Evidence map›Paper›PMID 38609170›Full record

Trial reportThe Journal of clinical endocrinology and metabolism2024

Impact of Distinct Antiandrogen Exposures on the Plasma Metabolome in Feminizing Gender-affirming Hormone Therapy.

Rebecca Shepherd, Lachlan M Angus, Toby Mansell, Bridget Arman, Bo Won Kim, Katherine Lange, David Burgner, Jessica A Kerr, Ken Pang, Jeffrey D Zajac and 3 more

Open access · hybridAbstract readRandomized Controlled Trial
In one paragraph

Trial report in The Journal of clinical endocrinology and metabolism, 2024. 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
2.7field-weighted citation impact, top 11% of its field
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, 5 citations in OpenAlex.

  1. Trial
  2. Cardiometabolic diseases in transgender populations.Cardiovascular diabetology. Endocrinology reports · 2026
    Review
  3. Article
  4. Article
  5. 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

13 authors at 2 institutions in 2 countries.

Rebecca ShepherdMolecular Immunity, Infection and Immunity Theme, Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, VIC 3052, Australia.
Lachlan M AngusDepartment of Medicine (Austin Health), The University of Melbourne, Parkville, VIC 3052, Australia.
Toby MansellDepartment of Paediatrics, The University of Melbourne, Parkville, VIC 3052, Australia.
Bridget ArmanTherapeutics Discovery and Vascular Function Group, Department of Obstetrics and Gynaecology, University of Melbourne, Mercy Hospital for Women, Heidelberg, VIC 3084, Australia.
Bo Won KimMolecular Immunity, Infection and Immunity Theme, Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, VIC 3052, Australia.
Katherine LangeDepartment of Paediatrics, The University of Melbourne, Parkville, VIC 3052, Australia.
David BurgnerDepartment of Paediatrics, The University of Melbourne, Parkville, VIC 3052, Australia.ORCID 0000-0002-8304-4302
Jessica A KerrDepartment of Paediatrics, The University of Melbourne, Parkville, VIC 3052, Australia.
Ken PangBrain and Mind Research, Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, VIC 3052, Australia.ORCID 0000-0002-6881-775X
Jeffrey D ZajacDepartment of Medicine (Austin Health), The University of Melbourne, Parkville, VIC 3052, Australia.
Richard SafferyMolecular Immunity, Infection and Immunity Theme, Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, VIC 3052, Australia.ORCID 0000-0002-9510-4181
Ada CheungDepartment of Medicine (Austin Health), The University of Melbourne, Parkville, VIC 3052, Australia.ORCID 0000-0001-5257-5525
Boris NovakovicMolecular Immunity, Infection and Immunity Theme, Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, VIC 3052, Australia.ORCID 0000-0002-5623-9008
Royal Children's Hospital · AUThe University of Melbourne · AU

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
Australian Government Research and Training ProgramNational Health and Medical Research Council 1175744National Health and Medical Research Council 2008956National Institute of Allergy And Infectious Diseases R21AI179004NHMRC 1173314NIAID NIH HHS R21 AI179004
6 · The paper itself

Abstract

contextThe plasma metabolome is a functional readout of metabolic activity and is associated with phenotypes exhibiting sexual dimorphism, such as cardiovascular disease. Sex hormones are thought to play a key role in driving sexual dimorphism.

objectiveGender-affirming hormone therapy (GAHT) is a cornerstone of transgender care, but longitudinal changes in the plasma metabolome with feminizing GAHT have not been described.

methodsBlood samples were collected at baseline and after 3 and 6 months of GAHT from transgender women (n = 53). Participants were randomized to different anti-androgens, cyproterone acetate or spironolactone. Nuclear magnetic resonance-based metabolomics was used to measure 249 metabolic biomarkers in plasma. Additionally, we used metabolic biomarker data from an unrelated cohort of children and their parents (n = 3748) to identify sex- and age-related metabolite patterns.

resultsWe identified 43 metabolic biomarkers altered after 6 months in both anti-androgen groups, most belonging to the very low- or low-density lipoprotein subclasses, with all but 1 showing a decrease. We observed a cyproterone acetate-specific decrease in glutamine, glycine, and alanine levels. Notably, of the metabolic biomarkers exhibiting the most abundant "sex- and age-related" pattern (higher in assigned female children and lower in assigned female adults, relative to assigned males), 80% were significantly lowered after GAHT, reflecting a shift toward the adult female profile.

conclusionOur results suggest an anti-atherogenic signature in the plasma metabolome after the first 6 months of feminizing GAHT, with cyproterone acetate also reducing specific plasma amino acids. This study provides novel insight into the metabolic changes occurring across feminizing GAHT.

Indexed as

Androgen AntagonistsBiomarkersCyproterone AcetateMetabolomeTransgender PersonsAdolescentAdultChildFemaleGender-Affirming ProceduresHormone Replacement TherapyHumansMaleMetabolomicsMiddle AgedSpironolactoneAndrogen AntagonistsBiomarkersCyproterone AcetateSpironolactoneestradiolGAHTmetabolismmetabolomesex hormonestransgender

Identifiers

PMID38609170
PMCPMC11479691
OpenAlexW4394785577

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.