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

Sponsor
University of Colorado, Denver (Other)
Overall Status
Recruiting
CT.gov ID
NCT04066283
Collaborator
National Institutes of Health (NIH) (NIH)
30
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41.5
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Study Details

Study Description

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.

Study Design

Study Type:
Observational
Anticipated Enrollment :
30 participants
Observational Model:
Cohort
Time Perspective:
Cross-Sectional
Official Title:
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
Actual Study Start Date :
Apr 17, 2019
Anticipated Primary Completion Date :
Oct 1, 2022
Anticipated Study Completion Date :
Oct 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Older transgender women

This cohort will consist of transgender women aged 50-75 years old who have taken estradiol and spironolactone for at least one year.

Younger transgender women

This cohort will consist of transgender women aged 18-40 years old who have taken estradiol and spironolactone for at least one year.

Outcome Measures

Primary Outcome Measures

  1. Evaluation of endothelial function (flow-mediated dilation (FMD) [Baseline]

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

Secondary Outcome Measures

  1. Evaluation of carotid artery compliance [Baseline]

    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).

  2. Evaluation of carotid artery beta stiffness index [Baseline]

    The carotid artery beta stiffness index indicates how stiff the artery is. Higher numbers are associated with worse outcomes (stiffer artery).

  3. Carotid artery intimal-medial thickness [Baseline]

  4. Evaluation of oxidant burden: oxidized LDL [Baseline]

    Oxidized low-density lipoprotein (LDL) measured in the blood and endothelial cells.

  5. Evaluation of oxidant burden: nitrotyrosine [Baseline]

    Nitrotyrosine measured in the blood and endothelial cells.

  6. Evaluation of vascular endothelial cell inflammation: NFkB [Baseline]

    Protein NFkB (nuclear factor kappa-light-chain-enhancer of activated B cells) measured in blood and endothelial cells.

  7. Evaluation of vascular endothelial cell inflammation: MCP-1 [Baseline]

    Monocyte Chemoattractant Protein-1 (MCP-1) measured in blood and endothelial cells.

  8. Evaluation of vascular endothelial cell inflammation: IL-6 [Baseline]

    Interleukin 6 (IL-6) measured in blood and endothelial cells.

  9. Evaluation of vascular endothelial cell inflammation: CRP [Baseline]

    C-reactive protein (CRP) measured in blood and endothelial cells.

  10. Blood pressure [Baseline]

  11. Plasma lipid concentrations: total cholesterol [Baseline]

    Total cholesterol will be determined at baseline.

  12. Plasma lipid concentrations: triglycerides [Baseline]

    Triglycerides will be determined at baseline.

  13. Insulin sensitivity [Baseline]

  14. Whole body composition: Percent Lean Mass [Baseline]

    Percent lean mass will be determined using dual energy x-ray absorptiometry.

  15. Whole body composition: Percent Fat Mass [Baseline]

    Percent fat mass will be determined using dual energy x-ray absorptiometry.

  16. Regional body composition: Percent Lean Mass [Baseline]

    Regional percent lean mass will be determined using dual energy x-ray absorptiometry.

  17. Regional body composition: Percent Fat Mass [Baseline]

    Regional percent fat mass will be determined using dual energy x-ray absorptiometry.

  18. Weight changes [Baseline]

  19. Appetite ratings [Baseline]

  20. Appetite-related peptides [Baseline]

  21. D-Dimer [Baseline]

  22. Alcohol use [Baseline]

  23. Depression symptoms [Baseline]

  24. Physical activity monitoring [7 days]

    Physical activity will me monitored for 7 days with an ActivPALmonitor

  25. Energy intake [3 days]

    Energy intake will be estimated with a 3-day food diary

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 75 Years
Sexes Eligible for Study:
All
Accepts 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 thromobembolism

  • Hypertriglyceridemia >500 mg/dL

  • Fasted plasma glucose >7.0 mmol/L or previously treated diabetes

  • Resting blood pressure >140/90 mmHg

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Colorado Aurora Colorado United States 80045

Sponsors and Collaborators

  • University of Colorado, Denver
  • National Institutes of Health (NIH)

Investigators

  • Principal Investigator: Sean Iwamoto, MD, University of Colorado, Denver

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of Colorado, Denver
ClinicalTrials.gov Identifier:
NCT04066283
Other Study ID Numbers:
  • 18-2258
First Posted:
Aug 26, 2019
Last Update Posted:
Oct 26, 2021
Last Verified:
Oct 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 26, 2021