Abrams DI, Shade SB, Couey P, McCune J, Lo J, Bacchetti
P, Chang B, Epling L, Liegler T, Grant RM.
Dehydroepiandrosterone (DHEA) and HIV: a randomized placebo-controlled
study.
Community Consortium, Positive Health Program,
University of California, San Francisco, 3180 18th St, Ste 201, San
Francisco, CA 94110. dabrams@php.ucsf.edu
PURPOSE: The study was designed in response
to preliminary data suggesting that DHEA inhibits the expression of
HIV in latently infected cells and might thus be a potential adjunct
to currently available antiretroviral therapy. The primary objective
was to determine DHEA's impact on latent HIV infection; additionally,
we examined its effect on persistent viral replication, host immunity
and non-immune aspects of host restoration.
METHODS: Forty HIV-infected subjects with suppressed
viremia on a stable antiretroviral regimen were randomized in double-blind
fashion to receive either DHEA or placebo for 12 weeks, followed by
open-label DHEA for an additional 12 weeks. Intensive virologic monitoring
included plasma viral load (lower limits of detection 50 copies/mL and
2.5 copies/mL) and quantitative cultures of replication competent virus
reservoirs in blood cells. A full battery of immunologic measurements
was performed. Hormonal measurements, body weight and body composition
were obtained. Quality of life was assessed with a variety of instruments.
RESULTS: DHEA was bioavailable as ascertained
by increased levels of DHEA, DHEA(S) and androstenedione in recipients'
plasma compared to the control group. HIV plasma viral load did not
decrease and may, in fact, have increased in the DHEA arm, and there
was no apparent immunologic effect compared to placebo recipients. There
appeared to be no benefit with regard to lean muscle mass or bone density
in the DHEA treated group. DHEA treatment had a positive impact on mood
and quality of life.
CONCLUSIONS: DHEA supplementation in fully suppressed
HIV patients was associated with an improvement in quality of life but
appeared to have no beneficial antiviral, immunomodulatory, hormonal
or body composition effects, suggesting that it not be routinely used
as an adjunctive therapy in this population.
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