ASIH may suffer from sexual dysfunction
(9)
, administration
of AIs in this population may still be considered, but proper
monitoring is advised.
Management of sexual dysfunction.
Erectile dysfunction
and decreased libido are common complaints of AAS users,
especially during the post-cycle period when endogenous T
levels are lowest. Adding to the complexity of evaluating
these patients, the types of AAS used may contribute uniquely
to the pathophysiology of AAS-induced sexual dysfunction.
Certain synthetic AASs, such as nandrolone, have a reputa-
tion for causing erectile dysfunction when used alone. This
effect is likely due to an unopposed progestin-like action of
the steroid along with the relatively lower androgenic activity
of its 5-alpha metabolite dihydronandrolone (compared with
dihydrotestosterone). By concurrently administering inject-
able T, AAS users attempt to mitigate the sexual side effect
pro
f
le of synthetic AASs such as nandrolone (
Table 2
).
More than 25% of users report using PDE5i either prophy-
lactically or as treatment for erectile dysfunction
(9, 17)
.
Several popular Internet AAS suppliers offer drugs such as
dapoxetine, bromocriptine, and cabergoline as well as
PDE5i. In addition, AAS users commonly purchase over the
counter herbal
‘‘
aphrodisiacs
’’
that have been previously
found to contain designer analogues of licensed PDE5i
(42)
.
Indeed,
for
AAS
users,
initial
therapy
for
erectile
dysfunction consists of PDE5i. Although controversial, the
restoration of a normal hormonal milieu may be important
for optimal response to oral PDE5i therapies.
Management of inferility and testicular atrophy.
AAS use
can be an important cause of male-factor infertility
(12)
.
Although several recent reviews have addressed the effects of
androgen consumption on male fertility
(6, 12, 29, 95, 96)
,
some clinicians remain unaware of the fact that the use of
exogenous androgens suppresses the HPG axis and, by
decreasing intratesticular T (ITT), results in infertility
(6, 97,
98)
. Because an adequate ITT concentration is necessary for
spermatogenesis
(52)
, it is not surprising that AAS users have
presented to fertility clinics with azoospermia or oligospermia
as well as sperm dysmorphia and dysmotility
(12, 95, 99)
.A
return of ITT is the most important factor for restoration of
spermatogenesis, and therefore initial management of AAS-
induced infertility should parallel strategies for the correction
of the underlying hypogonadotropic hypogonadism
(29, 52)
.
A review of the literature suggests that most cases of
AAS-induced oligospermia or azoospermia are likely to
resolve spontaneously within 4
12 months after AAS discon-
tinuation
(29)
. Although some authors have argued for
reserving medical treatment for cases of azoospermia lasting
>
24 months
(100)
, SERMs and/or gonadotropins have been
successfully used after much shorter intervals of AAS cessa-
tion
(67,
101,
102)
.
Spermatogenesis
recovery
time,
however, with or without medical treatment, appears to be
highly variable and is dif
f
cult or impossible to predict for
an individual patient.
In a case series of four azoospermic men, Gazvani et al.
reported on the spontaneous return of sperm concentration
to normal levels over a variable period of 5
18 months after
AAS cessation
(100)
. Turek et al. reported a single case of
AAS-induced azoospermia successfully treated with hCG,
and pregnancy was achieved after 3 months of therapy
(102)
. Menon et al. reported a return to normal semen param-
eters after 3 months of treatment with hCG and hMG in a
patient who had been untreated and azoospermic for 1 year
after stopping AAS
(67)
.
As far as we know, cases of persistent azoospermia
despite exhaustive medical treatment have not been described
in the literature. Clearly, the management of AAS-induced
male infertility should begin with conservative or medical
management. Histopathologic abnormalities, such as sperm
maturation arrest, have been described in AAS users and an-
imal models
(102, 103)
, and although there are no published
data con
f
rming the success of sperm retrieval techniques
with subsequent IVF-ICSI for cases of AAS-induced
TABLE 2
An example (considerable variations exist) of a bodybuilder's 12-week AAS cycle followed by 4 weeks of post-cycle therapy.
Week
Testosterone
cypionate, mg/wk
Nandrolone
(Deca-Durabolin), mg/wk
Metadienone
(Dianabol), mg/d
hCG
(IU/2
3d)
Anastrazole
(Arimidex), mg/d
Clomiphene
citrate (Clomid)
Tamoxifen
(Nolvadex), mg/d
1
500
500
25
2
750
500
25
3
750
500
25
4
750
500
25
5
1000
500
50
6
1000
500
50
7
1000
500
50
8
1000
500
50
9
1000
500
0
500
0.25
10
1000
500
0
500
0.25
11
750
500
0
500
0.25
12
500
500
0
500
0.25
13
200
40
14
100
40
15
50
20
16
50
20
Note:
AAS
¼
anabolic-androgenic steroid.
Rahnema. Anabolic steroid
induced hypogonadism. Fertil Steril 2014.
1276
VOL. 101 NO. 5 / MAY 2014
ORIGINAL ARTICLE: ANDROLOGY