Optimal final adult height achieved by low-dose recombinant human growth hormone therapy

被引:0
|
作者
Saengkaew, Tansit [1 ,2 ]
Aroonparkmongkol, Suparb [1 ]
Wacharasindhu, Suttipong [1 ]
机构
[1] Chulalongkorn Univ, Fac Med, Dept Pediat, Div Endocrinol, Bangkok 10330, Thailand
[2] Prince Songkla Univ, Fac Med, Dept Pediat, Endocrinol Unit, Hat Yai 90110, Thailand
关键词
growth hormone; growth hormone deficiency; growth hormone treatment; recombinant human growth hormone; short stature; ONSET GH DEFICIENCY; CHILDREN; EXPERIENCE;
D O I
10.2478/abm-2024-0011
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: Thailand has been administering the recombinant human growth hormone (rhGH) treatment for >20 years. Due to limited resources being available, efforts have been directed toward utilizing rhGH at the lowest feasible dose. However, there is currently a lack of evidence in terms of the efficacy and outcomes. Objective: To evaluate the auxological outcomes of growth hormone (GH) treatment and the GH secretion ability after reaching final adult height (FAH) and discontinuing rhGH. Methods Data of 40 patients were retrospectively reviewed. The clinical characteristics, auxological data, and results of biochemical and endocrine investigations before and during rhGH treatment were evaluated. In addition, GH retesting was performed in 24 patients using the insulin tolerance test. Results: Twenty patients (50%) had complete growth hormone deficiency (GHD), defined as peak stimulated GH level <5 ng/mL, and the remaining patients had partial GHD. Most patients were male (n = 25, 62.5%). The mean age at which rhGH was initiated was 8.9 years. Patients with partial GHD received a higher dose of rhGH than those with complete GHD (30.9 <mu>g/kg/d vs. 26.2 mu g/kg/d, P = 0.02). Patients with complete and partial GHD reached FAH at height standard deviation scores (SDSs) of -0.65 and -1.47, respectively. The factors associated with obtaining a good clinical response in terms of height gain included peak-stimulated GH level, age of puberty, and age of discontinuing rhGH. After completing the rhGH treatment, 13 of the 24 patients showed normal GH secretion. Patients with multiple pituitary hormone deficiency (MPHD) were likely to have persistent GHD through adulthood (n = 8, 88.9%). Conclusion: This study has demonstrated that the use of low-dose rhGH could result in healthy populations achieving optimal FAHs. Patients with MPHD might not require retesting as they were likely to have persistent GHD. The results obtained in this research highlight the benefits of the treatment. This treatment can be applied in resource-limited countries.
引用
收藏
页码:53 / 60
页数:8
相关论文
共 50 条
  • [1] The impact of recombinant human growth hormone treatment on final adult height
    R. K. Fine
    E. K. Sullivan
    A. Tejani
    [J]. Pediatric Nephrology, 2000, 14 : 679 - 681
  • [2] The impact of recombinant human growth hormone treatment on final adult height
    Fine, RN
    Sullivan, EK
    Tejani, A
    [J]. PEDIATRIC NEPHROLOGY, 2000, 14 (07) : 679 - 681
  • [3] Low-dose recombinant human growth hormone as adjuvant therapy to lifestyle modifications in the management of obesity
    Albert, SG
    Mooradian, AD
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2004, 89 (02): : 695 - 701
  • [4] Final height in children with idiopathic growth hormone deficiency treated with a fixed dose of recombinant growth hormone
    Rachmiel, Marianna
    Rota, Vanessa
    Atenafu, Eshetu
    Daneman, Denis
    Hamilton, Jill
    [J]. HORMONE RESEARCH, 2007, 68 (05) : 236 - 243
  • [5] Evaluation of the clinical and laboratory parameters and final adult height in patients treated with recombinant human growth hormone
    Sayin, Emine
    Altincik, Ayca
    Ozhan, Bayram
    [J]. HORMONE RESEARCH IN PAEDIATRICS, 2021, 94 (SUPPL 1): : 314 - 315
  • [6] Near final and final adult height in Egyptian children with isolated idiopathic growth hormone deficiency treated with recombinant growth hormone
    Ghali, Isis M.
    Salah, Nermin
    Hafez, Mona
    Anwar, Ghada M.
    Farid, Tarek
    Elmogy, Fatma
    AbduAllah, Nagwa
    [J]. HORMONE RESEARCH, 2009, 72 : 251 - 251
  • [7] Prevalence of low lean mass in patients with adult growth hormone deficiency with or without low-dose growth hormone therapy
    Zheng, Xiaoya
    Cheng, Qingfeng
    Long, Jian
    Wang, Yunting
    Gong, Lilin
    Wei, Qiang
    Luo, Rong
    Liao, Kun
    Ren, Wei
    [J]. CLINICAL ENDOCRINOLOGY, 2019, 90 (06) : 834 - 841
  • [8] Therapeutic effects of growth hormone combined with low-dose stanozolol on growth velocity and final height of girls with Turner syndrome
    Xiong, Hui
    Chen, Hong-Shan
    Du, Min-Lian
    Li, Yan-Hong
    Ma, Hua-Mei
    Su, Zhe
    Chen, Qiu-Li
    [J]. CLINICAL ENDOCRINOLOGY, 2015, 83 (02) : 223 - 228
  • [9] A multicentre trial of recombinant growth hormone and low dose oestrogen in Turner syndrome: near final height analysis
    Johnston, DI
    Betts, P
    Dunger, D
    Barnes, N
    Swift, PGF
    Buckler, JMH
    Butler, GE
    [J]. ARCHIVES OF DISEASE IN CHILDHOOD, 2001, 84 (01) : 76 - 80
  • [10] FINAL HEIGHT IN TURNER SYNDROME CONSIDERING RECOMBINANT HUMAN GROWTH HORMONE SUPPLEMENTATION
    Martins, Claudia
    Kury, Bruna
    Guimaraes, Marilia
    Brilhante, Ana Paula
    [J]. HORMONE RESEARCH IN PAEDIATRICS, 2017, 88 : 298 - 298