Davis Shanlee, Howell Susan, Janusz Jennifer, Lahlou Najiba, Reynolds Regina, Thompson Talia, Swenson Karli, Wilson Rebecca, Ross Judith, Zeitler Philip, Tartaglia Nicole
Department of Pediatrics, Section of Endocrinology, University of Colorado SOM, Aurora, Colorado, USA.
eXtraOrdinarY Kids Clinic and Research Program, Children's Hospital Colorado, Aurora, Colorado, USA.
medRxiv. 2025 Feb 6:2024.12.09.24318726. doi: 10.1101/2024.12.09.24318726.
47,XXY/Klinefelter syndrome (XXY) is associated with impaired testicular function and differences in physical growth, metabolism, and neurodevelopment. Clinical features of XXY may be attributable to inadequate testosterone during the mini-puberty period of infancy.
We tested the hypothesis that exogenous testosterone treatment positively effects short-term physical, hormonal, and neurodevelopmental outcomes in infants with XXY.
Double-blind randomized controlled trial, 2017-2021.
US tertiary care pediatric hospital.
Infants 30-90 days of age with prenatally identified, non-mosaic 47,XXY (n=71).
Testosterone cypionate 25mg intramuscular injections every 4 weeks for 3 doses.
The primary outcomes were change in percent fat mass (%FM) z-scores and change in the total composite percentile on Alberta Infant Motor Scales (AIMS) assessment from baseline to 12 weeks.
The between group difference in change in %FM z-scores was -0.57 [95% CI -1.1, -0.06], p=0.03), secondary to greater increases in lean mass in the testosterone-treated group (1.5±0.4 kg vs 1.2±0.4, p=0.001). Testosterone suppressed gonadotropins and inhibin B (p<0.001 for all). In contrast, there were no significant group differences in short term motor, cognitive, or language outcomes (p>0.15 for all).
In this double-blind randomized controlled trial in infants with XXY, testosterone injections resulted in physical effects attributable to systemic androgen exposure; however, there was no impact on neurodevelopmental outcomes and the hypothalamic-pituitary-gonadal axis was suppressed. These results do not support routine testosterone treatment in infants with XXY, however long term follow up on physical health, neurodevelopment and testicular function is needed.
47,XXY/克氏综合征(XXY)与睾丸功能受损以及身体生长、代谢和神经发育差异有关。XXY的临床特征可能归因于婴儿小青春期期间睾酮分泌不足。
我们检验了以下假设,即外源性睾酮治疗对患有XXY的婴儿的短期身体、激素和神经发育结局有积极影响。
2017年至2021年的双盲随机对照试验。
美国三级护理儿科医院。
30至90日龄、产前确诊为非嵌合型47,XXY的婴儿(n = 71)。
每4周肌肉注射25mg环戊丙酸睾酮,共3剂。
主要结局为从基线到12周时脂肪量百分比(%FM)z评分的变化以及艾伯塔婴儿运动量表(AIMS)评估中总综合百分位数的变化。
%FM z评分变化的组间差异为-0.57[95%CI -1.1,-0.06],p = 0.03),这是由于睾酮治疗组的瘦体重增加更多(1.5±0.4kg对1.2±0.4,p = 0.001)。睾酮抑制促性腺激素和抑制素B(所有p<0.001)。相比之下,短期运动、认知或语言结局无显著组间差异(所有p>0.15)。
在这项针对患有XXY的婴儿的双盲随机对照试验中,睾酮注射导致了全身雄激素暴露所致的身体效应;然而,对神经发育结局没有影响,并且下丘脑-垂体-性腺轴受到抑制。这些结果不支持对患有XXY的婴儿进行常规睾酮治疗,然而需要对身体健康、神经发育和睾丸功能进行长期随访。