眼科 ›› 2026, Vol. 35 ›› Issue (1): 40-47.doi: 10.13281/j.cnki.issn.1004-4469.2026.01.007

• 论著 • 上一篇    下一篇

重组人生长激素对近视矮小症儿童眼球发育的影响

李涛1 唐娟2 张琴琴3 戴传强3   

  1. 1资阳市中心医院眼科 资阳市眼科重点实验室 四川大学华西医院资阳医院,四川资阳641300;2资阳市中心医院内分泌科,四川资阳641300;3资阳市中心医院医教部,四川资阳641300
  • 收稿日期:2024-11-01 出版日期:2026-01-25 发布日期:2026-01-13
  • 通讯作者: 唐娟,Email:874548166@qq.com E-mail:874548166@qq.com
  • 基金资助:
    四川省成都医学院联合科研基金(25LHYW2-01; 25LHYW2-02);四川省卫生健康委员会科技项目(24WSXT096;24WSXT098);四川省医学会医学科研项目和青年创新项目(Q2024062);四川省医疗卫生与健康促进会科研课题(SCMHPI2025HT261)

Effect of recombinant human growth hormone on eye development in dwarfism children with myopia

Li Tao1, Tang Juan2, Zhang Qinqin3, Dai Chuanqiang3   

  1. 1 Department of Ophthalmology, Ziyang Central Hospital, Ziyang Key Laboratory of Ophthalmology, West China Hospital of Sichuan University-Ziyang Hospital, Ziyang Sichuan 641300, China; 2 Department of Endocrinology, Ziyang Central Hospital, Ziyang Sichuan 641300, China; 3 Department of Medical Education, Ziyang Central Hospital, Ziyang Sichuan 641300, China
  • Received:2024-11-01 Online:2026-01-25 Published:2026-01-13
  • Contact: Tang Juan, Email: 874548166@qq.com E-mail:874548166@qq.com
  • Supported by:
    Chengdu Medical College Joint Research Fund of Sichuan Province (25LHYW2-01; 25LHYW2-02); Sichuan Provincial Health Commission Science and Technology Project (24WSXT096; 24WSXT098); Sichuan Medical Association Medical Research and Youth Innovation Project (Q2024062); Sichuan Medical and Health Care Promotion Institute Scientific Research Project (SCMHPI2025HT261)

摘要: 目的 探讨第二性征背景下重组人生长激素(recombinant human growth hormone,rhGH)对于近视矮小症儿童眼球发育的影响。设计 病例对照研究。 研究对象 资阳市中心医院2021年2月至2024年5月收治的第二性征年龄阶段的矮小症儿童60例(120眼),另设置发育正常的儿童60例为正常对照组。方法 60例矮小症儿童随机分为治疗组(30例)和非治疗组(30例),治疗组予以rhGH干预生长发育。对比各组治疗前和治疗后1年和2年儿童身高、生长激素(growth hormone deficiency,GH)、血清胰岛素样生长因子-1(insulin like growth factor-1,IGF-1)和胰岛素样生长因子结合蛋白-3(insulin-like growth factor binding protein-3,IGFBP-3)以及眼部生物学指标[角膜曲率(corneal curvature,CC)、等效球镜度数(spherical equivalent , SE)、角膜散光(astigmatism,AST)、前房深度(anterior chamber depth,AD)、玻璃体深度(vitreous thickness,VT)、眼轴(axial length,AL)]的变化趋势。主要指标 儿童身高、GH、IGF-1和IGFBP-3以及眼部生物学指标。结果 治疗前矮小组儿童平均身高、IGF-1、GH、和IGFBP-3明显低于正常对照组(P均<0.05)。Pearson 相关分析和线性回归分析显示治疗前矮小组和正常对照组儿童CC(r=0.681、0.375,P=0.001、0.003)、SE(r=0.474、0.427,P=0.007、0.003)、AST(r=0.392、0.394,P=0.002、0.001)、AL(r=0.369、0.369,P=0.003、0.001)、AD(r=0.385、0.275,P=0.017、0.001)和VT(r=0.175、0.258,P=0.003、0.021)均与身高呈正相关。 予以rhGH治疗1年和2年后,治疗组儿童身高、IGF-1、GH和IGFBP-3均明显升高,其中2年后身高的增加量为(27.53±3.02)cm,明显高于非治疗组(17.14±1.95)cm(P=0.001)。与基线比较,治疗组、非治疗组和正常对照组儿童随访1年和2年CC、SE、AL值、AD、VT均增加(P均<0.05),其中治疗组、非治疗组和正常对照组儿童随访1年的SE增加量分别为(0.87±0.13)D、(0.33±0.07)D和(0.32±0.09)D,随访2年的SE增加量分别为(1.72±0.49)D、(0.54±0.12)D和(0.79±18)D;AL 1年的增加量分别为(0.64±0.12)cm、(0.22±0.06)cm、(0.33±0.09)cm;AL 2年的增加量分别为(1.17±0.28)cm、(0.51±0.13)cm、(0.56±0.15)cm(P均<0.05);此外,在1年和2年随访时间点,与非治疗组相比,治疗组患儿CC、AST、AD、VT增加量与SE和AL变化趋势一致(P均<0.05)。结论 rhGH治疗可导致第二性征背景下近视矮小症儿童近视发展加速,针对该类患儿需高度关注眼部生物学指标变化趋势,避免眼轴过度发育,及时采取近视防控措施。

