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Sleep Deprivation or antisocial behavior in males is linked to higher levels of tes-
Sleep deprivation is commonly cited as a factor associated tosterone. Further, evidence to support concepts such as “roid
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with difficulties experienced during SOF training and SU- rage” from the use of testosterone or AAS is often complicated
SOPS. Daily sleep has been estimated to be 2–4 hours during by the use of additional drugs, whether licit or illicit, and re-
SOF training (Table 1). Sleep deprivation may also include ported incidences of criminal or antisocial behavior.
psychological stresses such as realistic battlefield simulations
and captivity. It is clear that both sleep deprivation and de- Although days of demanding SOF training may result in re-
creased HPG function occur at least temporally during SOF duced testosterone that arguably contributes to decreased
training and likely during SUSOPS. A modest reduction in LBM, at present little data exist on the effects of short-term
normal sleep volume, from 8 to 5 hours daily, reduces testos- testosterone therapy on LBM and strength. A majority of stud-
terone levels after 1 week in healthy young males, suggesting ies supplementing testosterone or AAS with or without resis-
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that the significant sleep deprivation experienced during SOF tance training treated subjects well in excess of 6 weeks. It is
training is a key factor in the reduction of testosterone. unknown whether days of testosterone therapy would reverse
or attenuate the anthropometric and functional changes asso-
Testosterone Therapy ciated with SOF training.
Data clearly demonstrate the additive effects of testosterone or
AAS to increase LBM and strength when combined with resis- One of the most glaring limitations of exogenous testoster-
tance training (Table 3). However, testosterone independent one therapy in SOF would be its use in females entering SOF.
of resistance training has been reported to increase LBM and The androgenic effects of testosterone in female candidates
strength (Table 2). More importantly, in diseased populations entering SOF training would likely be an unwelcome risk, par-
(e.g., COPD, HIV) exhibiting cachexia, low LBM, and fatigue, ticularly in terms of disrupting the normal female HPG axis
the use of testosterone or AAS reportedly increases LBM and and the potential for the development of male secondary sex
strength. Therefore, the use of exogenous testosterone or AAS characteristics in females. This limitation is unavoidable and
may reverse or attenuate cachexia and diminished muscle should not discount the potential benefit of short-term exoge-
function in SOF during or following SUSOPS. nous testosterone to assist the combat performance of males in
SOF. Data specific to changes in females during SOF training
Although data show positive results in diseased and SOF pop- and SUSOPS need to be gathered and strategies developed to
ulations, the occurrence of adverse reactions in therapy should attenuate losses in LBM and strength in female SOF.
not be disregarded. There is a risk for prostate cancer and
worsening symptoms of benign prostatic hypertrophy, liver Acknowledgments
toxicity, and tumor and worsening symptoms of sleep apnea The views expressed in this article are those of the authors and
and congestive heart failure, gynecomastia, infertility, and do not necessarily reflect the official policy or position of the
skin diseases. Without proper dosage and close monitoring Air Force, the Department of Defense, or the US Government.
46
of vital endocrine systems, these negative effects can become
quickly exacerbated. Disclosure
The authors have no financial relationships relevant to this
Recommendations article to disclose.
Data support the relationship between altered HPG function
and decreases in LBM and functional capacity during SOF
training. Further, it appears that reductions in testosterone pre- References
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