Evidence map›Paper›PMID 34125226›Full record

ArticleThe Journal of clinical endocrinology and metabolism2021

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

Suzanne M E Kuijpers, Chantal M Wiepjes, Elfi B Conemans, Alessandra D Fisher, Guy T'Sjoen, Martin den Heijer

Open access · greenAbstract readMulticenter Study
In one paragraph

Article in The Journal of clinical endocrinology and metabolism, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
9.7field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

30 citing papers in PubMed, 1 synthesis or guideline pooled it, 60 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 3 countries.

Suzanne M E KuijpersDepartment of Endocrinology and Center of Expertise on Gender Dysphoria, Amsterdam University Medical Center, location VUmc, 1007 MB Amsterdam, the Netherlands.ORCID 0000-0002-6821-0405
Chantal M WiepjesDepartment of Endocrinology and Center of Expertise on Gender Dysphoria, Amsterdam University Medical Center, location VUmc, 1007 MB Amsterdam, the Netherlands.ORCID 0000-0002-8280-0065
Elfi B ConemansDepartment of Endocrinology and Center of Expertise on Gender Dysphoria, Amsterdam University Medical Center, location VUmc, 1007 MB Amsterdam, the Netherlands.
Alessandra D FisherSexual Medicine and Andrology Unit, Department of Experimental, Clinical and Biomedical Sciences, University of Florence, Florence, Italy.ORCID 0000-0003-3446-5132
Guy T'SjoenDepartment of Endocrinology and Center for Sexology and Gender, Ghent University Hospital, Ghent, Belgium.ORCID 0000-0002-9250-4403
Martin den HeijerDepartment of Endocrinology and Center of Expertise on Gender Dysphoria, Amsterdam University Medical Center, location VUmc, 1007 MB Amsterdam, the Netherlands.ORCID 0000-0003-3620-5617
Amsterdam University Medical Centers · NLGhent University Hospital · BEUniversity of Florence · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

contextCyproterone 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.

objectiveTo assess the lowest effective dose of CPA in trans women to prevent side effects.

methodsThis 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.

resultsUsing 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.

conclusionCompared 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.

Indexed as

Androgen AntagonistsBelgiumCohort StudiesCyproterone AcetateDose-Response Relationship, DrugFemaleGender-Affirming ProceduresGender DysphoriaGender IdentityHormone Replacement TherapyHumansItalyLongitudinal StudiesMaleNetherlandsTranssexualismAndrogen AntagonistsCyproterone Acetateanti-androgencyproterone acetatehormone therapytestosteronetrans people

Identifiers

PMID34125226
PMCPMC8571811
OpenAlexW3167349204

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.