Xu Qingbo, Yang Yu, Xie Liling, Zhang Dongguang, Zou Haiying, Cao LanFang, Yang Li
Department of Endocrinology, Genetics and Metabolism, Jiangxi Provincial Children's Hospital, Nanchang, Jiangxi, 330038, People's Republic of China.
Department of Endocrinology, The Affiliated Children's Hospital of Nanchang Medical College, Nanchang, Jiangxi, 330038, People's Republic of China.
Int J Gen Med. 2025 Sep 12;18:5433-5446. doi: 10.2147/IJGM.S541514. eCollection 2025.
Growth hormone (GH) therapy affects linear growth and may influence hematopoiesis, but dynamic hemoglobin (Hb) changes in children remain unclear.
To characterize longitudinal Hb trajectories during weekly GH treatment in short stature, including idiopathic short stature (ISS) and growth hormone deficiency (GHD), and to assess their associations with growth response.
This retrospective cohort study included 165 children with short stature who received once-weekly PEGylated GH therapy for at least 12 months. Hematologic/growth-related parameters were collected at baseline, 6 and 12 months. Group-based trajectory modeling (GBTM) identified Hb trajectory groups. Spearman correlation analysis was performed to evaluate the association between Hb, red blood cell (RBC) count, and insulin-like growth factor 1 (IGF-1). Multivariate logistic regression was used to identify predictors of Hb improvement (≥5 g/L).
Three distinct Hb trajectory groups were identified: ascending (n = 82), ascending-then-descending (n = 51), and stable (n = 32). The ascending group demonstrated the most favorable height SDS improvement at 12 months (mean ΔHtSDS = 1.01), while the ascending-then-descending and stable groups showed more modest gains. IGF-1 levels were moderately correlated with Hb at 12 months ( = 0.308, = 0.001) and RBC counts ( = 0.236, = 0.014). Logistic regression revealed no independent baseline predictor of Hb improvement; however, the inclusion of Hb trajectory group significantly enhanced the predictive model for growth response (adjusted increased from 0.129 to 0.240; = 0.018).
Hb trajectories vary significantly among children receiving GH therapy and are moderately associated with height outcomes. Longitudinal monitoring of Hb may serve as a cost-effective dynamic biomarker to guide personalized GH dose titration in pediatric growth disorders. If validated, Hb monitoring may serve as a practical biomarker for personalized GH dosing in pediatric growth disorders.
生长激素(GH)治疗会影响线性生长,可能还会影响造血功能,但儿童血红蛋白(Hb)的动态变化仍不明确。
描述身材矮小儿童(包括特发性矮小症(ISS)和生长激素缺乏症(GHD))在每周接受GH治疗期间Hb的纵向变化轨迹,并评估其与生长反应的相关性。
这项回顾性队列研究纳入了165例身材矮小儿童,他们接受了至少12个月的每周一次聚乙二醇化GH治疗。在基线、6个月和12个月时收集血液学/生长相关参数。基于组的轨迹建模(GBTM)确定了Hb轨迹组。进行Spearman相关性分析以评估Hb、红细胞(RBC)计数和胰岛素样生长因子1(IGF-1)之间的相关性。使用多变量逻辑回归来确定Hb改善(≥5g/L)的预测因素。
确定了三个不同的Hb轨迹组:上升组(n = 82)、先上升后下降组(n = 51)和稳定组(n = 32)。上升组在12个月时身高标准差积分(SDS)改善最为明显(平均ΔHtSDS = 1.01),而先上升后下降组和稳定组的增长则较为适度。IGF-1水平在12个月时与Hb(r = 0.308,P = 0.001)和RBC计数(r = 0.236,P = 0.014)中度相关。逻辑回归显示,没有独立的基线指标可预测Hb改善;然而,纳入Hb轨迹组显著增强了生长反应的预测模型(调整后的R²从0.129增加到0.240;P = 0.018)。
接受GH治疗的儿童中,Hb轨迹差异显著,且与身高结果中度相关。对Hb进行纵向监测可能作为一种经济有效的动态生物标志物,用于指导儿科生长障碍中GH剂量的个性化滴定。如果得到验证,Hb监测可能成为儿科生长障碍中个性化GH给药的实用生物标志物。