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Scand J Med Sci Sports 2004: 14: 16–23 COPYRIGHT & BLACKWELL MUNKSGAARD 2004

Printed in Denmark . All rights reserved


DOI: 10.1046/j.1600-0838.2003.00328.x

Regional bone mineral density after resistive training in young


and older men and women
Alice S. Ryan1, Fred M. Ivey2, Diane E. Hurlbut2, Gregory F. Martel2, Jeffrey T. Lemmer2, John D. Sorkin1,
E. Jeffrey Metter3, Jerome L. Fleg3, Ben F. Hurley2
1
Department of Medicine, Division of Gerontology at the University of Maryland School of Medicine, and the Geriatric Research,
Education and Clinical Center (GRECC), Baltimore VA Medical Center, Baltimore, MD, USA,
2
The University of Maryland, Department of Kinesiology, College Park, MD, USA
3
The National Institutes of Aging, Gerontology Research Center, Baltimore, MD, USA
Corresponding author: Alice S. Ryan, PhD, Division of Gerontology, BT/18/GR, Baltimore Veterans Affairs Medical Center,
Baltimore, MD 21201, USA. Tel: (410) 605-7851, Fax: (410) 605-7913, E-mail: aryan@grecc.umaryland.edu
Accepted for publication 7 February 2003

Purpose: The purpose of this study was to determine the after training in young men and women and older men
effects of 6 months of whole-body resistive training (RT) (Po0.05) but did not change significantly in older women.
on total and regional bone mineral density (BMD) and bone Upper- and lower-body 1RM strength increased in all
mineral content (BMC) by age and gender in young and groups (Po0.01). Overall, there was a significant increase
older men and women. Methods: Younger men (n 5 10) in BMD at the femoral neck, ward’s triangle and greater
and women (n 5 7) aged 20–29 years (2571 years) and trochanter BMD, as well as total body BMC and leg BMC
older men (n 5 10) and women (n 5 10) aged 65–74 years (Po0.05). Total-body BMD and L2–L4 spine BMD
(6971 years) participated in 6 months of progressive did not change with RT. There were no gender differences
whole-body RT. Upper- and lower-body strength was in the training response between men and women for
assessed by the one repetition maximum (1RM) test, and any of the BMD regions and no age differences in the
total body fat, lean tissue mass, femoral neck BMD, training response, except for a trend between young and
Ward’s triangle BMD, greater trochanter BMD, total- older subjects for femoral neck (Po0.08). Conclusion: A
body BMD, and L2–L4 spine BMD were determined by 6-month RT program increases muscle mass and improves
dual-energy X-ray absorptiometry before and after 6 BMD of the femoral region in young and healthy older men
months of RT. Results: Percent body fat decreased only and women as a group, with a trend for this to be greater in
in the young men (Po0.05). Lean tissue mass increased young subjects.

Introduction enhancing bone mass (Rubin et al., 1987). Resistive


training (RT), which places heavy loads on the
Peak bone mass is a major determinant of future risk skeleton during a training session and increases both
for bone fracture. Reducing the risk for osteoporosis strength and muscle mass, may increase BMD
may involve increasing bone mass at skeletal (Nelson et al., 1994; Treuth et al., 1994; McCartney
maturity, and preventing or slowing the loss of bone et al., 1995; Ryan et al., 1995). However, a clear
mineral density (BMD) with advancing age. Age- consensus of the effects of RT on BMD has not been
associated losses in BMD (Mazess, 1982) are reached. In prior studies, RT increased (Snow-
accompanied by a loss of fat-free mass (Steer, Harter et al., 1992; Lohman et al., 1995), did not
1988), muscle strength (Lindle et al., 1997), and change (Gleeson et al., 1990) or decreased (Rockwell
muscle quality (Lynch et al., 1999). Collectively, et al., 1990) BMD in premenopausal women and
these concomitants of aging may increase both falls increased (Nelson, 1994) or maintained BMD
and fracture risk in the elderly. Therefore, it is (Notelovitz et al., 1991; Ryan et al., 1998) in
optimal to not only maximize the bone mineral postmenopausal women. Relatively little informa-
status of young men and women but also to tion is available concerning the effects of RT on
minimize decreases in bone density and loss of BMD in men. RT of 16 weeks increased femoral
muscle mass with advancing age. neck BMD in middle-aged men (Menkes et al., 1993;
Exercise training is increasingly recommended for Ryan et al., 1994) but did not change the BMD in
older persons to strengthen bones. Regular exercise this region in elderly men (Yarasheski et al., 1997).
that accentuates muscular skeletal loading with few Furthermore, no age or gender comparisons of the
repetitions and high stress may be optimal for BMD response to RT have been made in the same

