Clinical Features of Transient Growth Hormone Deficiency

Yuki Sakai, K. Ikegawa, Kazuhiro Shimura, Y. Hasegawa
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Abstract

Background: Most patients with idiopathic growth hormone deficiency (iGHD) in childhood have normal GH stimulation test results in adulthood. The present study aimed to investigate the characteristics and possible etiology of transient iGHD. Methods: Patients with childhood-onset iGHD who completed their GH treatment between March 2010 and March 2021 were retrospectively studied. Patients with a clear history of child abuse or constitutional delay of growth and puberty were excluded. Ten patients with a diagnosis of iGHD based on a decreased growth rate and growth hormone stimulation test findings at the time of onset were included. Retesting demonstrated that these patients had a normal GH level. Results: Five patients had insufficient weight gain (BMI SD score < −1.0 at the start of treatment or a decrease in BMI SD score > 1.0 from one year before treatment to the start of treatment). The other five patients had no remarkable clinical features. One patient had decreased height velocity at the same time as their sibling. Conclusion: Insufficient pre-treatment weight gain or a familial cluster of cases may be related to low GH peaks of GHST, leading to a diagnosis of transient GHD.
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短暂性生长激素缺乏症的临床特点
背景:大多数儿童期特发性生长激素缺乏症(iGHD)患者成年后GH刺激测试结果正常。本研究旨在探讨短暂性iGHD的特点和可能的病因。方法:对2010年3月至2021年3月期间完成GH治疗的儿童期发病iGHD患者进行回顾性研究。有明显虐待儿童史或生长发育和青春期发育迟缓的患者被排除在外。包括10名根据发病时生长速率下降和生长激素刺激测试结果诊断为iGHD的患者。重新测试表明这些患者的生长激素水平正常。结果:5名患者的体重增加不足(治疗开始时BMI SD评分<−1.0,或从治疗前一年到治疗开始,BMI SD评分下降>1.0)。其他5例患者无明显临床特征。一名患者的身高速度与他们的兄弟姐妹同时下降。结论:治疗前体重增加不足或家族性聚集性病例可能与GHST的GH峰值低有关,从而诊断为短暂性GHD。
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