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重组生长激素长期治疗对小于胎龄儿生长结局的影响:一项系统评价

Effects of long-term treatment with recombinant growth hormone on growth outcome in children born small for gestational age: a systematic review.

作者信息

Ferrigno Rosario, Savage Martin O, Cioffi Daniela, Pellino Valeria, Savanelli Maria Cristina, Klain Antonella

机构信息

UOSD di Auxologia ed Endocrinologia, AORN Santobono-Pausilipon, Via M. Fiore, 4, Napoli, 80016, Italy.

William Harvey Research Institute, Queen Mary,, London, UK.

出版信息

Rev Endocr Metab Disord. 2025 Apr;26(2):147-159. doi: 10.1007/s11154-024-09911-y. Epub 2024 Sep 17.

DOI:10.1007/s11154-024-09911-y
PMID:39285087
Abstract

Children born small for gestational age (SGA) are defined as those having birth weight and/or length below -2 SD for gestational age. In approximately 90% of cases, SGA children experience catch-up growth in the first two years of life and a subsequent regular growth rate, reaching normal adult height. However, in the remaining 10% of cases, SGA children fail to have catch-up growth, showing persistent short stature and a constantly impaired growth rate, leading to decreased adult height compared with both general population and their mid-parental height. Therefore, in these children GH treatment may be indicated to improve growth outcome. As it can be started in most countries from the age of 4 years and is usually recommended until the completion of puberty, long-term GH treatment in SGA children (namely, longer than three years) showed a persistent improvement in height and an initial improvement in growth rate in the first year of treatment, followed by a stable, regular growth rate over time. In the present article, we systematically reviewed the currently available reports about efficacy of long-term GH treatment in SGA children, with a particular focus on growth rate over time and adult height.

摘要

小于胎龄儿(SGA)是指出生体重和/或身长低于同孕周-2标准差的儿童。在大约90%的病例中,SGA儿童在生命的头两年经历追赶生长,并随后保持正常的生长速度,达到正常成人身高。然而,在其余10%的病例中,SGA儿童未能实现追赶生长,表现为持续身材矮小和生长速度持续受损,导致与普通人群及其父母平均身高相比成人身高降低。因此,对于这些儿童,可能需要使用生长激素(GH)治疗以改善生长结局。由于在大多数国家可以从4岁开始使用,并且通常建议持续到青春期结束,SGA儿童的长期GH治疗(即超过三年)显示身高持续改善,治疗第一年生长速度初步改善,随后随着时间推移生长速度稳定、正常。在本文中,我们系统回顾了目前关于SGA儿童长期GH治疗疗效的现有报告,特别关注随时间变化的生长速度和成人身高。

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Safety and Effectiveness of a Biosimilar Recombinant Human Growth Hormone in Children Requiring Growth Hormone Treatment: Analysis of Final Data from PATRO Children, an International, Post-Marketing Surveillance Study.在需要生长激素治疗的儿童中,一种生物类似重组人生长激素的安全性和有效性:来自 PATRO 儿童的国际上市后监测研究的最终数据分析。
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Long-Term Efficacy and Safety of Recombinant Human Growth Hormone in Children Born Small for Gestational Age.重组人生长激素治疗小于胎龄儿的长期疗效和安全性
Horm Metab Res. 2023 Sep;55(9):599-609. doi: 10.1055/a-2136-8654. Epub 2023 Sep 7.
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Growth response of syndromic versus non-syndromic children born small for gestational age (SGA) to growth hormone therapy: a Belgian study.
综合征型与非综合征型小于胎龄儿(SGA)对生长激素治疗的生长反应:一项比利时研究。
Front Endocrinol (Lausanne). 2023 Jun 2;14:1112938. doi: 10.3389/fendo.2023.1112938. eCollection 2023.
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Growth Hormone Dose Modulation and Final Height in Short Children Born Small for Gestational Age: French Real-Life Data.生长激素剂量调节与胎龄小导致身材矮小儿童的最终身高:法国真实数据。
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Childhood growth hormone treatment and metabolic and cardiovascular risk in adults born small for gestational age after growth hormone cessation in the Netherlands: a 12-year follow-up study.荷兰小于胎龄儿成年后生长激素治疗停止后的儿童期生长激素治疗与代谢及心血管风险:一项12年随访研究
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Safety and Efficacy of Pediatric Growth Hormone Therapy: Results From the Full KIGS Cohort.儿科生长激素治疗的安全性和疗效:来自完整 KIGS 队列的结果。
J Clin Endocrinol Metab. 2022 Nov 25;107(12):3287-3301. doi: 10.1210/clinem/dgac517.
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PLoS One. 2022 Apr 26;17(4):e0266329. doi: 10.1371/journal.pone.0266329. eCollection 2022.
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Clin Pediatr Endocrinol. 2020;29(4):159-171. doi: 10.1297/cpe.29.159. Epub 2020 Oct 3.
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