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BMD and resistive training in men and women
study using an identical RT intervention for all RT program
groups. Thus, it is unclear as to whether BMD The RT program consisted of three exercise sessions per week
responds differently to an RT program in men vs. on nonconsecutive days for approximately 6 months using 11
women or in younger vs. older individuals. There- exercises of pneumatic variable-resistance machines (Keiser
fore, the purpose of this study was to compare age K-300, Keiser Sports Health Inc., Fresno, CA, USA),
dumbbells, and floor exercises, as previously described (Ryan
and gender BMD responsiveness to RT by compar- et al., 1995), with some modifications. The training included
ing the effects of 6 months of RT on total and the following exercises: leg press, chest press, leg curl,
regional BMD in young men, young women, older latissimus pulldown, leg extension, military press, seated
men, and older women. row, triceps pushdown, abdominal crunch, biceps curl, and
sit-ups. To minimize the risk of staleness and boredom during
the study, the ST program was divided into two 12-week
periods. During the first 12 weeks of the program, subjects
Methods performed two sets of leg exercises and one set of upper-body
Subjects exercises as previously described (Ryan et al., 1995). After
Subjects were recruited through advertisements in the approximately 12 weeks, the protocol was varied so that not
Washington area newspapers for participation in this Uni- all exercises were performed during every training session. On
versity- and hospital-based study. The study began with 23 Mondays, subjects performed one set of the chest press,
older men (n 5 12) and women (n 5 11) aged 65–74 years latissimus pulldown, and shoulder press exercises and two sets
(6971 years) and 21 younger men (n 5 13) and women (n 5 8) of the three leg exercises. On Wednesdays, subjects performed
aged 20–29 years (2571 years). Two older subjects (one male one set of all upper- and lower-body exercises. On Fridays, the
and one female) and four younger subjects (three males and ST session consisted of one set of triceps, upper back,
one female) did not complete the training protocol due to abdominal, and biceps curls and two sets of the leg exercises.
illness, personal reasons, and/or time constraints. These Biceps curls and abdominal crunches were performed in the
subjects did not differ in age, BMI, or BMD compared with same manner as during the first 12 weeks of training.
those who completed the protocol. Body composition and Abdominal crunches were performed on all training days.
BMD data are missing for one older male who completed the Subjects gradually increased the resistance, following a warm-
intervention. Therefore, these seven subjects were excluded up at 50% of their 1RM, until failure to complete a repetition.
from the data analysis. The majority of the men and women This resulted in 12–15RM, including the warm-up repetitions.
were Caucasian with the exception of three African-Amer- During both phases of training, the beginning and ending
icans (one older male, two older females) and three Asians weights were recorded after each session in order to assess the
(two young men, one older female). Subjects were screened by increases in muscular strength that were occurring. The
medical history, physical examination, fasting blood profile, decision to increase the load was based on whether they
2 h oral glucose tolerance test, and a graded exercise treadmill could achieve the minimum and maximum repetitions of 12–
test. All subjects were nonsmokers, free of cardiovascular 15 while using maximal effort (i.e., 12–15RM). Subjects were
disease (CVD), and were not on any medications known to weighed at every third exercise session. Younger and older
influence calcium or bone metabolism with the exception of subjects underwent the RT program in similar seasons.
two older women who were on hormone-replacement therapy. Attendance at the training sessions was 470% in the young
All older women were at least 2 years postmenopausal. Only subjects and 485% in the older men and women.
persons who were weight stable and had not participated in a
regular exercise program for a minimum of 6 months prior to
the study were included. All methods and procedures were Body composition and BMD
approved by the Institutional Review Boards of the University Total body fat mass, lean tissue mass, and bone mineral
of Maryland and all subjects provided written informed content (BMC) (g) were determined by dual-energy X-ray
consent. absorptiometry (DXA) (Model DPX-L LUNAR Radiation
Corp., Madison, WI, USA). All DXA scans were analyzed by
the same investigator using the LUNAR Corporation Version
Strength tests 1.3Z DPX-L extended analysis program for body composi-
tion. The coefficients of variation (CV) for total body percent
Prior to the strength assessment, subjects participated in five
fat, fat tissue mass, lean tissue mass, and BMC are 1.4%,
training sessions using light resistance to become familiar with
1.4%, 0.7%, and 0.4%, respectively, which was determined by
the equipment and the exercise techniques and to control for
five repeat scans with repositioning of one individual.
artificially high initial strength gains due to motor learning
The same DXA scanner and software were used to scan the
effects. Upper-body and lower-body strength were assessed by
total body, anterioposterior (AP) lumbar spine (L2–L4) and
the one repetition maximum (1RM) test, defined as the
femur (femoral neck, Ward’s triangle, greater trochanter) to
maximum amount of resistance that could be moved
obtain total and regional BMD (g cm 2). The CVs for these
successfully through the full range of motion at one time.
regions are 0.5%, 0.8%, 1.3%, 4.2%, and 1.3%, respectively,
Subjects attempted lifts with gradually increasing loads.
which was determined by five repeat scans with repositioning
Successive attempts were made with B30 s rest between
of two individuals and analyzed by the same investigator.
attempts until failure to complete another repetition occurred.
Regions of interest, including arms, legs, and trunk BMC, were
Approximately the same number of trials was used to reach
analyzed using the extended analysis of the LUNAR software.
the 1RM before compared to after training. Strength was
assessed for both the upper and lower body using the
following exercise machines: leg press, leg extension, chest
press, latissimus pulldown, and triceps pushdown. Leg Statistical analyses
strength on both leg machines was tested unilaterally, but Initial analyses were designed to determine if RT changed
the summed values were used in the analysis. The biceps were regional bone density in the entire study population. If
tested with free weights using a biceps curl. a change in the entire study population was detected,

