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this is possibly the best study on testosterone injections i've seen.
http://ajpendo.physiology.org/cgi/reprint/281/6/E1172
Testosterone dose-response relationships
in healthy young men
SHALENDER BHASIN,1 LINDA WOODHOUSE,1 RICHARD CASABURI,3 ATAM B. SINGH,1
DIMPLE BHASIN,3 NANCY BERMAN,3 XIANGHONG CHEN,4 KEVIN E. YARASHESKI,4
LYNNE MAGLIANO,2 CONNIE DZEKOV,1 JEANNE DZEKOV,1 RACHELLE BROSS,3
JEFFREY PHILLIPS,3 INDRANI SINHA-HIKIM,1 RUOQUING SHEN,1
AND THOMAS W. STORER2
1Division of Endocrinology, Metabolism, and Molecular Medicine, Charles R. Drew University
of Medicine and Science, Los Angeles 90059; 2Laboratory for Exercise Sciences, El Camino
College, and 3Harbor-University of California Los Angeles Medical Center,
Torrance, California 90502; and 4Biomedical Mass Spectrometric Research Resource, Department
of Internal Medicine, Washington University, School of Medicine, St. Louis, Missouri 63110
Received 13 March 2001; accepted in final form 27 July 2001
Bhasin, Shalender, Linda Woodhouse, Richard
Casaburi, Atam B. Singh, Dimple Bhasin, Nancy Berman,
Xianghong Chen, Kevin E. Yarasheski, Lynne
Magliano, Connie Dzekov, Jeanne Dzekov, Rachelle
Bross, Jeffrey Phillips, Indrani Sinha-Hikim, Ruoquing
Shen, and Thomas W. Storer. Testosterone dose-response
relationships in healthy young men. Am J Physiol
Endocrinol Metab 281: E1172–E1181, 2001.—Testosterone
increases muscle mass and strength and regulates other
physiological processes, but we do not know whether testosterone
effects are dose dependent and whether dose requirements
for maintaining various androgen-dependent processes
are similar. To determine the effects of graded doses of
testosterone on body composition, muscle size, strength,
power, sexual and cognitive functions, prostate-specific antigen
(PSA), plasma lipids, hemoglobin, and insulin-like
growth factor I (IGF-I) levels, 61 eugonadal men, 18–35 yr,
were randomized to one of five groups to receive monthly
injections of a long-acting gonadotropin-releasing hormone
(GnRH) agonist, to suppress endogenous testosterone secretion,
and weekly injections of 25, 50, 125, 300, or 600 mg of
testosterone enanthate for 20 wk. Energy and protein intakes
were standardized. The administration of the GnRH
agonist plus graded doses of testosterone resulted in mean
nadir testosterone concentrations of 253, 306, 542, 1,345, and
2,370 ng/dl at the 25-, 50-, 125-, 300-, and 600-mg doses,
respectively. Fat-free mass increased dose dependently in
men receiving 125, 300, or 600 mg of testosterone weekly
(change 13.4, 5.2, and 7.9 kg, respectively). The changes in
fat-free mass were highly dependent on testosterone dose
(P 5 0.0001) and correlated with log testosterone concentrations
(r 5 0.73, P 5 0.0001). Changes in leg press strength,
leg power, thigh and quadriceps muscle volumes, hemoglobin,
and IGF-I were positively correlated with testosterone
concentrations, whereas changes in fat mass and plasma
high-density lipoprotein (HDL) cholesterol were negatively
correlated. Sexual function, visual-spatial cognition and
mood, and PSA levels did not change significantly at any
dose. We conclude that changes in circulating testosterone
concentrations, induced by GnRH agonist and testosterone
administration, are associated with testosterone dose- and
concentration-dependent changes in fat-free mass, muscle
size, strength and power, fat mass, hemoglobin, HDL cholesterol,
and IGF-I levels, in conformity with a single linear
dose-response relationship. However, different androgen-dependent
processes have different testosterone dose-response
relationships.
sexual function; testosterone effects on muscle; cognitive
function; plasma lipids; prostate-specific antigen; testosterone
effects on insulin-like growth factor I; testosterone and
hemoglobin
TESTOSTERONE regulates many physiological processes,
including muscle protein metabolism, some aspects of
sexual and cognitive functions, secondary sex characteristics,
erythropoiesis, plasma lipids, and bone metabolism
(7, 50). However, testosterone dose dependency
of various androgen-dependent processes is not
well understood (6). Administration of replacement
doses of testosterone to hypogonadal men (10, 12, 30,
45, 49) and of supraphysiological doses to eugonadal
men (9, 22–23, 26) increases fat-free mass, muscle size,
and strength. Conversely, suppression of endogenous
testosterone concentrations is associated with loss of
fat-free mass and a decrease in fractional muscle protein
synthesis (33). However, not known are whether
testosterone effects on the muscle are dose dependent,
or the nature of the testosterone dose-response relationships
(6). Androgen receptors in most tissues are
either saturated or downregulated at physiological testosterone
concentrations (2, 18, 39, 50); this leads to
speculation that there might be two separate doseresponse
curves: one in hypogonadal range, with
Address for reprint requests and other correspondence: S. Bhasin,
Professor of Medicine, UCLA School of Medicine, and Chief, Division
of Endocrinology, Metabolism, and Molecular Medicine, Charles R.
Drew Univ. of Medicine and Science, 1731 E. 120th St., Los Angeles,
CA 90059 (E-mail: [email protected]).
The costs of publication of this article were defrayed in part by the
payment of page charges. The article must therefore be hereby
marked ‘‘advertisement’’ in accordance with 18 U.S.C. Section 1734
solely to indicate this fact.
Am J Physiol Endocrinol Metab
281: E1172–E1181, 2001.
E1172 0193-1849/01 $5.00 Copyright © 2001 the American Physiological Society http://www.ajpendo.org
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maximal response at low normal testosterone concentrations,
and a second in supraphysiological range,
representing a separate mechanism of action (1). However,
testosterone dose-response relationships for a
range of androgen-dependent functions in humans
have not been studied.
Animal studies suggest that different androgen-dependent
processes have different androgen dose-response
relationships (6, 8, 21). Sexual function in male
mammals is maintained at serum testosterone concentrations
that are at the lower end of the male range (3,
6, 8, 13, 21, 31). However, it is not known whether the
low normal testosterone levels that normalize sexual
function are sufficient to maintain muscle mass and
strength, or whether the higher testosterone concentrations
required to maintain muscle mass and
strength might adversely affect plasma lipids, hemoglobin
levels, and the prostate. This information is
important for optimizing testosterone replacement regimens
for treatment of hypogonadal men. Also, for the
proposed use of testosterone in sarcopenia associated
with aging (46, 47) and chronic illness (11, 27), it is
important to know whether significant gains in muscle
mass and strength can be achieved at testosterone
doses that do not adversely affect plasma high-density
lipoprotein (HDL) and prostate-specific antigen (PSA)
levels.
Therefore, the primary objective of this study was to
determine the dose dependency of testosterone’s effects
on fat-free mass and muscle performance. We hypothesized
that changes in circulating testosterone concentrations
would be associated with dose-dependent
changes in fat-free mass, muscle strength, and power
in conformity with a single linear dose-response relationship,
and that the dose requirements for maintaining
other androgen-dependent processes would be different.
We treated young men with a long-acting
gonadotropin-releasing hormone (GnRH) agonist to
suppress endogenous testosterone secretion, and concomitantly
also with one of five testosterone-dose regimens
to create different levels of serum testosterone
concentrations extending from subphysiological to the
supraphysiological range. The lowest testosterone
dose, 25 mg weekly, was selected because this dose had
been shown to maintain sexual function in GnRH antagonist-
treated men (37). The selection of the 600-mg
weekly dose was based on the consideration that this
was the highest dose that had been safely administered
to men in controlled studies (9).
METHODS
This was a double-blind, randomized study consisting of a
4-wk control period, a 20-wk treatment period, and a 16-wk
recovery period. Each participant provided informed consent,
approved by the institutional review boards of Drew University
and Harbor-UCLA Research and Education Institute.
Participants. The participants were healthy men, 18–35 yr
of age, with prior weight-lifting experience and normal testosterone
levels. These men had not used any anabolic agents
and had not participated in competitive sports events in the
preceding year, and they were not planning to participate in
competitive events in the following year.
Randomization. Sixty-one eligible men were randomly assigned
to one of five groups. All received monthly injections of
a long-acting GnRH agonist to suppress endogenous testosterone
production. In addition, group 1 received 25 mg of
testosterone enanthate intramuscularly weekly; group 2, 50
mg testosterone enanthate; group 3, 125 mg testosterone
enanthate; group 4, 300 mg testosterone enanthate; and
group 5, 600 mg testosterone enanthate. Twelve men were
assigned to group 1, 12 to group 2, 12 to group 3, 12 to group
4, and 13 to group 5. Testosterone and GnRH agonist injections
were administered by the General Clinical Research
Center staff to assure compliance.
Nutritional intake. Energy and protein intakes were standardized
at 36 kcalzkg21 zday21 and 1.2 gzkg21 zday21, respectively.
The standardized diet was initiated 2 wk before
treatment was started; dietary instructions were reinforced
every 4 wk. The nutritional intake was verified by analysis of
3-day food records and 24-h food recalls every 4 wk by use of
the Minnesota Nutritional Software.
Exercise stimulus. The participants were asked not to
undertake strength training or moderate-to-heavy endurance
exercise during the study. These instructions were reinforced
every 4 wk.
Outcome measures. Body composition and muscle performance
were assessed at baseline and during week 20. Fatfree
mass and fat mass were measured by underwater weighing
and dual-energy X-ray absorptiometry (DEXA, Hologic
4500, Waltham, MA). Total thigh muscle and quadriceps
muscle volumes were measured by MRI scanning.
