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Do Transitioned Athletes Compete at an Advantage or Disadvantage

Do Transitioned Athletes Compete at an Advantage or Disadvantage

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<strong>Tr<strong>an</strong>sitioned</strong> <strong>Athletes</strong> <strong>an</strong>d Competition 13<br />

spectrum, physically b<strong>or</strong>n women had smaller muscle cross-sectional area; <strong>at</strong> the high end of the<br />

spectrum muscle cross-sectional area was equal between tr<strong>an</strong>sitioned women <strong>an</strong>d physically b<strong>or</strong>n<br />

women (37). This finding is of imp<strong>or</strong>t<strong>an</strong>ce as individuals (both tr<strong>an</strong>sitioned <strong>an</strong>d physically b<strong>or</strong>n<br />

women) taking part in sp<strong>or</strong>t would likely have gre<strong>at</strong>er muscle mass th<strong>an</strong> the average popul<strong>at</strong>ion,<br />

thus as difference did not exist <strong>at</strong> the upper end of the muscle cross-sectional area spectrum,<br />

differences in muscle cross-sectional area may not exist between tr<strong>an</strong>sitioned women <strong>an</strong>d<br />

physically b<strong>or</strong>n women <strong>at</strong>hletes. However, as the af<strong>or</strong>ementioned trial did not compare muscle<br />

cross-sectional area in tr<strong>an</strong>sitioned <strong>an</strong>d physically b<strong>or</strong>n women <strong>at</strong>hletes, this premise remains<br />

unsubst<strong>an</strong>ti<strong>at</strong>ed.<br />

Estrogen <strong>an</strong>d <strong>an</strong>ti-<strong>an</strong>drogen administr<strong>at</strong>ion also alters body f<strong>at</strong> content <strong>an</strong>d distribution<br />

(28, 30). Specifically, in tr<strong>an</strong>sitioned women estrogen supplement<strong>at</strong>ion increased both<br />

subcut<strong>an</strong>eous (28, 30) <strong>an</strong>d visceral f<strong>at</strong> (28) content, resulting in <strong>an</strong> overall increase in percent<br />

body f<strong>at</strong>. Additionally, the increase in subcut<strong>an</strong>eous f<strong>at</strong> was most prominent in the gynoid region<br />

(66% vs 57% increase); however, the waist-to-hip r<strong>at</strong>io did not ch<strong>an</strong>ge in tr<strong>an</strong>sitioned women<br />

(28). Additionally, total subcut<strong>an</strong>eous f<strong>at</strong> content still appeared to be lower in tr<strong>an</strong>sitioned<br />

women following one year of estrogen tre<strong>at</strong>ment as compared with physically b<strong>or</strong>n women (28).<br />

Looking <strong>at</strong> individual <strong>an</strong><strong>at</strong>omical loc<strong>at</strong>ions, estrogen <strong>an</strong>d <strong>an</strong>ti-<strong>an</strong>drogen administr<strong>at</strong>ion increased<br />

percent body f<strong>at</strong> <strong>at</strong> the triceps, biceps, subscapula, suprailiac <strong>an</strong>d para-umbilical regions (28).<br />

Estrogen <strong>an</strong>d <strong>an</strong>ti-<strong>an</strong>drogen supplement<strong>at</strong>ion also increased individual adipocyte size <strong>an</strong>d<br />

decreased basal lipolytic activity of gluteal <strong>an</strong>d abdominal f<strong>at</strong> cells (30). However, similar to the<br />

effect of testosterone supplement<strong>at</strong>ion to tr<strong>an</strong>sitioned men, estrogen <strong>an</strong>d <strong>an</strong>ti-<strong>an</strong>drogen<br />

supplement<strong>at</strong>ion to tr<strong>an</strong>sitioned women did not alter r<strong>at</strong>es of stimul<strong>at</strong>ed lipolysis (30).<br />

Despite women generally being lighter th<strong>an</strong> men (26, 27), total body weight increased in<br />

response to estrogen <strong>an</strong>d <strong>an</strong>ti-<strong>an</strong>drogen supplement<strong>at</strong>ion in tr<strong>an</strong>sitioned women, despite a<br />

decrease in muscle mass (28). Thus, f<strong>or</strong> sp<strong>or</strong>ting events where <strong>an</strong> <strong>at</strong>hlete would have to carry<br />

their own body weight (i.e. running) <strong>an</strong> increase in body weight following estrogen <strong>an</strong>d <strong>an</strong>ti<strong>an</strong>drogen<br />

tre<strong>at</strong>ment may be detrimental to perf<strong>or</strong>m<strong>an</strong>ce. However, again, to d<strong>at</strong>e no study has<br />

been conducted investig<strong>at</strong>ing the effect of estrogen supplement<strong>at</strong>ion on body weight in<br />

tr<strong>an</strong>sitioned women <strong>at</strong>hletes. As <strong>at</strong>hletes are very active <strong>an</strong>d proper nutrition plays <strong>an</strong> imp<strong>or</strong>t<strong>an</strong>t<br />

role in <strong>at</strong>hletic perf<strong>or</strong>m<strong>an</strong>ce, it is likely th<strong>at</strong> body weight would decrease in this subset of<br />

tr<strong>an</strong>sitioned women. Additionally, the body weight decrease would likely be due to the effect of<br />

estrogen to decrease muscle mass, while body f<strong>at</strong> st<strong>or</strong>es would not increase as dram<strong>at</strong>ically as<br />

th<strong>at</strong> found in non-<strong>at</strong>hletic tr<strong>an</strong>sitioned women. However, this the<strong>or</strong>y needs to be tested.<br />

To d<strong>at</strong>e no study has been conducted investig<strong>at</strong>ing the long term effects of estrogen<br />

supplement<strong>at</strong>ion on carbohydr<strong>at</strong>e <strong>or</strong> lipid metabolism during endur<strong>an</strong>ce exercise. However, as<br />

described in detail above (see “metabolic effects of estrogen), E2 supplement<strong>at</strong>ion to men c<strong>an</strong><br />

spare liver glucose/glycogen utiliz<strong>at</strong>ion (17, 25), resulting in lower carbohydr<strong>at</strong>e <strong>an</strong>d higher lipid<br />

oxid<strong>at</strong>ion during a bout of endur<strong>an</strong>ce exercise (25). However, these E2 supplement<strong>at</strong>ion trials<br />

have used dosing periods of 72h to 11 days (18, 25, 71, 89), thus their applicability to<br />

metabolism during exercise in tr<strong>an</strong>sitioned women needs further investig<strong>at</strong>ion.

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