Evidence map›Paper›PMID 39389223›Full record

Observational studyAmerican journal of preventive medicine2025

Hormones, Stress, and Heart Disease in Transgender Women with HIV in LITE Plus.

Tonia C Poteat, Molly Ehrig, Hedyeh Ahmadi, Mannat Malik, Sari L Reisner, Asa E Radix, Jowanna Malone, Christopher Cannon, Carl G Streed, Mabel Toribio and 7 more

Abstract readMulticenter StudyObservational Study
In one paragraph

Observational study in American journal of preventive medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Cardiometabolic diseases in transgender populations.Cardiovascular diabetology. Endocrinology reports · 2026
    Review
  2. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors.

Tonia C PoteatDivision of Healthcare in Adult Populations, Duke University School of Nursing, Durham, North Carolina. Electronic address: tonia.poteat@duke.edu.
Molly EhrigDepartment of Biostatistics and Bioinformatics, Duke University, Durham, North Carolina.
Hedyeh AhmadiUniversity Statistical Consulting, Irvine, California.
Mannat MalikDepartment of Health Behavior, University of North Carolina Gillings School of Global Public Health, Chapel Hill, North Carolina.
Sari L ReisnerDepartment of Epidemiology, University of Michigan School of Public Health, Ann Arbor, Michigan; The Fenway Institute, Fenway Health, Boston, Massachusetts.
Asa E RadixCallen Lorde Community Health Center, New York, New York; Epidemiology Department, Columbia University Mailman School of Public Health, New York, New York.
Jowanna MaloneWhitman-Walker Institute, Washington, District of Columbia.
Christopher CannonWhitman-Walker Institute, Washington, District of Columbia.
Carl G StreedDepartment of General Internal Medicine, Boston University Chobanian and Avedisian School of Medicine, Boston, Massachusetts; GenderCare Center, Boston Medical Center, Boston, Massachusetts.
Mabel ToribioMetabolism Unit, Massachusetts General Hospital, Boston, Massachusetts.
Christopher CortinaDepartment of Biostatistics, University of North Carolina Gillings School of Global Public Health, Chapel Hill, North Carolina.
Ashleigh RichDivision of Healthcare in Adult Populations, Duke University School of Nursing, Durham, North Carolina.
Kenneth H MayerThe Fenway Institute, Fenway Health, Boston, Massachusetts; Department of Medicine, Harvard Medical School, Boston, Massachusetts; Beth Israel Deaconess Medical Center, Boston, Massachusetts.
L Zachary DuBoisDepartment of Anthropology, University of Oregon, Eugene, Oregon.
Robert-Paul JusterDepartment of Psychiatry and Addictology, University of Montreal, Montreal, Canada.
Andrea L WirtzDepartment of Epidemiology, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, Maryland.
Krista M PerreiraDepartment of Social Medicine, University of North Carolina School of Medicine, Chapel Hill, North Carolina.

Funding

Connecting the Dots: HIV, COVID-19, and Structural Racism in Gender Minority WomenR01MD013498 · NIMHD · UNIV OF NORTH CAROLINA CHAPEL HILL · PI PERREIRA, KRISTA M, POTEAT, TONIA C · 2018 to 2022
$3.8M
NIMHD NIH HHS R01 MD013498
6 · The paper itself

Abstract

introductionCardiovascular disease (CVD) is a leading cause of death among transgender women and people with HIV. Exogenous estrogen and psychosocial stressors are known risk factors for CVD. Yet, few studies have used biomarkers to examine the role of stress in CVD risk among transgender women with HIV (TWHIV). This analysis examined whether stress moderates relationships between gender-affirming hormone therapy (GAHT) duration and CVD risk among TWHIV.

methodsThis cross-sectional analysis of baseline data from an observational cohort of 108 Black and Latina TWHIV in Boston, New York, and Washington, DC, enrolled December 2020 to June 2022, measured sociodemographics, medical diagnoses, medications, smoking history, and perceived stress via interviewer-administered surveys. Physiological stress was measured with 14 biomarkers to calculate allostatic load indices (ALI). Forty participants provided saliva samples used to calculate cortisol awakening response and cortisol daily decline. The 2018 American College of Cardiology Revised Pooled Cohort Equation estimated 10-year CVD risk. Data were analyzed in 2024.

resultsGAHT duration was positively associated with CVD risk scores in bivariate regression. In multivariable linear regression models (adjusting for age, income, education), only age and ALI remained significantly associated with CVD risk scores (β 1.13, CI: 1.05, 1.21). No stress measure significantly interacted with GAHT duration to affect CVD risk scores. In visual plots, GAHT duration increased CVD risk scores only for TWHIV experiencing the highest ALI.

conclusionsStress plays an important role in CVD in TWHIV. More research is needed on non-GAHT factors, which influence CVD health among transgender women.

Indexed as

Cardiovascular DiseasesHIV InfectionsStress, PsychologicalTransgender PersonsAdultBiomarkersCross-Sectional StudiesFemaleHeart Disease Risk FactorsHumansHydrocortisoneMaleMiddle AgedRisk FactorsSalivaBiomarkersHydrocortisone

Identifiers

PMID39389223
PMCPMC11757083

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.