Current evidence indicates that thyroid cells are sensitive to human c
horionic gonadotropin (hCG) stimulation. In turn, thyroid hormones app
ear to influence ovarian and endometrial physiology and reproductive f
unction. Our studies addressed the possible effect of endogenous and e
xogenous hCG on in vivo thyroid function in normal pregnancy and contr
olled ovarian hyperstimulation, respectively. Circulating concentratio
ns of hCG in pregnant women during gestation were positively correlate
d with serum free thyroxine (r = 0.43, p = 0.02) and negatively correl
ated with thyrotropin levels in the same patients (r = 0.42, p = 0.02)
. By contrast, exogenous administration of hCG to effect follicular ma
turation in non-pregnant patients undergoing ovarian hyperstimulation
resulted in lower circulating hCG concentrations than seen in pregnanc
y and failed to alter free thyroxine or thyrotropin levels (p > 0.22).
Endogenous isoforms of hCG in early pregnancy appear to have thyrotro
pic activity in vivo. However, the results indicate that, under clinic
al conditions of controlled ovarian hyperstimulation for assisted repr
oduction, exogenous hCG does not affect the hypothalamic-pituitary-thy
roid axis.