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[生长激素治疗期间预测特纳综合征患者最终身高良好的人体测量参数]

[Anthropometric parameters prognosticating a good final height in patients with Turner syndrome during growth hormone therapy].

作者信息

Kucharska Anna M, Majcher Anna, Rymkiewicz-Kluczyńska Barbara

机构信息

Katedra i Klinika Pediatrii i Endokrynologii AM w Warszawie.

出版信息

Pediatr Endocrinol Diabetes Metab. 2007;13(3):165-70.

PMID:17880828
Abstract

INTRODUCTION

Growth hormone treatment in Turner girls is a widely accepted method of their final height improvement. However some patients do not reach satisfactory final height. The aim of the study was to evaluate the anthropometric parameters which would be prognostic for final height in children with Turner syndrome treated with growth hormone.

MATERIAL AND METHODS

Data of 18 girls with Turner syndrome who completed growth hormone therapy and reached a final height were analysed. Mean age was 11.32+/-3.04 years. Correlations of final height with following parameters were analysed: trunk to limbs ratio, lower limbs length (in SDS), growth velocity in the first years of GH therapy. From among other characteristics which could determine the final height the karyotype, age at the start of GH therapy were evaluated.

RESULTS

The mean height gain in the group was 8.4 cm (range: 0.6-19.9 cm). Final height over 3rd percentile for the healthy population achieved 33.3% patients. Growth velocity in first 2 years of therapy correlated negatively with final height. Patients with final height over 3rd percentile had statistically significant greater mean height gain. Patients with low final height had a significantly greater deficit of leg length and increased Trunk/Leg Length index. Age at the beginning and duration of therapy had no influence on final height.

CONCLUSIONS

Better final height reach the patients who have more advantageous Trunk/Leg Length index before and during therapy, and reduction of leg length deficiency is relatively greater than height deficiency reduction.

摘要

引言

对特纳综合征女童进行生长激素治疗是一种被广泛认可的改善其最终身高的方法。然而,一些患者并未达到令人满意的最终身高。本研究的目的是评估那些对接受生长激素治疗的特纳综合征患儿的最终身高具有预后价值的人体测量参数。

材料与方法

分析了18例完成生长激素治疗并达到最终身高的特纳综合征女童的数据。平均年龄为11.32±3.04岁。分析了最终身高与以下参数的相关性:躯干与四肢比例、下肢长度(以标准差计分)、生长激素治疗最初几年的生长速度。从其他可能决定最终身高的特征中,评估了核型、开始生长激素治疗时的年龄。

结果

该组的平均身高增长为8.4厘米(范围:0.6 - 19.9厘米)。最终身高超过健康人群第3百分位数的患者占33.3%。治疗前两年的生长速度与最终身高呈负相关。最终身高超过第3百分位数的患者平均身高增长在统计学上显著更高。最终身高较低的患者腿部长度明显更短,且躯干/腿长指数增加。治疗开始时的年龄及治疗持续时间对最终身高无影响。

结论

治疗前及治疗期间躯干/腿长指数更有利、腿部长度不足减少相对大于身高不足减少的患者,最终身高更好。

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[Anthropometric parameters prognosticating a good final height in patients with Turner syndrome during growth hormone therapy].[生长激素治疗期间预测特纳综合征患者最终身高良好的人体测量参数]
Pediatr Endocrinol Diabetes Metab. 2007;13(3):165-70.
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Experience with growth hormone therapy in Turner syndrome in a single centre: low total height gain, no further gains after puberty onset and unchanged body proportions.单一中心特纳综合征生长激素治疗的经验:总身高增长较低,青春期开始后无进一步增长且身体比例无变化。
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Homozygosity of the d3-growth hormone receptor polymorphism is associated with a high total effect of GH on growth and a low BMI in girls with Turner syndrome.d3生长激素受体多态性的纯合性与特纳综合征女孩中生长激素对生长的高总体效应及低体重指数相关。
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GH treatment to final height produces similar height gains in patients with SHOX deficiency and Turner syndrome: results of a multicenter trial.GH 治疗对 SHOX 缺乏症和 Turner 综合征患者的最终身高产生相似的身高增长:一项多中心试验的结果。
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Final height of growth hormone-treated GH-deficient children and girls with Turner's syndrome: the Dutch experience. The Dutch Advisory Group on Growth Hormone.生长激素治疗的生长激素缺乏儿童及特纳综合征女童的最终身高:荷兰的经验。荷兰生长激素咨询小组。
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Major determinants of height development in Turner syndrome (TS) patients treated with GH: analysis of 987 patients from KIGS.生长激素治疗的特纳综合征(TS)患者身高发育的主要决定因素:对国际生长数据库(KIGS)中987例患者的分析
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[Prediction of final height in girls with Turner syndrome treated with growth hormone].[生长激素治疗特纳综合征女孩最终身高的预测]
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[Effect of estrogen therapy on the growth of Turner syndrome in girls treated with growth hormone].雌激素疗法对接受生长激素治疗的特纳综合征女童生长情况的影响
Medicina (B Aires). 2001;61(3):271-4.
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Growth hormone and low dose estrogen in Turner syndrome: results of a United States multi-center trial to near-final height.生长激素与低剂量雌激素治疗特纳综合征:一项美国多中心试验关于接近最终身高的结果
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