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Ryan et al.
subsequent analyses were run to determine if the change (Po0.005), but similar body weight and lean tissue
varied by age group or gender. These analyses were performed mass than the young women.
using ANOVA. The dependent variable in each ANOVA was Body weight and fat mass did not significantly
the change in bone density for each region; the independent
variables included the BMD or BMC before RT, an age term change after training in any group. Percent body fat
(young vs. old), a gender term (male vs. female), and an age by decreased significantly in the young men (Po0.05),
gender interaction. Differences in BMD at baseline within but did not change significantly in the other groups.
each sex and within each age group were determined by t- Lean tissue mass increased significantly after training
tests. Pearson correlation coefficients were determined to in young men, young women, and older men (all
evaluate relationships among variables of body composition,
BMD, and strength. All statistical tests were two-tailed. Data Po0.05), but did not change significantly in older
are expressed as mean7standard error of the mean (SEM) women.
and significance was set at the Po0.05 level.

Muscular strength
Results The men had significantly higher baseline 1RM
Subject characteristics values than the women for all strength tests
Subject characteristics are presented in Table 1. The (Po0.01), except that no differences were observed
average age did not differ between young men and for leg extension strength between the two young
young women or between older men and older groups (Table 2). Moreover, the younger subjects
women. Although baseline BMI was similar between were stronger than older subjects at baseline (all
young men and young women and between older Po0.05) with a few exceptions. There were no
men and older women, baseline body weight was significant differences in leg extension in young
higher in the men (Po0.01). In the comparisons by and older men and no differences in biceps curl,
age group, there were no significant differences in latissimus pulldown, and leg press between young
body weight, lean tissue mass, or fat mass between and older women prior to training.
the young and older men. However, older women RT increased muscular strength significantly in all
had higher fat mass (Po0.05) and percent body fat four groups for all exercises tested (Table 2; all

Table 1. Subject characteristics before and after training in all four age and gender groups

Young men Young women Older men Older women

Before After Before After Before After Before After


training training training training training training training training

Age (years) 2571 2671 7071 6871


Weight (kg) 82.875.2 83.074.9 63.475.0 65.475.2 80.873.0 81.072.9 70.272.1 70.772.3
Height (cm) 177.472.5 F 166.571.6 F 173.771.4 F 161.072.3 F
BMI (kg cm 2) 26.571.3 26.971.4 23.471.5 23.971.5 26.971.0 26.771.0 27.370.8 27.770.9
Body fat (%) 24.072.5 22.272.2* 31.972.2 31.772.1 28.971.5 28.171.6 40.771.2 40.071.4
Fat mass (kg) 20.973.5 19.273.0 20.973.0 21.473.0 23.872.2 23.272.1 28.771.4 28.571.7
Lean tissue mass (kg) 58.872.4 60.672.3* 40.072.0 41.572.2* 54.071.1 54.970.9* 39.471.0 40.170.9

Values are means7SEM. Significantly dierent compared to before training (*Po0.05).

