Cited by 75Adipokines, Inflammation, and Metabolic DiseasesHormonal and reproductive studiesLGBTQ Health, Identity, and Policy

Effects of sex hormone treatment on the metabolic syndrome in transgender individuals: focus on metabolic cytokines

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Auer, Matthias K, Ebert, Thomas, Pietzner, Maik, Defreyne, Justine, Fuss, Johannes, Stalla, Günter K, T’Sjoen, Guy·2018·The Journal of Clinical Endocrinology & Metabolism

Abstract

Context: Hormonal treatment in transgender persons affects many components of the metabolic syndrome (MS). Objective: To determine the role of direct hormonal effects, changes in metabolic cytokines, and body composition on metabolic outcomes. Design, Setting, and Participants: 24 transwomen and 45 transmen from the European Network for the Investigation of Gender Incongruence were investigated at baseline and after 12 months of hormonal therapy. Outcome Measures: Best predictors for changes in components of MS, applying least absolute shrinkage and selection operator regression. Results: In transwomen, a decrease in triglyceride levels was best explained by a decrease in fat mass and an increase in fibroblast growth factor 21 (FGF-21); the decrease in total and low-density lipoprotein cholesterol levels was principally due to a decrease in resistin. A decrease in high-density lipoprotein cholesterol depended on an inverse association with fat mass. In contrast, in transmen, an increase in low-density lipoprotein cholesterol was predicted by a decrease in FGF-21 and an increase in the waist/hip ratio; a decrease in the high-density lipoprotein/total cholesterol ratio depended on a decline in adiponectin levels. In transwomen, worsened insulin resistance and increased early insulin response seemed to be due to a direct treatment effect; however, improvements in hepatic insulin sensitivity in transmen were best predicted by a positive association with chemerin, resistin, and FGF-21 and were inversely related to changes in the waist/hip ratio and leptin and adipocyte fatty acid-binding protein levels. Conclusions: The effects of hormonal therapy on different components of the MS are sex-specific and involve a complex interplay of direct hormonal effects, changes in body composition, and metabolic cytokine secretion.

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Crossref · 10.1210/jc.2017-01559

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  • Seven of the follow-up studies, including the large ENIGI study, and two studies with high post-GAHT testosterone, showed that total lean body mass was decreased by 3.0%-5.4% following hormone transition (p<0.05).

    “Seven of these studies,15 36 39–41 44 51 including the large (n=179) ENIGI study,15 and two studies40 51 with high post-GAHT testosterone (~8 nmol/L), showed that total LBM was decreased by 3.0%–5.4% following hormone transition (p<0.05).”

    From How does hormone transition in transgender women change body composition, muscle strength and haemoglobin? Systematic review with a focus on the implications for sport participation (2021) · cites this paper as [39]

    The Markers of the MS section reports that lean mass remained unchanged in transwomen and increased in transmen after GAHT, contrary to the attributed decrease. The Patients section describes a cohort of 69, not the n=179 ENIGI study named in the citing sentence. No page numbers are available in our copy. (LLM, conf=0.90)

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  • Twelve longitudinal studies have examined the effects of testosterone suppression on lean body mass or muscle size in transgender women.

    “Including Gooren and Bunck [62], 12 longitudinal studies [53, 63–73] have examined the effects of testosterone suppression on lean body mass or muscle size in transgender women.”

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Authors
Auer, M. K., Ebert, T., Pietzner, M., Defreyne, J., Fuss, J., Stalla, G. K., & T’Sjoen, G.
Affiliations
  • LMU Klinikum (DE)
  • University Hospital Leipzig (DE)
  • Universitätsmedizin Greifswald (DE)
  • Ghent University Hospital (BE)
  • University Medical Center Hamburg-Eppendorf (DE)
  • Max Planck Institute of Psychiatry (DE)
Corresponding author
Auer, Matthias K
Venue
The Journal of Clinical Endocrinology & Metabolism
Published
2017-12-05
Volume
103
Issue
2
Pages
790-802
ISSN
  • 0021-972X (ISSN-L)
  • 1945-7197
OpenAlex
W2775773328
Cited by
75
References
52
Citations by year
2026: 7 · 2025: 9 · 2024: 10 · 2023: 9 · 2022: 12 · 2021: 9 · 2020: 10 · 2019: 6 · 2018: 3
FWCI
4.07
Type
journal article
Language
en
Open access
Locations
  • The Journal of Clinical Endocrinology & Metabolism (publishedVersion)
  • PubMed (publishedVersion)
  • Ghent University Academic Bibliography (Ghent University) (submittedVersion)
Topics
  • Health Sciences › Medicine › Epidemiology › Adipokines, Inflammation, and Metabolic Diseases
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Hormonal and reproductive studies
  • Social Sciences › Psychology › Social Psychology › LGBTQ Health, Identity, and Policy
Keywords
metabolic syndrome, transgender people, sex hormone therapy, FGF21, resistin, adiponectin, chemerin, leptin, adipocyte fatty acid-binding protein, body composition, fat mass, triglycerides, cholesterol, insulin resistance, hepatic insulin sensitivity, sex differences
MeSH terms
Adult, Body Composition, Europe, Female, Humans, Insulin Resistance, Longitudinal Studies, Male, Gonadal Steroid Hormones, Cohort Studies, Cytokines, Metabolic Syndrome, Transgender Persons

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