For estimation of total body water, the men ingested 10 g
of 2H2O (10, 11), and plasma samples were drawn at 215, 0,
120, 180, and 240 min. We measured 2H abundance in
plasma by nuclear magnetic resonance spectroscopy (10, 11),
with a correction factor of 0.985 for exchangeable hydrogen.
We measured bilateral leg press strength by use of the
one-repetition maximum (1-RM) method (11). A seated leg
press exercise with pneumatic resistance (Keiser Sport,
Fresno, CA) was used for this purpose. Subjects performed
5–10 min of leg cycling and stretching warm-up and received
instruction and practice in lifting mechanics before performing
progressive warm-up lifts leading to the 1-RM. Seat
position and the ensuing knee and hip angles, as well as foot
placement, were measured and recorded for use in subsequent
testing. To ensure reliability in this highly effortdependent
test, the 1-RM score was reassessed within 7 days,
but not sooner than 2 days, after the first evaluation. If
duplicate scores were within 5%, the higher of the two values
was accepted as the strength score. If the two tests differed
by .5%, additional studies were conducted, $2 days apart
but within 7 days, until the two highest scores were within
5%. No subject required .2 days of strength assessment.
We also measured leg power, because power in the lower
extremity is strongly related to performance of functional
activities in the elderly (4). The sarcopenia that accompanies
aging is due in large part to a loss of the fast-twitch type II
fibers and the coincident decrease in explosive force. Muscular
power is important in performing such daily activities as
rising from a chair, climbing stairs, and walking with speed
(4). Leg power was measured with a previously validated (4,
5) Nottingham leg extensor power rig. Subjects performed
10–15 trials of right leg and hip extension, attempting to
generate as much force as possible by accelerating the leg
rig’s weighted flywheel from rest. The power score (in watts)
was taken as the highest value observed during these trials
with evidence of a plateau. As with the strength tests, power
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measurements were preceded by a 5- to 10-min warm-up,
stretching, and practice. The power tests were repeated
within 7 days, but not sooner than 2 days, after the first tests
to reduce the effect of familiarization. To minimize test-retest
variability, the angle of knee flexion and the seat position
were recorded and maintained constant across tests.
Sexual function was assessed by daily logs of sexual activity
and desire that were maintained for 7 consecutive days at
baseline and during treatment by use of a published instrument
(13). Spatial cognition was assessed by a computerized
checkerboard test (38) and mood by Hamilton’s depression
(20) and Young’s mania scales (24).
Adverse experiences, blood counts and chemistries, PSA,
plasma lipids, total and free testosterone, luteinizing hormone
(LH), sex steroid-binding globulin (SHBG), and insulinlike
growth factor I (IGF-I) levels were measured periodically
during control and treatment periods. Serum total testosterone
was measured by an immunoassay (8–11); free testosterone
by equilibrium dialysis (43); LH, SHBG, and PSA by
immunoradiometric assays (9–11); and IGF-I by acid-ethanol
extraction and immunoassay (28). The sensitivities and intra-
and interassay coefficients of variation for hormone assays
were as follows: total testosterone (0.6 ng/dl), 8.2 and
13.2%; free testosterone (0.22 pg/ml), 4.2 and 12.3%; LH (0.05
U/l), 10.7 and 13.0%; SHBG (6.25 nmol/l), 4 and 6%; PSA
(0.01 ng/ml), 5.0 and 6.4%; and IGF-I (80 ng/ml), 4 and 6%,
respectively. These assays have been validated previously
(8–11).
Statistical analyses. All variables were examined for their
distribution characteristics. Variables not meeting the assumption
of a normal distribution were log-transformed and
retested. An ANOVA was used to compare change from
baseline in outcome measures among the five groups. All
outcome measures were analyzed using a paired t-test to
detect a nonzero change from baseline within each group.
P , 0.05 was considered statistically significant.
To describe the relationship between testosterone concentrations
(T) and change in fat-free mass (Y) during
testosterone administration, we tested three models: a
linear model (Y 5 a 1 bT); a logarithmic model, Y 5 a 1
b z X, where X 5 log (T), and a and b represent the intercept
and slope, respectively; and a growth model, Y 5 a/(1 1
b z e2k zX). The logarithmic model provided the best fit for
the data and was used to model the effects of testosterone
concentrations on the change in other outcome variables.
The correlations between testosterone concentrations and
change in outcome variables are derived from this model.
We also modeled the linear dependence of the change in
outcome variables on testosterone dose by use of linear
regression.
RESULTS
Participant characteristics. Of 61 men enrolled, 54
completed the study: 12 in group 1, 8 in group 2, 11 in
group 3, 10 in group 4, and 13 in group 5. One man
discontinued treatment because of acne; other subjects
were unable to meet the demands of the protocol. The
five groups did not significantly differ with respect to
their baseline characteristics (Table 1).
Compliance. All evaluable subjects received 100% of
their GnRH agonist injections, and only one man in the
125-mg group missed one testosterone injection.
Nutritional intake. Daily energy intake and proportion
of calories derived from protein, carbohydrate, and
fat were not significantly different among the five
groups at baseline. There was no significant change in
daily caloric, protein, carbohydrate, or fat intake in any
group during treatment (data not shown).
Hormone levels. Serum total and free testosterone
levels (Table 2), measured during week 16, 1 wk after
the previous injection, were linearly dependent on the
testosterone dose (P 5 0.0001). Serum total and free
testosterone concentrations decreased from baseline in
men receiving the 25- and 50-mg doses and increased
at 300- and 600-mg doses. Serum LH levels were suppressed
in all groups. Serum SHBG levels decreased
dose dependently at the 300- and 600-mg doses but did
not change in other groups. Serum IGF-I concentrations
increased dose dependently at the 300- and 600-mg doses
(correlation between log testosterone level and change in
IGF-I 5 0.55, P 5 0.0001). IGFBP-3 levels did not change
significantly in any group.
Body composition. Fat-free mass, measured by underwater
weighing, did not change significantly in men
receiving the 25- or 50-mg testosterone dose, but it
increased dose dependently at higher doses (Table 3).
The changes in fat-free mass were highly dependent on
testosterone dose (P 5 0.0001) and correlated with log
total testosterone concentrations during treatment
(r 5 0.73, P 5 0.0001, see Fig. 2).
Changes in fat-free mass, measured by DEXA scan,
were qualitatively similar to those obtained from underwater
weighing (Table 3, Fig. 1). The measurements of
fat-free mass by DEXA were highly correlated with values
obtained from underwater weighing (r 5 0.94, P ,
0.0001).
Table 1. Baseline characteristics of the participants
GnRH Agonist 1 1 1 1 1
Testosterone Enanthate 25 mg 50 mg 125 mg 300 mg 600 mg P Value
Age, yr 2865 2965 2863 2465 2564 0.0583
Height, cm 17565 17769 17867 17767 17568 0.7230
Weight, kg 68.068.4 77.068.1 78.9610.6 78.4610.1 74.8612.5 0.1014
Body mass index, kg/m2 2363 2563 2563 2563 2563 0.3680
Serum testosterone
levels, nmol/l 5936161 5666220 5536182 6546157 6326228 0.7093
Fat-free mass, kg 59.166.7 65.165.1 66.067.2 67.368.9 64.268.0 0.1506
Leg press strength, kg 355.56103.8 407.8662.2 419.2686.2 439.8681.4 431.6699.3 0.2149
Hemoglobin, g/l 144612 151611 14269 14468 14168 0.1428
No. in group 12 12 12 12 13
Values are means 6 SD. GnRH, gonadotropin-releasing hormone.
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To determine whether the apparent changes in fatfree
mass by DEXA scan and underwater weighing
represented water retention, we measured total body
water and compared the ratios of total body water to
fat-free mass before and after treatment in each group.
The ratios of total body water to fat-free mass by
underwater weighing did not significantly change with
treatment in any treatment group (Table 3), indicating
that the apparent increase in fat-free mass measured
by underwater weighing did not represent water retention
in excess of that associated with protein accretion.
Fat mass, measured by underwater weighing, increased
significantly in men receiving the 25- and
50-mg doses but did not change in men receiving the
higher doses of testosterone (Table 3, Fig. 1). There
was an inverse correlation between change in fat mass
by underwater weighing and log testosterone concentrations
(r 5 20.60, P 5 0.0001, Fig. 2).
Muscle size. The thigh muscle volume and quadriceps
muscle volume did not significantly change in men
receiving the 25- or 50-mg doses but increased dose
dependently at higher doses of testosterone (Table 4,
Fig. 1). The changes in thigh muscle and quadriceps
muscle volumes correlated with log testosterone levels
during treatment (r 5 0.66, P 5 0.0001, and r 5 0.55,
P 5 0.0001, respectively, Fig. 2).
Muscle performance. The leg press strength did not
change significantly in the 25- and 125-mg-dose groups
but increased significantly in those receiving the 50-,
300-, and 600-mg doses (Table 5). The changes in leg
press strength correlated with log testosterone levels
during treatment (r 5 0.48, P 5 0.0005, Fig. 2) and
changes in muscle volume (r 5 0.54, P 5 0.003) and
fat-free mass (r 5 0.74, P , 0.0001).
