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以重组人生长激素治疗生长激素缺乏症婴儿至接近成人身高:生长模式。

Treatment of growth hormone-deficient infants with recombinant human growth hormone to near-adult height: patterns of growth.

机构信息

Department of Pediatrics, University of South Florida College of Medicine, Tampa, Fla., USA.

出版信息

Horm Res Paediatr. 2011;75(4):276-83. doi: 10.1159/000322881. Epub 2011 Jan 18.

Abstract

BACKGROUND/AIMS: To determine adult statures and linear growth patterns of children with growth hormone deficiency (GHD) who began treatment with recombinant human growth hormone (rhGH) in infancy.

METHODS

Forty-seven patients with GHD in whom administration of rhGH was initiated at or before 2 years of age and who had achieved near-adult heights (NAH) were identified in the database of the Genentech National Cooperative Growth Study.

RESULTS

After beginning treatment at a mean age of 0.9 years and height of -2.3 SD, these subjects achieved mean statures of -0.6, -0.3, and -0.4 SD at 5 and 10 years of age and at NAH, respectively. In 23 patients whose parental heights were known, mean NAH was comparable to the target height. Patients with uncomplicated courses whose heights were normal or tall when spontaneous puberty occurred or was induced realized the tallest NAHs. Patients with severe prenatal or perinatal, congenital and acquired neurologic insults, sexual precocity, or associated illnesses achieved less optimal NAHs.

CONCLUSION

A normal pattern of linear growth during childhood and adolescence and satisfactory NAHs can be achieved in the majority of patients when treatment of the GHD subject is begun during infancy.

摘要

背景/目的:确定在婴儿期开始接受重组人生长激素(rhGH)治疗的生长激素缺乏症(GHD)儿童的成人身高和线性生长模式。

方法

在 Genentech 国家合作生长研究数据库中确定了 47 名 GHD 患者,这些患者在 2 岁或 2 岁之前开始接受 rhGH 治疗,并且已经达到接近成人身高(NAH)。

结果

这些患者在平均年龄为 0.9 岁和身高为-2.3SD 时开始治疗,分别在 5 岁、10 岁和 NAH 时达到平均身高-0.6、-0.3 和-0.4SD。在已知父母身高的 23 名患者中,平均 NAH 与靶身高相当。在自然青春期发生或诱导发生时身高正常或较高的无并发症患者实现了最高的 NAH。患有严重的产前或围产期、先天性和获得性神经损伤、性早熟或相关疾病的患者实现了不太理想的 NAH。

结论

当 GHD 患者在婴儿期开始治疗时,大多数患者可以在儿童期和青春期实现正常的线性生长模式,并达到满意的 NAH。

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