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[垂体功能减退症患儿早期生长激素治疗的结果]

[Results of early growth hormone treatment in children with hypopituitarism].

作者信息

Huet Frédéric, Bensignor Candace, Polak Michel, Carel Jean-Claude

机构信息

Pédiatrie 1 et Génétique Médicale, Hôpital d'Enfants, Bd de Lattre de Tassigny--21079 Dijon cedex.

出版信息

Bull Acad Natl Med. 2012 Jan;196(1):117-23; discussion 123-5.

Abstract

Hypopituitarism is an interesting pathological model because it allows us to examine the long-term effects of hormone replacement therapy in this population. However, the impact of growth hormone replacement therapy started before 1 year of age on final height has not been studied. The France-Hypophyse database contains the files of 59 children who started growth hormone therapy before one year of age between 1977 and 1992, and the complete growth profile of 49 patients could be analyzed Twenty girls (age at diagnosis: 6.1 +/- 3.8 months) and 29 boys (4.5 +/- 3.3 months) were treated with growth hormone for an average of 16 +/- 1.6 years. Catch-up growth was maximal during the first 3 years. At 10 years of age the patients had reached or even exceeded their target size Puberty was spontaneous (14 children) or stimulated (33 children), and occurred at an estimated bone age of 11.7 +/- 1.8 years. During puberty we observed an acceptable growth spurt but no further catch-up growth. Final height was 159 +/- 8 cm in girls and 173 +/- 7 cm in boys. No adverse effects of growth hormone therapy were reported Thanks to early GH treatment, children with hypopituitarism had a mean gap between final size and parental target size of only 0.1 +/- 1.1 SD. Early diagnosis and treatment are therefore essential in this setting.

摘要

垂体功能减退是一种有趣的病理模型,因为它使我们能够研究该人群中激素替代疗法的长期效果。然而,1岁前开始的生长激素替代疗法对最终身高的影响尚未得到研究。法国垂体数据库包含了1977年至1992年间59名1岁前开始生长激素治疗的儿童的档案,其中49名患者的完整生长情况可以进行分析。20名女孩(诊断时年龄:6.1±3.8个月)和29名男孩(4.5±3.3个月)接受了平均16±1.6年的生长激素治疗。追赶生长在最初3年最为显著。10岁时,患者达到甚至超过了他们的目标身高。青春期为自发(14名儿童)或促发(33名儿童),估计骨龄为11.7±1.8岁。青春期期间,我们观察到有可接受的生长突增,但没有进一步的追赶生长。女孩的最终身高为159±8厘米,男孩为173±7厘米。未报告生长激素治疗的不良反应。由于早期生长激素治疗,垂体功能减退儿童的最终身高与父母目标身高之间的平均差距仅为0.1±1.1标准差。因此,在这种情况下,早期诊断和治疗至关重要。

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