Lipoprotein(a) [Lp(a)] has recently emerged as Lan important risk fact
or for atherosclerotic cardiovascular disease.(1) Lp(a) levels are lar
gely under genetic control and have proved remarkably resistant to the
rapeutic manipulations.(1) Of the commonly used lipid-lowering medicat
ions, only high-dose niacin appears to reduce Lp(a) levels.(2) Others
have demonstrated that estrogen(3) and the anabolic-androgenic steroid
stanozolol(4) reduce Lp(a) concentrations in postmenopausal women, bu
t to our knowledge, the effect of androgenic hormone administration on
Lp(a) in men has not been examined. Testosterone is normally aromatiz
ed to estradiol, and peripheral aromatization of testosterone is the m
ajor source of circulating estrogen in men.(5) We recently examined th
e effect of testosterone aromatization on serum lipid and lipoprotein
levels in men by administering testosterone alone or in combination wi
th the aromatase inhibitor testolactone.(6) Recent reports that estrog
en decreases Lp(a)(3) prompted us to examine Lp(a) levels from our stu
dy to determine the effects of testosterone and its aromatization to e
stradiol on Lp(a) levels.