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Gonadorelin

GnRH, Luteinizing Hormone-Releasing Hormone, LHRH, Factrel

Quick Stats
Studies 192
Trials 100
Score 3
2025 pubmed

Metabolic safety of gender-affirming hormonal treatment in transgender females.

Milionis. Charalampos C; Barouti. Konstantina K; Papadopoulou. Vassiliki V; Pouliasi. Foteini F; Karlafti. Efthymia E; Makrydima. Sofia S; Karampa. Stavroula S; Venaki. Evaggelia E; Koukkou. Eftychia E

Key Findings

  • After ~18 months, estradiol averaged 85.65 pg/mL and testosterone dropped to 24 ng/dL, staying within therapeutic targets.
  • Triglycerides rose significantly, but no participants developed severe hypertriglyceridemia.
  • Hemoglobin and hematocrit fell significantly, yet no cases of clinically relevant anemia occurred.
  • Total, HDL, and LDL cholesterol, glucose, and liver enzymes showed no significant changes.

Practical Outcomes

  • If you’re using a GnRH agonist like gonadorelin with estradiol, keep an eye on triglyceride levels and blood‑cell counts through regular labs. Staying within the recommended estradiol and testosterone ranges appears important for metabolic safety. Adjust diet or consider lipid‑lowering strategies if triglycerides climb, and monitor for any signs of anemia.

Summary

A study of transgender women who took oral estradiol and a GnRH‑agonist (similar to gonadorelin) for about a year and a half showed that the hormone mix kept estrogen and testosterone in the desired range, but it did raise triglyceride levels a bit and lowered red‑blood‑cell counts, though not enough to cause serious problems. Other health markers like cholesterol, blood sugar, and liver enzymes stayed stable.

Abstract

Background Gender incongruence results from the mismatch between gender identity and thesex assigned at birth. The process of gender affirmation includes a series of procedures during which the transgender individual acquires phenotypic features of the desired sex. Hormonal therapy for transgender women aims to suppress endogenous androgens and replace them with estrogens. The present study sought to investigate the safety of feminizing therapy in transgender women in relation to somatometric and metabolic parameters. Methods The medical records of transgender women who received oral estradiol valerate and a gonadotropin-releasing hormone (GnRH) agonist for at least 18months were reviewed. The study population had estradiol levels within the normal limits of the follicular phase of cisgender women of reproductive age and suppressed blood testosterone levels after 18months of treatment. Changes in body mass index, glycemic and lipid profiles, hemoglobin and hematocrit, and liver function tests were examined. The paired t -test was used for statistical analysis. Results The mean blood estradiol and testosterone levels after approximately 18months of treatment were 85.65pg/mL and 24ng/dL, respectively. There was a statistically significant increase in blood triglycerides as well as a statistically significant decrease in hemoglobin and hematocrit. However, none of the participants developed severe hypertriglyceridemia or anemia. No significant changes were found in blood cholesterol (total, high-density lipoprotein, and low-density lipoprotein cholesterol), glucose, and liver enzymes. Conclusions Treatment with oral estradiol valerate and an intramuscular GnRH agonist is used in daily clinical practice to promote feminizing physical changes in transgender women. However, the possibility of side effects is not well documented. The present study demonstrated that achieving estradiol and testosterone levels within therapeutic targets is important for the safety of gender-affirming therapy.

Study Information

Provider

pubmed

Year

2025

DOI

10.1071/sh25113