zyxwvutsr
zyxwvuts
zyxwvuts
zyxwvut
British Journal of Nutrition (1996), 75, 793-802
793
zyx
zyxwvu
zyxwvut
zyxw
Body composition assessment in lean and normal-weight young
women
BY G. MIKAEL FOGELHOLM, T. K A T R I I N A KUKKONEN-HARJULA,
H A R R I T. SIEVANEN, P E K K A OJA A N D I L K K A M.VUORI
UKK Institute for Health Promotion Research, PO Box 30, FIN-33501 Tampere, Finland
(Received 27 September 1994 - Revised 13 April 1995 - Accepted 6 October 1995)
Using percentage body fat (BF YO)
from a three-compartment (3C) model (body density from underwater
weighing (vww)
and bone-mineral mass from duaI-energy X-ray absorptiometry (DXA)) as a criterion,
we studied the accuracy of UWW, DXA, two skinfold equations, and two bioimpedance (BIA) equations.
Thirty-four women (aged 16-20 years) with BF% 135-31.1 volunteered. UWW underestimated BF%
by -0.5 BF YO(95 % CI : - 1.0; -0.02), whereas DXA overestimated it by 7-3BF % (95 YOCI 5-8;88).
Skinfolds underestimated and BIA overpredicted BF%. The differences between 3C and UWW,
skinfolds (Durnin & Womersley, 1974) and BIA (Deurenberg et uf. 1990) were dependent (range of r
values: -0.63 to -079; P < 0.0001) on BF%, causing an overestimation of lean subjects’ (UWW,
BIA) or an underestimation of normal-weight subjects’ (UWW, skinfolds) BF%. The 3C model and
UWW gave comparable body-composition results for healthy young women with BF % of approximately
20-25. Based on a significant mean difference from the 3C model, and a large standard error of the
estimate, we do not regard DXA as superior to skinfolds or BIA to assess BFYo.
Bioimpedance: Body composition: Bone: Dual-energy X-ray absorptiometry
Information about body composition in lean and normal-build young women is needed in
clinical and scientific work with, for instance, athletes and patients with eating disorders.
Information on body composition is also important in metabolic studies, and for
calculating drug dose in pharmaceutical studies. Underwater weighing (UWW) and
skinfold measurements are the most frequently used methods in laboratory and. field
respectively. New alternatives include bioelectrical impedance analysis (BIA), dual-energy
X-ray absorptiometry (DXA) and multicompartment models (e.g. UWW and DXA in
combination).
Variation in total bone-mineral content (TBMC), especially in young or postmenopausal
women, is a major factor affecting the accuracy of UWW (two-compartment model), in
which the densities of fat and fat-free compartments are assumed to be constant (Martin
& Drinkwater, 1991). TBMC in women is affected by several factors in early adulthood,
such as weight, biological maturation, oestrogen production, nutrient intakes and physical
exercise (Suominen, 1993).
Combining values for body density (by UWW) and TBMC yields a three-compartment
(3C) model (fat, bone, fat-free soft tissue), in which TBMC from a whole-body DXA scan
is used to correct for variation in bone minerals (Lohman, 1986). Body composition can
also be assessed using DXA only (Mazess et al. 1990), but to the best of our knowledge the
accuracy of this method in young women has not been examined.
Use of skinfolds and BIA to assess BF % in young women raises practical problems. For
instance, it may be inappropriate to use adult equations which assume a fixed chemical
composition of the fat-free compartment or a certain pattern of subcutaneous fat
794
zyxwvuts
zyxwv
zyxwvu
zyxwv
zyxwv
zyxw
G. M. FOGELHOLM A N D OTHERS
distribution (Lohman, 1986; Martin & Drinkwater, 1991; Webster & Barr, 1993). In
particular adolescent females and athletes favouring lean body image are at risk of eating
disorders, and improper use of body composition analysis by, for instance, trainers or
teachers might aggravate this problem (Webster & Barr, 1993). Therefore, more research
is needed to examine the validity of skinfolds and BIA in relation to multicompartment
models in young women.
