Impact of Testosterone on Endothelial Function Varies by GnRH Agonist Treatment

睾酮对内皮功能的影响因促性腺激素释放激素激动剂治疗而异

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Abstract

CONTEXT: Transgender adults taking testosterone have impaired endothelial function, a triggering mechanism for cardiovascular disease. The impact of testosterone with and without gonadotropin-releasing hormone agonists (GnRHa) on endothelial function in transgender adolescents is unknown. OBJECTIVE: To evaluate the effects of 12 months of testosterone therapy on endothelial function among transgender adolescents and whether the effects differ based on exposure to GnRHa. DESIGN: Longitudinal, observational study with assessments prior to and after 1 and 12 months of testosterone therapy. SETTING: Academic regional referral center. PARTICIPANTS: Nineteen adolescents with a female sex (8 receiving GnRHa, 11 not receiving GnRHa). INTERVENTIONS: Clinically prescribed testosterone. MAIN OUTCOME MEASURES: Endothelial function assessed by brachial artery flow mediated dilation (FMD) at baseline and after 1 and 12 months testosterone therapy. Differences between groups were assessed at baseline by t-test and over time with a linear regression model with a time*group interaction. RESULTS: FMD was lower in GnRHa + compared to GnRHa- individuals at baseline (7.9 ± 2.5% vs 10.9 ± 2.9%, P = .029) and after 1 month (P = .042) of testosterone therapy. After 12 months of testosterone, FMD was similar between groups: 9.9 ± 4.2% for GnRHa + and 9.8 ± 2.8% for GnRHa- (P = .965). There was a significant interaction in the linear regression model for FMD (P = .030) with an increase in FMD for GnRHa + individuals and a decrease in FMD for GnRHa- individuals after 12 months of testosterone. CONCLUSION: Prior to testosterone therapy, GnRHa + individuals had lower endothelial function compared to GnRHa- individuals. The effects of testosterone on endothelial function were modulated by GnRHa status.

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