Longitudinal Changes in Hematologic Parameters Among Transgender People Receiving Hormone Therapy.
hematocrit
hemoglobin
hormone therapy
longitudinal
transgender
Journal
Journal of the Endocrine Society
ISSN: 2472-1972
Titre abrégé: J Endocr Soc
Pays: United States
ID NLM: 101697997
Informations de publication
Date de publication:
01 Nov 2020
01 Nov 2020
Historique:
received:
01
06
2020
accepted:
13
08
2020
entrez:
9
4
2021
pubmed:
10
4
2021
medline:
10
4
2021
Statut:
epublish
Résumé
The effect of gender-affirming hormone therapy (HT) on erythropoiesis is an area of priority in transgender health research. To compare changes in hematologic parameters and rates of erythrocytosis and anemia among transgender people to those of cisgender controls. Longitudinal observational study. We compared 559 transfeminine (TF) and 424 transmasculine (TM) people enrolled in 3 integrated health care systems to matched cisgender referents. Hormone therapy receipt was ascertained from filled prescriptions. Hemoglobin (Hb) and hematocrit (Hct) levels were examined from the first blood test to HT initiation, and from the start of HT to the most recent blood test. Rates of erythrocytosis and anemia in transgender participants and referents were compared by calculating adjusted hazard ratios and 95% confidence intervals (CI). In the TF group, there was a downward trend for both Hb and Hct. The corresponding changes in the TM cohort were in the opposite direction. TM study participants experienced a 7-fold higher rate (95% CI: 4.1-13.4) of erythrocytosis relative to matched cisgender males, and an 83-fold higher rate (95% CI: 36.1-191.2) compared to cisgender females. The corresponding rates for anemia were elevated in TF subjects but primarily relative to cisgender males (hazard ratio 5.9; 95% CI: 4.6-7.5). Our results support previous recommendations that hematological parameters of transgender people receiving HT should be interpreted based on their affirmed gender, rather than their sex documented at birth. The clinical significance of erythrocytosis following testosterone therapy, as well as anemia following feminizing HT, requires further investigation.
Identifiants
pubmed: 33834151
doi: 10.1210/jendso/bvaa119
pii: bvaa119
pmc: PMC8011434
doi:
Types de publication
Journal Article
Langues
eng
Pagination
bvaa119Subventions
Organisme : NICHD NIH HHS
ID : R21 HD076387
Pays : United States
Informations de copyright
© The Author(s) 2020. Published by Oxford University Press on behalf of the Endocrine Society.
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