Pediatric Endocrinology Section, University Children's Hospital, Eberhard Karls University, Hoppe Seyler Strasse 1, Tuebingen D-72076, Germany.
J Clin Endocrinol Metab. 2010 Mar;95(3):1229-37. doi: 10.1210/jc.2009-1471. Epub 2010 Jan 22.
Information about the expected growth response of children to GH therapy is currently inadequate.
The aim of the study was to compare observed and expected growth in response to GH in prepubertal children and to propose how these parameters can be used to optimize GH therapy. Indices considered were observed growth, observed growth relative to reference data [height sd score (Ht SDS), change in (Delta) Ht SDS, height velocity (HV)], and observed growth relative to growth predicted from prediction models [Studentized residual (SR)]. Design/Setting/Patients/Intervention: Growth data from KIGS-Pfizer International Growth Database-on prepubertal children aged 1-13 yr with severe GH deficiency (GHD; maxGH <5 microg/liter; n = 2129), with less-severe GHD (maxGH of 5-10 microg/liter; n = 3075), and with Turner syndrome (n = 2350), and short children born small for gestational age (n = 993) were analyzed before and during 2 yr of GH treatment.
For each patient group, growth responses during the first 2 yr of GH treatment were established. The relationships of HV and DeltaHt SDS with SR were determined.
Reference data were generated for assessing adequate individual responses. Responses to GH in terms of HV and DeltaHt SDS were greatest in children with severe GHD. HV and DeltaHt SDS were highly correlated with SR during only the first year of GH treatment (R approximately 0.7; P < 0.001).
Decisions on GH therapy regimens should be made using both traditional (HV or DeltaHt SDS) and prediction model-derived (SR) indices of growth response.
目前,有关儿童对 GH 治疗反应的预期生长情况的信息还不充分。
本研究旨在比较青春期前儿童对 GH 治疗的实际生长与预期生长,并提出如何利用这些参数来优化 GH 治疗。所考虑的指标包括实际生长、与参考数据(身高标准差评分(Ht SDS)、Ht SDS 的变化(Delta Ht SDS)、身高速度(HV))的相对生长,以及基于预测模型预测的生长(学生残差(SR))。
设计/设置/患者/干预:分析了 KIGS-Pfizer 国际生长数据库中年龄为 1-13 岁的严重 GH 缺乏症(maxGH <5 microg/liter;n = 2129)、轻度 GH 缺乏症(maxGH 为 5-10 microg/liter;n = 3075)、特纳综合征(n = 2350)和因宫内生长受限而身材矮小的儿童(n = 993)在接受 2 年 GH 治疗前和治疗期间的生长数据。
为每个患者组确定了头 2 年 GH 治疗期间的生长反应。确定了 HV 和 DeltaHt SDS 与 SR 的关系。
为评估个体反应的充分性生成了参考数据。在严重 GH 缺乏症儿童中,HV 和 DeltaHt SDS 对 GH 的反应最大。HV 和 DeltaHt SDS 仅在 GH 治疗的第一年与 SR 高度相关(R 约为 0.7;P <0.001)。
GH 治疗方案的决策应同时使用传统(HV 或 DeltaHt SDS)和基于预测模型的(SR)生长反应指标。