Valenzise M, Nasso C, Scarfone A, Rottura M, Cafarella G, Pallio G, Visalli G, Di Prima E, Nasso E, Squadrito V, Wasniewska M, Irrera P, Arcoraci V, Squadrito F
Department of Human Pathology and Evolutive Age "Gaetano Barresi", University of Messina, Messina, Italy.
Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy.
Front Pediatr. 2023 May 17;11:1170025. doi: 10.3389/fped.2023.1170025. eCollection 2023.
Central precocious puberty (CPP) results from premature activation of hypothalamic-pituitary-gonadal axis, with the consequent increase of gonadotropin-releasing hormone (GnRH); GnRH agonists (GnRHa) represent the gold-standard therapy in children with CPP although their use might be responsible for pituitary GnRH receptors down-regulation, that in turn suppresses luteinizing hormone (LH) and follicle stimulating hormone (FSH) and blocks of gonadal sex hormones release. The most prescribed GnRHa in the clinical practice are leuprolide and triptorelin, whose use is generally safe and well tolerated; however, mild menopausal-like side effects could appear. The aim of the present study was to investigate and compare the efficacy and tolerability profile of leuprolide and triptorelin in CPP patients.
110 girls affected by CPP were enrolled in this retrospective study, carried out from 2018 to 2020. The enrolled patients received leuprolide ( = 48) or triptorelin ( = 62). Efficacy was investigated by the means of clinical parameters and radiological changes and side effects were also recorded to evaluate the possible relationship between the two GnRHa treatments and side effects appearance.
At baseline triptorelin patients had significantly higher LH and LH peak levels than leuprolide patients, whereas no significant difference in other patient characteristics was observed between the two groups. The leuprolide treatment lasted 971 days [790-1,171 days] while the duration of triptorelin administration was 792 days [760-1,003 days] ( < 0.001). Overall 46 (41.8%) of the studied patients reported mild menopausal-like symptoms: among these 27 were treated with triptorelin and 19 with leuprolide ( = 0.558). Patients treated with triptorelin, or leuprolide showed headache (27.4% vs. 16.7%), mood swings (12.9% vs. 16.7%), increased appetite (12.9% vs. 18.8%) and nausea (1.6% vs. 10.4%) respectively. Moreover, the onset of side effects appearance related to GnRHa therapy significantly reduces with the increase of the initial bone age ( = 0.038).
Leuprolide and triptorelin treatment appear to be effective and safe without significant difference between the two drugs in term of efficacy and tolerability, making both good options for treating CPP.
中枢性性早熟(CPP)是由下丘脑 - 垂体 - 性腺轴过早激活导致促性腺激素释放激素(GnRH)增加引起的;GnRH激动剂(GnRHa)是CPP患儿的金标准治疗药物,尽管其使用可能导致垂体GnRH受体下调,进而抑制黄体生成素(LH)和卵泡刺激素(FSH),并阻断性腺性激素的释放。临床实践中最常用的GnRHa是亮丙瑞林和曲普瑞林,其使用通常安全且耐受性良好;然而,可能会出现轻度的类绝经副作用。本研究的目的是调查和比较亮丙瑞林和曲普瑞林在CPP患者中的疗效和耐受性。
本回顾性研究纳入了110例受CPP影响的女孩,研究时间为2018年至2020年。纳入的患者接受亮丙瑞林(n = 48)或曲普瑞林(n = 62)治疗。通过临床参数和影像学变化来研究疗效,并记录副作用,以评估两种GnRHa治疗与副作用出现之间的可能关系。
基线时,曲普瑞林组患者的LH和LH峰值水平显著高于亮丙瑞林组患者,而两组患者的其他特征无显著差异。亮丙瑞林治疗持续971天[790 - 1171天],而曲普瑞林给药持续时间为792天[760 - 1003天](P < 0.001)。总体而言,46例(41.8%)研究患者报告有轻度类绝经症状:其中27例接受曲普瑞林治疗,19例接受亮丙瑞林治疗(P = 0.558)。接受曲普瑞林或亮丙瑞林治疗的患者分别出现头痛(27.4%对16.7%)、情绪波动(12.9%对16.7%)、食欲增加(12.9%对18.8%)和恶心(1.6%对10.4%)。此外,与GnRHa治疗相关的副作用出现与初始骨龄的增加显著减少有关(P = 0.038)。
亮丙瑞林和曲普瑞林治疗似乎有效且安全,两种药物在疗效和耐受性方面无显著差异,都是治疗CPP的良好选择。