关键词: 近视, 眼球发育, 矮小症, 重组人生长激素, 眼生物学指标

Abstract: Objective To explore the effect of recombinant human growth hormone (rhGH) on eye development in children with myopia and dwarfism under the background of secondary sexual characteristics. Design Case-control study. Participants Sixty children (120 eyes) with dwarfism in the age stage of secondary sexual characteristics admitted to Ziyang Central Hospital from February 2021 to May 2024, while 60 children with normal development were set as the normal control group. Methods Sixty children (120 eyes) with dwarfism were randomly divided into treatment group and observed group. The treatment group received rhGH intervention for growth and development. The changes in height, growth hormone (GH), serum insulin-like growth factor-1 (IGF-1), insulin-like growth factor binding protein-3 (IGFBP-3), and ocular biological indicators [including corneal curvature(CC), spherical equivalent (SE), astigmatism (AST), axial length (AL), anterior chamber depth (AD), vitreous thickness (VT)] were compared and analyzed before and after treatment for 1 and 2 years. Main Measure Outcomes Height, GH, IGF-1, IGFBP-3, and ocular biological indicators. Results Before treatment, the average height, IGF-1, GH, and IGFBP-3 of children in the dwarfism group were significantly lower than those in the normal control group (all P<0.05); Pearson correlation analysis and linear regression analysis showed that CC (r=0.681, 0.375; P=0.001, 0.003), SE (r=0.474, 0.427; P=0.007, 0.003), AST (r=0.392, 0.394; P=0.002, 0.001), AL (r=0.369, 0.369; P=0.003, 0.001), AD (r=0.385, 0.275; P=0.017, 0.001), and VT (r=0.175, 0.258; P=0.003, 0.021) were positively correlated with height in both the dwarfism group and the normal control group of children. After 1 and 2 years of treatment with rhGH, the height, IGF-1, GH, and IGFBP-3 of the treatment group significantly increased (all P<0.05). The increase in height after 2 years was (27.53±3.02) cm, which was significantly higher than that of the non treatment group (17.14±1.95 cm) (P=0.001). Compared with baseline, the CC, SE, AL, AD and VT of children in the treatment group, non treatment group, and normal control group increased at 1-year and 2-year follow-up, and the differences were statistically significant (all P<0.05). The SE increases in the treatment group, non treatment group, and normal control group at 1-year follow-up were (0.87±0.13) D, (0.33±0.07) D and (0.32±0.09) D, respectively, and at 2-year follow-up were (1.72±0.49) D, (0.54±0.12) D and (0.79±18) D, respectively. The annual increase in AL was (0.64±0.12) cm, (0.22±0.06) cm and (0.33±0.09) cm, respectively. The two-year increase in AL was (1.17±0.28) cm, (0.51±0.13) cm, and (0.56±0.15) cm, respectively (all P<0.05). In addition, at the 1-year and 2-year follow-up time points, compared with the non treatment group, the increase in CC, AST, AD, and VT in the treatment group was consistent with the trend of SE and AL changes, and the differences were statistically significant (all P<0.05). Conclusion rhGH therapy can accelerate the progression of myopia in dwarfism children under the background of secondary sexual characteristics. For such patients, close monitoring of ocular biological indicators is essential to prevent excessive axial length growth and to implement timely myopia prevention measures.

Key words: Myopia, Ocular development, Dwarfism, Recombinant human growth hormone, Eye biological indicators