Table 2. 1RM strength values (kg) before and after training in all four age and gender groups

Young men Young women Older men Older women

Before After Before After Before After Before After


training training training training training training training training

Leg extension 148715 200718* 145714 187720* 15878 205710** 9276 11778**
Leg press 697726 871735** 419738 585750* 534725 636726** 349729 445726**
Chest press 7275 8977** 3472 4773* 4572 5372** 2771 3171**
Latissimus pulldown 7475 9276** 3473 4673* 5171 6373** 2971 3671**
Biceps curl 3573 4674** 1572 2472* 2771 3471** 1571 2071**
Triceps pushdown 8178 110710** 4273 5975* 5172 6673** 3172 3971**

Values are means7SEM. 1RM values for leg strength on both leg machines are the results from the sum of both legs. Significantly dierent compared to
before training (*Po0.01, **Po0.001).

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BMD and resistive training in men and women
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Table 3. Bone mineral density values (g cm ) before and after training in all four age and gender groups

Young men Young women Older Men Older women

Before After Before After Before After Before After


training training training training training training training Training

Total body 1.25670.027 1.26370.025 1.17870.029 1.18170.032 1.20570.020 1.21070.018 1.04170.029 1.04770.031
Lumbar spine 1.26070.047 1.26270.045 1.23970.036 1.27370.036 1.24070.035 1.25070.035 1.04970.044 1.04670.046
Femoral neck 1.14170.047 1.16870.048 1.00570.067 1.01870.069 0.92670.039 0.92870.040 0.82570.047 0.82670.045
Ward’s triangle 1.07070.052 1.10270.050 0.93270.074 0.96370.079 0.74370.047 0.74970.052 0.71370.051 0.71770.051
Greater trochanter 0.93970.057 0.95270.054 0.79270.052 0.80970.052 0.91970.031 0.93570.029 0.72770.044 0.72470.041

Values are means7SEM.

Po0.01). The relative increases in strength did not greater trochanter BMD than older women prior to
differ between young men and young women, or training (Po0.005). As expected, differences in
between older men and older women. In age BMD were observed with age. Total body, L2–L4
comparisons, relative changes in strength were spine, femoral neck, and Ward’s triangle BMD were
similar between the young men and the older men. significantly lower in older women than young
In addition, relative improvements in strength were women (all Po0.05). Femoral neck and Ward’s
similar for each exercise between young and older triangle BMD were lower in older men than young
women, except that younger women had a larger men (Po0.001).
percent increase in chest press strength than older Overall, there was a significant increase in femoral
women. neck BMD (0.97270.025 vs. 0.98270.032 g cm 2,
Po0.05, Fig. 1). Simple t-tests, not corrected for
multiple comparisons, indicate that the increase was
Bone mineral density limited to the young men (Po0.05). However, after
There were no differences in total body, lumbar adjustment for multiple comparisons using ANOVA,
spine, or the femoral regions of BMD between the there was a trend for a difference between the young
young groups at baseline (Table 3). In contrast, older and older subjects (Po0.08) with no gender differ-
men had higher total BMD, L2–L4 spine BMD, and ence. There was also a significant increase in Ward’s

Fig. 1. BMD ( g cm 2) after RT of the femoral neck, Ward’s triangle, and greater trochanter in young and older men and
women. Values are means 7 SEM. *Po0.05 before vs. after resistive training.

