No discrete event marks a transition to male reproductive senescence;
however, a number of investigations have suggested that male fertility
and reproductive hormone secretion decrease with age, giving rise to
the term male menopause. Nearly all studies of seminiferous tubular fu
nction and morphology have found evidence of an age-related deteriorat
ion including anatomical lesions, reduced semen quality, elevated seru
m levels of inhibin, and diminished fertility. The question of altered
androgen secretion remains controversial with evidence both for and a
gainst age-related reductions in testosterone (T), free T, and/or DHT
in multiple investigations. Much of this controversy probably stems fr
om noncomparable populations, especially with regard to confounding va
riables such as stress, illness, and medication use. Published finding
s to date agree that in healthy aging men there is a small but signifi
cant increase in basal levels of LH and a diminished T response to exo
genous gonadotropin, suggesting an intrinsic loss of Leydig cell reser
ve. Moreover, there is evidence of a gradual loss of function of the h
ypothalamic/pituitary gonadotropic axis as well. Despite these changes
, healthy aging men appear to maintain normal circulating total and fr
ee T and DHT levels, despite modest increases in sex hormone binding g
lobulin (SHBG) and an small downward trend in serum androgens. Whether
there are metabolic consequences such as altered body composition, mu
scle strength, and lipid profiles in the portion of the aging male pop
ulation with larger androgen decrements requires further investigation
.