Evidence map›Paper›PMID 41115957›Full record

ArticleNature medicine2026

Plasma proteome adaptations during feminizing gender-affirming hormone therapy.

Nhi N L Nguyen, Den Celestra, Lachlan M Angus, Toby Mansell, Rebecca Shepherd, Bo Won Kim, Bridget Arman, Georgiana Cabau, Tania O Crișan, Leo A B Joosten and 9 more

Abstract read
In one paragraph

Article in Nature medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
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

19 authors.

Nhi N L NguyenMolecular Immunity, Infection, Immunity and Global Health Theme, Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, Victoria, Australia.
Den CelestraMolecular Immunity, Infection, Immunity and Global Health Theme, Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, Victoria, Australia.ORCID 0009-0008-4245-981X
Lachlan M AngusDepartment of Medicine (Austin Health), The University of Melbourne, Heidelberg, Victoria, Australia.
Toby MansellDepartment of Paediatrics, The University of Melbourne, Parkville, Victoria, Australia.ORCID 0000-0002-1282-6331
Rebecca ShepherdMolecular Immunity, Infection, Immunity and Global Health Theme, Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, Victoria, Australia.
Bo Won KimMolecular Immunity, Infection, Immunity and Global Health Theme, Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, Victoria, Australia.
Bridget ArmanTherapeutics Discovery and Vascular Function Group, Department of Obstetrics and Gynaecology, University of Melbourne, Mercy Hospital for Women, Heidelberg, Victoria, Australia.ORCID 0000-0003-0314-378X
Georgiana CabauDepartment of Medical Genetics, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Tania O CrișanDepartment of Medical Genetics, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Leo A B JoostenDepartment of Medical Genetics, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.ORCID 0000-0001-6166-9830
Camille LaberthonnièreDepartment of Cell Biology, Faculty of Science, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, the Netherlands.
David BurgnerDepartment of Paediatrics, The University of Melbourne, Parkville, Victoria, Australia.ORCID 0000-0002-8304-4302
Gilda TachedjianLife Sciences Discipline, Burnet Institute, Melbourne, Victoria, Australia.ORCID 0000-0002-7733-7037
Musa MhlangaDepartment of Internal Medicine, Radboud University Medical Center, Nijmegen, the Netherlands.ORCID 0000-0003-1381-3409
Rachel A DaveyDepartment of Medicine (Austin Health), The University of Melbourne, Heidelberg, Victoria, Australia.
Ken C PangDepartment of Paediatrics, The University of Melbourne, Parkville, Victoria, Australia.
Ada S CheungDepartment of Medicine (Austin Health), The University of Melbourne, Heidelberg, Victoria, Australia. adac@unimelb.edu.au.ORCID 0000-0001-5257-5525
Richard SafferyMolecular Immunity, Infection, Immunity and Global Health Theme, Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, Victoria, Australia.ORCID 0000-0002-9510-4181
Boris NovakovicMolecular Immunity, Infection, Immunity and Global Health Theme, Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, Victoria, Australia. boris.novakovic@mcri.edu.au.ORCID 0000-0002-5623-9008

Funding

Understanding the effects of Gender Affirming Hormone Therapy (GAHT) on immune function using a systems immunology approachR21AI179004 · NIAID · MURDOCH CHILDREN'S RESEARCH INSTITUTE · PI NOVAKOVIC, BORIS · 2023 to 2024
$272k
NIAID NIH HHS R21 AI179004Paul G. Allen Family Foundation Allen Distinguished Investigator programU.S. Department of Health & Human Services | NIH | National Institute of Allergy and Infectious Diseases (NIAID) R21AI179004
6 · The paper itself

Abstract

Sex differences manifest in various traits, as well as in the risk of cardiovascular, metabolic and immunological conditions. Despite the clear physical changes induced by gender-affirming hormone therapy (GAHT), little is known about how it affects underlying physiological and biochemical processes. Here we examined plasma proteome changes over 6 months of feminizing GAHT in 40 transgender individuals treated with estradiol plus one of two antiandrogens: cyproterone acetate or spironolactone. Testosterone levels dropped markedly in the cyproterone group, but less so in those receiving spironolactone. Among 5,279 total proteins measured, feminizing GAHT changed the levels of 245 and 91, in the cyproterone and spironolactone groups, respectively, with most (>95%) showing a decrease. Proteins associated with male spermatogenesis showed a marked decrease in the cyproterone group, attributable specifically to loss of testosterone. Changes in body fat percentage and breast volume following GAHT were also reflected in the plasma proteome, including an increase in leptin expression. We show that feminizing GAHT remodels the proteome toward a cis-female profile, altering 36 (cyproterone) and 22 (spironolactone) of the top 100 sex-associated proteins in UK Biobank adult data. Moreover, 43% of cyproterone-affected proteins overlapped with those altered by menopausal hormone therapy in cis women, showing the same directional changes, with notable exceptions including CXCL13 and NOS3. Feminizing GAHT skewed the protein profile toward that linked to asthma and autoimmunity, while GAHT with cyproterone specifically skewed it away from an atherosclerosis-associated profile, suggesting a protective effect. These results reveal that feminizing GAHT reshapes the plasma proteome in a hormone-dependent manner, with implications for reproductive capacity, immune regulation and long-term health outcomes.

Indexed as

Gender-Affirming ProceduresProteomeTranssexualismAdultAndrogen AntagonistsCyproterone AcetateEstradiolFemaleHormone Replacement TherapyHumansMaleMiddle AgedTestosteroneTransgender PersonsAndrogen AntagonistsCyproterone AcetateEstradiolProteomeTestosterone

Identifiers

PMID41115957
PMCPMC12823392

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.