Testosterone Restores Body Composition, Bone Mass, and Bone Strength Following Early Puberty Suppression in a Mouse Model Mimicking the Clinical Strategy in Trans Boys

IF 5.1 1区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Vanessa Dubois, Silvia Ciancia, Stefanie Doms, Sarah El Kharraz, Vera Sommers, Na Ri Kim, Karel David, Jolien Van Dijck, Roger Valle-Tenney, Christa Maes, Leen Antonio, Brigitte Decallonne, Geert Carmeliet, Frank Claessens, Martine Cools, Dirk Vanderschueren
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引用次数: 3

Abstract

Transgender youth increasingly present at pediatric gender services. Some of them receive long-term puberty suppression with gonadotropin-releasing hormone analogues (GnRHa) before starting gender-affirming hormones (GAH). The impact of GnRHa use started in early puberty on bone composition and bone mass accrual is unexplored. It is furthermore unclear whether subsequent GAH fully restore GnRHa effects and whether the timing of GAH introduction matters. To answer these questions, we developed a mouse model mimicking the clinical strategy applied in trans boys. Prepubertal 4-week-old female mice were treated with GnRHa alone or with GnRHa supplemented with testosterone (T) from 6 weeks (early puberty) or 8 weeks (late puberty) onward. Outcomes were analyzed at 16 weeks and compared with untreated mice of both sexes. GnRHa markedly increased total body fat mass, decreased lean body mass, and had a modest negative impact on grip strength. Both early and late T administration shaped body composition to adult male levels, whereas grip strength was restored to female values. GnRHa-treated animals showed lower trabecular bone volume and reduced cortical bone mass and strength. These changes were reversed by T to female levels (cortical bone mass and strength) irrespective of the time of administration or even fully up to adult male control values (trabecular parameters) in case of earlier T start. The lower bone mass in GnRHa-treated mice was associated with increased bone marrow adiposity, also reversed by T. In conclusion, prolonged GnRHa use started in prepubertal female mice modifies body composition toward more fat and less lean mass and impairs bone mass acquisition and strength. Subsequent T administration counteracts GnRHa impact on these parameters, shaping body composition and trabecular parameters to male values while restoring cortical bone architecture and strength up to female but not male control levels. These findings could help guide clinical strategies in transgender care. © 2023 American Society for Bone and Mineral Research (ASBMR).

Abstract Image

睾酮在模仿跨性别男孩临床策略的小鼠模型中恢复青春期早期抑制后的身体成分、骨量和骨强度
越来越多的跨性别青年参加儿科性别服务。其中一些人在开始使用性别确认激素(GAH)之前,接受促性腺激素释放激素类似物(GnRHa)的长期青春期抑制。青春期早期开始使用GnRHa对骨成分和骨量增加的影响尚未探索。此外,尚不清楚随后的GAH是否完全恢复GnRHa效应,以及GAH引入的时间是否重要。为了回答这些问题,我们开发了一个模仿跨性别男孩临床策略的小鼠模型。青春期前4周龄雌性小鼠单独用GnRHa或用补充了睾酮(T)的GnRHa从6 周(青春期早期)或8周 数周后(青春期晚期)。在16岁时分析结果 周,并与未经治疗的两性小鼠进行比较。GnRHa显著增加了全身脂肪量,减少了瘦体重,并对握力产生了适度的负面影响。早期和晚期服用T使身体成分达到成年男性水平,而握力恢复到女性水平。GnRHa治疗的动物表现出较低的骨小梁体积和较低的皮质骨量和强度。这些变化被T逆转为女性水平(皮质骨量和强度),而与给药时间无关,甚至在T开始较早的情况下完全达到成年男性对照值(小梁参数)。GnRHa治疗小鼠的较低骨量与骨髓肥胖增加有关,T也逆转了这一点。总之,青春期前雌性小鼠开始长期使用GnRHa会改变身体成分,使其变得更胖、更瘦,并损害骨量的获取和强度。随后的T给药抵消了GnRHa对这些参数的影响,使身体组成和小梁参数达到男性值,同时使皮质骨结构和强度恢复到女性而不是男性的控制水平。这些发现可能有助于指导跨性别护理的临床策略。©2023美国骨与矿物研究学会(ASBMR)。
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来源期刊
Journal of Bone and Mineral Research
Journal of Bone and Mineral Research 医学-内分泌学与代谢
CiteScore
11.30
自引率
6.50%
发文量
257
审稿时长
2 months
期刊介绍: The Journal of Bone and Mineral Research (JBMR) publishes highly impactful original manuscripts, reviews, and special articles on basic, translational and clinical investigations relevant to the musculoskeletal system and mineral metabolism. Specifically, the journal is interested in original research on the biology and physiology of skeletal tissues, interdisciplinary research spanning the musculoskeletal and other systems, including but not limited to immunology, hematology, energy metabolism, cancer biology, and neurology, and systems biology topics using large scale “-omics” approaches. The journal welcomes clinical research on the pathophysiology, treatment and prevention of osteoporosis and fractures, as well as sarcopenia, disorders of bone and mineral metabolism, and rare or genetically determined bone diseases.
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