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. 2019 Sep 19;10:638. doi: 10.3389/fendo.2019.00638

Table 1.

Initial clinical and laboratorial characteristics.

Characteristics Group 1 (N = 20) Group 2 (N = 62) Group 3 (N = 33) p-value
Sex (F/M) 3/17 19/43 9/24 NS
Target height (cm) 161.9 ± 9 165.6 ± 9.6 166.1 ± 7.1 NS
Target height SDS −1.7 ± 0.9 −1 ± 1.1 −1 ± 0.8 <0.05*
Peak GH to ITT(μg/L) 19.4 ± 8.3 3.6 ± 2.6 6.4 ± 8.9 <0.05
Peak GH to CT (μg/L) 18.7 ± 15.9 4 ± 3.1 9 ± 11.8 <0.05
*

p < 0.05 (group 1 vs. other groups).

p < 0.05 (between all groups).

Group 1: children diagnosed with FSS or CDGP; Group 2: children who gained 0.3 SD in height after 1 year of rhGH treatment; Group 2: children who gained <0.3 SD in height after 1 year of rhGH treatment. F, Female; M, Male; IGF-1, Insulin-like Growth Factor I; ITT, Insulin Tolerance Test; CT, Clonidine Test; NS, Not Significant; FSS, Familial Short Stature; CDGP, Constitutional delay of growth and puberty; rhGH, Recombinant Human Growth Hormone.