Cardiovascular outcomes in transgender individuals in Sweden after initiation of gender-affirming hormone therapy.


Journal

European journal of preventive cardiology
ISSN: 2047-4881
Titre abrégé: Eur J Prev Cardiol
Pays: England
ID NLM: 101564430

Informations de publication

Date de publication:
08 11 2022
Historique:
received: 17 05 2022
revised: 22 06 2022
accepted: 28 06 2022
pubmed: 3 7 2022
medline: 11 11 2022
entrez: 2 7 2022
Statut: ppublish

Résumé

We compared the incidence of cardiovascular disease (CVD) in transgender participants with a diagnosis of gender dysphoria (GD) with and without gender-affirming hormone therapy (GAHT) to the incidence observed in the general population. The population-based cohort included all individuals >10 years in Sweden linked to Swedish nationwide healthcare Registers (2006-16). Two comparator groups without GD/GAHT were matched (1:10) on age, county of residence, and on male and female birth-assigned sex, respectively. Cox proportional models provided hazard ratios (HRs) and 95% confidence intervals (CI) for CVD outcomes. Among 1779 transgender individuals [48% birth-assigned males (AMAB), 52% birth-assigned females (AFAB)], 18 developed CVD, most of which were conduction disorders. The incidence of CVD for AFAB individuals with GD was 3.7 per 1000 person-years (95% CI: 1.4-10.0). Assigned male at birth individuals with GD had an incidence of CVD event of 7.1 per 1000 person-years (95% CI: 4.2-12.0). The risk of CVD event was 2.4 times higher in AMAB individuals (HR: 2.4, 95% CI: 1.3-4.2) compared with cisgender women, and 1.7 higher compared with cisgender men (HR: 1.7, 95% CI: 1.0-2.9). Analysis limited to transgender individuals without GAHT yielded similar results to those with GAHT treatment. The incidence of CVD among GD/GAHT individuals was low, although increased compared with matched individuals without GD and similar to the incidence among GD/no GAHT individuals, thus not lending support for a causal relationship between treatment and CVD outcomes. Larger studies with longer follow-up are needed to verify these findings, as well as possible effect modification by comorbidity.

Identifiants

pubmed: 35778824
pii: 6627156
doi: 10.1093/eurjpc/zwac133
doi:

Substances chimiques

Hormones 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2017-2026

Commentaires et corrections

Type : CommentIn

Informations de copyright

© The Author(s) 2022. Published by Oxford University Press on behalf of the European Society of Cardiology.

Déclaration de conflit d'intérêts

Conflict of interest: None declared.

Auteurs

Maria A Karalexi (MA)

Department of Women's and Children's Health, Uppsala University, 753 09 Uppsala, Sweden.

Thomas Frisell (T)

Clinical Epidemiology Division, Department of Medicine Solna, Karolinska Institutet, 171 77 Stockholm, Sweden.

Sven Cnattingius (S)

Clinical Epidemiology Division, Department of Medicine Solna, Karolinska Institutet, 171 77 Stockholm, Sweden.

Dag Holmberg (D)

Department of Molecular Medicine and Surgery, Karolinska Institutet, Karolinska University Hospital, 171 76 Stockholm, Sweden.

Mats Holmberg (M)

ANOVA, Andrology, Sexual Medicine and Transgender Medicine, Karolinska University Hospital, 171 76 Stockholm, Sweden.
Department of Medicine, Huddinge, Karolinska Institutet, 171 77 Stockholm, Sweden.

Natasa Kollia (N)

Department of Nutrition and Dietetics, School of Health Science and Education, Harokopio University, 176 71 Athens, Greece.

Alkistis Skalkidou (A)

Department of Women's and Children's Health, Uppsala University, 753 09 Uppsala, Sweden.

Fotios C Papadopoulos (FC)

Department of Medical Sciences, Psychiatry, Uppsala University, Uppsala University Hospital, 751 85 Uppsala, Sweden.

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