Em. Kouri et al., CHANGES IN LIPOPROTEIN-LIPID LEVELS IN NORMAL MEN FOLLOWING ADMINISTRATION OF INCREASING DOSES OF TESTOSTERONE CYPIONATE, Clinical journal of sport medicine, 6(3), 1996, pp. 152-157
Objective: The objective of this study was to examine the relationship
between anabolic-androgenic steroids and lipoprotein levels in men re
ceiving weekly injections of gradually escalating doses of up to 600 m
g/week of testosterone cypionate. Design: The design was a placebo-con
trolled, double-blind, 24-week cross-over design in which subjects wer
e randomized to one of two treatment sequences: (a) weekly testosteron
e cypionate injections for 6 weeks, no treatment for 6 weeks, weekly p
lacebo injections for 6 weeks, and then again no treatment for 6 weeks
; or (b) placebo, no treatment, testosterone, and then no treatment, w
ith each interval also lasting 6 weeks as in the first sequence. Setti
ng: The setting was a private hospital. Participants: Participants wer
e normal male volunteers. Interventions: Testosterone cypionate inject
ions were given in gradually increasing doses of 150 mg/week for 2 wee
ks, 300 mg/week for 2 weeks, and 600 mg/week for 2 weeks. Eight subjec
ts received testosterone injections during the first injection phase a
nd placebo during the second injection phase, and the remaining eight
subjects received placebo first and testosterone second. Results: We f
ound a 21% depression of high-density lipoprotein cholesterol (HDL-C)
levels following the first 300-mg testosterone dose. This depression r
emained unchanged after the two 600-mg doses. In contrast, we did not
find any changes in low-density lipoprotein or total cholesterol level
s at any of the time points studied. Subjects' total cholesterol/HDL-C
ratios were significantly elevated during testosterone administration
and even 4 weeks following the last injection. Conclusion: Our findin
gs suggest that testosterone cypionate adversely affects cholesterol f
ractions, that this effect reaches its full magnitude even at very mod
estly supraphysiologic doses, and that this effect persists for severa
l weeks after discontinuation of the drug.