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Impact of Hormonal Contraception on HIV Acquisition, Cervico-Vaginal Viral Shedding, and Disease Progression
Elizabeth Stringer
Univ of Alabama at Birmingham, Lusaka, Zambia
Background: This
presentation will review pertinent studies on the effect of hormonal
contraception on HIV acquisition, infectivity, and disease progression. Whether
hormonal contraception increases susceptibility to HIV acquisition has been
the subject of numerous studies in animals and humans. Results from 2 large,
prospective studies that produced conflicting results—the Mombasa Cohort Study
and the Hormonal Contraception-HIV (HC-HIV) Study—will be reviewed. Few
well-executed studies have used an incident HIV outcome to assess the influence
of hormonal contraception on HIV transmissibility. Most instead rely on
cervico-vaginal viral shedding as a surrogate marker for infectivity. Data in
this area suggest that hormonal contraception may increase shedding of
cell-associated virus. Moreover, data from the Mombasa Cohort Study suggest
that women using depot medroxyprogesterone acetate (DMPA) at the time of HIV
acquisition had a higher viral set-point than women using non-hormonal methods
and that they were more likely to acquire multiple viral variants, which in
turn was associated with faster disease progression. A recent randomized trial
of the intrauterine contraceptive device (IUD) versus hormonal contraception
conducted in Zambia found an increased risk of disease progression (defined as
either death or CD4 falling below 200 cells/mm3) in women allocated
to hormonal contraception.
Conclusions: Data from
these studies, as well as a large multi-country HIV treatment cohort, will be
reviewed.
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