Table 3. Body composition analysis
Testosterone
Dose Baseline Week 20
Change from
Baseline
P vs. Zero
Change
Fat-free mass (kg) by underwater weighing
(overall ANOVA P 5 0.0001)
25 mg 61.162.7 58.161.7 21.060.5 0.0695
50 mg 66.162.5 65.762.0 10.660.4 0.1324
125 mg 66.062.1 67.962.7 13.460.8 0.0024
300 mg 66.962.4 72.462.8 15.260.8 0.0001
600 mg 64.262.2 72.162.4 17.960.6 0.0001
Fat mass (kg) by underwater weighing
(overall ANOVA P 5 0.0001)
25 mg 8.361.4 11.361.6 13.160.7 0.0014
50 mg 10.961.4 14.361.7 13.561.0 0.0096
125 mg 12.262.0 10.962.1 10.0160.5 0.9820
300 mg 11.461.6 10.961.7 20.560.6 0.4134
600 mg 9.461.9 8.861.9 21.160.7 0.1132
Fat-free mass (kg) by DEXA scan (overall ANOVA P 5 0.0001)
25 mg 53.661.8 53.462.0 10.460.3 0.2198
50 mg 58.662.3 59.262.5 11.160.9 0.2313
125 mg 60.162.1 63.162.3 12.960.8 0.0054
300 mg 59.062.7 64.362.2 15.560.7 0.0001
600 mg 57.461.9 66.362.4 18.960.8 0.0001
Fat mass (kg) by DEXA scan (overall ANOVA P 5 0.0004)
25 mg 10.061.8 13.761.4 13.661.5 0.0326
50 mg 15.461.2 17.961.2 12.661.0 0.0324
125 mg 15.262.0 15.261.9 20.360.8 0.6882
300 mg 16.361.2 15.4161.5 20.960.6 0.1834
600 mg 14.261.9 12.061.5 22.060.7 0.0141
Ratio of total body water to fat-free mass (percent)
(overall ANOVA for change from baseline, P 5 0.270)
25 mg 62.762.7 63.762.1 11.162.4
50 mg 62.061.9 63.862.4 12.062.0
125 mg 67.061.7 63.563.0 23.861.6
300 mg 61.662.7 64.663.1 12.162.5
600 mg 65.362.4 67.462.8 12.561.7
Values on each day represent the mean (6SE) of all available
values on that day. However, the change represents the difference
between paired values only. Ratios of total body water assessed by
deuterium water dilution to fat-free mass measured by underwater
weighing were calculated for each subject and averaged across subjects
within each group. DEXA, dual-energy X-ray absorptiometry.
Table 2. Serum total and free testosterone, LH, FSH,
SHBG, and IGF-I levels
Testosterone
Dose Baseline Week 16
Change from
Baseline
P vs. Zero
Change
Testosterone (ng/dl) (overall ANOVA P 5 0.0001)
25 mg 593648 253666 2340685 0.0029
50 mg 566678 306658 2260664 0.0037
125 mg 553653 570675 57675 0.7425
300 mg 653650 1,3456139 6916143 0.0005
600 mg 632663 2,3706150 1,7376156 0.0001
Free testosterone (pg/ml) (overall ANOVA P 5 0.0001)
25 mg 6266 2965 23368 0.0014
50 mg 5766 3263 22565 0.0009
125 mg 4965 5268 367 0.8601
300 mg 7167 138621 67618 0.0012
600 mg 6465 275630 211631 0.0001
LH (U/l) (overall ANOVA P 5 0.8054)
25 mg 3.560.4 0.360.1 23.260.4 0.0001
50 mg 3.860.3 0.660.3 23.060.4 0.0008
125 mg 3.460.3 0.560.1 22.860.4 0.0001
300 mg 3.760.5 0.660.1 23.560.5 0.0002
600 mg 3.360.3 0.660.4 22.960.4 0.0001
SHBG (nmol/l) (overall ANOVA P 5 0.0001)
25 mg 29.162.9 28.563.6 20.662.9 0.8497
50 mg 24.463.4 21.163.2 23.361.1 0.0202
125 mg 33.164.2 28.963.8 24.262.6 0.1410
300 mg 31.463.8 22.463.9 29.163.7 0.0348
600 mg 40.164.9 20.663.2 219.562.8 0.0001
IGF-I (ng/ml) (overall ANOVA P 5 0.0001)
25 mg 268626 261635 27619 0.7462
50 mg 246614 225612 220610 0.0797
125 mg 299624 282631 218617 0.3284
300 mg 314624 388630 74628 0.0272
600 mg 227620 304621 77613 0.0001
Values on each day represent the mean (6SE) of all available
values on that day. However, the change represents the difference
between paired values only. Treatment values represent the day 113
(week 16) values, obtained 1 wk after the previous testosterone
injection. We used week 16 rather than week 20 values because week
20 values were not always drawn exactly 1 wk after the previous
injection. LH and FSH, luteinizing and follicle-stimulating hormones,
respectively; SHBG, sex hormone-binding globulin; IGF-I,
insulin-like growth factor I. To convert total testosterone levels to
nmol/l, multiply by 0.03467. To convert free testosterone levels to
pg/ml, multiply by 3.467.
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Leg power, measured by the Nottingham leg rig, did
not change significantly in men receiving the 25-, 50-, and
125-mg doses of testosterone weekly, but it increased
significantly in those receiving the 300- and 600-mg
doses. The increase in leg power correlated with log
testosterone concentrations (r 5 0.39, P 5 0.0105, Fig. 2)
and changes in fat-free mass (r 5 0.30, P 5 0.0392) and
muscle strength (r 5 0.42, P 5 0.0020).
Behavioral measures. The scores for sexual activity
and sexual desire measured by daily logs did not
change significantly at any dose. Similarly, visualspatial
cognition (Table 6) and mood, as assessed by
Hamilton’s depression and Young’s manic scales (data
not shown), did not change significantly in any group.
Adverse experiences and safety measures. Hemoglobin
levels decreased significantly in men receiving the
50-mg dose but increased at the 600-mg dose; the
changes in hemoglobin were positively correlated with
testosterone concentrations (r 5 0.66, P 5 0.0001) (Table
7). Changes in plasma HDL cholesterol, in contrast, were
negatively dependent on testosterone dose (P 5 0.0049)
and correlated with testosterone concentrations (r 5
Fig. 1. Change in fat-free mass (A), fat
mass (B), leg press strength (C), thigh
muscle volume (D), quadriceps muscle
volume (E), sexual function (F), insulin-
like growth factor I (G), and prostate-
specific antigen (H). Data are
means 6 SE. *Significant differences
from all other groups (P , 0.05); vsignificant
difference from 25-, 50-, and
125-mg doses (P , 0.05); 1significant
difference from 25- and 50-mg doses
(P , 0.05); and > significant difference
from 25-mg dose (P , 0.05).
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20.40, P 5 0.0054). Total cholesterol, plasma lowdensity
lipoprotein cholesterol, and triglyceride levels
did not change significantly at any dose. Serum PSA,
creatinine, bilirubin, alanine aminotransferase, and
alkaline phosphatase did not change significantly in
any group, but aspartate aminotransferase decreased
significantly in the 25-mg group. Two men in the 25-mg
group, five in the 50-mg group, three in the 125-mg
group, seven in the 300-mg group, and two in the
600-mg group developed acne. One man receiving the
50-mg dose reported decreased ability to achieve erections.
DISCUSSION
GnRH agonist administration suppressed endogenous
LH and testosterone secretion; therefore, circulating
testosterone concentrations during treatment
were proportional to the administered dose of testosterone
enanthate. This strategy of combined administration
of GnRH agonist and graded doses of testosterone
enanthate was effective in establishing different
levels of serum testosterone concentrations among the
five treatment groups. The different levels of circulating
testosterone concentrations created by this regimen
were associated with dose- and concentration-
Fig. 2. Relationship between serum
testosterone concentrations (T) during
treatment (week 16) and change in fatfree
mass (A), fat mass (B), leg press
strength (C), thigh muscle volume (D),
quadriceps muscle volume (E), sexual
function (F), insulin-like growth factor
I (G), and prostate-specific antigen (H).
The correlation coefficient, r, was calculated
using the logarithmic model,
Y 5 a 1 bzX, where X 5 log (T), and a
and b represent the intercept and
slope.
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dependent changes in fat-free mass, fat mass, thigh
and quadriceps muscle volume, muscle strength, leg
power, hemoglobin, circulating IGF-I, and plasma
HDL cholesterol. Serum PSA levels, sexual desire and
activity, and spatial cognition did not change significantly
at any dose. The changes in fat-free mass, muscle
volume, leg press strength and power, hemoglobin,
and IGF-I were positively correlated, whereas changes
in plasma HDL cholesterol and fat mass were negatively
correlated with testosterone dose and total and
free testosterone concentrations during treatment.
The compliance with the treatment regimen was
high. The participants received 100% of their scheduled
GnRH agonist, and 99% of testosterone injections.
Serum LH levels were suppressed in all men, demonstrating
the effectiveness of GnRH agonist treatment.
The treatment regimen was well tolerated. There were
no significant changes in PSA or liver enzymes at any
dose. However, long-term effects of androgen administration
on the prostate, cardiovascular risk, and behavior
are unknown.
Serum testosterone levels were measured 7 days
after previous injection; they reflect the lowest testosterone
levels after an injection. Testosterone concentrations
were higher at other time points. Weekly injections
of testosterone enanthate are associated with
fluctuations in testosterone levels (44). Although nadir
testosterone concentrations were highly correlated
with testosterone enanthate dose, it is possible that
sustained testosterone delivery by a patch or gel might
reveal different dose-response relationships, particularly
with respect to hemoglobin and HDL cholesterol
(19).
There were no significant changes in overall sexual
activity or sexual desire in any group, including those
receiving the 25-mg dose. Testosterone replacement of
hypogonadal men improves frequency of sexual acts
and fantasies, sexual desire, and response to visual
erotic stimuli (3, 13, 15, 17, 31, 41). Our data demonstrate
that serum testosterone concentrations at the
lower end of male range can maintain some aspects of
sexual function (3, 13). Testosterone has been shown to
regulate nitric oxide synthase activity in the cavernosal
smooth muscle (32), and it is possible that optimum
penile rigidity might require higher testosterone
levels than those produced by the 25-mg dose.
