Potential for Optimization of Growth Hormone Treatment in Children with Growth Hormone Deficiency (GHD), Small for Gestational Age (SGA), and Turner Syndrome (TS) in Germany - Data from the PATRO® Children Study.

IF 2.6 3区 医学 Q3 ENDOCRINOLOGY & METABOLISM Hormone Research in Paediatrics Pub Date : 2024-04-25 DOI:10.1159/000539068
Carl-Joachim Partsch, Christof Land, Roland Pfäffle, Karl Otfried Schwab, Heide Sommer
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Abstract

INTRODUCTION Growth hormone (GH) treatment in children with growth hormone deficiency (GHD), short children born small for gestational age (SGA), and Turner syndrome (TS) is well established. However, a variety of parameters are still under discussion to achieve optimal growth results and efficiency of GH use in real world treatment. METHODS German GH-treatment naïve patients of the PATRO Children database were grouped according to their start of treatment into groups of 3 years from 2007 to 2018. Time trends in age, gender, GH dose, height standard deviation score (SDS), first year growth response, and Index of Responsiveness (IoR) were investigated in children with GHD, short children born SGA, and TS starting GH treatment in the German patient population of the PATRO Children database from 2007 - 2018 to determine specific parameters for GH treatment optimization. RESULTS All patient groups started GH treatment at a relatively high chronological age (2007 - 2009: GHD 8.33 ± 3.19, SGA 7.32 ± 2.52, TS 8.65 ± 4.39) with a slight but not significant trend towards younger therapy start up to 2016 to 2018 (GHD 8.04 ± 3.36, SGA 6.67 ± 2.65, TS 7.85 ± 3.38). In the GHD and SGA groups female patients were underrepresented compared to male patients (GHD 32.3 %, SGA 43.6 %) with no significant change over the 4 time periods. Patients with GHD started GH treatment at a low dose (0.026 mg/kg/day). In SGA and TS patients GH therapy was started below the registered dose recommendation (0.030 mg/kg/day and 0.0337 mg/kg/day, respectively). In the first year of treatment the mean GH dose was increased moderately (GHD: 0.0307, SGA: 0.0357, TS: 0.0408 mg/kg/day). There was no significant change of GH dosing over time from 2007 - 2018. The IoR was comparable between time-groups for all three diagnoses. DISCUSSION This study shows potential for improvement of GH treatment results in GHD, SGA, and TS patients in terms of early dose adjustment and younger age at start of treatment. This is in accordance with important parameters used in prediction models.
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德国生长激素缺乏症 (GHD)、小于胎龄 (SGA) 和特纳综合征 (TS) 患儿的生长激素治疗优化潜力--来自 PATRO® 儿童研究的数据。
导言:生长激素(GH)治疗生长激素缺乏症(GHD)、胎龄不足矮小儿童(SGA)和特纳综合征(TS)已得到广泛认可。然而,为了在实际治疗中达到最佳的生长效果和 GH 使用效率,各种参数仍在讨论之中。方法:将 PATRO 儿童数据库中接受过 GH 治疗的德国患者按照开始治疗的时间分组,从 2007 年到 2018 年每 3 年为一组。研究了2007-2018年PATRO儿童数据库德国患者群体中GHD儿童、SGA出生的矮小儿童和开始接受GH治疗的TS儿童的年龄、性别、GH剂量、身高标准差评分(SDS)、第一年生长反应和反应指数(IoR)的时间趋势,以确定GH治疗优化的具体参数。结果所有患者组开始接受 GH 治疗的年龄都相对较高(2007 - 2009 年:GHD 8.33 ± 3.19,SGA 7.32 ± 2.52,TS 8.65 ± 4.39),到 2016 年至 2018 年,治疗开始年龄有轻微但不显著的年轻化趋势(GHD 8.04 ± 3.36,SGA 6.67 ± 2.65,TS 7.85 ± 3.38)。在GHD和SGA组中,女性患者的比例低于男性患者(GHD为32.3%,SGA为43.6%),4个时间段内没有明显变化。GHD 患者开始接受 GH 治疗时剂量较低(0.026 毫克/千克/天)。SGA 和 TS 患者开始接受 GH 治疗时的剂量低于建议的注册剂量(分别为 0.030 毫克/千克/天和 0.0337 毫克/千克/天)。在治疗的第一年,GH 的平均剂量适度增加(GHD:0.0307 毫克/千克/天,SGA:0.0357 毫克/千克/天,TS:0.0408 毫克/千克/天)。从2007年到2018年,GH剂量没有明显变化。该研究表明,GHD、SGA 和 TS 患者的 GH 治疗效果有可能在早期剂量调整和开始治疗时的年龄降低方面得到改善。这与预测模型中使用的重要参数相符。
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来源期刊
Hormone Research in Paediatrics
Hormone Research in Paediatrics ENDOCRINOLOGY & METABOLISM-PEDIATRICS
CiteScore
4.90
自引率
6.20%
发文量
88
审稿时长
4-8 weeks
期刊介绍: The mission of ''Hormone Research in Paediatrics'' is to improve the care of children with endocrine disorders by promoting basic and clinical knowledge. The journal facilitates the dissemination of information through original papers, mini reviews, clinical guidelines and papers on novel insights from clinical practice. Periodic editorials from outstanding paediatric endocrinologists address the main published novelties by critically reviewing the major strengths and weaknesses of the studies.
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