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使用生长激素治疗长达三年的软骨发育不全儿童的生长情况。

Growth of children with hypochondroplasia treated with growth hormone for up to three years.

作者信息

Bridges N A, Hindmarsh P C, Brook C G

机构信息

Middlesex Hospital, London, UK.

出版信息

Horm Res. 1991;36 Suppl 1:56-60. doi: 10.1159/000182190.

Abstract

Hypochondroplasia is a skeletal dysplasia characterised by poor childhood growth and an inadequate pubertal growth spurt. 31 children with a radiological diagnosis of hypochondroplasia have been treated for up to 3 years with recombinant human growth hormone, mean dose 17.9 U/m2/week as daily subcutaneous injections. Mean pre-treatment height velocity standard deviation score (SDS) was -0.51; this increased to +1.58 after 1 year of treatment. This improvement diminishes over the next 2 years. The effect on final height remains unknown. There was a considerable variation in clinical response within the group treated.

摘要

软骨发育不全是一种骨骼发育异常,其特征为儿童期生长缓慢以及青春期生长突增不足。31名经放射学诊断为软骨发育不全的儿童接受了重组人生长激素治疗,治疗时间长达3年,平均剂量为每周17.9 U/m²,每日皮下注射。治疗前平均身高增长速度标准差评分(SDS)为-0.51;治疗1年后增至+1.58。在接下来的2年中,这种改善逐渐减弱。对最终身高的影响尚不清楚。治疗组内临床反应存在相当大的差异。

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