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Ryan et al.
triangle BMD (0.85970.036 vs. 0.876 7 0.038 g cm 2,
Po0.05) and greater trochanter BMD (0.84870.027
vs. 0.85970.027 g cm 2, Po0.05) in the entire study
population (Fig. 1). There were no age or gender
differences in Ward’s triangle or greater trochanter
BMD and their response to RT. Total body BMD
(1.16970.019 vs. 1.17570.019 g cm 2) and L2–L4
spine BMD (1.19470.025 vs. 1.20270.025 g cm 2)
did not change with RT and there were no age or
gender differences in their response to RT. Total body
BMC (2.72670.009 vs. 2.74570.009 kg, Po0.05)
and leg BMC (1.08670.004 vs. 1.09770.004 kg,
Po0.05) also significantly increased with RT in the
entire study population. Simple t-tests, not corrected for
multiple comparisons, indicate that the increase in total
BMC was limited to the young men (Po0.05). Yet, Fig. 2. Relationship between baseline leg press strength (kg)
after adjustment for multiple comparisons using and femoral neck BMD (g cm 2) in young and older men
ANOVA, there was no age or gender difference in and women (r 5 0.58, Po0.001).
total BMC. There was no age or gender difference in
the change in leg BMC to RT. Arm BMC and trunk
BMC (data not shown) did not change significantly
with RT.

Relationships of BMD with body composition and


muscular strength
Body weight was significantly associated with greater
total body BMD (r 5 0.52, Po0.005), L2–L4 BMD
(r 5 0.33, Po0.05), and greater trochanter BMD
(r 5 0.51, Po0.005), but not with the BMD of either
the femoral neck or Ward’s triangle in the entire
group before training. Lean tissue mass was sig-
nificantly associated with total body BMD (r 5 0.71,
Po0.0001), lumbar spine BMD (r 5 0.46, Po0.005),
and all three regions of the femur at baseline Fig. 3. Relationship between baseline chest press strength
(femoral neck, Ward’s triangle, and greater trochan- (kg) and L2–L4 BMD (g cm 2) in young and older men and
ter BMD, r 5 0.51, 0.43, and 0.66, respectively, all women (r 5 0.47, Po0.005).
Po0.01).
Initial 1RM strength values for the leg press
were highly correlated with baseline total body with the increase in femoral neck BMD (r 5 0.46,
BMD (r 5 0.66, Po0.0001), L2–L4 BMD (r 5 0.49, Po0.01) and total body BMD (r 5 0.37, Po0.05).
Po0.005) and femoral neck (Fig. 2), Ward’s triangle No other significant associations were observed
and the greater trochanter BMD in all subjects between changes in muscular strength and changes
(r 5 0.58, 0.56, 0.47, respectively, all Po0.001). in total or regional BMD.
Significant associations were found at baseline
between 1RM values for the chest press and L2–L4
BMD (Fig. 3), femoral neck, Ward’s triangle, and Discussion
greater trochanter before RT (r 5 0.47, 0.58, 0.60,
0.49, respectively, all Po0.005). Initial latissimus Maximizing the peak bone mineral status of young
pulldown 1RM values were also significantly asso- men and women, as well as increasing strength and
ciated with baseline L2–L4, femoral neck, Ward’s muscle mass, may optimize factors to reduce fracture
triangle, and greater trochanter BMD (r 5 0.42–0.53, risk in later years. The loss of BMD with aging that
all Po0.05). Increases in 1RM values for the leg may coincide with the increased inactivity, loss of
press were associated with the increase in Ward’s muscle mass, and decline in strength with aging may
triangle BMD (r 5 0.35, Po0.05). The increase in lead to falls and the development of osteoporosis.
1RM values for the leg extension was associated The current results indicate that gender and age do

