Efficacy of leuprolide acetate versus triptorelin pamoate administered every 3 months for treatment of central precocious puberty.

IF 3.2 Q1 PEDIATRICS Clinical and Experimental Pediatrics Pub Date : 2025-01-01 Epub Date: 2024-11-06 DOI:10.3345/cep.2024.00822
Thanaporn Thaneetrakool, Suphab Aroonparkmongkol, Nattakarn Numsriskulrat, Vichit Supornsilchai, Suttipong Wacharasindhu, Khomsak Srilanchakon
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Abstract

Background: Central precocious puberty (CPP) is typically treated with gonadotropin-releasing hormone (GnRH) agonists. Although numerous GnRH agonist variants are available, limited research has compared the efficacy of leuprolide acetate and triptorelin pamoate administered at 3-month intervals.

Purpose: This study aimed to assess the efficacy of CPP treatment with triptorelin pamoate and leuprolide acetate administered at 3-month intervals.

Methods: This retrospective cohort study included 116 girls with CPP: 71 treated with leuprolide acetate every 3 months and 45 treated with triptorelin pamoate every 3 months. Anthropometric measurements were compared before and after therapy. At 6 months after the therapy, luteinizing hormone (LH) suppression was evaluated.

Results: When administered every 3 months, leuprolide acetate and triptorelin pamoate significantly suppressed LH. The predicted adult height (PAH) and degree of bone age advancement at the end of treatment were comparable.

Conclusion: Treatment with leuprolide acetate and triptorelin pamoate every 3 months did not have significantly different effects on LH suppression or PAH.

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在治疗中枢性性早熟方面,醋酸亮丙瑞林与帕莫酸曲普瑞林每 3 个月给药一次的疗效对比。
背景:中枢性性早熟(CPP)通常采用促性腺激素释放激素(GnRH)激动剂治疗。目的:本研究旨在评估醋酸曲普瑞林和醋酸亮丙瑞林治疗中枢性性早熟的疗效:这项回顾性队列研究包括116名CPP女孩:71名每3个月接受一次醋酸亮丙瑞林治疗,45名每3个月接受一次帕莫酸曲普瑞林治疗。对比了治疗前后的人体测量数据。治疗 6 个月后,对黄体生成素(LH)抑制情况进行了评估:结果:醋酸亮丙瑞林和帕莫酸曲普瑞林每 3 个月给药一次,可显著抑制 LH。结论:醋酸亮丙瑞林和帕莫酸曲普瑞林治疗可明显抑制促性腺激素(LH),治疗结束时的预测成人身高(PAH)和骨龄增长程度相当:结论:每 3 个月服用醋酸亮丙瑞林和帕莫酸曲普瑞林对抑制 LH 或 PAH 的效果没有明显差异。
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来源期刊
CiteScore
8.00
自引率
2.40%
发文量
88
审稿时长
60 weeks
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