2003
DOI: 10.1046/j.1365-2265.2003.01773.x
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Growth hormone secretory pattern and response to treatment in children with short stature followed to adult height

Abstract: Long-term administration of GH to short children with normal spontaneous GH secretion is not associated with an appreciable increase in adult height.

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Cited by 23 publications
(29 citation statements)
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“…Onset of puberty during treatment was not evaluated and could account for much or all of this acceleration. A similar first-year growth acceleration was reported in 2 other studies of children diagnosed by the same criteria [79][80][81] , and both of these studies suffered from the same limitations.…”
Section: (Strong Recommendation ••⚪⚪)supporting
confidence: 60%
See 1 more Smart Citation
“…Onset of puberty during treatment was not evaluated and could account for much or all of this acceleration. A similar first-year growth acceleration was reported in 2 other studies of children diagnosed by the same criteria [79][80][81] , and both of these studies suffered from the same limitations.…”
Section: (Strong Recommendation ••⚪⚪)supporting
confidence: 60%
“…We could find a report of the effects on AH in only one retrospective study [80] that showed a mean AH gain of 1.03 SDS following GH treatment in children who met the criteria for neurosecretory dysfunction, compared to untreated ISS cases with normal spontaneous secretion. This gain is virtually identical to that obtained in treated ISS (see discussion below) making the contribution of the spontaneous GH measurement very questionable.…”
Section: (Strong Recommendation ••⚪⚪)mentioning
confidence: 99%
“…W procesie diagnostycznym wykonuje się zazwyczaj dwa testy i ocenia się maksymalne stężenie GH. Obecnie w Polsce i w większości krajów do rozpoznania niedoboru GH przyjmuje się wartość poniżej 10 ng/ml [9][10][11][12][13]. Przy tym za ciężki niedobór GH (sGHD) u dziecka przyjmuje się zazwyczaj maksymalny wyrzut GH poniżej 5 ng/ml, a za częściowy niedobór GH (pGHD) maksymalny wyrzut GH pomiędzy 5 a 10 ng/ml [14][15][16].…”
Section: Wstępunclassified
“…Além disso, os critérios diagnósticos utilizados na maior parte das vezes -pico de GH máximo em testes de estímulo < 10 ng/ml -são arbitrários, inespecíficos (33,34), provavelmente inadequados para os ensaios monoclonais atuais (28), além de não necessariamente levarem em consideração os critérios clínicos e auxoló-gicos sabidamente importantes para a definição do diagnóstico de DGH. Sendo assim, diversos autores (8,23,25,34-36) têm apontado evidências de que uma proporção considerá-vel de indivíduos considerados como tendo DGH nesses estudos apresentem na verdade condições como baixa estatura idiopática ou retardo constitucional do crescimento e puberdade, o que prejudica a interpretação dos dados levantados e, conseqüentemente, a qualidade da previsão de resposta.…”
Section: Análise Crítica Dos Modelos Preditivos Atuais Vieses De Seleunclassified