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BMD and resistive training in men and women
not influence BMD responsiveness to RT. Specifi- aerobic training (Rikli & McManis, 1990; Peterson et
cally, results of this study demonstrate that 6 months al., 1991; Svendsen et al., 1993) or estrogen therapy
of RT increases BMD in the femoral region in (Notelovitz et al., 1991). Of the studies that
healthy young and older men and women. The RT employed RT alone, we (Ryan et al., 1998) and
program did not change total and lumbar spine others (Pruitt et al., 1992; McCartney et al., 1995)
BMD in any group. have observed no significant changes in the total-
Cross-sectional studies indicate that young male body, lumbar spine, or femoral neck BMD. In
strength-trained athletes have higher BMD (Colletti contrast, Nelson et al. (1994) observed small
et al., 1989; Karlsson et al., 1993) and serum increases in femoral neck (0.9%) and lumbar spine
osteocalcin levels (a marker of bone formation) (1.0%) BMD after a 1 year 2-day per week RT
(Karlsson et al., 1995) than controls. To our knowl- program in 50–70-year-old postmenopausal women.
edge, only one longitudinal investigation (Fujimura Although these changes were within the range of
et al., 1997) has previously examined the effects of precision of the technique to detect changes, the
RT on BMD in young men. In that study, 4 months preservation of BMD in the exercise group was
of RT did not change total, lumbar spine, or femoral significant only when contrasted with the decrease in
neck BMD (Fujimura et al., 1997). The reasons for BMD in these regions in sedentary controls (Nelson
the discrepancy in changes in femoral neck BMD et al., 1994). Our study differs from that of Nelson et
between these findings and those of the present study al. (1994) in sample size of the exercise group (10 vs.
are not known since intensity and type of training 20 women), lack of control group for comparison,
appeared to be similar. However, the training and differences in age because the women in our
protocol in the present study was 2 months longer study were older by almost 10 years (65–74 vs. 50–70
in duration. years.).
Only a few prospective studies have been reported Although a limitation of the present study is the
in older men. RT of 16 weeks increased lumbar spine lack of age- and gender-matched control groups, we
BMD by 2% (Menkes et al., 1993) and femoral neck have preliminary evidence that the increases in BMD
BMD by B3% (Menkes et al., 1993; Ryan et al., and BMC are clinically significant. In the Baltimore
1994) but did not change total body, Ward’s triangle, Longitudinal Study of Aging (BLSA), femoral neck
or greater trochanter BMD in middle-aged men. BMD declines B1.5% and 0.8% per year in young
Ward’s triangle BMD increased after 16 weeks of RT (25 years of age) men and women, respectively.
in elderly men, but whole-body, lumbar spine, and Lumbar spine BMD had minimal increases per year
femoral neck BMD were unchanged (Yarasheski in young men or women (B0.2–0.4%). These
et al., 1997). Our results confirm those that showed findings contrast the 2–3% increases in femoral neck
that 10 months of RT did not change total-body BMD in our RT young subjects, which suggests that
or lumbar spine bone mass in 60–80-year old men RT may have accelerated bone formation in the
(McCartney et al., 1995). young group. Likewise, in older men and women
Our results in premenopausal women confirm (B67 years old) participating in the BLSA there was,
previous studies, which report a maintenance of in general, a loss of BMD in the trochanter (B0.9%
lumbar spine (Gleeson et al., 1990; Rockwell et al., and 0.7% per year in men and women) and femoral
1990) after RT. In contrast, others have reported neck (B0.53% and 0.03%). Although a large
an increase (Snow-Harter et al., 1992; Lohman et al., variation exists in both the BLSA population and
1995) or a decrease in lumbar BMD (Rockwell et al., ours with respect to changes in BMD over 1 year, it
1990), and a maintenance of femoral BMD (Snow- appears that RT may have slowed bone loss in the
Harter et al., 1992; Chilibeck et al., 1996) with RT older men and women. We also recognize that our
in premenopausal women. In general, the intensity sample sizes are too low to adequately detect age and
and duration of training were similar in each of gender differences in the response to RT.
these studies such that 2–3 sets were performed at Bone density is positively associated with the
initial resistances of B70% 1RM for 5–12 months. strength of the anatomically related structures (Sinaki
Thus, the intensity or duration of the resistance et al., 1986; Zimmermann et al., 1990). Furthermore,
training probably does not explain the disparate positive associations between bone mass and fat-free
results. mass (Aloia et al., 1995) and between BMD and
Previous studies that have examined the effects of muscular strength (Ryan et al., 1998) have been
RT on BMD in older women have also reported reported previously. We also found significant
disparate results (Dalsky et al., 1988; Rikli, & associations between lean tissue mass and total
McManis, 1990; Notelovitz et al., 1991; Peterson et BMD and all regional measures of BMD in young
al., 1991; Pruitt et al., 1992; Svendsen et al., 1993; and older men and women. The present study
Nelson et al., 1994; Ryan et al., 1998), perhaps confirms the previous associations of baseline leg
because, in some cases, RT was combined with press strength with femoral BMD and chest press

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16000838, 2004, 1, Downloaded from https://onlinelibrary.wiley.com/doi/10.1111/j.1600-0838.2003.00328.x by Pontificia Universidade Catolica De Goias, Wiley Online Library on [07/12/2023]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License
Ryan et al.
strength with spinal BMD in postmenopausal women at skeletal maturity, then perhaps significant reduc-
(Ryan et al., 1998), and extends them to include tions in fracture risk may occur in later years.
young men and women and older men. Additional Additional studies are needed to examine the effects
research is needed to examine whether these two of the combination of RT with other exercise
exercises may be important to include in RT regimens or other treatment strategies on regional
programs attempting to induce increases in BMD. BMD in older people.