Using a 3C model (fat, bone and fat-free soft tissue from UWW and DXA) as the
criterion model, we addressed two questions concerning body composition (in the present
study : percentage body fat, BF Yo) assessment in lean and normal-weight young women :
(1) how large is the difference between the 3C model and the alternative methods (UWW,
DXA, two skinfold equations, two BIA equations) ; (2) are the differences dependent on the
magnitude of BF % ?
METHODS
Subjects
Thirty-four women volunteered. To obtain a sample with a wide variation in the level and
type of physical activity, both non-athletes and athletes were recruited : twelve participants
(35 Yo)were high-school students not engaged in regular sports training, twelve (35 Yo)were
gymnasts (n 9) or figure-skaters (n 3) at elite national level, and ten (30 %) played soccer in
a team in the Finnish national league. None of the subjects followed a completely
vegetarian diet or was under treatment for a clinical eating disorder. Five subjects were
oligomenorrheic (4-9 menstrual cycles during the past year) and two (both aged 16 years)
had not reached menarche. Contraceptive pills were used by four subjects.
For the menstruating participants (n 32) the measurements were done within 14 d of the
start of a menstrual period. The measurements began, after an overnight fast, with BIA,
followed by DXA, anthropometry (weight, height, skinfolds) and UWW. Alternatively,
anthropometry and UWW were done before DXA. The subjects had a light breakfast (one
slice of bread with cheese and one glass of juice) immediately after BIA. All measurements
for each participant were finished within 4 h.
The characteristics of the participants were: mean age 17 (range 1620) years, height 1.65
(range 1.52-1.76) m, weight 5 5 4 (range 38.9-66-6) kg and BMI 20.6 (range 16.823.8) kg/m2. After being informed about the study, all subjects (or if under 18 years, their
guardian) signed a written informed consent. The study was approved by the ethical
committee of the UKK Institute for Health Promotion Research, Tampere, Finland.
Underwater weighing
Before UWW the subject was weighed on a high-precision scale (Sartorius F 150S-D2,
Goettingen, Germany) in a swimming-suit. Then the subject was submerged to her neck in
a sitting position and the residual lung volume (RV) was determined by the He-dilution
method, using a wet spirometer (Pulmonet 111, Sensormedics BV, Bilthoven, The
Netherlands). Two to four trials were performed to obtain two readings with less than
0.1 litres of difference. RV was the mean of these two values.
The scale for UWW (Tamtron Inc., Tampere, Finland) was connected via a 12-bit A/Dconverter (DT2801, Data Translation Inc., Marlborough, MA, USA) to a microcomputer
which continuously acquired weight values at 20 samples/s. The resolution was 2.4 g. A
dedicated software program was used to record the underwater trials and to calculate the
average weight for each trial. All weight measurements were visually verified. The subject
performed eight successive underwater trials in a sitting position after full exhalation
(presumably at RV) and the mean of the three trials giving the highest results was used in
further calculations. Air volume in the gastrointestinal tract was assumed to be 0 1 litres.
zyxwvu
zy
BODY COMPOSITION I N YOUNG WOMEN
795
zy
zy
Dual-energy X-ray absorptiometry
TBMC and BFYo were determined with a DXA scanner (XR-26, Norland Corp, Fort
Atkinson, WI, USA) that uses an X-ray tube operating at 100 kVp coupled with a
multistage K-edge samarinium filter. The two effective energies were 47 and 80 keV. Subject
position and scanning were done by the same operator and according to the manufacturer's
recommendations. The scan speed was 80 mm/s and resolution (pixel size) 6 5 x 13 mm'.
Duration of the scan was about 20 min. According to the manufacturer, the precision in
vivo of the TBMC measurements is 0.8 YO.TBMC and BF YOwere calculated from the scan
data by the Norland total body composition scan software (versions 2.2.2 and 1.1.4
respectively). The scanner was calibrated daily using a dedicated calibration standard.
Skinfold thickness
Using Harpenden calipers (British Indicators Ltd, Luton, Beds.), skinfold measurements
were taken from the following five sites (Harrison et al. 1991): triceps (posterior aspect of
the arm, at the midpoint between the lateral projection of the acromial process and the
inferior border of the olecranon process of the ulna), biceps (anterior aspect of the arm,
same level as triceps skinfold), subscapula (inferior to the inferior angle of the scapula, 45"
angle), suprailiac (horizontal skinfold at the midaxillary line immediately superior to the
iliac crest) and mid-thigh (midpoint between the inguinal crease and the proximal border
of patella). The right side of the body was used for all measurements. Three readings (to
the nearest 0.1 mm) from each site were obtained and the mean value was used in
calculations. One technician carried out all measurements.
