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The Effects of Orchiectomy and Age on Vascular and Metabolic Health in Older Versus Younger Transgender Women

The Effects of Orchiectomy and Age on Vascular and Metabolic Health in Older Versus Younger Transgender Women

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05195164
Enrollment
17
Registered
2022-01-18
Start date
2021-03-22
Completion date
2023-12-31
Last updated
2024-09-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Appetitive Behavior, Blood Pressure, Gender Identity, Insulin Sensitivity, Lipid Disorder, Transgender, Vascular Inflammation, Vascular Stiffness

Brief summary

This study plans to learn more about differences in heart disease risk after gender-affirming orchiectomy (i.e., testes removal) in older transgender (trans) women compared to younger trans women.

Detailed description

The global aim of this study is to characterize cardiometabolic risk (measured by vascular, metabolic and biochemical factors-which have not been extensively studied prospectively) in trans women before and after orchiectomy. Trans women appear to be at greater risk for cardiovascular disease (CVD) and blood clots compared to non-trans adults. The effect of orchiectomy on CVD risk among trans women is unknown, but orchiectomy may change blood vessel function and metabolic health. The investigators will examine blood vessel function and metabolic profiles of trans women before and at several timepoints after orchiectomy to identify age-related differences in CVD risk factors. This knowledge may lead to new approaches to prevent CVD in trans women as well as all people regardless of gender identity.

Interventions

OTHERNo intervention

There was no intervention

Sponsors

Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
CollaboratorNIH
National Center for Advancing Translational Sciences (NCATS)
CollaboratorNIH
University of Colorado, Denver
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 99 Years
Healthy volunteers
Yes

Inclusion criteria

* Aged 18 years and older * Identify as a transgender woman * Have taken estradiol and spironolactone for at least one year * Currently taking oral or transdermal or injectable estradiol * Have not yet undergone but desire orchiectomy

Exclusion criteria

* Under 18 years of age * Don't identify as a transgender woman * Not currently taking estradiol or spironolactone * Have been on estradiol and spironolactone for less than one year * History of orchiectomy * Not deemed a candidate for orchiectomy * Current tobacco smoker * Current illicit drug use * History of prior or active estrogen-dependent neoplasms * Acute liver or gallbladder disease * Venous thromboembolism * Hypertriglyceridemia \>500 mg/dL * Fasted plasma glucose \>7.0 mmol/L or previously treated diabetes * Resting blood pressure \>140/90 mmHg

Design outcomes

Primary

MeasureTime frameDescription
Evaluation of endothelial function (flow-mediated dilation (FMD) at BaselineBaselineBrachial artery flow-mediated dilation (FMD), as measured by ultrasound.
Evaluation of endothelial function (flow-mediated dilation (FMD) at 1 Month1 monthBrachial artery flow-mediated dilation (FMD), as measured by ultrasound.
Evaluation of endothelial function (flow-mediated dilation (FMD) at 6 Months6 monthBrachial artery flow-mediated dilation (FMD), as measured by ultrasound.
Evaluation of endothelial function (flow-mediated dilation (FMD) at 12 Months12 monthBrachial artery flow-mediated dilation (FMD), as measured by ultrasound.

Secondary

MeasureTime frameDescription
Carotid artery intimal-medial thicknessBaseline, 1 mo., 6 mo., 12 mo.
Evaluation of oxidant burden: oxidized LDLBaseline, 1 mo., 6 mo., 12 mo.Oxidized low-density lipoprotein (LDL) measured in the blood and endothelial cells.
Evaluation of oxidant burden: nitrotyrosineBaseline, 1 mo., 6 mo., 12 mo.Nitrotyrosine measured in the blood and endothelial cells.
Evaluation of vascular endothelial cell inflammation: nuclear factor kappa-light-chain-enhancer of activated B cells (NFkB)Baseline, 1 mo., 6 mo., 12 mo.Protein NFkB (nuclear factor kappa-light-chain-enhancer of activated B cells) measured in blood and endothelial cells.
Evaluation of vascular endothelial cell inflammation: CRPBaseline, 1 mo., 6 mo., 12 mo.C-reactive protein (CRP) measured in blood and endothelial cells.
Blood pressureBaseline, 1 mo., 6 mo., 12 mo.Blood pressure will be measured at baseline, 1 mo., 6 mo. 12 mo.
Plasma lipid concentrations: total cholesterolBaseline, 1 mo., 6 mo., 12 mo.Total cholesterol will be determined at baseline, 1 mo., 6 mo., 12 mo.
Plasma lipid concentrations: triglyceridesBaseline, 1 mo., 6 mo., 12 mo.Triglycerides will be determined at baseline, 1 mo., 6 mo., 12 mo.
Insulin sensitivityBaseline, 1 mo., 6 mo., 12 mo.
Whole body composition: Percent Lean MassBaseline, 6 mo., 12 mo.Percent lean mass will be determined using dual energy x-ray absorptiometry.
Whole body composition: Percent Fat MassBaseline, 6 mo., 12 mo.Percent fat mass will be determined using dual energy x-ray absorptiometry.
Evaluation of vascular endothelial cell inflammation: MCP-1Baseline, 1 mo., 6 mo., 12 mo.Monocyte Chemoattractant Protein-1 (MCP-1) measured in blood and endothelial cells.
Regional body composition: Percent Fat MassBaseline, 6 mo., 12 mo.Regional percent fat mass will be determined using dual energy x-ray absorptiometry.
Bone densityBaseline, 12 mo.Bone density of femur and spine will be determined using dual energy x-ray absorptiometry.
Weight changesBaseline, 1 mo., 6 mo., 12 mo.Body weight will be measured at baseline, 1 mo., 6 mo., 12 mo.
Appetite ratingsBaseline, 1 mo., 6 mo., 12 mo.
Appetite-related peptidesBaseline, 1 mo., 6 mo., 12 mo.
D-DimerBaseline, 1 mo., 6 mo., 12 mo.
Alcohol useBaseline, 1 mo., 6 mo., 12 mo.
Depression symptomsBaseline, 1 mo., 6 mo., 12 mo.
Physical activity monitoring7 days at baseline, 1 mo., 6 mo., 12 mo.Physical activity will me monitored for 7 days with an ActivPAL monitor
Energy intake3 days at baseline, 1 mo., 6 mo., 12 mo.Energy intake will be estimated with a 3-day food diary
Sex hormone concentrationsBaseline, 1 mo., 6 mo., 12 mo.Sex hormone concentrations of estradiol, testosterone, follicle stimulating hormone (FSH), luteinizing hormone (LH) and sex hormone-binding globulin (SHBG) will be measured
Regional body composition: Percent Lean MassBaseline, 6 mo., 12 mo.Regional percent lean mass will be determined using dual energy x-ray absorptiometry.
Evaluation of vascular endothelial cell inflammation: IL-6Baseline, 1 mo., 6 mo., 12 mo.Interleukin 6 (IL-6) measured in blood and endothelial cells.
Evaluation of carotid artery complianceBaseline, 1 mo., 6 mo., 12 mo.The carotid artery compliance index indicates how elastic the artery is. The index describes the change in arterial blood volume in response to a change in arterial blood pressure. Lower numbers are associated with worse outcomes (less elastic arteries).
Evaluation of carotid artery beta stiffness indexBaseline, 1 mo., 6 mo., 12 mo.The carotid artery beta stiffness index indicates how stiff the artery is. Higher numbers are associated with worse outcomes (stiffer artery).

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026