Response to Recombinant Human Growth Hormone (rhGH) Therapy in Children with Growth Hormone Deficiency.

Maira Riaz, Mohsina Noor Ibrahim, Versha Rani Rai, Safia Bibi, Zubair Ahmed Khoso, Taj Mohammad Laghari
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Abstract

Objective: To determine the auxological response to recombinant human growth hormone (rhGH) therapy in children with growth hormone deficiency (GHD) presenting at the National Institute of Child Health, Karachi, Pakistan.

Study design:  Observational study. Place and Duration of the Study: Department of Paediatric Endocrinology, National Institute of Child Health, Karachi, Pakistan, from January 2022 to December 2023.

Methodology:  All pre-pubertal children with short stature aged 3-12 years diagnosed with GHD and who were prescribed rhGH therapy were included in the study. Children with any other underlying reason for short stature or any other comorbidity were excluded. Patients' demographics and baseline growth parameters were recorded in a pre-designed proforma. Patients were then followed up every three months till one year. Response to rhGH therapy was evaluated through comparison of growth parameters before and after one year of therapy.

Results: A total of 90 children including 47 (52.2%) males and 43 (47.8%) females with GHD were enrolled. Mean age of these patients was 7.92 ± 2.647 years. A statistically significant change in height (SD), Weight (SD), and BMI (SD) was observed before and after one year of therapy (p <0.001). Response to therapy in terms of height did not differ significantly with respect to gender (p = 0.955) or stimulated growth hormone levels (p = 0.911). However, response to rhGH therapy was significantly better in terms of increase in height, weight, and BMI in patients presenting earlier i.e. at age ≤8 years.

Conclusion: Recombinant human growth hormone therapy was effective in children with short stature to achieve desirable growth. Children diagnosed and treated at a younger age (≤8years) achieve better height outcomes as compared to those presenting late.

Key words:  Short stature, Growth hormone deficiency, Recombinant human growth hormone.

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生长激素缺乏症儿童对重组人生长激素(rhGH)疗法的反应。
研究目的研究设计: 研究设计:观察性研究。研究地点和时间:研究地点和时间:巴基斯坦卡拉奇国立儿童健康研究所儿科内分泌科,2022 年 1 月至 2023 年 12 月: 研究对象:所有被诊断为GHD并接受rhGH治疗的3-12岁青春期前身材矮小儿童。排除了因其他原因导致身材矮小或患有其他合并症的儿童。研究人员在预先设计的表格中记录了患者的人口统计学特征和基线生长参数。然后每三个月对患者进行一次随访,直至一年。通过比较治疗前后一年的生长参数,评估对 rhGH 治疗的反应:共有90名GHD患儿接受了治疗,其中包括47名男性(52.2%)和43名女性(47.8%)。这些患者的平均年龄为(7.92 ± 2.647)岁。在治疗一年前后,观察到身高(标清)、体重(标清)和体重指数(标清)发生了统计学意义上的明显变化(P 结语):重组人生长激素疗法对身材矮小的儿童能有效实现理想的生长。在较小年龄(≤8 岁)接受诊断和治疗的儿童与较晚接受诊断和治疗的儿童相比,能获得更好的身高结果: 短身材 生长激素缺乏 重组人生长激素
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