Abstract

ContextThe safety and efficacy of feminizing hormone therapy in aging transgender (trans) individuals is unclear. Current recommendations suggest transdermal estradiol beyond the age of 45 years, especially if cardiometabolic risk factors are present.ObjectiveTo evaluate feminizing hormone therapy regimens and cardiovascular risk factors in aging trans individuals.DesignRetrospective cross-sectional analysis.SettingPrimary care and endocrine specialist clinic in Melbourne, Australia.ParticipantsTrans individuals on feminizing therapy for ≥6 months.Main Outcomes MeasuresFeminizing hormone regimens and serum estradiol concentrations by age group: (a) ≥45 years, (b) <45 years, and prevalence of cardiometabolic risk factors in individuals ≥45 years.Results296 individuals were stratified by age group: ≥45 years (n=55) and <45 years (n=241). There was no difference in median estradiol concentration between groups (328 nmol/L vs. 300 nmol/L, p=0.22). However, there was a higher proportion of individuals ≥45 years treated with transdermal estradiol (31% vs. 8%, p<0.00001). Of those treated with oral estradiol, the median dose was lower in the ≥45 years group (4mg vs. 6mg, p=0.01). The most prevalent cardiometabolic risk factor in the ≥45 years group was hypertension (29%), followed by current smoking (24%), obesity (20%), dyslipidaemia (16%) and diabetes (9%).ConclusionsA greater proportion of trans individuals ≥45 years of age were treated with transdermal estradiol. Of those who received oral estradiol, the median dose was lower. This is important given the high prevalence of cardiometabolic risk factors in this age group, however cardiovascular risk management guidelines in this demographic are lacking.

Highlights

  • The intersection of aging and healthcare in transgender individuals is a novel area of research, and there is a paucity of data regarding the safety and efficacy of feminizing hormone therapy in older trans individuals

  • Individuals in the

  • Of those treated with oral estradiol, the median dose was lower in the ≥45 years group (4mg vs. 6mg, p=0.01), and the sex hormone binding globulin (SHBG) was higher (88nmol/L vs. 46nmol/L, p=0.004)

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Summary

Introduction

The intersection of aging and healthcare in transgender (trans) individuals is a novel area of research, and there is a paucity of data regarding the safety and efficacy of feminizing hormone therapy in older trans individuals Important considerations in this demographic include estradiol dose, formulation, route of administration, target sex steroid concentrations and duration of treatment. In the trans population, individuals on feminizing therapy (presumed male at birth) have a greater incidence of cardiovascular mortality than those on masculinizing therapy (123 per 100,000 person years vs 15 per 100,000 person years respectively) (1). The mechanisms underlying this discrepancy are poorly understood

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