Bioelectrical impedance
After an overnight fast and within 30 min of the last voiding, a standard whole-body rightsided tetrapolar BIA was performed using the RJL BIA-106 analyser (RJL Systems Inc.,
Detroit, MI, USA) with subjects in a supine position after a 15 min resting period. The
procedure was done as described by Lukaski et al. (1985).
zyxwv
zyxw
Calculation of percentage body fat
In addition to the data obtained using DXA software, BFYo was calculated from six
different equations :
(1) 3C model, used as the criterion method, with the Lohman (1986) equation:
BF YO= (6.386/Db + 3.961 BMF - 6.090) x 100,
where D, is body density (g/cm3) from UWW and BMF is body mineral fraction (kg),
calculated as (TBMC/(O.824 x body weight)).
(2) UWW (two-compartment model) with the Siri (1956) equation:
BF Yo = (4.95/Db - 4.50) x 100.
(3) Skinfolds,.,
D,
=
with the Jackson et al. (1980) equation:
1.0994921- 00009929 CS + 0.0000023 XS2-00000714 age,
where CS is sum of triceps, suprailiac and thigh skinfold thicknesses.
(4) Skinfolds,,
with the Durnin & Womersley (1974) equation:
D,
=
1.1549-0.0678 (lOgCS),
where CS is sum of triceps, biceps, subscapular and suprailiac skinfold thicknesses. BF YO
was calculated from D, with the Siri (1956) equation.
796
zyxwvut
zyxwvutsr
zyxwv
zyxw
zyx
G . M. FOGELHOLM A N D O T H E R S
(5) BIA,,,
with the Lukaski et al. (1986) equation:
FFM = 4.917+0.821 x height2/Ry
Height is expressed in cm.
where FFM is fat-free mass (kg) and R is resistance (0).
(6) BIA,,,
with the Deurenberg et al. (1990) equation:
FFM = 2580 x height2/impedance + 0.375 weight + 105 height -0.164 age -6.5,
where impedance = (resistance2+ reactance2)05. Height is expressed in m. BF YO=
((weight - FFM)/weight) x 100.
Statistical analyses
Method comparisons were done as recommended by Altman & Bland (1983). The
difference between the 3C and an alternative method was calculated by subtracting the 3C
result from the alternative result. The difference was considered significant when the 95 OO/
CI of the mean difference did not include the zero value. The statistical associations
between the magnitude of measurement (average of the 3C and alternative results) and
difference (alternative minus 3C), and between the 3C and alternative results were
calculated by Pearson product-moment correlations. Standard error of the estimate was
calculated as SEE = SD,, x (1 -r2)05, where SD,, is the SD of the 3C model and r is the
correlation coefficient between the 3C model and the alternative method (Clark et al. 1993).
BMDP Statistical Software (BMDP Statistical Software Inc., Los Angeles, CAYUSA)
(1990 version) was used for statistical analyses. The 95% CI for mean values and for
correlation coefficients were calculated according to Gardner & Altman (1989).
RESULTS
zyxwvu
zyx
Mean values, 95% CI for the mean and ranges for body density, TBMC, skinfold
thicknesses and impedance index (height'/resistance) are presented in Table 1. The mean
BF%, calculated by 3C, was 22.7, with a range from 13.5 to 31.1 (Table 2). The mean BF%
values of alternative methods varied between 17.2 (skinfolds,,)
and 30.0 (DXA). All
alternative methods were significantly different (P < 005) from the 3C model (Table 2).
However, the difference between UWW (two-compartments) and the 3C model was only
0-5 BF% (2.2%).
UWW gave higher results than the 3C model for the lean and lower results for the
normal-weight volunteers (Fig. 1 (a)) : the correlation coefficient between the magnitude of
measurement and the difference between the models was r -0.63 (95 YOCI : -0.37; -0.80,
P = 0.0001). The mean BF YOvalues for subjects with a 3C model result below 20 % were
166 and 16-2for UWW and 3C respectively. For subjects with a 3C result above 25 %, the
corresponding results were 27.1 and 29.1.
