Oestradiol concentrations in trans women with HIV suppressed on unboosted integrase inhibitor regimens versus trans women without HIV taking oral oestradiol: a pilot study

Author:

Loutfy Mona123,Lacombe-Duncan Ashley14,Tseng Alice56,Persad Yasmeen1,Underhill Angela1,Kennedy V Logan1,Armstrong Ian7,Fung Raymond8,Bourns Amy39,Nguyen Quang39,Hranilovic Sue10,Weisdorf Thea10,Chan L Y L311,Kia Hannah12ORCID,Halpenny Roberta2,Iyer Harshita1,Jeyarajah Nirubini2,Kovchazov George2,McCully Jennifer2,Scarsi Kimberly K13ORCID

Affiliation:

1. Women’s College Research Institute, Women's College Hospital , Toronto, Ontario , Canada

2. Maple Leaf Research , Toronto, Ontario , Canada

3. Department of Medicine, University of Toronto , Toronto, Ontario , Canada

4. School of Social Work, University of Michigan , Ann Arbor, MI , USA

5. Toronto General Hospital, Unity Health Network , Toronto, Ontario , Canada

6. Leslie Dan Faculty of Pharmacy, University of Toronto , Toronto, Ontario , Canada

7. Maple Leaf Medical Clinic , Toronto, Ontario , Canada

8. Michael Garron Hospital , Toronto, Ontario , Canada

9. Sherbourne Health , Toronto, Ontario , Canada

10. Academic Family Health, St. Michael’s Hospital , Toronto, Ontario , Canada

11. Church-Wellesley Medical Clinic , Toronto, Ontario , Canada

12. School of Social Work, University of British Columbia , Vancouver, British Columbia , Canada

13. College of Pharmacy, University of Nebraska Medical Center , Omaha, NE , USA

Abstract

Abstract Background Feminizing hormone therapy (FHT) is essential to many trans women. Concern about negative drug interactions between FHT and ART can be an ART adherence barrier among trans women with HIV. Objectives In this single-centre, parallel group, cross-sectional pilot study, we measured serum oestradiol concentrations in trans women with HIV taking FHT and unboosted integrase strand transfer inhibitor (INSTI)-based ART versus trans women without HIV taking FHT. Methods We included trans women with and without HIV, aged ≥18 years, taking ≥2 mg/day of oral oestradiol for at least 3 months plus an anti-androgen. Trans women with HIV were on suppressive ART ≥3 months. Serum oestradiol concentrations were measured prior to medication dosing and 2, 4, 6 and 8 h post-dose. Median oestradiol concentrations were compared between groups using Wilcoxon rank-sum tests. Results Participants (n = 8 with HIV, n = 7 without) had a median age of 32 (IQR: 28, 39) years. Among participants, the median oral oestradiol dose was 4 mg (range 2–6 mg). Participants had been taking FHT for a median of 4 years (IQR: 2, 8). Six trans women with HIV were taking bictegravir/emtricitabine/tenofovir alafenamide and two were taking dolutegravir/abacavir/lamivudine. All oestradiol concentrations were not significantly different between groups. Eleven (73%) participants had target oestradiol concentrations in the range 200–735 pmol/L at C4h (75% among women with HIV, 71% among those without HIV). Conclusions Oestradiol concentrations were not statistically different in trans women with HIV compared with those without HIV, suggesting a low probability of clinically relevant drug–drug interactions between FHT and unboosted INSTI-based ART.

Funder

Canadian Institutes of Health Research

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology,Microbiology (medical)

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