speci
f
c
‘‘
nutritionists
’’
who, for a fee, usually yearly, give
advice to these men about AAS, dietary supplements, and
nutritional plans.
The AAS user's rationale for choosing various drugs and
protocols is typically based on anecdotal evidence and inter-
pretations of quasiscienti
f
c literature propagated via Internet
forums. It is also apparent that some users achieve popular au-
thority within the Internet bodybuilding community and are
often consulted for medical advice via forums. Indeed, given
the minimal exposure that physicians have to AAS, coupled
with the fact that many
‘‘
expert
’’
users have experimented
with the majority of available AAS and their companion
medications, it is not too far-fetched to consider
f
rst-hand
experience of achievable gains, side effects, and
‘‘
optimal
’’
self-treatment regiments by seasoned AAS users to be of
perceived
‘‘
greater value
’’
than an average physician's recom-
mendation. Indeed, it is the general consensus within the
AAS community that experienced AAS users are more
educated than their physicians on AAS use, a sentiment that
may contribute to the AAS user's hesitancy to approach his
physician for advice when adverse symptoms occur
(17, 43)
.
Motivations for Use and Dependence: A Challenge
for Clinicians
Results from large surveys sampling AAS users on Internet
bodybuilding forums have reported that the most common
reason for beginning AAS use was to increase muscle mass
and decrease body fat
(9, 17)
. These users also reported
feeling compelled to continue their regimens for a fear of
the withdrawal that would result in excessive hypogonadal
symptoms and the loss of muscle mass
(6, 17)
.
When considering the concept of ASIH, the aggregate
AAS dose and duration likely portends the extent of the con-
dition; however, it must be recognized that there are substan-
tial variations in types and amounts of AAS used
(45)
.A
subset of aggressive users may develop a dependence syn-
drome of combined physiologic and psychologic etiology,
subjecting themselves to long-term or permanent endocrine
dysfunction
(9, 12, 14, 15, 17, 31, 44
46)
. Given these case
reports as well as the known AAS side effects, one might
wonder whether AAS users experience regret over their
decision to use AAS. If these suspicions are correct, then
determining the reasons for regret would be a valuable tool
in educating current patients previously on AAS who are
seeking TRT for hypogonadism.
In stark contrast to the classic drug abusers, most AAS
users show considerable forethought in their illicit substance
use
(47)
. Users typically obtain all of the necessary medica-
tions before beginning their self-determined
‘‘
treatment
’’
cy-
cle and follow calculated dosing schedules
(9, 17, 25, 48, 49)
.
AAS users are often hesitant to stop their regimens and often
present to physicians with requests for diagnostics or
unwarranted therapies without the intent of stopping illicit
AAS use. It is also common for AAS users to want to cycle
off all TRT, feeling that this enhances their responsiveness
and improves safety. As such, the treatment of AAS users
poses a unique challenge for physicians. It may be helpful
to gauge the patient's knowledge of AAS-associated compli-
cations while working to address misconceptions that often
stem from Internet forum trends and popular anecdotal evi-
dence. Central to this is the need for physicians to become
more educated about the psychology and pathophysiology
underlying AAS use.
Pathophysiology
Feedback suppression.
Use of AAS results in hypogonado-
tropic hypogonadism by feedback suppression of the
hypothalamic-pituitary-gonadal (HPG) axis via inhibition of
pulsatile GnRH release and a subsequent decrease in LH and
FSH (
Fig. 1
). The duration of suppression and the resultant
symptomatic ASIH is highly variable and due to multiple fac-
tors, including differences in the choices of drugs, amounts
used, and durations of use. Based on our experience, there
may be differences between individual users regarding the
response kinetics of the HPG axis. Our experience and that of
other investigators suggests that younger men may have a
more
‘‘
elastic axis
’’
capable of recovering GnRH pulsation and
gonadotropin secretion faster and more completely than older
AAS users
(50)
. It is possible that shorter durations, lower doses,
youngerages,and higherT levelsatbaseline are associatedwith
a quicker recovery of HPG axis function after AAS use.
ASIH: a unique pathophysiology.
Considerable variation ex-
ists regarding drug combinations, dosing, and duration of use.
Up to 90% of AAS users combine or
‘‘
stack
’’
multiple andro-
gens, a practice that users believe provides the greatest results
while
minimizing
unwanted
side
effects
(19,
48)
.
Traditionally, a typical bodybuilding cycle includes a stack
of multiple AAS at a combined dose of 500
1,500 mg/wk
and lasts on average 4-12 weeks
(17, 19, 25, 32, 48, 51)
(
Table 1
). The most commonly used androgens reported by
multiple surveys are single-ester T, nandrolone, stanazolol,
metandienone, and trenbolone
(16, 17, 32)
. In contrast,
FIGURE 1
Illustrates the pathophysiology of anabolic-androgenic steroid (AAS)
induced hypogonadism (ASIH) and the mechanism of action of
selected treatment strategies. Recovery therapy focuses on estrogen
blockade at the level of the hypothalamus to encourage GnRH
pulsation and gonadotropin release to restart the hypothalamic-
pituitary-gonadal axis and increase testosterone production.
Rahnema. Anabolic steroid
induced hypogonadism. Fertil Steril 2014.
VOL. 101 NO. 5 / MAY 2014
1273
Fertility and Sterility®