The difference between the 3C model and the skinfolds,,, and that between the 3C
model and the BIA,,, were also dependent on the magnitude of measurement: r -0.75
(95 YoCI: -0.87; -0.56, P < 0.0001) and -0.79 (95% CI: -089; -0.61, P < 0.0001) for
skinfolds,, and BIA,,, respectively (Fig. 1(b) and 1(c)). Although both correlations were
underprediction
negative, the relation to zero difference was dissimilar : for skinfolds,,,
was greater with increasing BF %, whereas for BIA,,,,
overprediction increased with
decreasing BF %.
The differencebetween the 3C model and DXA, skinfolds,,, or BIA,,, was independent
of the magnitude of the measurements (range of r values: O.OM.25, P = 0.14-0.76). Hence,
zy
zyxwvuts
797
B O D Y COMPOSITION I N Y O U N G WOMEN
Table 1. Body density, mineral content, skinfold thickness and bioimpedance values used in
the assessment of body composition in thirty-four young women
zyxwvuts
zyx
Mean
Underwater weighing
Body density (g/cm3)
DXA
TBMC (kg)
Body mineral fraction*
Skinfolds
Triceps (mm)
Biceps (mm)
Subscapula (mm)
Suprailiac (mm)
Midthigh (mm)
Bioimpedance
Height2/resistance
95% CI
Range
1.048
1.045; 1.051
1.03Cb1.067
2.614
5.69
2.500; 2.728
5.57; 5.81
1.693-3.21 1
4.92-6.29
13.3
6.6
10.3
7.4
22.6
11.7; 14.9
58; 7.4
9.3; 11.3
6.3; 8.5
20.4; 24.8
1.2-24-7
3.1-1 5.1
6.0-16.9
3.7-1 6.5
10.5-35.5
45.3
43.7; 469
32.4-54.3
zy
zy
TBMC, total bone-mineral content; DXA, dual-energy X-ray absorptiometry.
* Calculated as: (TBMC/(0424 x weight)) x 100.
Table 2. Body fat content (% body weight) in thirty-jiouryoung women: comparison of results
from the criterion method (three-compartment model (3C) with underwater weighing (UW W )
and dual energy X-ray absorptiometry (DXA)) and the alternatives: UWW, DXA, two
skinfold equations and two bioimpedance (BIA) equations
Mean
Body fat (%)
3c
UWW
DXA
Skinfolds,,,
Skinfolds,,
B%"K
BIADE"
Alternative minus 3C (BF YO)
uww*
DXA
Skinfolds,,,
Skinfolds,,*
BIALlJK
BIA,,,*
22.7
22.2
30.0
17.4
17.2
24.1
27.2
-0.5
7.3
- 5.3
- 5.5
1.5
4.5
95% CI
20.8 ; 24.6
20.1; 23.7
27.8; 32.2
15.9; 18.9
16-4; 18.0
22.3; 25.9
26.4; 28.0
Range
13.5-3 1.1
14.&307
17.0-41.6
10.1-283
12.3-2 1.9
14.0-307
22'3-30.9
zyxwvu
-1.0; -002
5.8; 8.8
-6.6; -4.1
-7.0; -4.0
0.1 ; 2.9
3.1 ; 5.9
- 3.1
to
-6.7 to
- 16.2 to
-15.8to
-11.0to
-39 to
+2.6
+I51
+2.8
+3'8
+103
+124
BF%, percentage body fat; JPW, equation of Jackson et al. (1980); DW, equation of Durnin & Womersley
(1974); LUK, equation of Lukaski et al. (1986); DEU, equation of Deurenberg et al. (1990).
* Difference was dependent on the size of measurement.
zyxwv
differences from the 3C model (overestimation by DXA and BIA,,,, underestimation by
skinfolds,,,) were of a similar magnitude in both lean and normal-weight subjects.
The correlation between the 3C model and UWW was strong with a small SEE (Table 2).
The correlations between the 3C and the remaining alternative methods (DXA, skinfolds,
BIA) were lower and the SEE larger.
