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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-
                                                    14
              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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