Summary

To prepare its 2017 guideline on hormone treatment for trans people, the Endocrine Society (a body of hormone doctors) paid Mayo Clinic reviewers to gather all studies on cross-sex hormones and heart health. They found 29 studies. Almost all simply observed patients, and many had no comparison group. Testosterone in trans men worsened cholesterol, raising 'bad' cholesterol and blood fats and lowering 'good' cholesterol. Estrogen in trans women raised blood fats. Heart attacks, strokes, blood clots and deaths were too rarely reported to measure risk, though they were more common in trans women. The reviewers judged the evidence low quality. The review mainly shows how little was known about heart safety when the guideline was written. Larger studies published since (for example Getahun 2018 and Nota 2019) are not included.

Key findings

• انجمن غدد درون‌ریز هزینهٔ این مرور را برای پشتیبانی از رهنمود 2017 خود دربارهٔ درمان دیسفوریای جنسیتی (ناراحتی از جنس خود) با هورمون‌ها پرداخت.
• 29 مطالعه با 3,231 زن ترنس و 1,500 مرد ترنس را شامل شد؛ فقط 1 مطالعه درمان را تصادفی تخصیص داد، 17 مطالعه صرفاً افراد را پیش و پس مقایسه کردند و فقط 4 مطالعه گروه مقایسه داشت.
• در مردان ترنس، پس از 2 سال یا بیشتر، تستوسترون با چربی‌های خون بالاتر (تری‌گلیسرید، 21.4 mg/dL بالاتر)، کلسترول «بد» بالاتر (17.8 mg/dL بالاتر) و کلسترول «خوب» پایین‌تر (تا 8.5 mg/dL کمتر) مرتبط بود.
• در زنان ترنس، چربی‌های خون پس از 2 سال یا بیشتر بالاتر بود (31.9 mg/dL بالاتر)، بدون تغییر روشن در کلسترول.
• در زنان ترنس، مطالعات 56 لختهٔ خون در 1,767 نفر، 14 سکتهٔ قلبی در 1,073 نفر، 8 سکته در 859 نفر و 139 مرگ در 1,486 نفر را گزارش کردند، از جمله 23 مرگ قلبی و 26 خودکشی.
• در مردان ترنس، مطالعات فقط 1 لخته در 771 نفر، 1 سکتهٔ قلبی در 478 نفر، هیچ سکته در 340 نفر و 13 مرگ در 651 نفر را گزارش کردند.
• مرورگران شواهد کلی را کم‌کیفیت ارزیابی کردند، احتمالاً متأثر از گزارش گزینشی، با داده اندک دربارهٔ رویدادهای سلامتی که برای بیماران مهم‌ترند.

Abstract

BACKGROUND: Transgender individuals receive cross-sex hormonal therapy to induce desired secondary sexual characteristics despite limited data regarding its effects on cardiovascular health. METHODS: A comprehensive search of several databases up to 7 April 2015 was conducted for studies evaluating the effect of sex steroid use on lipids, myocardial infarction, stroke, venous thromboembolism (VTE), and mortality in transgender individuals. Pairs of reviewers selected and appraised the studies. A random-effects model was used to pool weighted mean differences and 95% confidence intervals (CIs). RESULTS: We found 29 eligible studies with moderate risk of bias. In female-to-male (FTM) individuals, sex steroid therapy was associated with statistically significant increases in serum triglyceride (TG) levels at 3 to 6 months and at ≥24 months (21.4 mg/dL; 95% CI: 0.14 to 42.6) and in low-density lipoprotein cholesterol (LDL-C) levels at 12 months and ≥24 months (17.8 mg/dL; 95% CI: 3.5 to 32.1). High-density lipoprotein cholesterol (HDL-C) levels decreased significantly across all follow-up periods (highest at ≥24 months, -8.5 mg/dL; 95% CI: -13.0 to -3.9). In male-to-female (MTF) individuals, serum TG levels were significantly higher at ≥24 months (31.9 mg/dL; 95% CI: 3.9 to 59.9) without any changes in other parameters. Few myocardial infarction, stroke, VTE, and death events were reported (more frequently in MTF individuals). CONCLUSIONS: Low-quality evidence suggests that sex steroid therapy may increase LDL-C and TG levels and decrease HDL-C level in FTM individuals, whereas oral estrogens may increase TG levels in MTF individuals. Data about important patient outcomes remain sparse.

Conclusion

Low-quality evidence suggests that sex steroid therapy may increase LDL-C and TG levels and decrease HDL-C level in FTM individuals, whereas oral estrogens may increase TG levels in MTF individuals. Data about important patient outcomes remain sparse.