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Gender-affirming hormonal therapy induces a gender-concordant fecal metagenome transition in transgender individuals.

Authors :
Liwinski T
Auer MK
Schröder J
Pieknik I
Casar C
Schwinge D
Henze L
Stalla GK
Lang UE
von Klitzing A
Briken P
Hildebrandt T
Desbuleux JC
Biedermann SV
Holterhus PM
Bang C
Schramm C
Fuss J
Source :
BMC medicine [BMC Med] 2024 Sep 02; Vol. 22 (1), pp. 346. Date of Electronic Publication: 2024 Sep 02.
Publication Year :
2024

Abstract

Background: Limited data exists regarding gender-specific microbial alterations during gender-affirming hormonal therapy (GAHT) in transgender individuals. This study aimed to investigate the nuanced impact of sex steroids on gut microbiota taxonomy and function, addressing this gap. We prospectively analyzed gut metagenome changes associated with 12 weeks of GAHT in trans women and trans men, examining both taxonomic and functional shifts.<br />Methods: Thirty-six transgender individuals (17 trans women, 19 trans men) provided pre- and post-GAHT stool samples. Shotgun metagenomic sequencing was used to assess the changes in gut microbiota structure and potential function following GAHT.<br />Results: While alpha and beta diversity remained unchanged during transition, specific species, including Parabacteroides goldsteinii and Escherichia coli, exhibited significant abundance shifts aligned with affirmed gender. Overall functional metagenome analysis showed a statistically significant effect of gender and transition (R <superscript>2</superscript>  = 4.1%, P = 0.0115), emphasizing transitions aligned with affirmed gender, particularly in fatty acid-related metabolism.<br />Conclusions: This study provides compelling evidence of distinct taxonomic and functional profiles in the gut microbiota between trans men and women. GAHT induces androgenization in trans men and feminization in trans women, potentially impacting physiological and health-related outcomes.<br />Trial Registration: Clinicaltrials.gov NCT02185274.<br /> (© 2024. The Author(s).)

Details

Language :
English
ISSN :
1741-7015
Volume :
22
Issue :
1
Database :
MEDLINE
Journal :
BMC medicine
Publication Type :
Academic Journal
Accession number :
39218875
Full Text :
https://doi.org/10.1186/s12916-024-03548-z