Evidence map›Paper›PMID 40768483›Full record

ArticlePloS one2025

Unveiling health disparities: Diagnostic prevalences in a transgender cohort versus matched controls.

Laurel Hiatt, Blessing S Ofori-Atta, Amanda V Bakian, Nicole L Mihalopoulos, Brooks R Keeshin, Anna Docherty, Michael Staley, Alison Fraser, Emily Sullivan, Erin A Kaufman and 2 more

Abstract read
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Laurel HiattDepartment of Human Genetics, University of Utah, Salt Lake City, Utah, United States of America.ORCID https://orcid.org/0000-0003-1321-0325
Blessing S Ofori-AttaStudy Design and Biostatistics Center, University of Utah, Salt Lake City, Utah, United States of America.
Amanda V BakianDepartment of Psychiatry, University of Utah, Salt Lake City, Utah, United States of America.
Nicole L MihalopoulosDepartment of Pediatrics, University of Utah, Salt Lake City, Utah, United States of America.
Brooks R KeeshinDivision of Child Protection and Family Health, University of Utah, Salt Lake City, Utah, United States of America.
Anna DochertyDepartment of Psychiatry, University of Utah, Salt Lake City, Utah, United States of America.
Michael StaleyOffice of the Medical Examiner, Utah Department of Human Health and Services, Salt Lake City, Utah, United States of America.
Alison FraserUtah Population Database, University of Utah, Salt Lake City, Utah, United States of America.
Emily SullivanZero Suicide Program, University of Utah, Salt Lake City, Utah, United States of America.
Erin A KaufmanDepartment of Psychiatry, University of Utah, Salt Lake City, Utah, United States of America.ORCID https://orcid.org/0000-0002-7636-6602
Hilary CoonDepartment of Psychiatry, University of Utah, Salt Lake City, Utah, United States of America.
Anne V KirbyDepartment of Occupational and Recreational Therapies, University of Utah, Salt Lake City, Utah, United States of America.

Funding

Examining Mechanisms of Change in Adolescent Self-Inflicted InjuryK23MH135225 · NIMH · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Erin Anne Kaufman · 2024 to 2026
$598k
NIMH NIH HHS K23 MH135225
6 · The paper itself

Abstract

importanceTransgender and gender-diverse (TGD) individuals are at risk for discrimination and inequities across legal, social, and medical contexts. Population-level resources have rarely been used for TGD health research and, therefore, data is lacking about prevalences of a wide range of clinical conditions among TGD populations.

objectiveTo leverage the Utah Population Database's demographic, vital, and health records and examine population-level diagnostic prevalences in TGD individuals and an age-matched general cohort.

participants6,664 TGD individuals were identified using ICD codes for gender incongruence between 1995 and 2021; 64,124 age-matched individuals comprised the control cohort.

designUsing Phecodes to collapse ICD codes, this study examined differences in the prevalence of medical, mental health, and neurodevelopmental clinical phenotypes in TGD and control cohorts using modified Poisson regression models.

settingAffiliated healthcare systems within the state of Utah. MAIN OUTCOME AND MEASURE: We evaluated adjusted prevalence ratios of identified Phecodes.

resultsThe TGD cohort showed broadly higher documented prevalences of medical, mental health, and neurodevelopmental conditions compared to controls. Medical diagnoses more common in the TGD cohort included sleep disorders and chronic pain. Disparities in diagnoses such as "other endocrine disorders" and "need for hormone replacement therapy" likely reflect gender-affirming treatments. Mental health conditions including mood, depression, anxiety, and personality disorders were significantly more prevalent in the TGD cohort. CONCLUSIONS AND RELEVANCE: This study highlights diagnostic disparities for TGD individuals across multiple clinical categories. Our findings may be driven by: 1) discrimination and over-medicalization of TGD individuals, 2) differences in accessing and interacting with the healthcare system, and 3) variation in the true incidence of medical and mental health outcomes in the TGD vs control cohorts.

Indexed as

Health Status DisparitiesTransgender PersonsAdolescentAdultAgedCase-Control StudiesCohort StudiesFemaleHumansMaleMental HealthMiddle AgedPrevalenceUtahYoung Adult

Identifiers

PMID40768483
PMCPMC12327606

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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.