Short stature with normal growth hormone stimulation testing: lack of evidence for partial growth hormone deficiency or insensitivity.
Short stature with normal growth hormone stimulation testing: lack of evidence for partial growth hormone deficiency or insensitivity.
复制标题
生长激素刺激试验正常的身材矮小:缺乏部分生长激素缺乏或不敏感的证据。
DOI:
10.1159/000079711
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发表时间:
2004
期刊:
影响因子:
--
通讯作者:
Baron,Jeffrey
中科院分区:
文献类型:
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作者:
Nwosu,BenjaminU;Coco,Marilena;Jones,Joy;Barnes,KevinM;Yanovski,JackA;Baron,Jeffrey
ObjectivesTo test the hypothesis that children with short stature and peak stimulated GH (pGH) of 7–10 µg/l have partial GH deficiency and to test the hypothesis that short children with normal pGH but low IGF-I levels have partial GH deficiency or partial GH insensitivity.Design and PatientsRetrospective analysis of the clinical and biochemical profiles of 76 children who underwent an evaluation for short stature (height< 5th percentile) that included two, sex steroid-primed GH stimulation tests.ResultsPatients with pGH< 7 µg/l (n= 14) differed significantly from those with pGH> 7 µg/l (n= 62), having greater midparental height (MPH) SDS, a greater disparity between height SDS and MPH SDS, and lower IGF-I SDS. Patients with pGH of 7–10 µg/l (n= 12) did not have characteristics intermediate between those with pGH< 7 µg/l and those with pGH≧ 10 µg/l, but instead resembled those with pGH≧ 10 µg/l. Patients with pGH≧ 7 µg/l, but low IGF-I (<–2 SDS)(n= 5), did not show characteristics intermediate between those with pGH< 7 µg/l and those with pGH≧ 7 µg/l and normal IGF-I.ConclusionsThese data do not support either the hypothesis that children with pGH of 7–10 µg/l have partial GH deficiency or the hypothesis that children with normal pGH but subnormal IGF-I levels have partial GH deficiency or insensitivity.