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Effects of Aging and Gender-Affirming Hormone Therapy on Vascular Endothelial Function and Metabolic Profiles in Transgender Women

Novel Evaluations of Aging and Gender-Affirming Hormone Therapy on Vascular Endothelial Function and Metabolic Profiles in Transgender Women Compared to Age Group-Matched Cisgender Adults

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04066283
Enrollment
29
Registered
2019-08-26
Start date
2019-04-17
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 will examine markers of vascular endothelial function (vascular health) and metabolic profiles in younger versus older transgender women (people who were assigned male at birth but whose gender identity is female). Data will also be compared to those from cisgender women and men.

Interventions

OTHERNo intervention

There was no intervention in this study

Sponsors

National Center for Advancing Translational Sciences (NCATS)
CollaboratorNIH
University of Colorado, Denver
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
Yes

Inclusion criteria

* Aged 18-40 years old or 50-75 years old * Identify as a transgender woman * Have taken estradiol and spironolactone for at least one year * Currently taking oral or transdermal estradiol

Exclusion criteria

* 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 * 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)BaselineBrachial artery flow-mediated dilation (FMD), as measured by ultrasound.

Secondary

MeasureTime frameDescription
Plasma lipid concentrations: triglyceridesBaselineTriglycerides will be determined at baseline.
Evaluation of carotid artery complianceBaselineThe 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 indexBaselineThe carotid artery beta stiffness index indicates how stiff the artery is. Higher numbers are associated with worse outcomes (stiffer artery).
Carotid artery intimal-medial thicknessBaseline
Evaluation of oxidant burden: oxidized LDLBaselineOxidized low-density lipoprotein (LDL) measured in the blood and endothelial cells.
Evaluation of oxidant burden: nitrotyrosineBaselineNitrotyrosine measured in the blood and endothelial cells.
Evaluation of vascular endothelial cell inflammation: NFkBBaselineProtein NFkB (nuclear factor kappa-light-chain-enhancer of activated B cells) measured in blood and endothelial cells.
Evaluation of vascular endothelial cell inflammation: MCP-1BaselineMonocyte Chemoattractant Protein-1 (MCP-1) measured in blood and endothelial cells.
Evaluation of vascular endothelial cell inflammation: IL-6BaselineInterleukin 6 (IL-6) measured in blood and endothelial cells.
Evaluation of vascular endothelial cell inflammation: CRPBaselineC-reactive protein (CRP) measured in blood and endothelial cells.
Blood pressureBaseline
Plasma lipid concentrations: total cholesterolBaselineTotal cholesterol will be determined at baseline.
Whole body composition: Percent Lean MassBaselinePercent lean mass will be determined using dual energy x-ray absorptiometry.
Whole body composition: Percent Fat MassBaselinePercent fat mass will be determined using dual energy x-ray absorptiometry.
Regional body composition: Percent Lean MassBaselineRegional percent lean mass will be determined using dual energy x-ray absorptiometry.
Regional body composition: Percent Fat MassBaselineRegional percent fat mass will be determined using dual energy x-ray absorptiometry.
Weight changesBaseline
Appetite ratingsBaseline
Appetite-related peptidesBaseline
D-DimerBaseline
Alcohol useBaseline
Depression symptomsBaseline
Physical activity monitoring7 daysPhysical activity will me monitored for 7 days with an ActivPALmonitor
Insulin sensitivityBaseline
Energy intake3 daysEnergy intake will be estimated with a 3-day food diary

Countries

United States

Outcome results

None listed

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