基础医学与临床 ›› 2026, Vol. 46 ›› Issue (5): 687-693.doi: 10.16352/j.issn.1001-6325.2026.05.0687

• 研究论文 • 上一篇    下一篇

生长激素治疗对生长激素缺乏症患儿血清抵抗素、瘦素及FGF-23水平的影响

郑泽延, 周智博, 孙宇欣, 郭晓湲, 朱惠娟*, 潘慧*   

  1. 中国医学科学院北京协和医学院 北京协和医院 内分泌科 国家卫生健康委内分泌重点实验室,北京 100730
  • 收稿日期:2026-01-23 修回日期:2026-03-24 出版日期:2026-05-05 发布日期:2026-04-28
  • 通讯作者: *panhui20111111@163.com;shengxin2004@163.com
  • 基金资助:
    癌症、心脑血管、呼吸和代谢性疾病防治研究国家科技重大专项(2023ZD0506800)

Effects of growth hormone therapy on serum resistin, leptin, and FGF-23 levels in children with growth hormone deficiency

ZHENG Zeyan, ZHOU Zhibo, SUN Yunxin, GUO Xiaoyuan, ZHU Huijuan*, PAN Hui*   

  1. Department of Endocrinology, Key Laboratory of Endocrinology of National health Commission, Peking union Medical College Hospital, Chinese Academy of Medical Science & Peking Union Medical College, Beijing 100730, China
  • Received:2026-01-23 Revised:2026-03-24 Online:2026-05-05 Published:2026-04-28
  • Contact: *panhui20111111@163.com;shengxin2004@163.com

摘要: 目的 比较生长激素缺乏症(GHD)患儿、特发性矮小症(ISS)患儿及健康对照(HC)儿童血清抵抗素(resistin)、瘦素(leptin)和成纤维细胞生长因子23(FGF-23)水平的差异,评估1年生长激素(GH)治疗对GHD患儿上述指标的动态影响及其临床意义。方法 本研究前瞻性纳入了25例GHD儿童、25例ISS儿童和30例HC儿童。GHD患儿接受1年GH治疗,于基线、治疗后6个月及12个月时进行随访。采用ELISA检测上述因子水平,并同步收集身高、体质量、生长速度(GV)、胰岛素样生长因子-1(IGF-1)、血脂谱、空腹血糖(FBG)及胰岛素抵抗指数(HOMA-IR)等临床资料。用线性混合效应模型校正混杂并评估指标变化。结果 基线时,GHD组血清resistin和FGF-23水平均显著高于HC组(P< 0.05),leptin水平显著高于ISS组(P<0.05)。GH治疗1年后,三者水平均显著下降(P< 0.01),校正年龄、性别、体质指数标准差评分(BMI SDS)及胰岛素样生长因子-1标准差评分(IGF-1 SDS)后差异仍显著(P< 0.001)。同期,GHD患儿身高标准差评分(Ht SDS)由(-1.8±0.7)升至(-1.5±2.2),年生长速度从(4.6±1.1)cm/年增至(9.3±1.7)cm/年,IGF-1 SDS水平显著升高(P< 0.001)。FBG和三酰甘油轻度升高(P<0.05,P<0.01),但仍在正常参考范围;其余代谢指标差异无统计学意义。结论 GH治疗显著改善GHD患儿线性生长并降低resistin、leptin和FGF-23水平,短期代谢安全性良好。

关键词: 生长激素缺乏症, 生长激素治疗, 抵抗素, 瘦素, 成纤维细胞生长因子23

Abstract: Objective To compare serum level of resistin, leptin, and fibroblast growth factor 23(FGF-23)in children with growth hormone deficiency(GHD), children with idiopathic short stature(ISS), and healthy(children) control(HC) in order to evaluate the dynamic effects and clinical significance of one-year growth hormone(GH) therapy on these biomarkers. Methods This prospective cohort study enrolled 25 children with GHD, 25 children with ISS and 30 healthy children. Children with GHD received one-year growth hormone therapy. Fasting venous blood samples were collected before growth hormone therapy and at 6 and 12 months during treatment. Serum resistin, leptin, and FGF-23 levels were measured using ELISA. Clinical parameters including height, weight, growth velocity(GV),insulin-like growth factor 1(IGF-1), lipid profiles, fasting blood glucose(FBG), and homeostatic model assessment of insulin resistance(HOMA-IR) were collected at the same time. A linear mixed-effects model was used to adjust for confounders and evaluate indicator changes. Results The baseline level of serum resistin and FGF-23 in the GHD group was significantly higher than those in the healthy controls group(P<0.05), leptin level was significantly higher than those in the ISS group(P<0.05). After one-year GH therapy all three biomarkers significantly decreased in GHD children(P<0.01) and was still significant after adjustment for age, gender, body mass index standard deviation score(BMI SDS), and IGF-1 standard deviation score(IGF-1 SDS). Concurrently, height standard deviation score(Ht SDS) improved from(-1.8±0.7) to(-1.5±2.2), annual growth velocity increased from(4.6±1.1)cm/year to(9.3±1.7)cm/year, and IGF-1 SDS significantly increased(P<0.001). During treatment, FBG and triglyceride level mildly increased(P<0.05,P<0.01), but still kept within normal reference ranges; other metabolic parameters showed no significant changes. Conclusions GH therapy significantly improves linear growth and reduces resistin, leptin, and FGF-23 levels in children with GHD, demonstrating good short-term metabolic safety.

Key words: growth hormone deficiency, growth hormone therapy, resistin, leptin, fibroblast growth factor 23

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