798
zyxwvu
zyxwv
zyxwvutsrq
zyxwvu
zyxwvu
zyxwv
G . M. FOGELHOLM AND OTHERS
Table 3. Body f a t content (YObody weight) in thirty-four young women: correlations of the
criterion method (3-compartment model with underwater weighing ( U W W ) and dual energy
X-ray absorptiometry (DXA)) with alternatives: UWW, D X A , two skinfold equations and
two bioimpedance (BIA) equations
UWW
DXA
Skinfolds,,,
Skinfolds,,
B'AL",
BIAD,"
r
95% CI
0.96
0.74
0.68
0.62
0.68
0.66
0.92; 0.98
0.54; 0-86
0.44;0.83
0.36; 0.80
0.44; 0.83
0.41 ;0.82
SEE
(BF%)
1.49
3.57
3.89
4.17
3.89
3.96
zyxw
zyxwvutsr
SEE, standard error of the estimate; BF%, percentage body fat; JF'W, equation of Jackson et ul. (1980); DW,
equation of Durnin & Womersley (1974); LUK, equation of Lukaski et al. (1986); DEU, equation of Deurenberg
et al. (1990).
:/__c_c
12
3
0
-;I,,
-3
m.
,
,
,
-1 5
-1 8
20
25
30
35
10
15
Mean of two- and three-compartment
results (BF%)
c
-18'
10
1
15
20
25
30
35
Mean of skinfold- and
three-compartment results (BF%)
-9
'i -12
-15
zyxwvutsrq
c
E -18
a
m
10
15
20
25
30
35
Mean of MA- and threecompartment results (BF%)
Fig. 1 . Comparison between a three-compartment model and (a) a two-compartment model (underwater
weighing) ( y = 3.7-0.19x), (b) skinfolds (Durnin & Womersley, 1974) ( y = 12.6-0.91~)and (c) bioimpedance
(Deurenberg et al. 1990) ( y = 28.0-0.94~) for measuring body composition. The figure illustrates a significant
relationship between the difference of the methods (alternative minus the three-compartment model) and their
mean in thirty-four young women.
zyxw
zyxwvu
zyx
zyxw
BODY COMPOSITION IN Y O U N G WOMEN
DISCUSSION
799
zyx
zyx
Underwater weighing and dual-energy X-ray absorptiometry
A 3C model (fat, bone and fat-free soft tissue measured with UWW and DXA) for body
composition was used as the criterion to evaluate the relative accuracy of two laboratory
(UWW, DXA) and two ‘field’ methods (skinfolds, BIA). Most (65 %) of our subjects were
female athletes on a high national level. Overweight (BMI 2 25 kg/m2) subjects were
excluded.
The 3C model (Lohman, 1986), with body density measured by UWW and specific
adjustment for variation in TBMC, was chosen as the criterion. Nevertheless, the accuracy
of this method is dependent on several assumptions. Therefore, an individual’s true body
composition remains unknown even when such a multicompartment model is used.
RV was measured while the subject was in the water tank, but not simultaneously with
the weighing. Differences between the measured RV and the actual lung volume during the
weighing might cause errors in assessment of body composition. We tried to reduce this
error by taking the mean value of two to four RV measurements, and by using the three
highest underwater weights (with lung volume as close to RV as possible) in calculations.
It was not possible to measure total body water by stable-isotope techniques in the
present study. Consequently, we could not use a four-compartment model which might be
considered a limitation. Nevertheless, during certain periods in women’s life (early
adulthood, after the menopause), interindividual variation in TBMC is apparently the most
important source of bias in body composition assessment (Martin & Drinkwater, 1991;
Vogel & Friedl, 1992). Moreover, by timing the measurements according to the participants’
menstruation, we controlled for the episodic increases in total body water during different
phases of the menstrual cycle (Vogel & Friedl, 1992).
A matter of debate is whether bone (or body) mineral content should be related to body
weight (Lohman, 1986; Friedl et al. 1992) or to FFM (Wang et al. 1989; Snead et al. 1993).
The latter approach seems logical, because TBMC affects the density of FFM, which then
alters calculations of BF %. When FFM is used as a correction factor for UWW, FFM
should be measured with an alternative method, such as DXA (Snead et al. 1993).