Key words: exercise, aging, osteoporosis, strength,


menopause.
Perspective
The high fracture risk in the elderly, especially in
women, should intensify the development of strate- Acknowledgements
gies to reduce this risk. Exercise, including RT, is Our appreciation is extended to the participants in the study
often recommended to provide loading forces as and to Andrew P. Goldberg (MD) for support. This study was
components of the osteogenic response in the supported by funds from: NIH grant KO1-A600747 (ASR);
prevention of osteoporosis. In the present study, a NIH training grant 1T32-AG00219 (FMI and JTL); Ger-
iatrics & Gerontology Education and Research Program at
6-month RT program increases BMD in the femoral the University of Maryland, Baltimore, the Department of
region in young and older men and women as a Veterans Affairs; and Contract N01-AG-4-2148 from the
group. If young men and women can increase BMD National Institute of Aging, NIH.

References
Aloia JF, Vaswani A, Ma R, Flaster E. formation in weight lifters. Calcif and older men. J Appl Physiol 1993: 74:
To what extent is bone mass Tissue Int 1995: 56: 177–180. 2478–2484.
determined by fat-free or fat mass? Am Lindle RS, Metter EJ, Lynch NA, Nelson ME, Fiatarone MA, Morganti
J Clin Nutr 1995: 61: 1110–1114. Fleg JL, Fozard JL, Tobin J, Roy TA, CM, Trice I, Greenberg RA, Evans WJ.
Chilibeck PD, Calder A, Sale DG, Hurley BF. Age and gender Effects of high-intensity strength
Webber CE. Twenty weeks of weight comparisons of muscle strength in training on multiple risk factors for
training increases lean tissue mass but 654 women and men aged 20–98. osteoporotic fractures: a randomized
not bone mineral mass or density in J. Appl. Physiol 1997: 88: 1581– controlled trial. JAMA 1994: 272:
healthy, active young women. Can J 1587. 1909–1914.
Physiol 1996: 74: 1180–1185. Lohman T, Going S, Pamenter R, Hall Notelovitz M, Martin D, Tesar R, Khan
Colletti LA, Edwards J, Gordon L, Shary M, Boyden T, Houtkooper L, FY, Probart C, Fields C, McKenzie L.
J, Bell NH. The effects of muscle- Ritenbaugh C, Bare L, Hill A, Aickin Estrogen therapy and variable-
building exercise on bone mineral M. Effects of resistance training resistance weight training increases
density of the radius, spine, and hip in on regional and total bone mineral bone mineral in surgically menopausal
young men. Calcif Tissue Int 1989: 45: density in premenopausal women: a women. J Bone Miner Res 1991: 6:
12–14. randomized prospective study. J Bone 583–590.
Dalsky GP, Stocke KS, Ehsani AA, Miner Res 1995: 10: 1015–1024. Peterson SE, Peterson MD, Raymond G,
Slatopolsky E, Lee WC, Birge SJ. Lynch NA, Metter EJ, Lindle RS, Fozard Gilligan C, Checovich MM, Smith EL.
Weight-bearing exercise training and JL, Tobin JD, Roy TA, Fleg JL, Hurley Muscular strength and bone density
lumbar bone mineral content in BF. Muscle quality. I. Age-associated with weight training in middle-aged
postmenopausal women. Ann Intern differences between arm and leg muscle women. Med Sci Sports Exerc 1991: 23:
Med 1988: 108: 824–828. groups. J Appl Physiol 1999: 86: 499–504.
Fujimura R, Ashizawa N, Watanabe M, 188–194. Pruitt LA, Jackson RD, Bartels RL,
Mukai N, Amagai H, Fukubayashi T, Martin AD, McCulloch RG. Bone Lehnhard HJ. Weight training effects
Hayashi K, Tokuyama K, Suzuki M. dynamics: stress, strain and fracture. on bone mineral density in early
Effect of resistance training on bone J Sports Sci 1987: 5: 155–163. postmenopausal women. J Bone Miner
formation and resorption in young Mazess RB. On aging bone loss. Clin Res 1992: 7: 179–185.
male subjects assessed by biomarkers of Orthop 1982: 165: 239–252. Rikli RE, McManis BG. Effects of
bone metabolism. J Bone Miner Res McCartney N, Hicks AL, Martin J, exercise on bone mineral content in
1997: 12: 656–662. Webber CE. Long-term resistance postmenopausal women. Res Quarterly
Gleeson PB, Protas EJ, LeBlanc AD, training in the elderly: effects on Exerc Sport 1990: 613: 243–249.
Schneider VS, Evans HJ. Effects of dynamic strength, exercise capacity, Rockwell JC, Sorensen AM, Baker S,
weight lifting on bone mineral density muscle, and bone. J Gerontol 1995: Leahey D, Stock JL, Michaels J,
in premenopausal women. J Bone 50A: B97–B104. Baran DT. Weight training decreases
Miner Res 1990: 5: 153–158. Menkes A, Mazel S, Redmond RA, vertebral bone density in
Karlsson MK, Johnell O, Obrant KJ. Koffler K, Libanati RCR, Gundberg premenopausal women: A prospective
Bone mineral density in weight lifters. CN, Zizic TM, Hagberg JM, Pratley study. J Clin Endocrinol Metab 1990:
Calcif Tissue Int 1993: 52: 212–215. RE, Hurley BF. Strength training 71: 988–993.
Karlsson MK, Vergnaud P, Delmas PD, increases regional bone mineral density Rubin CT, Lanyon LE. Regulation of
Obrant KJ. Indicators of bone and bone remodeling in middle-aged bone formation by applied dynamic

