Department of Clinical Paediatrics, Faculty of Medical Sciences, University of Warmia and Mazury, Poland.
Pediatr Endocrinol Diabetes Metab. 2024;30(3):116-124. doi: 10.5114/pedm.2024.142590.
For 35 years, recombinant human growth hormone (rhGH) has been successfully used worldwide to treat children with short stature related to growth hormone deficiency (GHD). Growth hormone therapy requires an individual approach to the patient due to varying responses to the treatment. Excessive body weight is one of the factors influencing the response.
To evaluate the impact of excessive body mass on rhGH therapy effectiveness in GHD children.
165 short-statured children with isolated GHD (mean age 10.72 ±3.33 years), treated with rhGH for at least one year (mean follow-up 4.32 ±1.80 years), were separated into 3 groups based on their BMI standard deviation score (SDS). Bone age, height, weight, insulin-like growth factor 1 level, and rhGH dose were obtained up to 10 years with one-year intervals.
The mean change in height SDS in the first year was 0.52 ±0.41 SD and 0.60 ±0.32 SD for normal and excessive body weight children, respectively. The mean height velocity, based on the height SDS measured over the consecutive 5 years, was 0.44±0.25 SD/year for the normal-weight group and 0.32 ±0.24 SD/year for the excessive body weight group (p < 0.1).
Excess body weight has a significant impact on rhGH therapy outcomes. This correlates with the height increase in the first year of observation; however, long-term observation has shown that children diagnosed with overweight or obesity achieve significantly worse results compared to their normal-weight peers.
35 年来,重组人生长激素(rhGH)已在全球范围内成功用于治疗与生长激素缺乏症(GHD)相关的身材矮小儿童。由于对治疗的反应不同,生长激素治疗需要对患者进行个体化治疗。超重是影响反应的因素之一。
评估超重对 GHD 儿童 rhGH 治疗效果的影响。
165 名身材矮小的孤立性 GHD 儿童(平均年龄 10.72 ±3.33 岁),接受 rhGH 治疗至少一年(平均随访 4.32 ±1.80 年),根据其 BMI 标准差评分(SDS)分为 3 组。在 10 年内以一年为间隔获得骨龄、身高、体重、胰岛素样生长因子 1 水平和 rhGH 剂量。
第一年身高 SDS 的平均变化分别为 0.52 ±0.41 SDS 和 0.60 ±0.32 SDS,正常体重和超重儿童分别为 0.52 ±0.41 SDS 和 0.60 ±0.32 SDS。连续 5 年身高 SDS 测量的平均身高增长率分别为正常体重组 0.44±0.25 SDS/年和超重组 0.32 ±0.24 SDS/年(p<0.1)。
超重对 rhGH 治疗结果有显著影响。这与观察期第一年的身高增长有关;然而,长期观察表明,与体重正常的同龄人相比,超重或肥胖的儿童的治疗结果明显较差。