Summary
The Amsterdam gender clinic, which pioneered puberty blockers for gender dysphoria (distress about one's sex), followed up adults who took blockers as teenagers and then cross-sex hormones for 9 to 15 years. As earlier studies found, bone density fell behind their peers while puberty was paused. Females given testosterone had caught back up to their starting level by about age 28. Males given estrogen recovered at the hip, but their lower-spine bone density stayed well below where it started and below average for their age. Depending on the comparison used, up to 18% of males had spine density far below normal for their age. The authors call the treatment 'safe' for bone in those taking testosterone. But only half of those eligible took part, people who stopped hormones were left out, there was no untreated comparison group, and broken bones were not measured.
Key findings
- O estudo acompanhou 75 adultos (25 nascidos do sexo masculino, 50 do feminino) que começaram bloqueadores da puberdade antes dos 18 anos e depois tomaram hormônios cruzados por cerca de 12 anos em média.
- Em comparação com outros da mesma idade, a densidade óssea ficou para trás durante os bloqueadores nos dois sexos, como estudos anteriores haviam mostrado.
- Nas pessoas do sexo masculino que receberam estrogênio, a densidade óssea da coluna lombar ainda estava claramente mais atrás de sua faixa etária do que antes dos bloqueadores, e abaixo da média, enquanto a densidade do quadril voltou ao ponto de partida.
- Dependendo do sexo com o qual foram comparados, 9% a 18% das pessoas do sexo masculino tinham densidade óssea da coluna muito abaixo da faixa normal para sua idade por volta dos 28 anos.
- Nas pessoas do sexo feminino que receberam testosterona, a densidade óssea da coluna e do quadril voltou ao que era antes do tratamento, próxima da média para a idade.
- Apenas 75 de 143 pessoas elegíveis (52%) participaram: 21% disseram não, 19% não puderam ser localizadas e 4% que haviam parado os hormônios foram deixadas de fora.
- Os autores concluíram que os bloqueadores seguidos de hormônios são 'seguros' para os ossos em quem toma testosterona, mas que quem toma estrogênio precisa de um tratamento mais bem ajustado e de mais estudo.
Abstract
IMPORTANCE: Bone mineral density (BMD) z scores in transgender adolescents decrease during puberty suppression with a gonadotropin-releasing hormone (GnRH) agonist. Previous research found that after short-term use of gender-affirming hormones (GAH), pretreatment z scores were not restored. Long-term follow-up studies are lacking.
OBJECTIVE: To assess BMD after long-term GAH treatment in transgender adults who used puberty suppression in adolescence.
DESIGN, SETTING, AND PARTICIPANTS: This single-center cohort study with follow-up duration of 15 years selected participants from a database containing all people visiting a gender identity clinic at an academic hospital in the Netherlands between 1972 and December 31, 2018. Recruitment occurred from March 1, 2020, to August 31, 2021. A total of 75 participants diagnosed with gender dysphoria who had used puberty suppression before age 18 years prior to receiving at least 9 years of long-term GAH were included.
EXPOSURES: Puberty suppression with a GnRH agonist followed by GAH treatment.
MAIN OUTCOMES AND MEASURES: Lumbar spine, total hip, and femoral neck BMD and z scores before the start of puberty suppression, at start of GAH, and at short- and long-term follow-up.
RESULTS: Among 75 participants, 25 were assigned male at birth, and 50 were assigned female at birth. At long-term follow-up, the median (IQR) age was 28.2 (27.0-30.8) years in participants assigned male at birth and 28.2 (26.6-30.6) years in participants assigned female at birth. The median (IQR) duration of GAH treatment was 11.6 (10.1-14.7) years among those assigned male at birth and 11.9 (10.2-13.8) years among those assigned female at birth. The z scores decreased during puberty suppression. In individuals assigned male at birth, the mean (SD) z score after long-term GAH use was -1.34 (1.16; change from start of GnRH agonist: -0.87; 95% CI, -1.15 to -0.59) at the lumbar spine, -0.66 (0.75; change from start of GnRH agonist: -0.12; 95% CI, -0.31 to 0.07) at the total hip, and -0.54 (0.84; change from start of GnRH agonist: 0.01; 95% CI, -0.20 to 0.22) at the femoral neck. In individuals assigned female at birth, after long-term GAH use, the mean (SD) z score was 0.20 (1.05; change from start of GnRH agonist: 0.09; 95% CI, -0.09 to 0.27) at the lumbar spine, 0.07 (0.91; change from start of GnRH agonist: 0.10; 95% CI, -0.06 to 0.26) at the total hip, and -0.19 (0.94; change from start of GnRH agonist: -0.20; 95% CI, -0.26 to 0.06) at the femoral neck.
CONCLUSIONS AND RELEVANCE: In this cohort study, after long-term use of GAH, z scores in individuals treated with puberty suppression caught up with pretreatment levels, except for the lumbar spine in participants assigned male at birth, which might have been due to low estradiol concentrations. These findings suggest that treatment with GnRH agonists followed by long-term GAH is safe with regard to bone health in transgender persons receiving testosterone, but bone health in transgender persons receiving estrogen requires extra attention and further study. Estrogen treatment should be optimized and lifestyle counseling provided to maximize bone development in individuals assigned male at birth.
Conclusion
In this cohort study, after long-term use of GAH, z scores in individuals treated with puberty suppression caught up with pretreatment levels, except for the lumbar spine in participants assigned male at birth, which might have been due to low estradiol concentrations. These findings suggest that treatment with GnRH agonists followed by long-term GAH is safe with regard to bone health in transgender persons receiving testosterone, but bone health in transgender persons receiving estrogen requires extra attention and further study. Estrogen treatment should be optimized and lifestyle counseling provided to maximize bone development in individuals assigned male at birth.