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78 名宫内生长受限且无追赶生长的患儿于青春期前阶段开始接受生长激素治疗直至成人身高年龄。对青春期和代谢特征变化的评估。

Seventy eight children born small for gestational age without catch-up growth treated with growth hormone from the prepubertal stage until adult height age. An evaluation of puberty and changes in the metabolic profile.

机构信息

Pediatric Endocrinology Unit, Vall d'Hebron University Hospital, Barcelona, Spain; Autonomous University of Barcelona, Barcelona, Spain.

Vall d'Hebron Research Institut, Paediatric Endocrinology, Vall d'Hebron University Hospital, Barcelona, Spain.

出版信息

Endocrinol Diabetes Nutr (Engl Ed). 2021 Nov;68(9):612-620. doi: 10.1016/j.endien.2021.11.024.

Abstract

UNLABELLED

A wide variation in height gain rate is observed in children small for gestational age (SGA) treated with growth hormone (GH). The aim of this study was to evaluate prepubertal and pubertal growth, height gain attained at adult age and to assess potential predictive factors in catch-up growth. Changes in metabolic profile were also analyzed.

PATIENTS AND METHODS

Seventy-eight children born SGA were treated with a GH median dose of 33.0±2.8mcg/kg/day at a mean age of 7.3±2.0 (boys) and 6.0±1.8 (girls).

RESULTS

Mean height (SDS) at GH onset was -3.31±0.7 for boys and -3.48±0.7 for girls. According to age at pubertal growth spurt onset patients were classified in their pubertal maturity group. Adult height attained expressed in SDS was -1.75±0.7 for boys and -1.69±1.0 for girls, both below the range of their mid-parental height. The greatest height gain occurred during the prepubertal period. Patients with greater height gain were lighter (p<0.001), shorter (p=0.005), and younger (p=0.02) at the start of GH, and also showed a greater increase in growth velocity during the first year on GH (p<0.001). SGA children started puberty at the same age and with the same distribution into pubertal maturity group as the reference population. No relevant GH-related adverse events were reported, including in the insulin resistance parameters evaluated. Differences were found in fasting plasma glucose values, but were without clinical relevance. IGF-I plasma values remained within the safety range.

CONCLUSIONS

GH therapy is safe and beneficial for SGA children. The response to GH therapy is widely heterogeneous, suggesting that GH should be started at a young age and the GH dose prescribed should be individualized. SGA children started puberty at the same age as the reference population. The only factor that predicts greater adult height is growth velocity during the first year of therapy.

摘要

未加标签

接受生长激素(GH)治疗的胎儿生长受限(SGA)儿童身高增长率存在广泛差异。本研究旨在评估青春期前和青春期的生长情况、成年时获得的身高增长,并评估追赶生长的潜在预测因素。还分析了代谢谱的变化。

患者和方法

78 名出生时 SGA 的儿童以 33.0±2.8mcg/kg/天的中位数剂量接受 GH 治疗,平均年龄为 7.3±2.0(男孩)和 6.0±1.8(女孩)。

结果

男孩 GH 起始时的平均身高(SDS)为-3.31±0.7,女孩为-3.48±0.7。根据青春期生长突增开始的年龄,患者被分为青春期成熟组。成年时获得的身高以 SDS 表示,男孩为-1.75±0.7,女孩为-1.69±1.0,均低于中亲身高范围。最大的身高增长发生在青春期前。身高增长较大的患者在开始使用 GH 时体重较轻(p<0.001)、身高较矮(p=0.005)且年龄较小(p=0.02),并且在使用 GH 的第一年生长速度也有更大的增加(p<0.001)。SGA 儿童的青春期开始年龄与参考人群相同,并且按照青春期成熟组分布。未报告与 GH 相关的不良事件,包括评估的胰岛素抵抗参数。空腹血糖值存在差异,但无临床意义。IGF-I 血浆值仍在安全范围内。

结论

GH 治疗对 SGA 儿童是安全且有益的。对 GH 治疗的反应差异很大,表明 GH 应在年轻时开始使用,并且应个体化规定 GH 剂量。SGA 儿童的青春期开始年龄与参考人群相同。唯一能预测更大成年身高的因素是治疗第一年的生长速度。

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