芳香化酶抑制剂联合r-hGH改善青春期后期男童终身高的有效性和安全性:回顾性队列研究

The Effectiveness and Safety of Aromatase Inhibitors Combined with r-hGH in Improving Final Adult Height in Late-Pubertal Boys: A Retrospective Cohort Study

  • 摘要: 目的研究芳香化酶抑制剂(aromatase inhibitors,AI)联合重组人生长激素(recombinant human growth hormone,r-hGH)改善青春期后期男童终身高(final height,FH)的有效性及安全性。方法连续性纳入2017年2月—2022年12月于福建医科大学附属漳州市医院儿童生长发育科就诊的青春期伴生长减速男童临床资料,根据治不同疗方案将患儿分为GH组、AI联合GH组和对照组: GH组单用r-hGH剂量0.18~0.2 U/(kg·d)治疗,至生长速率小于0.5 cm/3个月时停药; AI联合GH组采用阿那曲唑1 mg/d或来曲唑2.5 mg/d联合r-hGH剂量0.18~0.2 U/(kg·d)治疗,AI应用1年后停药,r-hGH持续应用至生长速率小于0.5 cm/3个月时停药;对照组不采用任何促身高药物。所有患儿每3个月门诊随访1次,直至FH,监测生长发育指标及不良反应,并比较GH组和AI联合GH组的有效性和安全性。结果共入选符合纳入和排除标准的青春期男童69例,其中GH组28例、AI联合GH组17例、对照组24例,三组在身高、骨龄、骨龄别身高标准差积分(height standard deviation scorefor bone age,HtSDSBA)、遗传靶身高(target height,TH)和骨龄网络首发时间: 2025-10-17 09:25:25网络首发地址: https://link.cnki.net/urlid/11.5882.R.20251016.1704.010预测成人身高(predict adult height for bone age,PAHBA)方面差异均无统计学意义(P均>0.05)。69例均随访至FH,其中GH组FH为(165.54±2.06) cm,FH—PAHBA为(3.45±1.20) cm; AI联合GH组FH为(167.57±2.20) cm,FH—PAHBA为(5.60±1.32) cm;对照组FH为(163.78±2.63) cm,FH—PAHBA为(1.49±2.57) cm,三组FH、FH-PAHBA差异均有统计学意义(P均<0.05),相比其他两组,AI联合GH组可更好地改善FH。不良反应方面,AI联合GH组不良反应发生率高于GH组(P <0.001),主要表现为体重增加。结论 AI联合r-hGH治疗可有效改善青春期后期男童的FH,但治疗期间需密切监测不良反应

     

    Abstract: Objective To investigate the efficacy and safety of aromatase inhibitors (AI) combined with recombinant human growth hormone (r-hGH) in improving the final height (FH) of boys in late puberty.Methods Clinical data of pubertal boys with growth deceleration,consecutively admitted to the Department of Child Growth and Development,Zhangzhou Affiliated Hospital of Fujian Medical University between February 2017 and December 2022,were collected.According to different treatment regimens,the patients were divided into the GH group,the AI+GH group,and the control group.The GH group received r-hGH monotherapydose 0.18-0.2 U/(kg·d)until the growth velocity was less than 0.5 cm/3 months.The AI+GH group received anastrozole 1 mg/d or letrozole 2.5 mg/d combined with r-hGHdose 0.18-0.2 U/(kg·d);AI was discontinued after 1 year,while r-hGH was continued until the growth velocity was less than 0.5 cm/3 months.The control group did not receive any height-promoting drugs.All patients were followed up outpatient every 3 months until FH was reached,monitoring growth development indicators and adverse reactions.The efficacy and safety were compared between the GH group and the AI+GH group.Results A total of 69 pubertal boys meeting the inclusion and exclusion criteria were enrolled,including 28 in the GH group,17 in the AI+GH group,and 24 in the control group.There were no statistically significant differences among the three groups in terms of height,bone age,height standard deviation score for bone age (HtSDSBA),target height (TH),and predicted adult height for bone age (PAHBA)(all P > 0.05).All 69 cases were followed up to FH.The FH was (165.54 ± 2.06) cm in the GH group,with FHPAHBA being (3.45 ± 1.20) cm;the FH was (167.57 ± 2.20) cm in the AI+GH group,with FH-PAHBA being (5.60 ± 1.32) cm;and the FH was (163.78 ± 2.63) cm in the control group,with FH-PAHBA being (1.49 ± 2.57) cm.The differences in FH and FH-PAHBA among the three groups were statistically significant (all P < 0.05).Compared with the other two groups,the AI+GH group resulted in better improvement of FH.Regarding adverse reactions,the incidence in the AI+GH group was higher than that in the GH group (P < 0.001),primarily manifested as weight gain.Conclusion Combination therapy with AI and r-hGH can effectively improve the FH of boys in late puberty,but adverse reactions require close monitoring during treatment.

     

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