مرور انجمن غدد درون‌ریز: تغییر اندک کوتاه‌مدت تراکم استخوان با هورمون‌ها، اما تقریباً هیچ داده‌ای دربارهٔ شکستگی

تأثیر استروئیدهای جنسی بر سلامت استخوان در افراد ترنس: مرور نظام‌مند و فراتحلیل

Authors
Naykky Singh-Ospina, Spyridoula Maraka, Rene Rodriguez-Gutierrez, Caroline Davidge-Pitts, Todd B. Nippoldt, Larry J. Prokop, Mohammad Hassan Murad
Journal
The Journal of Clinical Endocrinology & Metabolism
Year
2017

Summary

This review was one of the evidence reviews behind the Endocrine Society's 2017 guideline on treating gender dysphoria (distress about one's sex). The Mayo Clinic team combined 13 studies (639 people, mostly adults) that measured bone density before and after cross-sex hormones. Testosterone in females made no measurable difference to spine or hip bone density over one to two years. Estrogen in males slightly raised spine bone density. Only one study looked at broken bones (none in a year), and only one looked at teenagers given puberty blockers (drugs that pause puberty) and then hormones. That study found males had lower spine bone density at age 22 than before treatment. The authors said the effect on the risk of broken bones is uncertain. The review is reassuring about short-term bone density in adults, but cannot show long-term safety, fracture risk, or safety for teenagers.

Key findings

  • این مرور 13 مطالعه با 639 نفر را ترکیب کرد: 392 مردمتولد و 247 زن‌متولد.
  • در زن‌متولدهای مصرف‌کنندهٔ تستوسترون، تراکم استخوان در پایین ستون فقرات و لگن پس از یک یا دو سال تغییر قابل‌سنجشی نکرد.
  • در مردمتولدهای مصرف‌کنندهٔ استروژن، تراکم استخوان پایین ستون فقرات پس از یک سال اندکی و پس از دو سال کمی بیشتر بالا رفت.
  • فقط یک مطالعه، با 53 مردمتولد و 53 زن‌متولد، شکستگی‌ها را بررسی کرد و در 12 ماه هیچ نیافت.
  • فقط یک مطالعه نوجوانانی را که بلوکر بلوغ و سپس هورمون گرفتند پوشش داد، و یافت مردمتولدها در 22 سالگی تراکم استخوان ستون فقرات کمتری از پیش از درمان داشتند.
  • نویسندگان گفتند بیشتر شواهد از مطالعاتی آمد که خطر گمراه‌کننده بودنشان متوسط بود، و اثر بر خطر شکستگی نامطمئن است.
  • این مرور برای انجمن غدد درون‌ریز، با برنامه‌ای که با کارشناسانش ساخته شد، برای پشتیبانی از رهنمود 2017 آن انجام شد.

Abstract

BACKGROUND: The impact of sex steroids on bone health in transgender individuals is unclear.

METHODS: A comprehensive search of several databases to 7 April 2015 was conducted for studies evaluating bone health in transgender individuals receiving sex steroids. Pairs of reviewers selected and appraised studies. A random effects model was used to pool weighted mean differences and 95% confidence intervals (CIs).

RESULTS: Thirteen studies evaluating 639 transgender individuals were identified [392 male-to-female (MTF), 247 female-to-male (FTM)]. In FTM individuals and compared with baseline values before initiation of masculinizing hormone therapy, there was no statistically significant difference in the lumbar spine, femoral neck, or total hip bone mineral density (BMD) when assessed at 12 and 24 months. In MTF individuals and compared with baseline values before initiation of feminizing hormone therapy, there was a statistically significant increase in lumbar spine BMD at 12 months (0.04 g/cm2; 95% CI, 0.03 to 0.06 g/cm2) and 24 months (0.06 g/cm2; 95% CI, 0.04 to 0.08 g/cm2). Fracture rates were evaluated in a single cohort of 53 MTF and 53 FTM individuals, with no events at 12 months. The body of evidence is derived mostly from observational studies at moderate risk of bias.

CONCLUSION: In FTM individuals, masculinizing hormone therapy was not associated with significant changes in BMD, whereas in MTF individuals feminizing hormone therapy was associated with an increase in BMD at the lumbar spine. The impact of these BMD changes on patient-important outcomes such as fracture risk is uncertain.

Conclusion

In FTM individuals, masculinizing hormone therapy was not associated with significant changes in BMD, whereas in MTF individuals feminizing hormone therapy was associated with an increase in BMD at the lumbar spine. The impact of these BMD changes on patient-important outcomes such as fracture risk is uncertain.