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土耳其生长激素缺乏症儿童长期生长激素替代疗法的结果

The results of long-term growth hormone replacement therapy in Turkish children with growth hormone deficiency.

作者信息

Yordam N, Kandemir N, Alikaşifoğlu A

机构信息

Department of Pediatrics, Hacettepe University Faculty of Medicine, Ankara, Turkey.

出版信息

Turk J Pediatr. 1998 Jan-Mar;40(1):55-60.

PMID:9673529
Abstract

From a total of 118 patients treated for growth hormone deficiency, 37 (23 boys, 14 girls) have reached their final height. Twenty-five patients had isolated growth hormone deficiency (IGHD) and 12 had multiple pituitary hormone deficiency (MPHD). Growth hormone deficiency was diagnosed and treated late in both boys and girls. The mean height standard deviation score (SDS) for chronological age (CA) increased significantly from -4.43 to -1.94 during the therapy. The target height was not achieved in boys or girls nor in MPHD and IGHD groups, although they have reached the third percentile of the normal Turkish population. The height and chronological age of the patients at the start of the treatment correlated significantly with final height in all patients. Therefore, early diagnosis and treatment is important to complete catch-up growth in growth hormone deficient patients. The height prognosis is improved with administration of a recombinant form of human growth hormone (GH) as daily subcutaneous injections with a dose of 0.1 IU/kg, when compared to the earlier studies with pituitary GH.

摘要

在总共118例接受生长激素缺乏症治疗的患者中,37例(23名男孩,14名女孩)已达到最终身高。25例患者患有孤立性生长激素缺乏症(IGHD),12例患有多种垂体激素缺乏症(MPHD)。男孩和女孩的生长激素缺乏症均诊断较晚且治疗较晚。治疗期间,按实足年龄(CA)计算的平均身高标准差评分(SDS)从-4.43显著增加至-1.94。尽管患者已达到土耳其正常人群的第3百分位数,但男孩、女孩、MPHD组和IGHD组均未达到靶身高。所有患者治疗开始时的身高和实足年龄与最终身高显著相关。因此,早期诊断和治疗对于生长激素缺乏症患者完成追赶生长很重要。与早期使用垂体生长激素的研究相比,每天皮下注射剂量为0.1 IU/kg的重组人生长激素(GH)可改善身高预后。

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