22
16000838, 2004, 1, Downloaded from https://onlinelibrary.wiley.com/doi/10.1111/j.1600-0838.2003.00328.x by Pontificia Universidade Catolica De Goias, Wiley Online Library on [07/12/2023]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License
BMD and resistive training in men and women
loads. J. Bone Joint Surg Am 1984: 66: Sinaki M, McPhee MM, Hodgson S. overweight postmenopausal women.
397–402. Relationship between bone mineral Am J Med 1993: 95: 131–140.
Ryan AS, Pratley RE, Elahi D, Goldberg density of spine and strength of back Treuth MS, Ryan AS, Pratley RE, Rubin
AP. Resistive training increases fat-free extensors in healthy post-menopausal MA, Miller JP, Nicklas BJ, Sorkin J,
mass and maintains RMR despite women. Mayo Clin Proc 1986: 61: Harman SM, Koval S, Goldberg AP,
weight loss in postmenopausal 116–122. Hurley BF. Effects of strength training
women. J Appl Physiol 1995: 79 (3): Snow-Harter C, Bouxsein ML, Lewis BT, on body composition in middle-aged
818–823. Carter DR, Marcus R. Effects of and older men using DEXA and
Ryan AS, Treuth MS, Hunter GR, Elahi resistance and endurance exercise on MRI. J Appl Physiol 1994: 77 (2):
D. Resistive training maintains bone bone mineral status of young women: 614–620.
mineral density in postmenopausal a randomized exercise intervention Yarasheski KE, Campbell JA, Kohrt
women. Calcif Tissue Int 1998: 62: trial. J Clin Endocrinol Metab 1992: 7: WM. Effect of resistance exercise and
295–299. 761–769. growth hormone on bone density in
Ryan AS, Treuth MS, Rubin MA, Miller Steer B. Body composition and aging. older men. Clin Endocrinol 1997: 47:
JP, Nicklas BJ, Landis DM, Pratley Nutr Rev 1988: 46: 45–51. 223–229.
RE, Libanati CR, Gundberg CM, Svendsen OL, Hassager C, Christiansen Zimmermann CL, Smidt GL, Brooks JS,
Hurley BF. Effects of strength training C. Effect of an energy-restrictive Kinsey WJ, Eekhoff TL. Relationship
on bone mineral density: hormonal and diet, with or without exercise, on lean of extremity muscle torque and bone
bone turnover relationships. J Appl tissue mass, resting metabolic rate, mineral density in postmenopausal
Physiol 1994: 77 (4): 1678–1684. cardiovascular risk factors, and bone in women. Phys Ther 1990: 70: 302–309.

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