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接受生长激素治疗的特纳综合征患者的最终身高。

Final height in Turner syndrome patients treated with growth hormone.

作者信息

Rochiccioli P, Battin J, Bertrand A M, Bost M, Cabrol S, le Bouc Y, Chaussain J L, Chatelain P, Colle M, Czernichow P

机构信息

Service d'Endocrinologie infantile, CHU Purpan, Toulouse, France.

出版信息

Horm Res. 1995;44(4):172-6. doi: 10.1159/000184620.

Abstract

The first treatment trials on patients presenting with Turner syndrome were successful in accelerating growth velocity. It is therefore essential to know the final height of the patients who were treated in order to ascertain whether or not growth hormone treatment increases final height. We are reporting on a group of 117 patients with Turner syndrome whose growth hormone treatment was initiated in 1986. The mean growth hormone dose was 0.74 IU/kg/week for an average period of 4 years. At the start of treatment, the patients' chronological age was 129/12 years, height -3.8 +/- 1.0 standard deviation scores (SDS) and bone age 10.5 +/- 2.1 years. Mean final height was 147.7 +/- 5.6 cm, i.e. a gain of 1.5 SDS. We noted no significant difference due to the type of chromosomal abnormality, nor to oxandrolone or estrogen-associated treatment. A significant correlation was found between final height, mean parental height, the duration of the treatment, height SDS at the start of treatment and growth hormone peak during pharmacological stimulation tests. However, there was no correlation between growth hormone dosage, chronological age and bone age at the start of treatment. These results show that the growth hormone treatment improves the final heights of patients with Turner syndrome.

摘要

针对特纳综合征患者的首批治疗试验成功加快了生长速度。因此,了解接受治疗患者的最终身高对于确定生长激素治疗是否能增加最终身高至关重要。我们报告了一组于1986年开始接受生长激素治疗的117例特纳综合征患者。生长激素平均剂量为0.74 IU/kg/周,平均治疗时间为4年。治疗开始时,患者的实际年龄为12 9/12岁,身高为-3.8±1.0标准差评分(SDS),骨龄为10.5±2.1岁。平均最终身高为147.7±5.6厘米,即增长了1.5个SDS。我们发现,染色体异常类型、氧雄龙或雌激素相关治疗均无显著差异。最终身高与父母平均身高、治疗持续时间、治疗开始时的身高SDS以及药物刺激试验期间的生长激素峰值之间存在显著相关性。然而,治疗开始时的生长激素剂量、实际年龄和骨龄之间并无相关性。这些结果表明,生长激素治疗可改善特纳综合征患者的最终身高。

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