Literature DB >> 12792152

Assessing short-statured children for growth hormone deficiency.

W Chemaitilly1, C Trivin, J-C Souberbielle, R Brauner.   

Abstract

AIM: To optimize the workup of short-statured children by defining the most appropriate tools for diagnosing growth hormone (GH) deficiency.
METHODS: Patients were assigned to prepubertal (n = 113) or pubertal (n = 112, including 25 boys primed with testosterone) age groups. Mean plasma GH concentration during sleep, GH peak after provocative test, and insulin-like growth factor I (IGF-I) were measured in a single evaluation.
RESULTS: The mean GH concentration during sleep was more often normal (n = 155) than the GH peak after provocative tests (n = 105) or the IGF-I concentration (n = 88). Prepubertal patients with a normal body mass index (BMI) had mean GH concentrations during sleep that correlated positively with height, growth rate, GH peak after provocative tests, and IGF-I (p < 0.0005 for all) and negatively with the difference between target and patient heights (p = 0.01) and BMI (p < 0.05). Pubertal patients with a normal BMI had a mean GH concentration during sleep that correlated positively with GH after provocative tests (p < 0.0001) and IGF-I (p < 0.005). Mean GH concentration during sleep and IGF-I concentration for boys primed with testosterone were more often normal (n = 23) than the GH peak after provocative tests (n = 14). All 9 patients with pituitary stalk interruption had low IGF-I concentrations; 1 patient had a normal GH peak after provocative test, and 2 patients had normal mean GH concentrations during sleep.
CONCLUSIONS: Measuring the GH concentration during sleep and priming boys with pubertal delay can help to exclude idiopathic GH deficiency. Magnetic resonance imaging is needed to exclude anatomic abnormalities when GH and/or IGF-I concentrations are low. Copyright 2003 S. Karger AG, Basel

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Year:  2003        PMID: 12792152     DOI: 10.1159/000070825

Source DB:  PubMed          Journal:  Horm Res        ISSN: 0301-0163


  1 in total

1.  Isolated haploinsufficiency of exon 1 of the SHOX gene in a patient with idiopathic short stature.

Authors:  Y-M Tan; K-Y Loke
Journal:  J Clin Pathol       Date:  2006-07       Impact factor: 3.411

  1 in total

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