Body wasting and loss of lean body mass (LBM) have been associated with inc
reased mortality and disease progression, and reduced quality of life, in p
atients with human immunodeficiency virus (HIV) infection. The failure of n
utritional therapies and, more recently, of effective viral suppression, to
consistently restore LBM has prompted investigation of the pharmacologic u
se of a number of specific protein anabolic agents, including recombinant h
uman growth hormone (rhGH), insulinlike growth factor I (rhIGF-I), and synt
hetic testosterone derivatives, such as nandrolone decanoate, oxandrolone,
and oxymetholone. In a placebo-controlled trial, treatment with rhGH result
ed in a significant and sustained increase in weight that was accompanied b
y an even greater increase in LBM and a decrease in fat, and improvement in
treadmill work output. Preliminary data suggest that short-term rhGH treat
ment may be effective in mitigating weight loss in patients with secondary
infections. Open-label studies of nandrolone decanoate suggest that this in
jectable agent also can increase weight and LBM. Two oral agents, oxandrolo
ne and oxymetholone, can increase weight, but their effects on LBM in place
bo-controlled trials have not been reported. Taken together, these studies
demonstrate that HIV-infected individuals can regain weight and LBM under t
he proper therapeutic circumstances. The effects of reversal of wasting on
survival and disease progression, long-term safety, and the potential value
of these therapies in the treatment of fat redistribution remain to be det
ermined.