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 26 条
[1]  
[Anonymous], 1985, J PEDIATR-US, V107, P10
[2]   Adult height in growth hormone (GH)-deficient children treated with biosynthetic GH [J].
Blethen, SL ;
Baptista, J ;
Kuntze, J ;
Foley, T ;
LaFranchi, S ;
Johanson, A .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1997, 82 (02) :418-420
[3]   Final height of patients treated for isolated GH deficiency: Examination of 83 patients [J].
Cacciari, E ;
Cicognani, A ;
Pirazzoli, P ;
Zucchini, S ;
Salardi, S ;
Balsamo, A ;
Cassio, A ;
Pasini, A ;
Carla, G ;
Tassinari, D ;
Gualandi, S .
EUROPEAN JOURNAL OF ENDOCRINOLOGY, 1997, 137 (01) :53-60
[4]   Adult height after long term treatment with recombinant growth hormone for idiopathic isolated growth hormone deficiency:: observational follow up study of the French population based registry [J].
Carel, JC ;
Ecosse, E ;
Nicolino, M ;
Tauber, M ;
Leger, J ;
Cabrol, S ;
Bastié-Sigeac, IN ;
Chaussain, JL ;
Coste, J .
BMJ-BRITISH MEDICAL JOURNAL, 2002, 325 (7355) :70-73
[5]   Effects of dose and gender on the growth and growth factor response to GH in GH-deficient children: Implications for efficacy and safety [J].
Cohen, P ;
Bright, GM ;
Rogol, AD ;
Kappelgaard, AM ;
Rosenfeld, RG .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2002, 87 (01) :90-98
[6]   Final height in idiopathic growth hormone deficiency: the KIGS experience [J].
Cutfield, W ;
Lindberg, A ;
Wikland, KA ;
Chatelain, P ;
Ranke, MB ;
Wilton, P .
ACTA PAEDIATRICA, 1999, 88 :72-75
[7]   Natural History of Growth Hormone Deficiency in a Pediatric Cohort [J].
Deillon, Eva ;
Hauschild, Michael ;
Faouzi, Mohamed ;
Stoppa-Vaucher, Sophie ;
Elowe-Gruau, Eglantine ;
Dwyer, Andrew ;
Theintz, Gerald E. ;
Dubuis, Jean-Michel ;
Mullis, Primus E. ;
Pitteloud, Nelly ;
Phan-Hug, Franziska .
HORMONE RESEARCH IN PAEDIATRICS, 2015, 83 (04) :252-261
[8]   The Rationale for Growth Hormone Therapy in Children with Short Stature [J].
Deodati, Annalisa ;
Cianfarani, Stefano .
JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY, 2017, 9 :23-32
[9]  
Department of Health Ministry of Public Health, 2000, Reference for weight, height and nutritional indices in Thais aged 1 day to 19 years
[10]   Adult height after growth hormone treatment in Japanese children with idiopathic growth hormone deficiency: analysis from the KIGS Japan database [J].
Fujieda, Kenji ;
Tanaka, Toshiaki ;
Takano, Kazue ;
Chihara, Kazuo ;
Seino, Yoshiki ;
Irie, Minoru .
JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, 2011, 24 (7-8) :457-462