Toward a Lowest Effective Dose of Cyproterone Acetate in Trans Women: Results From the ENIGI Study

Autor: Elfi B. Conemans, Alessandra D. Fisher, Suzanne M E Kuijpers, Chantal M. Wiepjes, Guy T'Sjoen, Martin den Heijer
Přispěvatelé: Internal medicine, APH - Aging & Later Life, Amsterdam Gastroenterology Endocrinology Metabolism
Rok vydání: 2021
Předmět:
Male
Endocrinology
Diabetes and Metabolism

Clinical Biochemistry
cyproterone acetate
THERAPY
Biochemistry
Cohort Studies
chemistry.chemical_compound
0302 clinical medicine
Endocrinology
SEX HORMONE-TREATMENT
Belgium
Medicine and Health Sciences
Medicine
ENDOCRINE
Longitudinal Studies
030212 general & internal medicine
Gender Dysphoria
Prospective cohort study
Testosterone
Netherlands
trans people
Gender Identity
Cyproterone acetate
Effective dose (pharmacology)
Treatment Outcome
Italy
Female
anti-androgen
medicine.medical_specialty
Hormone Replacement Therapy
030209 endocrinology & metabolism
Context (language use)
03 medical and health sciences
Internal medicine
Humans
Cyproterone Acetate
SUPPRESSION
VENOUS THROMBOEMBOLISM
hormone therapy
Dose-Response Relationship
Drug

business.industry
Biochemistry (medical)
Androgen Antagonists
Prolactin
Androgen receptor
chemistry
Sex Reassignment Procedures
testosterone
business
Transsexualism
Lipoprotein
Zdroj: Journal of Clinical Endocrinology and Metabolism, 106(10), E3936-E3945. The Endocrine Society
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
Kuijpers, S M E, Wiepjes, C M, Conemans, E B, Fisher, A D, Tsjoen, G & den Heijer, M 2021, ' Toward a Lowest Effective Dose of Cyproterone Acetate in Trans Women : Results from the ENIGI Study ', Journal of Clinical Endocrinology and Metabolism, vol. 106, no. 10, pp. E3936-E3945 . https://doi.org/10.1210/clinem/dgab427
ISSN: 1945-7197
0021-972X
Popis: Context Cyproterone acetate (CPA) is a competitive inhibitor of the androgen receptor and exerts negative hypothalamic feedback. It is often used in combination with estrogens in trans women to achieve feminization. However, CPA has been associated with side effects such as changes in liver enzyme concentrations and increases in prolactin concentrations. The question is whether the testosterone-lowering effect, as well as these side effects, are dose dependent. Objective To assess the lowest effective dose of CPA in trans women to prevent side effects. Methods This longitudinal study, conducted at gender identity centers in Amsterdam, Ghent, and Florence, is part of the European Network for the Investigation of Gender Incongruence (ENIGI), a multicenter prospective cohort study. Participants were trans women (n = 882) using estrogens only or in combination with 10, 25, 50, or 100 mg CPA daily. The primary outcome measure was the concentration of testosterone at 3 and/or 12 months of hormone therapy. Results Using estrogens only (without CPA) led to testosterone concentrations of 5.5 nmol/L (standard error of the mean [SEM] 0.3). All doses of CPA resulted in testosterone concentrations below the predefined threshold of suppression of 2 nmol/L (10 mg, 0.9 nmol/L, SEM 0.7; 25 mg, 0.9 nmol/L, SEM 0.1; 50mg, 1.1 nmol/L, SEM 0.1; 100 mg, 0.9 nmol/L, SEM 0.7). Higher prolactin and lower high-density lipoprotein concentrations were observed with increasing doses of CPA. No differences in liver enzyme concentrations were found between the doses. Conclusion Compared with higher doses of CPA, a daily dose of 10 mg is equally effective in lowering testosterone concentrations in trans women, while showing fewer side effects.
Databáze: OpenAIRE