Biochemical liver damage during gender affirming therapy in trans adults assigned female at birth: a meta-analysis
Journal of Endocrinological Investigation, ISSN: 1720-8386, Vol: 48, Issue: 1, Page: 161-171
2025
- 8Captures
- 1Mentions
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Metrics Details
- Captures8
- Readers8
- Mentions1
- News Mentions1
- 1
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University of L'Aquila Reports Findings in Women's Health (Biochemical liver damage during gender affirming therapy in trans adults assigned female at birth: a meta-analysis)
2024 JUL 10 (NewsRx) -- By a News Reporter-Staff News Editor at Chemicals & Chemistry Daily Daily -- New research on Women's Health is the
Article Description
Purpose: To assess the effects of testosterone (T)-based gender affirming hormone therapy (GAHT) on liver blood tests (LBTs) in assigned female at birth adults, using a meta-analytic approach. Methods: Prospective and retrospective studies were selected that reported the prevalence of biochemical liver damage (BLD) and LBTs changes during T therapy. Data collected included pre-and-during therapy alanine-aminotransferase (ALT), aspartate-aminotransferase (AST), gamma-glutamyl-transferase (GGT), and alkaline phosphatase (ALP) mean concentration values. Results: The prevalence of BLD in 14 studies on 1698 subjects was 1% (95% CI 0.00–3.00; I = 14.1%; p = 0.82). In 17 studies on 2758 subjects, GAHT was associated with a statistically (but not clinically) significant increase in AST, GGT and ALP at 12 months and ALT at 3–7 (MD: 1.19 IU/l; 95% CI 0.31, 2.08; I: 0%), at 12 (MD: 2.31 IU/l; 95% CI 1.41, 3.21; I: 29%), but with no more significant increase at 24 months (MD: 1.71 IU/l; 95% CI −0.02, 3.44; I: 0%). Conclusions: Analysis of aggregate estimates confirms a low risk of BLD and abnormalities in LBTs, transient in most cases, during T-based GAHT, thus suggesting a limited need for careful liver monitoring in AFAB people.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85196650330&origin=inward; http://dx.doi.org/10.1007/s40618-024-02418-y; http://www.ncbi.nlm.nih.gov/pubmed/38909133; https://link.springer.com/10.1007/s40618-024-02418-y; https://dx.doi.org/10.1007/s40618-024-02418-y; https://link.springer.com/article/10.1007/s40618-024-02418-y
Springer Science and Business Media LLC
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