The antiretroviral drug efavirenz significantly reduces the levels
of both hormones in the vaginal ring contraceptive in women with HIV, Kimberly
Scarsi of University of Nebraska Medical Center reported on Wednesday at the Conference
on Retroviruses and Opportunistic Infections (CROI 2018) in Boston.
Atazanavir also affected levels of the hormones, but its
effect appeared less likely to undermine the contraceptive effectiveness of the
vaginal ring, the study showed.
“If I was a woman receiving an efavirenz-based
antiretroviral regimen I would be uncomfortable with the degree of
contraceptive protection I would be getting from the vaginal ring,” Kimberly
Scarsi told a press briefing following the presentation.
The vaginal ring (NuvaRing)
is a flexible plastic ring containing 120 mcg of a type of progestin called
etonogestrel and 15 mcg of ethinyl estradiol. The ring contains enough of the
hormones to provide contraception for one month.
Efavirenz is known to reduce levels of etonogestrel
released by subdermal contraceptive implants but its effect on etonogestrel
released by the vaginal ring is unknown. The boosted protease inhibitor lopinavir/ritonavir
increases etonogestrel levels but the effect of other boosted protease inhibitors
is unknown.
To answer these questions, the AIDS Clinical Trials Group
designed the A5316 study. The study recruited a control group of 27 women with
HIV not yet taking antiretroviral therapy, 28 women taking efavirenz and 29
women taking atazanavir/ritonavir as part of a three-drug regimen. All women
consented to use the vaginal ring with another form of non-hormonal
contraception. All women on antiretroviral therapy had viral load below 400
copies/ml.
The control group had a median age of 31 years and the
antiretroviral treatment groups a median age of 36 years. Participants were
predominantly black (44-64%) or Hispanic (32-40%).
Participants underwent pharmacokinetic assessments of plasma
concentrations of etonogestrel and ethinyl estradiol on the day they commenced
using the vaginal ring, day 7, day 14 and day 21.
Levels of ethinyl estradiol, the oestrogen component of the
vaginal ring hormonal contraceptive that suppresses ovulation, were reduced by
53-57% in the efavirenz group compared to the control group and suppression was
evident within seven days of first insertion and throughout the sampling period
(p < 0.001 for all measurements). Ethinyl estradiol levels were reduced by
29-35% in the atazanavir/ritonavir group, and this difference was significant compared
to the control group at days 14 and 21 (p = 0.032, p = 0.004).
Levels of etonogestrel, the progestin component of vaginal
ring contraceptive that suppresses ovulation and impedes fertilisation, were
reduced by 76-79% in the efavirenz group, but increased by 71-79% in the
atazanavir/ritonavir group (all p < 0.001).
Menstrual bleeding abnormalities were more frequent in the efavirenz
group but other adverse events were more common in the control group.
The researchers concluded that efavirenz-based antiretroviral therapy may decrease
the effectiveness of vaginal ring contraceptives and warned that combination
antiretroviral-hormonal contraceptive vaginal rings for HIV prevention could
also be affected by drug-drug interactions.