0.32

[0.1–12]

[0.0–11.5]

Duration of conventional therapy, years

12.6 ± 4.9

14.0 ± 3.0

0.20

[3.0–21.8]

[5.5–17.8]

Age at menarche, years

13.4 ± 1.3

12.8 ± 0.8

0.15

[9.8–15.1]

[11.3–14.4]

Age at rhGH start, years

9.8 ± 3.4

[2.5–15.2]

Duration of rhGH treatment, years

4.4 ± 2.9

[0.6–12]

Dose of rhGH (µg/kg/day)

77.4 ± 14.5

– at the beginning of treatment

77.4 ± 14.5

– at the end of treatment

66.8 ± 20.5

Patients treated with a GnRH, n (%)

15 (47%)

2 (7%)

< 0.000

  1. rhGH: Recombinant human growth hormone; aGnRH: gonadotropin-releasing hormone analog; SDS: standard deviation score or Z-score