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阿联酋阿布扎比身材矮小儿童的重组生长激素治疗:适应症及治疗结果的横断面研究

Recombinant growth hormone therapy in children with short stature in Abu Dhabi: a cross-sectional study of indications and treatment outcomes.

作者信息

Al Jneibi Sara Salem, Taha Fatima, Hammouri Marwa, Allami Zahraa, Weber Stefan, Aljubeh Jamal, Al Remeithi Sareea

机构信息

Department of Pediatrics, Division of Endocrinology, Sheikh Khalifa Medical City (SKMC), Abu Dhabi, United Arab Emirates.

出版信息

Front Pediatr. 2025 May 20;13:1516967. doi: 10.3389/fped.2025.1516967. eCollection 2025.

Abstract

UNLABELLED

Early diagnosis of the pathological cause, if any, of short stature in children can lead to prompt intervention with recombinant growth hormone (rGH) treatment, potentially allowing them to achieve their true genetic height potential. However, it is crucial to identify children most likely to benefit from rGH treatment.

METHODS

This cross-sectional, retrospective study provides a broad overview of rGH prescribing patterns and evaluates both short- and long-term treatment outcomes in children treated at the Pediatric Endocrinology Clinic, Sheikh Khalifa Medical City, Abu Dhabi, UAE, between January 2011 and December 2022. One- and three-year outcome data for children treated with rGH for different diagnoses of short stature were assessed.

RESULTS

Idiopathic short stature (ISS) accounted for 34.8% of the cases for which rGH was prescribed. A significant response [mean height gain of ≥0.3 standard deviation score (SDS)/year] was seen across all assessed short-stature diagnoses, with the highest gain seen in the growth hormone deficiency (GHD) diagnosis group at the 1-year and 3-year treatment time points. More than 90% of the children diagnosed with GHD and ISS achieved normal final adult height. Younger age at rGH initiation, lower height SDS at baseline, and pre-pubertal status were associated with better outcomes post 1 and 3 years of rGH therapy. Greater response at 1 year of rGH therapy was associated with better final adult height outcome.

CONCLUSIONS

ISS was the most common indication for which rGH was prescribed in this study. A favorable increment in the height SDS of the rGH-treated children during their 1- and 3-year follow-ups was observed. Age, pubertal status, baseline height SDS, and rGH response at 1 year were directly associated with significantly improved short- and long-term response to rGH treatment. These findings provide a broad overview of the baseline and therapeutic response characteristics of rGH-treated children with short stature in the UAE and can help in optimizing and personalizing treatment strategies.

摘要

未标注

早期诊断儿童身材矮小的病理原因(若有),可促使及时采用重组生长激素(rGH)治疗进行干预,有可能使他们达到其真正的遗传身高潜力。然而,确定最有可能从rGH治疗中获益的儿童至关重要。

方法

这项横断面回顾性研究全面概述了rGH的处方模式,并评估了2011年1月至2022年12月期间在阿联酋阿布扎比谢赫哈利法医疗城儿科内分泌诊所接受治疗的儿童的短期和长期治疗结果。评估了因不同身材矮小诊断接受rGH治疗的儿童的1年和3年结局数据。

结果

特发性身材矮小(ISS)占rGH处方病例的34.8%。在所有评估的身材矮小诊断中均观察到显著反应[平均身高增长≥0.3标准差评分(SDS)/年],在生长激素缺乏(GHD)诊断组中,1年和3年治疗时间点的身高增长最高。超过90%被诊断为GHD和ISS的儿童达到了正常的最终成人身高。rGH起始治疗时年龄较小、基线身高SDS较低以及青春期前状态与rGH治疗1年和3年后的更好结局相关。rGH治疗1年时反应较大与更好的最终成人身高结局相关。

结论

ISS是本研究中rGH处方最常见的指征。观察到接受rGH治疗的儿童在1年和3年随访期间身高SDS有良好增加。年龄、青春期状态、基线身高SDS以及1年时的rGH反应与rGH治疗的短期和长期反应显著改善直接相关。这些发现全面概述了阿联酋接受rGH治疗的身材矮小儿童的基线和治疗反应特征,有助于优化和个性化治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f70/12129925/be96b267130e/fped-13-1516967-g001.jpg

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