This study demonstrates that an increase in circulating
testosterone concentrations results in dose-de-
Table 4. Thigh and quadriceps muscle volume
measured by MRI
Testosterone
Dose Baseline Week 20
Change from
Baseline
P vs. zero
change
Thigh muscle volume (overall ANOVA P 5 0.0001)
25 mg 753646 739644 214610 0.1958
50 mg 833653 844658 1168 0.2332
125 mg 890649 966660 56610 0.0004
300 mg 849639 933639 84612 0.0001
600 mg 802645 928648 126612 0.0001
Quadriceps muscle volume (overall ANOVA P 5 0.0001)
25 mg 436630 427627 2969 0.3524
50 mg 489634 493636 467 0.5889
125 mg 508629 546636 2165 0.0027
300 mg 497625 540622 4369 0.0008
600 mg 472627 540631 6868 0.0001
Values (in cm3) on each day represent the mean (6SE) of all
available values on that day. However, the change represents the
difference between paired values only.
Table 5. Change in measures of muscle performance
Testosterone
Dose Baseline Treatment
Change from
Baseline
P vs. Zero
Change
Leg press strength (kg) (overall ANOVA P 5 0.0003)
25 mg 355.5131.3 354.2627.9 21.267.4 0.8701
50 mg 407.8122.0 430.5622.3 122.767.6 0.0204
125 mg 419.2624.4 444.6632.2 118.4610.0 0.4195
300 mg 439.8625.7 525.5624.9 172.2612.4 0.0004
600 mg 431.6127.6 508.1628.1 176.5612.2 0.0001
Leg power (W) (overall ANOVA P 5 0.0419)
25 mg 183.6610.6 188.9612.9 5.368.4 0.5429
50 mg 234.4614.2 249.6617.8 15.2615.0 0.3468
125 mg 253.8620.6 265.6625.2 8.5615.3 0.5935
300 mg 233.8620.2 272.4627.8 38.669.4 0.0033
600 mg 212.4611.0 256.2613.8 48.1611.8 0.0015
Values on each day represent the mean (6SE) of all available
values on that day. However, the change represents the difference
between paired values only.
Table 6. Change in scores for sexual activity, sexual
desire, and spatial cognition
Testosterone
Dose Baseline Treatment
Change from
Baseline
P vs. zero
change
Sexual activity scores (overall ANOVA P 5 0.7842)
25 mg 10.761.7 8.262.9 22.563.2 0.4729
50 mg 14.162.1 13.761.8 20.462.8 0.9017
125 mg 9.862.7 12.062.9 2.263.1 0.5151
300 mg 11.661.6 12.061.9 0.760.9 0.4761
600 mg 16.163.7 15.660.5 0.762.2 0.7891
Intensity of sexual desire scores (overall ANOVA P 5 0.477)
25 mg 1.960.1 1.360.4 20.660.4 0.2253
50 mg 2.360.1 2.260.3 20.060.3 0.9615
125 mg 2.160.1 2.060.3 20.160.4 0.9078
300 mg 2.260.2 2.460.2 0.160.1 0.3559
600 mg 2.760.2 2.260.1 0.260.2 0.4075
Spatial cognition scores
1. No. of trial levels on the checkerboard test that the participant
reached before the test was terminated
(overall ANOVA P 5 0.235)
25 mg 6.860.3 6.460.3 20.460.3 0.284
50 mg 6.760.3 6.760.3 0.360.3 0.284
125 mg 6.660.3 6.660.2 0.060.4 1.0
300 mg 7.360.2 6.760.2 20.660.3 0.103
600 mg 6.660.2 6.960.2 0.360.3 0.278
2. No. of checkerboard squares correctly marked in all trials
(overall ANOVA P 5 0.6309)
25 mg 28.662.2 30.462.1 1.862.1 0.4272
50 mg 30.062.3 34.764.9 2.763.5 0.5236
125 mg 27.363.0 28.162.2 0.963.8 0.7292
300 mg 32.662.1 33.361.8 0.763.1 0.8241
600 mg 26.762.7 32.562.1 5.862.2 0.0265
Values are means 6 SE.
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pendent increases in fat-free mass, muscle size,
strength, and power. The relationships between circulating
testosterone concentrations and changes in fatfree
mass and muscle size conform to a single log-linear
dose-response curve. Our data do not support the notion
of two separate dose-response curves reflecting
two independent mechanisms of testosterone action on
the muscle. Forbes et al. (22) predicted 25 years ago
that the muscle mass accretion during androgen administration
is related to the cumulative androgen
dose, the product of daily dose and treatment duration.
Our data are consistent with Forbes’s hypothesis of a
linear relationship between testosterone dose and lean
mass accretion; however, we do not know whether
increasing the treatment duration would lead to further
gains in muscle mass.
In addition, we do not know whether responsiveness
to testosterone is attenuated in older men. Testosterone
dose-response relationships might be modulated
by other muscle growth regulators, such as nutritional
status, exercise and activity level, glucocorticoids, thyroid
hormones, and endogenous growth hormone secretory
status.
Serum PSA levels decrease after androgen withdrawal,
and testosterone replacement of hypogonadal
men increases PSA levels into the normal range (16,
34). We did not find significant changes in PSA at any
dose, indicating that the lowest dose of testosterone
maintained PSA levels. We did not measure prostate
volume in this study; therefore, we do not know
whether prostate volume exhibits the same relationship
with testosterone dose as PSA levels.
Hemoglobin levels changed significantly in relation
to testosterone dose and concentration. Testosterone
regulates erythropoiesis through its effects on erythropoietin
and stem cell proliferation (14, 35, 40). Although
modest increments in hemoglobin might be
beneficial in androgen-deficient men with chronic illness
who are anemic, marked increases in hemoglobin
levels could increase the risk of cerebrovascular events
(25) and hypertension (42).
Although men, on average, perform better on tests of
spatial cognition than women, testosterone replacement
has not been consistently shown to improve spatial
cognition in hypogonadal men (1, 29, 48). We did
not find changes in spatial cognition at any dose. The
effect size of gender differences in spatial cognition is
small; it is possible that our study did not have sufficient
power to detect small differences. We cannot
exclude the possibility that gender differences in spatial
cognition might be due to organizational effects of
testosterone and might not respond to changes in testosterone
levels in adult men.
Although mean change in fat-free mass and muscle
size correlated with testosterone dose and concentration,
there was considerable heterogeneity in response
to testosterone administration within each group.
These individual differences in response to androgen
administration might reflect differences in activity
level, testosterone metabolism, nutrition, or polymorphisms
in androgen receptor, myostatin, 5-a-reductase,
or other muscle growth regulators.
Our data demonstrate that different androgendependent
processes have different testosterone
dose-response relationships. Some aspects of sexual
function and spatial cognition, and PSA levels, were
maintained by relatively low doses of testosterone in
GnRH agonist-treated men and did not increase further
with administration of higher doses of testosterone.
In contrast, graded doses of testosterone
were associated with dose and testosterone concentration-
dependent changes in fat-free mass, fat
mass, muscle volume, leg press strength and power,
hemoglobin, IGF-I, and plasma HDL cholesterol. The
precise mechanisms for the tissue- and functionspecific
differences in testosterone dose dependence
are not well understood (36). Although only a single
androgen receptor protein is expressed in all androgen-
responsive tissues, tissue specificity of androgen
action might be mediated through combinatorial recruitment
of tissue-specific coactivators and corepressors
(36).
Testosterone doses associated with significant gains
in fat-free mass, muscle size, and strength were associated
with significant reductions in plasma HDL concentrations.
Further studies are needed to determine
whether clinically significant anabolic effects of testosterone
can be achieved without adversely affecting
cardiovascular risk. Selective androgen receptor modulators
that preferentially augment muscle mass and
strength, but only minimally affect prostate and cardiovascular
risk factors, are desirable (36).
This study was supported primarily by National Institutes of
Health (NIH) Grant 1RO1-AG-14369; additional support was pro-
Table 7. Changes in hemoglobin, plasma HDL
cholesterol, and PSA
Testosterone
Dose Baseline Week 20
Change from
Baseline
P vs. Zero
Change
Hemoglobin (g/l), (overall ANOVA P 5 0.0001)
25 mg 143.563.5 139.062.5 25.263.5 0.1759
50 mg 150.863.3 146.662.0 27.462.3 0.0153
125 mg 141.962.6 146.163.1 2.562.4 0.3061
300 mg 143.562.2 149.663.1 6.162.9 0.0639
600 mg 141.562.3 155.762.2 14.262.0 0.0001
PSA (ng/ml), (overall ANOVA P 5 0.5290)
25 mg 1.060.2 1.060.2 20.160.2 0.6870
50 mg 0.860.1 1.160.2 0.360.1 0.0186
125 mg 0.760.1 0.860.1 0.160.1 0.1721
300 mg 0.760.1 0.960.3 0.260.2 0.4525
600 mg 0.560.1 0.760.1 0.160.0 0.0010
Plasma HDL cholesterol (mg/dl) (overall ANOVA P 5 0.0049)
25 mg 4663 5164 14.562.6 0.1202
50 mg 4863 4765 20.764.0 0.8653
125 mg 4862 4363 24.061.7 0.0476
300 mg 4763 4162 25.762.8 0.0690
600 mg 4362 3462 28.461.8 0.0005
Values on each day represent the mean (6SE) of all available
values on that day. However, the change from baseline represents
the difference between paired values only. PSA, prostate-specific
antigen; HDL, high-density lipoprotein.
TESTOSTERONE DOSE-RESPONSE RELATIONSHIPS E1179
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vided by Grants 1RO1-DK-49296, 1RO1-DK-59297–01, Federal
Drug Administration Grant ODP 1397, a General Clinical Research
Center Grant MO-00425, NIH-National Center for Research Resources-
00954, RCMI Grants P20-RR-11145–01 (RCMI Clinical Research
Initiative) and G12-RR-03026. BioTechnology General (Iselin,
NJ) provided testosterone enanthate, and R. P. Debio (Martigny,
Switzerland) provided the GnRH agonist (Decapeptyl).
