Growth hormone secretion and growth hormone treatment in children with intrauterine growth retardation. Swedish Paediatric Study Group for Growth Hormone Treatment.

K Albertsson-Wikland
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引用次数: 79

Abstract

Few children with intrauterine growth retardation (IUGR) fail to show catch-up growth during the first year of life. There may be many reasons for this, ranging from disturbances of hormone production to hormonal unresponsiveness of target cells. This report presents preliminary data on growth hormone (GH) secretion and responses to GH treatment in 16 children with IUGR and poor catch-up growth, six of whom had Silver-Russell stigmata. GH secretion was assessed by measurement of the GH response to an arginine-insulin test and determination of spontaneous GH secretion over 24 hours. GH production was heterogeneous but, more often than expected, children showed both a low response to GH provocation and low spontaneous secretion of GH. Five out of six of the children with Silver-Russell syndrome and seven out of 10 of the children with non-Silver-Russell IUGR gained more than 2 cm in height during 1 year of treatment with GH at a dose of 0.1 IU/kg/day. These results clearly demonstrate that some children with IUGR and poor catch-up growth secrete insufficient amounts of GH, and that many of these very short children show an improvement in growth rate during treatment with physiological doses of GH.

宫内发育迟缓患儿生长激素分泌及生长激素治疗。瑞典儿科生长激素治疗研究小组。
很少有宫内生长迟缓(IUGR)的儿童在出生后的第一年没有表现出追赶性生长。这可能有很多原因,从激素产生的干扰到靶细胞的激素无反应。本文介绍了16例IUGR患儿的生长激素(GH)分泌和对GH治疗的反应的初步数据,其中6例患有银罗素斑痕。通过测量生长激素对精氨酸胰岛素试验的反应和测定24小时内生长激素的自发分泌来评估生长激素的分泌。生长激素的产生是不均匀的,但比预期的更常见的是,儿童对生长激素的刺激反应低,生长激素的自发分泌也低。在以0.1 IU/kg/天剂量的生长激素治疗1年期间,6名患有银罗素综合征的儿童中有5名,10名非银罗素IUGR儿童中有7名身高增加超过2厘米。这些结果清楚地表明,一些患有IUGR和追赶性生长不良的儿童分泌的生长激素量不足,许多这些非常矮小的儿童在使用生理剂量的生长激素治疗期间,生长速度有所改善。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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