Differential Endocrine and Metabolic Effects of Testosterone Suppressive Agents in Transgender Women.

Yael Sofer, Iris Yaish, Marianna Yaron, Michal Yacobi Bach, Naftali Stern, Yona Greenman
Author Information
  1. Yael Sofer: From the Institute of Endocrinology, Diabetes, Metabolism and Hypertension, Tel Aviv-Sourasky Medical Center, Tel Aviv, Israel; the Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  2. Iris Yaish: From the Institute of Endocrinology, Diabetes, Metabolism and Hypertension, Tel Aviv-Sourasky Medical Center, Tel Aviv, Israel.
  3. Marianna Yaron: From the Institute of Endocrinology, Diabetes, Metabolism and Hypertension, Tel Aviv-Sourasky Medical Center, Tel Aviv, Israel.
  4. Michal Yacobi Bach: From the Institute of Endocrinology, Diabetes, Metabolism and Hypertension, Tel Aviv-Sourasky Medical Center, Tel Aviv, Israel.
  5. Naftali Stern: From the Institute of Endocrinology, Diabetes, Metabolism and Hypertension, Tel Aviv-Sourasky Medical Center, Tel Aviv, Israel; the Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  6. Yona Greenman: From the Institute of Endocrinology, Diabetes, Metabolism and Hypertension, Tel Aviv-Sourasky Medical Center, Tel Aviv, Israel; the Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.. Electronic address: yonagr@tlvmc.gov.il.

Abstract

OBJECTIVE: Suppression of testosterone secretion and/or action in transgender women using cyproterone acetate (CPA), spironolactone, or gonadotropin-releasing hormone analogues (GA) is achieved through various mechanisms. Our objective was to characterize possible differential effects of these compounds on metabolic and endocrine variables.
METHODS: We conducted a historic cohort study of transgender patients treated in a tertiary referral center. A longitudinal analysis of treatment naïve patients and a cross-sectional analysis of the whole cohort at the last visit was carried out.
RESULTS: Among 126 transgender women (75 treatment-naïve), CPA was the predominant androgen suppressive therapy (70%), followed by spironolactone (17.6%), and GA (10.2%). Among those who were treatment-naïve, the increase in serum prolactin levels over baseline was greater at 3 months following CPA initiation (mean change 397 ± 335 mIU/L) than following spironolactone (20.1 ± 87 mIU/L) or GA initiation (64.6 ± 268 mIU/L; P = .0002). Prolactin levels remained higher in the CPA-treated group throughout follow-up, irrespective of estradiol levels, which were similar between the groups. A worse metabolic profile was associated with treatment with CPA than with spironolactone or GA. In the CPA compared to the spironolactone and GA groups, high-density lipoprotein-cholesterol levels were lower (47.1 ± 10.4, 54.4 ± 12.2, and 60.3 ± 13, respectively; P = .0076), while body mass index levels (24.3 ± 5, 21.7 ± 2.3, and 20.7±3.1 kg/m; P = .03), and systolic (117 ± 12.1, 109 ± 12.2, and 105 ± 13.3mm Hg; P = .01) and diastolic (74 ± 9, 65.6 ± 5.5, and 65.4 ± 11 mm Hg; P = .0008) blood pressure levels were higher at the last visit.
CONCLUSION: Treatment of transgender women with CPA was associated with hyperprolactinemia and a worse cardiovascular risk profile than treatment with spironolactone or GA.
ABBREVIATIONS: BMI = body mass index; CPA = cyproterone acetate; E2 = estradiol; FSH = follicle-stimulating hormone; GA = gonadotropin-releasing hormone analogues; LH = luteinizing hormone.

MeSH Term

Cohort Studies
Cross-Sectional Studies
Female
Follicle Stimulating Hormone
Humans
Luteinizing Hormone
Testosterone
Transgender Persons

Chemicals

Testosterone
Luteinizing Hormone
Follicle Stimulating Hormone

Word Cloud

Created with Highcharts 10.0.0±=CPAGAspironolactonelevelsPtransgenderhormone31womentreatmentmIU/L41225cyproteroneacetategonadotropin-releasinganaloguesmetaboliccohortpatientsanalysislastvisitAmongtreatment-naïve10followinginitiation206higherestradiolgroupsworseprofileassociated13bodymassindexHg65OBJECTIVE:Suppressiontestosteronesecretionand/oractionusingachievedvariousmechanismsobjectivecharacterizepossibledifferentialeffectscompoundsendocrinevariablesMETHODS:conductedhistoricstudytreatedtertiaryreferralcenterlongitudinalnaïvecross-sectionalwholecarriedoutRESULTS:12675predominantandrogensuppressivetherapy70%followed176%2%increaseserumprolactinbaselinegreatermonthsmeanchange39733587642680002ProlactinremainedCPA-treatedgroupthroughoutfollow-upirrespectivesimilarcomparedhigh-densitylipoprotein-cholesterollower475460respectively0076242177±3kg/m03systolic1171091053mm01diastolic74911mm0008bloodpressureCONCLUSION:TreatmenthyperprolactinemiacardiovascularriskABBREVIATIONS:BMIE2FSHfollicle-stimulatingLHluteinizingDifferentialEndocrineMetabolicEffectsTestosteroneSuppressiveAgentsTransgenderWomen

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