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TESTOSTERONE DOSE-RESPONSE RELATIONSHIPS E1181
AJP-
http://ajpendo.physiology.org/cgi/reprint/281/6/E1172
Testosterone dose-response relationships
in healthy young men
SHALENDER BHASIN,1 LINDA WOODHOUSE,1 RICHARD CASABURI,3 ATAM B. SINGH,1
DIMPLE BHASIN,3 NANCY BERMAN,3 XIANGHONG CHEN,4 KEVIN E. YARASHESKI,4
LYNNE MAGLIANO,2 CONNIE DZEKOV,1 JEANNE DZEKOV,1 RACHELLE BROSS,3
JEFFREY PHILLIPS,3 INDRANI SINHA-HIKIM,1 RUOQUING SHEN,1
AND THOMAS W. STORER2
1Division of Endocrinology, Metabolism, and Molecular Medicine, Charles R. Drew University
of Medicine and Science, Los Angeles 90059; 2Laboratory for Exercise Sciences, El Camino
College, and 3Harbor-University of California Los Angeles Medical Center,
Torrance, California 90502; and 4Biomedical Mass Spectrometric Research Resource, Department
of Internal Medicine, Washington University, School of Medicine, St. Louis, Missouri 63110
Received 13 March 2001; accepted in final form 27 July 2001
Bhasin, Shalender, Linda Woodhouse, Richard
Casaburi, Atam B. Singh, Dimple Bhasin, Nancy Berman,
Xianghong Chen, Kevin E. Yarasheski, Lynne
Magliano, Connie Dzekov, Jeanne Dzekov, Rachelle
Bross, Jeffrey Phillips, Indrani Sinha-Hikim, Ruoquing
Shen, and Thomas W. Storer. Testosterone dose-response
relationships in healthy young men. Am J Physiol
Endocrinol Metab 281: E1172–E1181, 2001.—Testosterone
increases muscle mass and strength and regulates other
physiological processes, but we do not know whether testosterone
effects are dose dependent and whether dose requirements
for maintaining various androgen-dependent processes
are similar. To determine the effects of graded doses of
testosterone on body composition, muscle size, strength,
power, sexual and cognitive functions, prostate-specific antigen
(PSA), plasma lipids, hemoglobin, and insulin-like
growth factor I (IGF-I) levels, 61 eugonadal men, 18–35 yr,
were randomized to one of five groups to receive monthly
injections of a long-acting gonadotropin-releasing hormone
(GnRH) agonist, to suppress endogenous testosterone secretion,
and weekly injections of 25, 50, 125, 300, or 600 mg of
testosterone enanthate for 20 wk. Energy and protein intakes
were standardized. The administration of the GnRH
agonist plus graded doses of testosterone resulted in mean
nadir testosterone concentrations of 253, 306, 542, 1,345, and
2,370 ng/dl at the 25-, 50-, 125-, 300-, and 600-mg doses,
respectively. Fat-free mass increased dose dependently in
men receiving 125, 300, or 600 mg of testosterone weekly
(change 13.4, 5.2, and 7.9 kg, respectively). The changes in
fat-free mass were highly dependent on testosterone dose
(P 5 0.0001) and correlated with log testosterone concentrations
(r 5 0.73, P 5 0.0001). Changes in leg press strength,
leg power, thigh and quadriceps muscle volumes, hemoglobin,
and IGF-I were positively correlated with testosterone
concentrations, whereas changes in fat mass and plasma
high-density lipoprotein (HDL) cholesterol were negatively
correlated. Sexual function, visual-spatial cognition and
mood, and PSA levels did not change significantly at any
dose. We conclude that changes in circulating testosterone
concentrations, induced by GnRH agonist and testosterone
administration, are associated with testosterone dose- and
concentration-dependent changes in fat-free mass, muscle
size, strength and power, fat mass, hemoglobin, HDL cholesterol,
and IGF-I levels, in conformity with a single linear
dose-response relationship. However, different androgen-dependent
processes have different testosterone dose-response
relationships.
sexual function; testosterone effects on muscle; cognitive
function; plasma lipids; prostate-specific antigen; testosterone
effects on insulin-like growth factor I; testosterone and
hemoglobin
TESTOSTERONE regulates many physiological processes,
including muscle protein metabolism, some aspects of
sexual and cognitive functions, secondary sex characteristics,
erythropoiesis, plasma lipids, and bone metabolism
(7, 50). However, testosterone dose dependency
of various androgen-dependent processes is not
well understood (6). Administration of replacement
doses of testosterone to hypogonadal men (10, 12, 30,
45, 49) and of supraphysiological doses to eugonadal
men (9, 22–23, 26) increases fat-free mass, muscle size,
and strength. Conversely, suppression of endogenous
testosterone concentrations is associated with loss of
fat-free mass and a decrease in fractional muscle protein
synthesis (33). However, not known are whether
testosterone effects on the muscle are dose dependent,
or the nature of the testosterone dose-response relationships
(6). Androgen receptors in most tissues are
either saturated or downregulated at physiological testosterone
concentrations (2, 18, 39, 50); this leads to
speculation that there might be two separate doseresponse
curves: one in hypogonadal range, with
Address for reprint requests and other correspondence: S. Bhasin,
Professor of Medicine, UCLA School of Medicine, and Chief, Division
of Endocrinology, Metabolism, and Molecular Medicine, Charles R.
Drew Univ. of Medicine and Science, 1731 E. 120th St., Los Angeles,
CA 90059 (E-mail: [email protected]).
The costs of publication of this article were defrayed in part by the
payment of page charges. The article must therefore be hereby
marked ‘‘advertisement’’ in accordance with 18 U.S.C. Section 1734
solely to indicate this fact.
Am J Physiol Endocrinol Metab
281: E1172–E1181, 2001.
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maximal response at low normal testosterone concentrations,
and a second in supraphysiological range,
representing a separate mechanism of action (1). However,
testosterone dose-response relationships for a
range of androgen-dependent functions in humans
have not been studied.
Animal studies suggest that different androgen-dependent
processes have different androgen dose-response
relationships (6, 8, 21). Sexual function in male
mammals is maintained at serum testosterone concentrations
that are at the lower end of the male range (3,
6, 8, 13, 21, 31). However, it is not known whether the
low normal testosterone levels that normalize sexual
function are sufficient to maintain muscle mass and
strength, or whether the higher testosterone concentrations
required to maintain muscle mass and
strength might adversely affect plasma lipids, hemoglobin
levels, and the prostate. This information is
important for optimizing testosterone replacement regimens
for treatment of hypogonadal men. Also, for the
proposed use of testosterone in sarcopenia associated
with aging (46, 47) and chronic illness (11, 27), it is
important to know whether significant gains in muscle
mass and strength can be achieved at testosterone
doses that do not adversely affect plasma high-density
lipoprotein (HDL) and prostate-specific antigen (PSA)
levels.
Therefore, the primary objective of this study was to
determine the dose dependency of testosterone’s effects
on fat-free mass and muscle performance. We hypothesized
that changes in circulating testosterone concentrations
would be associated with dose-dependent
changes in fat-free mass, muscle strength, and power
in conformity with a single linear dose-response relationship,
and that the dose requirements for maintaining
other androgen-dependent processes would be different.
We treated young men with a long-acting
gonadotropin-releasing hormone (GnRH) agonist to
suppress endogenous testosterone secretion, and concomitantly
also with one of five testosterone-dose regimens
to create different levels of serum testosterone
concentrations extending from subphysiological to the
supraphysiological range. The lowest testosterone
dose, 25 mg weekly, was selected because this dose had
been shown to maintain sexual function in GnRH antagonist-
treated men (37). The selection of the 600-mg
weekly dose was based on the consideration that this
was the highest dose that had been safely administered
to men in controlled studies (9).
METHODS
This was a double-blind, randomized study consisting of a
4-wk control period, a 20-wk treatment period, and a 16-wk
recovery period. Each participant provided informed consent,
approved by the institutional review boards of Drew University
and Harbor-UCLA Research and Education Institute.
Participants. The participants were healthy men, 18–35 yr
of age, with prior weight-lifting experience and normal testosterone
levels. These men had not used any anabolic agents
and had not participated in competitive sports events in the
preceding year, and they were not planning to participate in
competitive events in the following year.
Randomization. Sixty-one eligible men were randomly assigned
to one of five groups. All received monthly injections of
a long-acting GnRH agonist to suppress endogenous testosterone
production. In addition, group 1 received 25 mg of
testosterone enanthate intramuscularly weekly; group 2, 50
mg testosterone enanthate; group 3, 125 mg testosterone
enanthate; group 4, 300 mg testosterone enanthate; and
group 5, 600 mg testosterone enanthate. Twelve men were
assigned to group 1, 12 to group 2, 12 to group 3, 12 to group
4, and 13 to group 5. Testosterone and GnRH agonist injections
were administered by the General Clinical Research
Center staff to assure compliance.
Nutritional intake. Energy and protein intakes were standardized
at 36 kcalzkg21 zday21 and 1.2 gzkg21 zday21, respectively.
The standardized diet was initiated 2 wk before
treatment was started; dietary instructions were reinforced
every 4 wk. The nutritional intake was verified by analysis of
3-day food records and 24-h food recalls every 4 wk by use of
the Minnesota Nutritional Software.
Exercise stimulus. The participants were asked not to
undertake strength training or moderate-to-heavy endurance
exercise during the study. These instructions were reinforced
every 4 wk.
Outcome measures. Body composition and muscle performance
were assessed at baseline and during week 20. Fatfree
mass and fat mass were measured by underwater weighing
and dual-energy X-ray absorptiometry (DEXA, Hologic
4500, Waltham, MA). Total thigh muscle and quadriceps
muscle volumes were measured by MRI scanning.
