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生长激素治疗胎龄小的儿童的长期疗效:LG 生长研究数据的分析。

Long-term effectiveness of growth hormone therapy in children born small for gestational age: An analysis of LG growth study data.

机构信息

Department of Pediatrics, Ajou University School of Medicine, Ajou University Hospital, Suwon, Korea.

出版信息

PLoS One. 2022 Apr 26;17(4):e0266329. doi: 10.1371/journal.pone.0266329. eCollection 2022.

Abstract

PURPOSE

Growth hormone (GH) treatment has been used to improve growth in short children who were born small for gestational age (SGA). The aim of this study was to investigate the long-term efficacy of GH treatment in these children.

METHODS

Data from a multicenter observational clinical trial (ClinicalTrials.gov NCT01604395, LG growth study) were analyzed for growth outcome and prediction model in response to GH treatment. One hundred fifty-two children born SGA were included.

RESULTS

The mean age of patients born SGA was 7.13 ± 2.59 years. Height standard deviation score (SDS) in patients born SGA increased from -2.55 ± 0.49 before starting treatment to -1.13 ± 0.76 after 3 years of GH treatment. Of the 152 patients with SGA, 48 who remained prepubertal during treatment used model development. The equation describing the predicted height velocity during 1st year of GH treatment is as follows: the predictive height velocity (cm) = 10.95 + [1.12 x Height SDS at initial treatment (score)] + [0.03 x GH dose (ug/kg/day)] + [0.30 x TH SDS at initial treatment (score)] + [0.05 x age (year)] + [0.15 x Weight SDS at initial treatment (score)] ± 1.51 cm.

CONCLUSIONS

GH treatment improved growth outcome in short children born SGA. We also developed a prediction model that is potentially useful in determining the optimal growth outcome for each child born SGA.

TRIAL REGISTRATION

ClinicalTrials.gov Identifier: NCT01604395.

摘要

目的

生长激素(GH)治疗已被用于改善因宫内生长受限(SGA)而出生身材矮小的儿童的生长。本研究旨在探讨 GH 治疗对这些儿童的长期疗效。

方法

对一项多中心观察性临床试验(ClinicalTrials.gov NCT01604395,LG 生长研究)的数据进行分析,以评估 GH 治疗的生长结果和预测模型。共纳入 152 例 SGA 出生的儿童。

结果

SGA 出生的患者平均年龄为 7.13±2.59 岁。SGA 出生患者的身高标准差评分(SDS)从治疗前的-2.55±0.49 增加到 3 年后的-1.13±0.76。在 152 例 SGA 患者中,48 例在治疗期间仍处于青春前期,用于模型开发。描述 GH 治疗第 1 年预测身高速度的方程如下:预测身高速度(cm)=10.95+[1.12x 初始治疗时的身高 SDS(评分)]+[0.03xGH 剂量(ug/kg/天)]+[0.30x 初始治疗时的甲状腺刺激激素 SDS(评分)]+[0.05x 年龄(岁)]+[0.15x 初始治疗时的体重 SDS(评分)]±1.51cm。

结论

GH 治疗改善了 SGA 出生矮小儿童的生长结局。我们还开发了一种预测模型,对于确定每个 SGA 出生儿童的最佳生长结局可能具有一定的实用价值。

试验注册

ClinicalTrials.gov 标识符:NCT01604395。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db74/9041836/1b6b333f9b5b/pone.0266329.g001.jpg

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