타비스톡 사춘기 억제제 연구는 심리적 이점을 찾지 못했는데도 98%가 교차 성호르몬으로 이어감

영국에서 지속적 성별 불쾌감이 있는 12~15세 선별 코호트의 사춘기 억제 단기 결과

Authors
Polly Carmichael, Gary Butler, Una Masic, Tim J. Cole, Bianca L. De Stavola, Sarah Davidson, Elin M. Skageberg, Sophie Khadr, Russell M. Viner
Journal
PLOS ONE
Year
2021

Summary

This was the UK's own test of puberty blockers, run by the Tavistock's gender clinic for children from 2011. Forty-four carefully chosen 12–15-year-olds were given a blocker drug and followed until they were over 16. The blockers paused puberty as intended. But there was no measurable change in emotional distress, self-harm, quality of life or gender distress, and bone density fell behind other teens their age. Most young people spoke positively about the treatment in interviews, and 43 of 44 went on to cross-sex hormones. The authors call for larger studies. There was no comparison group, numbers fell sharply after the first year, and a later re-analysis found up to a third got worse. So the study offers no evidence that blockers help mental health.

Key findings

  • 심각하고 오래 지속되는 성별 불쾌감이 있는 12~15세 44명(출생 시 남성 25명, 여성 19명)이 클리닉에서 통상 2년의 평가를 거친 뒤 2011년부터 2015년 사이에 사춘기 차단제를 시작했습니다.
  • 부모도 청소년 본인도 1년, 2년, 3년 후 정서 또는 행동 문제나 자해에 어떤 변화도 보고하지 않았습니다.
  • 삶의 질, 자신의 몸에 대한 느낌, 성별 불쾌감, (임상의가 판단한) 대처 정도도 거의 변하지 않았습니다. 저자들은 차단제가 몸을 원하는 성 쪽으로 바꾸지 않는다고 지적합니다.
  • 허리 아래쪽 골밀도는 다른 10대보다 더디게 자라 나이에 비해 뒤처졌고, 키 성장도 느려졌습니다.
  • 두통, 안면 홍조, 피로 같은 예상된 부작용이 흔했습니다. 15~24개월 후 인터뷰에서 38%가 기력이 낮다고 말했습니다.
  • 44명 중 43명(98%)이 반대 성 호르몬으로 넘어갔으며, 이는 차단제 후에 중단하는 사람이 거의 없다는 네덜란드의 결과와 일치합니다.
  • 2년 시점에는 24명, 3년 시점에는 14명만 자료에 남아 있었고(3년 시점에 직접 설문지를 작성한 사람은 6명뿐), 장기 효과에 대해서는 말할 수 있는 것이 거의 없습니다.
  • 같은 자료에 대한 McPherson과 Freedman의 2024년 재분석은 측정 방법, 시점, 보고자에 따라 젊은이의 15~34%가 분명히 나빠졌다고 밝혔습니다.

Abstract

BACKGROUND: In adolescents with severe and persistent gender dysphoria (GD), gonadotropin releasing hormone analogues (GnRHa) are used from early/middle puberty with the aim of delaying irreversible and unwanted pubertal body changes. Evidence of outcomes of pubertal suppression in GD is limited. METHODS: We undertook an uncontrolled prospective observational study of GnRHa as monotherapy in 44 12-15 year olds with persistent and severe GD. Prespecified analyses were limited to key outcomes: bone mineral content (BMC) and bone mineral density (BMD); Child Behaviour CheckList (CBCL) total t-score; Youth Self-Report (YSR) total t-score; CBCL and YSR self-harm indices; at 12, 24 and 36 months. Semistructured interviews were conducted on GnRHa. RESULTS: 44 patients had data at 12 months follow-up, 24 at 24 months and 14 at 36 months. All had normal karyotype and endocrinology consistent with birth-registered sex. All achieved suppression of gonadotropins by 6 months. At the end of the study one ceased GnRHa and 43 (98%) elected to start cross-sex hormones. There was no change from baseline in spine BMD at 12 months nor in hip BMD at 24 and 36 months, but at 24 months lumbar spine BMC and BMD were higher than at baseline (BMC +6.0 (95% CI: 4.0, 7.9); BMD +0.05 (0.03, 0.07)). There were no changes from baseline to 12 or 24 months in CBCL or YSR total t-scores or for CBCL or YSR self-harm indices, nor for CBCL total t-score or self-harm index at 36 months. Most participants reported positive or a mixture of positive and negative life changes on GnRHa. Anticipated adverse events were common. CONCLUSIONS: Overall patient experience of changes on GnRHa treatment was positive. We identified no changes in psychological function. Changes in BMD were consistent with suppression of growth. Larger and longer-term prospective studies using a range of designs are needed to more fully quantify the benefits and harms of pubertal suppression in GD.

Conclusion

Treatment with GnRHa was efficacious in suppressing pubertal progression; anticipated effects of sex-hormone withdrawal were common and there were no unexpected adverse events. BMD increased in the lumbar spine and was stable at the hip, while BMD z-scores fell, consistent with delayed puberty. Overall participant experience was positive, but the authors identified no changes in psychological function, quality of life or degree of gender dysphoria. The great majority went on to cross-sex hormones; one did not, which the authors took as evidence that gender identity development continues on GnRHa. Larger, longer-term studies using a range of designs are needed to quantify benefits and harms.