For estimation of total body water, the men ingested 10 g
of 2H2O (10, 11), and plasma samples were drawn at 215, 0,
120, 180, and 240 min. We measured 2H abundance in
plasma by nuclear magnetic resonance spectroscopy (10, 11),
with a correction factor of 0.985 for exchangeable hydrogen.
We measured bilateral leg press strength by use of the
one-repetition maximum (1-RM) method (11). A seated leg
press exercise with pneumatic resistance (Keiser Sport,
Fresno, CA) was used for this purpose. Subjects performed
5–10 min of leg cycling and stretching warm-up and received
instruction and practice in lifting mechanics before performing
progressive warm-up lifts leading to the 1-RM. Seat
position and the ensuing knee and hip angles, as well as foot
placement, were measured and recorded for use in subsequent
testing. To ensure reliability in this highly effortdependent
test, the 1-RM score was reassessed within 7 days,
but not sooner than 2 days, after the first evaluation. If
duplicate scores were within 5%, the higher of the two values
was accepted as the strength score. If the two tests differed
by .5%, additional studies were conducted, $2 days apart
but within 7 days, until the two highest scores were within
5%. No subject required .2 days of strength assessment.
We also measured leg power, because power in the lower
extremity is strongly related to performance of functional
activities in the elderly (4). The sarcopenia that accompanies
aging is due in large part to a loss of the fast-twitch type II
fibers and the coincident decrease in explosive force. Muscular
power is important in performing such daily activities as
rising from a chair, climbing stairs, and walking with speed
(4). Leg power was measured with a previously validated (4,
5) Nottingham leg extensor power rig. Subjects performed
10–15 trials of right leg and hip extension, attempting to
generate as much force as possible by accelerating the leg
rig’s weighted flywheel from rest. The power score (in watts)
was taken as the highest value observed during these trials
with evidence of a plateau. As with the strength tests, power
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measurements were preceded by a 5- to 10-min warm-up,
stretching, and practice. The power tests were repeated
within 7 days, but not sooner than 2 days, after the first tests
to reduce the effect of familiarization. To minimize test-retest
variability, the angle of knee flexion and the seat position
were recorded and maintained constant across tests.
Sexual function was assessed by daily logs of sexual activity
and desire that were maintained for 7 consecutive days at
baseline and during treatment by use of a published instrument
(13). Spatial cognition was assessed by a computerized
checkerboard test (38) and mood by Hamilton’s depression
(20) and Young’s mania scales (24).
Adverse experiences, blood counts and chemistries, PSA,
plasma lipids, total and free testosterone, luteinizing hormone
(LH), sex steroid-binding globulin (SHBG), and insulinlike
growth factor I (IGF-I) levels were measured periodically
during control and treatment periods. Serum total testosterone
was measured by an immunoassay (8–11); free testosterone
by equilibrium dialysis (43); LH, SHBG, and PSA by
immunoradiometric assays (9–11); and IGF-I by acid-ethanol
extraction and immunoassay (28). The sensitivities and intra-
and interassay coefficients of variation for hormone assays
were as follows: total testosterone (0.6 ng/dl), 8.2 and
13.2%; free testosterone (0.22 pg/ml), 4.2 and 12.3%; LH (0.05
U/l), 10.7 and 13.0%; SHBG (6.25 nmol/l), 4 and 6%; PSA
(0.01 ng/ml), 5.0 and 6.4%; and IGF-I (80 ng/ml), 4 and 6%,
respectively. These assays have been validated previously
(8–11).
Statistical analyses. All variables were examined for their
distribution characteristics. Variables not meeting the assumption
of a normal distribution were log-transformed and
retested. An ANOVA was used to compare change from
baseline in outcome measures among the five groups. All
outcome measures were analyzed using a paired t-test to
detect a nonzero change from baseline within each group.
P , 0.05 was considered statistically significant.
To describe the relationship between testosterone concentrations
(T) and change in fat-free mass (Y) during
testosterone administration, we tested three models: a
linear model (Y 5 a 1 bT); a logarithmic model, Y 5 a 1
b z X, where X 5 log (T), and a and b represent the intercept
and slope, respectively; and a growth model, Y 5 a/(1 1
b z e2k zX). The logarithmic model provided the best fit for
the data and was used to model the effects of testosterone
concentrations on the change in other outcome variables.
The correlations between testosterone concentrations and
change in outcome variables are derived from this model.
We also modeled the linear dependence of the change in
outcome variables on testosterone dose by use of linear
regression.
RESULTS
Participant characteristics. Of 61 men enrolled, 54
completed the study: 12 in group 1, 8 in group 2, 11 in
group 3, 10 in group 4, and 13 in group 5. One man
discontinued treatment because of acne; other subjects
were unable to meet the demands of the protocol. The
five groups did not significantly differ with respect to
their baseline characteristics (Table 1).
Compliance. All evaluable subjects received 100% of
their GnRH agonist injections, and only one man in the
125-mg group missed one testosterone injection.
Nutritional intake. Daily energy intake and proportion
of calories derived from protein, carbohydrate, and
fat were not significantly different among the five
groups at baseline. There was no significant change in
daily caloric, protein, carbohydrate, or fat intake in any
group during treatment (data not shown).
Hormone levels. Serum total and free testosterone
levels (Table 2), measured during week 16, 1 wk after
the previous injection, were linearly dependent on the
testosterone dose (P 5 0.0001). Serum total and free
testosterone concentrations decreased from baseline in
men receiving the 25- and 50-mg doses and increased
at 300- and 600-mg doses. Serum LH levels were suppressed
in all groups. Serum SHBG levels decreased
dose dependently at the 300- and 600-mg doses but did
not change in other groups. Serum IGF-I concentrations
increased dose dependently at the 300- and 600-mg doses
(correlation between log testosterone level and change in
IGF-I 5 0.55, P 5 0.0001). IGFBP-3 levels did not change
significantly in any group.
Body composition. Fat-free mass, measured by underwater
weighing, did not change significantly in men
receiving the 25- or 50-mg testosterone dose, but it
increased dose dependently at higher doses (Table 3).
The changes in fat-free mass were highly dependent on
testosterone dose (P 5 0.0001) and correlated with log
total testosterone concentrations during treatment
(r 5 0.73, P 5 0.0001, see Fig. 2).
Changes in fat-free mass, measured by DEXA scan,
were qualitatively similar to those obtained from underwater
weighing (Table 3, Fig. 1). The measurements of
fat-free mass by DEXA were highly correlated with values
obtained from underwater weighing (r 5 0.94, P ,
0.0001).
Table 1. Baseline characteristics of the participants
GnRH Agonist 1 1 1 1 1
Testosterone Enanthate 25 mg 50 mg 125 mg 300 mg 600 mg P Value
Age, yr 2865 2965 2863 2465 2564 0.0583
Height, cm 17565 17769 17867 17767 17568 0.7230
Weight, kg 68.068.4 77.068.1 78.9610.6 78.4610.1 74.8612.5 0.1014
Body mass index, kg/m2 2363 2563 2563 2563 2563 0.3680
Serum testosterone
levels, nmol/l 5936161 5666220 5536182 6546157 6326228 0.7093
Fat-free mass, kg 59.166.7 65.165.1 66.067.2 67.368.9 64.268.0 0.1506
Leg press strength, kg 355.56103.8 407.8662.2 419.2686.2 439.8681.4 431.6699.3 0.2149
Hemoglobin, g/l 144612 151611 14269 14468 14168 0.1428
No. in group 12 12 12 12 13
Values are means 6 SD. GnRH, gonadotropin-releasing hormone.
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To determine whether the apparent changes in fatfree
mass by DEXA scan and underwater weighing
represented water retention, we measured total body
water and compared the ratios of total body water to
fat-free mass before and after treatment in each group.
The ratios of total body water to fat-free mass by
underwater weighing did not significantly change with
treatment in any treatment group (Table 3), indicating
that the apparent increase in fat-free mass measured
by underwater weighing did not represent water retention
in excess of that associated with protein accretion.
Fat mass, measured by underwater weighing, increased
significantly in men receiving the 25- and
50-mg doses but did not change in men receiving the
higher doses of testosterone (Table 3, Fig. 1). There
was an inverse correlation between change in fat mass
by underwater weighing and log testosterone concentrations
(r 5 20.60, P 5 0.0001, Fig. 2).
Muscle size. The thigh muscle volume and quadriceps
muscle volume did not significantly change in men
receiving the 25- or 50-mg doses but increased dose
dependently at higher doses of testosterone (Table 4,
Fig. 1). The changes in thigh muscle and quadriceps
muscle volumes correlated with log testosterone levels
during treatment (r 5 0.66, P 5 0.0001, and r 5 0.55,
P 5 0.0001, respectively, Fig. 2).
Muscle performance. The leg press strength did not
change significantly in the 25- and 125-mg-dose groups
but increased significantly in those receiving the 50-,
300-, and 600-mg doses (Table 5). The changes in leg
press strength correlated with log testosterone levels
during treatment (r 5 0.48, P 5 0.0005, Fig. 2) and
changes in muscle volume (r 5 0.54, P 5 0.003) and
fat-free mass (r 5 0.74, P , 0.0001).
