Seok Eun Mi, Park Hong Kyu, Rho Jung Gi, Kum Change Dae, Lee Hae Sang, Hwang Jin Soon
Department of Pediatrics, Ajou University Hospital, Ajou University School of Medicine, Suwon, Korea.
Department of Pediatrics, Gyeongsang National University Changwon Hospital, Changwon, Korea.
Ann Pediatr Endocrinol Metab. 2020 Sep;25(3):182-186. doi: 10.6065/apem.1938154.077. Epub 2020 Jul 29.
PURPOSE: Recombinant human growth hormone (rhGH) has been used to improve growth in children with Noonan syndrome (NS). This study aimed to investigate the efficacy of rhGH therapy in Korean children with NS. METHODS: Seventeen prepubertal children (10 boys, 7 girls) with NS who received rhGH therapy for at least 3 years between 2008 and 2017 were included. To compare the response, age- and sex-matched children with GH deficiency (GHD; n=31) were included. Height and growth velocity before and during treatment were analyzed. RESULTS: The mean age of NS patients was 6.34±2.32 years. After treatment, the height standard deviation score (SDS) increased from -2.93±0.81 to -1.51±1.00 in patients with NS and from -2.45±0.42 to -1.09±0.47 in patients with GHD. There were no significant differences in growth velocity or change in height SDS between patients with NS and GHD. Growth velocity in the first year of treatment was higher in patients with PTPN11 mutations than those without PTPN11 mutations, but the change in height SDS was not significantly different between those 2 groups. CONCLUSION: rhGH therapy can increase linear growth in prepubertal children with NS. The growth response between patients with NS and patients with GHD was not significantly different. Furthermore, we observed that lower doses of growth hormone have a similar effect on height compared to previous studies in patients with NS. Our study indicates that rhGH treatment is useful for growth promotion.
目的:重组人生长激素(rhGH)已被用于改善努南综合征(NS)患儿的生长情况。本研究旨在调查rhGH治疗对韩国NS患儿的疗效。 方法:纳入了17例青春期前NS患儿(10例男孩,7例女孩),这些患儿在2008年至2017年间接受rhGH治疗至少3年。为了进行反应比较,纳入了年龄和性别匹配的生长激素缺乏症(GHD)患儿(n = 31)。分析了治疗前和治疗期间的身高及生长速度。 结果:NS患者的平均年龄为6.34±2.32岁。治疗后,NS患者的身高标准差评分(SDS)从-2.93±0.81增加到-1.51±1.00,GHD患者从-2.45±0.42增加到-1.09±0.47。NS患者和GHD患者在生长速度或身高SDS变化方面无显著差异。PTPN11突变患者治疗第一年的生长速度高于无PTPN11突变的患者,但两组间身高SDS的变化无显著差异。 结论:rhGH治疗可增加青春期前NS患儿的线性生长。NS患者和GHD患者的生长反应无显著差异。此外,我们观察到与之前关于NS患者的研究相比,较低剂量的生长激素对身高有类似的影响。我们的研究表明rhGH治疗对促进生长有用。
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