Gender-affirming hormone therapy decreases d-dimer but worsens insulin sensitivity in transgender women.


Journal

HIV medicine
ISSN: 1468-1293
Titre abrégé: HIV Med
Pays: England
ID NLM: 100897392

Informations de publication

Date de publication:
Nov 2023
Historique:
received: 21 04 2023
accepted: 12 06 2023
medline: 16 11 2023
pubmed: 30 6 2023
entrez: 30 6 2023
Statut: ppublish

Résumé

Gender-affirming hormonal therapies (GAHT) and HIV increase cardiovascular risk for transgender women (TW), yet there is a paucity of data quantifying cardiometabolic changes following GAHT initiation, particularly among TW with HIV. The Féminas study enrolled TW from October 2016 to March 2017 in Lima, Peru. Participants reported sexual activity that was high risk for HIV acquisition or transmission. All were tested for HIV/ sexually transmitted infection and were given access to GAHT (oestradiol valerate and spironolactone), HIV pre-exposure prophylaxis (PrEP) or antiretroviral therapy (ART) for 12 months. Biomarker measurement was done on stored serum, whereas fasting glucose and lipids were measured in real time. In all, 170 TW (32 with HIV, 138 without HIV) had median age 27 years and 70% prior GAHT use. At baseline, PCSK9, sCD14, sCD163, IL-6, sTNFRI/II, CRP and EN-RAGE levels were significantly higher in TW with HIV than in TW without HIV. High-density lipoprotein and total cholesterol were lower and insulin and glucose parameters were similar. All TW with HIV started ART, but only five achieved virological suppression at any time. No TW without HIV initiated PrEP. Over 6 months, all participants initiated GAHT and had worsening insulin, glucose and HOMA-IR. Large d-dimer decreases also occurred. Similar changes occurred in TW with and without HIV. In this unique cohort of TW, GAHT decreased d-dimer but worsened insulin sensitivity. Because PrEP uptake and ART adherence were very low, observed effects are primarily attributed to GAHT use. Further study is needed to better understand cardiometabolic changes in TW by HIV serostatus.

Identifiants

pubmed: 37386803
doi: 10.1111/hiv.13522
doi:

Substances chimiques

PCSK9 protein, human EC 3.4.21.-
Proprotein Convertase 9 EC 3.4.21.-
fibrin fragment D 0
Estradiol 4TI98Z838E
Glucose IY9XDZ35W2
Insulins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1144-1149

Subventions

Organisme : NIH HHS
Pays : United States
Organisme : NIH HHS
Pays : United States

Informations de copyright

© 2023 British HIV Association.

Références

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Auteurs

Jordan E Lake (JE)

UTHealth McGovern School of Medicine, Houston, Texas, USA.

Hongyu Miao (H)

Florida State University, Tallahassee, Florida, USA.

Emily R Bowman (ER)

The Ohio State University, Columbus, Ohio, USA.

Jesse L Clark (JL)

University of California, Los Angeles, California, USA.

Ana N Hyatt (AN)

UTHealth McGovern School of Medicine, Houston, Texas, USA.

Aaren Kettelhut (A)

The Ohio State University, Columbus, Ohio, USA.

Javier R Lama (JR)

Asociación Civil Impacta Salud y Educación, Lima, Peru.

Sari L Reisner (SL)

Brigham and Women's Hospital, Boston, Massachusetts, USA.

Kenneth H Mayer (KH)

Fenway Health, Boston, Massachusetts, USA.

Amaya Perez-Brumer (A)

University of Toronto, Toronto, Ontario, Canada.

Nicholas Funderburg (N)

The Ohio State University, Columbus, Ohio, USA.

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Classifications MeSH