Table 3. Body composition analysis
Testosterone
Dose Baseline Week 20
Change from
Baseline
P vs. Zero
Change
Fat-free mass (kg) by underwater weighing
(overall ANOVA P 5 0.0001)
25 mg 61.162.7 58.161.7 21.060.5 0.0695
50 mg 66.162.5 65.762.0 10.660.4 0.1324
125 mg 66.062.1 67.962.7 13.460.8 0.0024
300 mg 66.962.4 72.462.8 15.260.8 0.0001
600 mg 64.262.2 72.162.4 17.960.6 0.0001
Fat mass (kg) by underwater weighing
(overall ANOVA P 5 0.0001)
25 mg 8.361.4 11.361.6 13.160.7 0.0014
50 mg 10.961.4 14.361.7 13.561.0 0.0096
125 mg 12.262.0 10.962.1 10.0160.5 0.9820
300 mg 11.461.6 10.961.7 20.560.6 0.4134
600 mg 9.461.9 8.861.9 21.160.7 0.1132
Fat-free mass (kg) by DEXA scan (overall ANOVA P 5 0.0001)
25 mg 53.661.8 53.462.0 10.460.3 0.2198
50 mg 58.662.3 59.262.5 11.160.9 0.2313
125 mg 60.162.1 63.162.3 12.960.8 0.0054
300 mg 59.062.7 64.362.2 15.560.7 0.0001
600 mg 57.461.9 66.362.4 18.960.8 0.0001
Fat mass (kg) by DEXA scan (overall ANOVA P 5 0.0004)
25 mg 10.061.8 13.761.4 13.661.5 0.0326
50 mg 15.461.2 17.961.2 12.661.0 0.0324
125 mg 15.262.0 15.261.9 20.360.8 0.6882
300 mg 16.361.2 15.4161.5 20.960.6 0.1834
600 mg 14.261.9 12.061.5 22.060.7 0.0141
Ratio of total body water to fat-free mass (percent)
(overall ANOVA for change from baseline, P 5 0.270)
25 mg 62.762.7 63.762.1 11.162.4
50 mg 62.061.9 63.862.4 12.062.0
125 mg 67.061.7 63.563.0 23.861.6
300 mg 61.662.7 64.663.1 12.162.5
600 mg 65.362.4 67.462.8 12.561.7
Values on each day represent the mean (6SE) of all available
values on that day. However, the change represents the difference
between paired values only. Ratios of total body water assessed by
deuterium water dilution to fat-free mass measured by underwater
weighing were calculated for each subject and averaged across subjects
within each group. DEXA, dual-energy X-ray absorptiometry.
Table 2. Serum total and free testosterone, LH, FSH,
SHBG, and IGF-I levels
Testosterone
Dose Baseline Week 16
Change from
Baseline
P vs. Zero
Change
Testosterone (ng/dl) (overall ANOVA P 5 0.0001)
25 mg 593648 253666 2340685 0.0029
50 mg 566678 306658 2260664 0.0037
125 mg 553653 570675 57675 0.7425
300 mg 653650 1,3456139 6916143 0.0005
600 mg 632663 2,3706150 1,7376156 0.0001
Free testosterone (pg/ml) (overall ANOVA P 5 0.0001)
25 mg 6266 2965 23368 0.0014
50 mg 5766 3263 22565 0.0009
125 mg 4965 5268 367 0.8601
300 mg 7167 138621 67618 0.0012
600 mg 6465 275630 211631 0.0001
LH (U/l) (overall ANOVA P 5 0.8054)
25 mg 3.560.4 0.360.1 23.260.4 0.0001
50 mg 3.860.3 0.660.3 23.060.4 0.0008
125 mg 3.460.3 0.560.1 22.860.4 0.0001
300 mg 3.760.5 0.660.1 23.560.5 0.0002
600 mg 3.360.3 0.660.4 22.960.4 0.0001
SHBG (nmol/l) (overall ANOVA P 5 0.0001)
25 mg 29.162.9 28.563.6 20.662.9 0.8497
50 mg 24.463.4 21.163.2 23.361.1 0.0202
125 mg 33.164.2 28.963.8 24.262.6 0.1410
300 mg 31.463.8 22.463.9 29.163.7 0.0348
600 mg 40.164.9 20.663.2 219.562.8 0.0001
IGF-I (ng/ml) (overall ANOVA P 5 0.0001)
25 mg 268626 261635 27619 0.7462
50 mg 246614 225612 220610 0.0797
125 mg 299624 282631 218617 0.3284
300 mg 314624 388630 74628 0.0272
600 mg 227620 304621 77613 0.0001
Values on each day represent the mean (6SE) of all available
values on that day. However, the change represents the difference
between paired values only. Treatment values represent the day 113
(week 16) values, obtained 1 wk after the previous testosterone
injection. We used week 16 rather than week 20 values because week
20 values were not always drawn exactly 1 wk after the previous
injection. LH and FSH, luteinizing and follicle-stimulating hormones,
respectively; SHBG, sex hormone-binding globulin; IGF-I,
insulin-like growth factor I. To convert total testosterone levels to
nmol/l, multiply by 0.03467. To convert free testosterone levels to
pg/ml, multiply by 3.467.
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Leg power, measured by the Nottingham leg rig, did
not change significantly in men receiving the 25-, 50-, and
125-mg doses of testosterone weekly, but it increased
significantly in those receiving the 300- and 600-mg
doses. The increase in leg power correlated with log
testosterone concentrations (r 5 0.39, P 5 0.0105, Fig. 2)
and changes in fat-free mass (r 5 0.30, P 5 0.0392) and
muscle strength (r 5 0.42, P 5 0.0020).
Behavioral measures. The scores for sexual activity
and sexual desire measured by daily logs did not
change significantly at any dose. Similarly, visualspatial
cognition (Table 6) and mood, as assessed by
Hamilton’s depression and Young’s manic scales (data
not shown), did not change significantly in any group.
Adverse experiences and safety measures. Hemoglobin
levels decreased significantly in men receiving the
50-mg dose but increased at the 600-mg dose; the
changes in hemoglobin were positively correlated with
testosterone concentrations (r 5 0.66, P 5 0.0001) (Table
7). Changes in plasma HDL cholesterol, in contrast, were
negatively dependent on testosterone dose (P 5 0.0049)
and correlated with testosterone concentrations (r 5
Fig. 1. Change in fat-free mass (A), fat
mass (B), leg press strength (C), thigh
muscle volume (D), quadriceps muscle
volume (E), sexual function (F), insulin-
like growth factor I (G), and prostate-
specific antigen (H). Data are
means 6 SE. *Significant differences
from all other groups (P , 0.05); vsignificant
difference from 25-, 50-, and
125-mg doses (P , 0.05); 1significant
difference from 25- and 50-mg doses
(P , 0.05); and > significant difference
from 25-mg dose (P , 0.05).
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20.40, P 5 0.0054). Total cholesterol, plasma lowdensity
lipoprotein cholesterol, and triglyceride levels
did not change significantly at any dose. Serum PSA,
creatinine, bilirubin, alanine aminotransferase, and
alkaline phosphatase did not change significantly in
any group, but aspartate aminotransferase decreased
significantly in the 25-mg group. Two men in the 25-mg
group, five in the 50-mg group, three in the 125-mg
group, seven in the 300-mg group, and two in the
600-mg group developed acne. One man receiving the
50-mg dose reported decreased ability to achieve erections.
DISCUSSION
GnRH agonist administration suppressed endogenous
LH and testosterone secretion; therefore, circulating
testosterone concentrations during treatment
were proportional to the administered dose of testosterone
enanthate. This strategy of combined administration
of GnRH agonist and graded doses of testosterone
enanthate was effective in establishing different
levels of serum testosterone concentrations among the
five treatment groups. The different levels of circulating
testosterone concentrations created by this regimen
were associated with dose- and concentration-
Fig. 2. Relationship between serum
testosterone concentrations (T) during
treatment (week 16) and change in fatfree
mass (A), fat mass (B), leg press
strength (C), thigh muscle volume (D),
quadriceps muscle volume (E), sexual
function (F), insulin-like growth factor
I (G), and prostate-specific antigen (H).
The correlation coefficient, r, was calculated
using the logarithmic model,
Y 5 a 1 bzX, where X 5 log (T), and a
and b represent the intercept and
slope.
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dependent changes in fat-free mass, fat mass, thigh
and quadriceps muscle volume, muscle strength, leg
power, hemoglobin, circulating IGF-I, and plasma
HDL cholesterol. Serum PSA levels, sexual desire and
activity, and spatial cognition did not change significantly
at any dose. The changes in fat-free mass, muscle
volume, leg press strength and power, hemoglobin,
and IGF-I were positively correlated, whereas changes
in plasma HDL cholesterol and fat mass were negatively
correlated with testosterone dose and total and
free testosterone concentrations during treatment.
The compliance with the treatment regimen was
high. The participants received 100% of their scheduled
GnRH agonist, and 99% of testosterone injections.
Serum LH levels were suppressed in all men, demonstrating
the effectiveness of GnRH agonist treatment.
The treatment regimen was well tolerated. There were
no significant changes in PSA or liver enzymes at any
dose. However, long-term effects of androgen administration
on the prostate, cardiovascular risk, and behavior
are unknown.
Serum testosterone levels were measured 7 days
after previous injection; they reflect the lowest testosterone
levels after an injection. Testosterone concentrations
were higher at other time points. Weekly injections
of testosterone enanthate are associated with
fluctuations in testosterone levels (44). Although nadir
testosterone concentrations were highly correlated
with testosterone enanthate dose, it is possible that
sustained testosterone delivery by a patch or gel might
reveal different dose-response relationships, particularly
with respect to hemoglobin and HDL cholesterol
(19).
There were no significant changes in overall sexual
activity or sexual desire in any group, including those
receiving the 25-mg dose. Testosterone replacement of
hypogonadal men improves frequency of sexual acts
and fantasies, sexual desire, and response to visual
erotic stimuli (3, 13, 15, 17, 31, 41). Our data demonstrate
that serum testosterone concentrations at the
lower end of male range can maintain some aspects of
sexual function (3, 13). Testosterone has been shown to
regulate nitric oxide synthase activity in the cavernosal
smooth muscle (32), and it is possible that optimum
penile rigidity might require higher testosterone
levels than those produced by the 25-mg dose.
