Evidence map›Paper›PMID 36766819›Full record

ArticleCells2023

Risk Assessment of Transgender People: Development of Rodent Models Mimicking Gender-Affirming Hormone Therapies and Identification of Sex-Dimorphic Liver Genes as Novel Biomarkers of Sex Transition.

Roberta Tassinari, Alessia Tammaro, Gabriele Lori, Sabrina Tait, Andrea Martinelli, Luigia Cancemi, Paolo Frassanito, Francesca Maranghi

Abstract read
In one paragraph

Article in Cells, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

10 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. A systematic review of transgender male rodent model methodology.Animal models and experimental medicine · 2025
    Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Roberta TassinariCenter for Gender Specific Medicine, Istituto Superiore di Sanità, 00144 Rome, Italy.ORCID 0000-0002-4121-2144
Alessia TammaroCenter for Gender Specific Medicine, Istituto Superiore di Sanità, 00144 Rome, Italy.
Gabriele LoriCenter for Gender Specific Medicine, Istituto Superiore di Sanità, 00144 Rome, Italy.ORCID 0000-0002-7997-6983
Sabrina TaitCenter for Gender Specific Medicine, Istituto Superiore di Sanità, 00144 Rome, Italy.ORCID 0000-0001-8029-8625
Andrea MartinelliExperimental Animal Welfare Sector, Istituto Superiore di Sanità, 00144 Rome, Italy.
Luigia CancemiExperimental Animal Welfare Sector, Istituto Superiore di Sanità, 00144 Rome, Italy.
Paolo FrassanitoExperimental Animal Welfare Sector, Istituto Superiore di Sanità, 00144 Rome, Italy.
Francesca MaranghiCenter for Gender Specific Medicine, Istituto Superiore di Sanità, 00144 Rome, Italy.ORCID 0000-0003-1736-2262

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Transgender (TG) describes individuals whose gender identity differs from the social norms. TG people undergoing gender-affirming hormone therapy (HT) may be considered a sub-group of the population susceptible to environmental contaminants for their targets and modes of action. The aim of this study is to set appropriate HT doses and identify specific biomarkers to implement TG animal models. Four adult rats/group/sex were subcutaneously exposed to three doses of HT (plus control) selected starting from available data. The demasculinizing-feminizing models (dMF) were β-estradiol plus cyproterone acetate, at 0.09 + 0.33, 0.09 + 0.93 and 0.18 + 0.33 mg, respectively, five times/week. The defeminizing-masculinizing models (dFM) were testosterone (T) at 0.45, 0.95 and 2.05 mg, two times/week. Clitoral gain and sperm count, histopathological analysis of reproductive organs and liver, hormone serum levels and gene expression of sex-dimorphic CYP450 were evaluated. In the dMF model, the selected doses-leading to T serum levels at the range of the corresponding cisgender-induced strong general toxicity and cannot be used in long-term studies. In the dFM model, 0.45 mg of T represents the correct dose. In addition, the endpoints selected are considered suitable and reliable to implement the animal model. The sex-specific CYP expression is a suitable biomarker to set proper (de)masculinizing/(de)feminizing HT and to implement TG animal models.

Indexed as

Transgender PersonsAnimalsBiomarkersFemaleGender IdentityHumansLiverMaleRatsRisk AssessmentRodentiaSemenTestosteroneBiomarkersTestosteronecyproterone acetatecytochrome P450estrogenfeminizingmasculinizingsex-specific genestestosterone

Identifiers

PMID36766819
PMCPMC9913858

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.