This study demonstrates that an increase in circulating
testosterone concentrations results in dose-de-
Table 4. Thigh and quadriceps muscle volume
measured by MRI
Testosterone
Dose Baseline Week 20
Change from
Baseline
P vs. zero
change
Thigh muscle volume (overall ANOVA P 5 0.0001)
25 mg 753646 739644 214610 0.1958
50 mg 833653 844658 1168 0.2332
125 mg 890649 966660 56610 0.0004
300 mg 849639 933639 84612 0.0001
600 mg 802645 928648 126612 0.0001
Quadriceps muscle volume (overall ANOVA P 5 0.0001)
25 mg 436630 427627 2969 0.3524
50 mg 489634 493636 467 0.5889
125 mg 508629 546636 2165 0.0027
300 mg 497625 540622 4369 0.0008
600 mg 472627 540631 6868 0.0001
Values (in cm3) on each day represent the mean (6SE) of all
available values on that day. However, the change represents the
difference between paired values only.
Table 5. Change in measures of muscle performance
Testosterone
Dose Baseline Treatment
Change from
Baseline
P vs. Zero
Change
Leg press strength (kg) (overall ANOVA P 5 0.0003)
25 mg 355.5131.3 354.2627.9 21.267.4 0.8701
50 mg 407.8122.0 430.5622.3 122.767.6 0.0204
125 mg 419.2624.4 444.6632.2 118.4610.0 0.4195
300 mg 439.8625.7 525.5624.9 172.2612.4 0.0004
600 mg 431.6127.6 508.1628.1 176.5612.2 0.0001
Leg power (W) (overall ANOVA P 5 0.0419)
25 mg 183.6610.6 188.9612.9 5.368.4 0.5429
50 mg 234.4614.2 249.6617.8 15.2615.0 0.3468
125 mg 253.8620.6 265.6625.2 8.5615.3 0.5935
300 mg 233.8620.2 272.4627.8 38.669.4 0.0033
600 mg 212.4611.0 256.2613.8 48.1611.8 0.0015
Values on each day represent the mean (6SE) of all available
values on that day. However, the change represents the difference
between paired values only.
Table 6. Change in scores for sexual activity, sexual
desire, and spatial cognition
Testosterone
Dose Baseline Treatment
Change from
Baseline
P vs. zero
change
Sexual activity scores (overall ANOVA P 5 0.7842)
25 mg 10.761.7 8.262.9 22.563.2 0.4729
50 mg 14.162.1 13.761.8 20.462.8 0.9017
125 mg 9.862.7 12.062.9 2.263.1 0.5151
300 mg 11.661.6 12.061.9 0.760.9 0.4761
600 mg 16.163.7 15.660.5 0.762.2 0.7891
Intensity of sexual desire scores (overall ANOVA P 5 0.477)
25 mg 1.960.1 1.360.4 20.660.4 0.2253
50 mg 2.360.1 2.260.3 20.060.3 0.9615
125 mg 2.160.1 2.060.3 20.160.4 0.9078
300 mg 2.260.2 2.460.2 0.160.1 0.3559
600 mg 2.760.2 2.260.1 0.260.2 0.4075
Spatial cognition scores
1. No. of trial levels on the checkerboard test that the participant
reached before the test was terminated
(overall ANOVA P 5 0.235)
25 mg 6.860.3 6.460.3 20.460.3 0.284
50 mg 6.760.3 6.760.3 0.360.3 0.284
125 mg 6.660.3 6.660.2 0.060.4 1.0
300 mg 7.360.2 6.760.2 20.660.3 0.103
600 mg 6.660.2 6.960.2 0.360.3 0.278
2. No. of checkerboard squares correctly marked in all trials
(overall ANOVA P 5 0.6309)
25 mg 28.662.2 30.462.1 1.862.1 0.4272
50 mg 30.062.3 34.764.9 2.763.5 0.5236
125 mg 27.363.0 28.162.2 0.963.8 0.7292
300 mg 32.662.1 33.361.8 0.763.1 0.8241
600 mg 26.762.7 32.562.1 5.862.2 0.0265
Values are means 6 SE.
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pendent increases in fat-free mass, muscle size,
strength, and power. The relationships between circulating
testosterone concentrations and changes in fatfree
mass and muscle size conform to a single log-linear
dose-response curve. Our data do not support the notion
of two separate dose-response curves reflecting
two independent mechanisms of testosterone action on
the muscle. Forbes et al. (22) predicted 25 years ago
that the muscle mass accretion during androgen administration
is related to the cumulative androgen
dose, the product of daily dose and treatment duration.
Our data are consistent with Forbes’s hypothesis of a
linear relationship between testosterone dose and lean
mass accretion; however, we do not know whether
increasing the treatment duration would lead to further
gains in muscle mass.
In addition, we do not know whether responsiveness
to testosterone is attenuated in older men. Testosterone
dose-response relationships might be modulated
by other muscle growth regulators, such as nutritional
status, exercise and activity level, glucocorticoids, thyroid
hormones, and endogenous growth hormone secretory
status.
Serum PSA levels decrease after androgen withdrawal,
and testosterone replacement of hypogonadal
men increases PSA levels into the normal range (16,
34). We did not find significant changes in PSA at any
dose, indicating that the lowest dose of testosterone
maintained PSA levels. We did not measure prostate
volume in this study; therefore, we do not know
whether prostate volume exhibits the same relationship
with testosterone dose as PSA levels.
Hemoglobin levels changed significantly in relation
to testosterone dose and concentration. Testosterone
regulates erythropoiesis through its effects on erythropoietin
and stem cell proliferation (14, 35, 40). Although
modest increments in hemoglobin might be
beneficial in androgen-deficient men with chronic illness
who are anemic, marked increases in hemoglobin
levels could increase the risk of cerebrovascular events
(25) and hypertension (42).
Although men, on average, perform better on tests of
spatial cognition than women, testosterone replacement
has not been consistently shown to improve spatial
cognition in hypogonadal men (1, 29, 48). We did
not find changes in spatial cognition at any dose. The
effect size of gender differences in spatial cognition is
small; it is possible that our study did not have sufficient
power to detect small differences. We cannot
exclude the possibility that gender differences in spatial
cognition might be due to organizational effects of
testosterone and might not respond to changes in testosterone
levels in adult men.
Although mean change in fat-free mass and muscle
size correlated with testosterone dose and concentration,
there was considerable heterogeneity in response
to testosterone administration within each group.
These individual differences in response to androgen
administration might reflect differences in activity
level, testosterone metabolism, nutrition, or polymorphisms
in androgen receptor, myostatin, 5-a-reductase,
or other muscle growth regulators.
Our data demonstrate that different androgendependent
processes have different testosterone
dose-response relationships. Some aspects of sexual
function and spatial cognition, and PSA levels, were
maintained by relatively low doses of testosterone in
GnRH agonist-treated men and did not increase further
with administration of higher doses of testosterone.
In contrast, graded doses of testosterone
were associated with dose and testosterone concentration-
dependent changes in fat-free mass, fat
mass, muscle volume, leg press strength and power,
hemoglobin, IGF-I, and plasma HDL cholesterol. The
precise mechanisms for the tissue- and functionspecific
differences in testosterone dose dependence
are not well understood (36). Although only a single
androgen receptor protein is expressed in all androgen-
responsive tissues, tissue specificity of androgen
action might be mediated through combinatorial recruitment
of tissue-specific coactivators and corepressors
(36).
Testosterone doses associated with significant gains
in fat-free mass, muscle size, and strength were associated
with significant reductions in plasma HDL concentrations.
Further studies are needed to determine
whether clinically significant anabolic effects of testosterone
can be achieved without adversely affecting
cardiovascular risk. Selective androgen receptor modulators
that preferentially augment muscle mass and
strength, but only minimally affect prostate and cardiovascular
risk factors, are desirable (36).
This study was supported primarily by National Institutes of
Health (NIH) Grant 1RO1-AG-14369; additional support was pro-
Table 7. Changes in hemoglobin, plasma HDL
cholesterol, and PSA
Testosterone
Dose Baseline Week 20
Change from
Baseline
P vs. Zero
Change
Hemoglobin (g/l), (overall ANOVA P 5 0.0001)
25 mg 143.563.5 139.062.5 25.263.5 0.1759
50 mg 150.863.3 146.662.0 27.462.3 0.0153
125 mg 141.962.6 146.163.1 2.562.4 0.3061
300 mg 143.562.2 149.663.1 6.162.9 0.0639
600 mg 141.562.3 155.762.2 14.262.0 0.0001
PSA (ng/ml), (overall ANOVA P 5 0.5290)
25 mg 1.060.2 1.060.2 20.160.2 0.6870
50 mg 0.860.1 1.160.2 0.360.1 0.0186
125 mg 0.760.1 0.860.1 0.160.1 0.1721
300 mg 0.760.1 0.960.3 0.260.2 0.4525
600 mg 0.560.1 0.760.1 0.160.0 0.0010
Plasma HDL cholesterol (mg/dl) (overall ANOVA P 5 0.0049)
25 mg 4663 5164 14.562.6 0.1202
50 mg 4863 4765 20.764.0 0.8653
125 mg 4862 4363 24.061.7 0.0476
300 mg 4763 4162 25.762.8 0.0690
600 mg 4362 3462 28.461.8 0.0005
Values on each day represent the mean (6SE) of all available
values on that day. However, the change from baseline represents
the difference between paired values only. PSA, prostate-specific
antigen; HDL, high-density lipoprotein.
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vided by Grants 1RO1-DK-49296, 1RO1-DK-59297–01, Federal
Drug Administration Grant ODP 1397, a General Clinical Research
Center Grant MO-00425, NIH-National Center for Research Resources-
00954, RCMI Grants P20-RR-11145–01 (RCMI Clinical Research
Initiative) and G12-RR-03026. BioTechnology General (Iselin,
NJ) provided testosterone enanthate, and R. P. Debio (Martigny,
Switzerland) provided the GnRH agonist (Decapeptyl).
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