However, because of the large difference between UWW and DXA results for BF % in the
present study, we were unwilling to express TBMC as a fraction of FFM,,,. If, as seemed
obvious, DXA overestimated BF %, FFM,,,
results would have been underestimations.
This would have increased the mineral fraction artifically and affected the accuracy of the
3C model.
The assumption that TBMC represents 82.4 % of total body minerals (Brozek et al. 1963)
is not necessarily correct. For instance, using neutron activation analysis, UWW and dualphoton absorptiometry, Heymsfield et al. (1989) found TBMC to be about 87 % of body
minerals. Moreover, the ratio between body and bone minerals is not essentially similar in
people with large differences in body frame. Unfortunately, we did not find a 3C model
with TBMC as a fraction of body weight. We considered the potential bias associated with
FFM,,, measurement to have a greater impact on the 3C model than the assumed ratio
between TBMC and true total body-mineral content.
The mean difference in BF% between UWW and the 3C model was rather small (0.5
percentage units or 2.2%). Nevertheless, we found an association between BF% and the
difference : compared with the 3C model, UWW showed a tendency to overestimate BF %
in lean and underestimate BF% in normal-weight subjects. This implies that the body
mineral fraction was smaller in lighter subjects.
Bunt et al. (1990) estimated the theoretical differences between models with and without
z
800
zyxwv
zyxwvuts
zyxw
zyxw
zyxwv
zy
G. M. F O G E L H O L M AND OTHERS
adjustment for bone minerals to be about 2.5 percentage units ( 5 4 % ) in those female
athletes whose bone density deviated most from the mean. Our divergence for the lean
subjects (0-65 percentage units) was smaller than found by Bunt et al. (1990) which might
be explained by the fact that they included subjects with secondary amenorrhoea.
There has been considerable interest concerning the validity of DXA in BF%
assessment. We found a large systematicdifference (overestimation) between DXA and the
3C model. Moreover, the random discrepancies (based on correlation and SEE for DXA
against the 3C model) were of similar magnitude as found for less expensive and faster field
methods, i.e. skinfolds and BIA. Hence, we do not regard DXA as superior to either of the
field methods in assessment of BF YO.
The difference between DXA and the criterion model (UWW, three or four
compartments) has been proposed to be due to several factors, including subjects’ sex, age,
BF% and the DXA instrument (manufacturer, version of software, X-ray spectrum,
calibration standards) used for measurement (Pritchard et al. 1993; Snead et al. 1993). The
number of method comparisons with Norland XR-26 is limited. Clark et al. (1993) found
XR-26 to overestimate BF% in adult males by 3.9 percentage units, with UWW as the
criterion. The large overestimation in the present study, independent of BF % within the
range of lean and normal-weight women, was in agreement with the apparent systematic
bias in Norland software converting the raw scan data to BF YO,
as suggested by Clark et
al. (1993). We are not aware of any technical explanations for this bias.
Skinfold thicknesses and bioelectrical impedance
The quadratic skinfold equations by Jackson et al. (1980) have been proposed to be the
most appropriate for field assessment of body composition in physically active women
(Wilmore, 1992; Webster & Barr, 1993). In comparison with UWW (Graves et al. 1987;
Clark et al. 1993; Eaton et al. 1993) or BIA (Graves et al. 1987; Eaton et al. 1993; Webster
& Barr, 1993), the equations by Jackson et al. (1980) appear to give lower BF % estimations
for females, thus agreeing with our results.
In contrast to our results, higher BF% estimations were obtained when Durnin &
Womersley (1974) equations were used against UWW or BIA in adult women (McNeill et
al. 1991; Pritchard et al. 1993). It is clear that the age of the subjects, different measuring
techniques and skinfold calipers affect the results. More interesting, however, was that the
two equations used in the present study showed a different association with the size of the
measurement. The skinfold sites of Durnin & Womersley (1974) did not include thigh,
which is an important fat store of women with normal or high fat mass.
Choice of the regression equation also affects BF% results obtained from BIA. A
difficulty when measuring women during their early adulthood is to choose between adult
and child equations. In the present study the sex-specific adult equation of Lukaski et al.
(1986) gave higher BF% values compared with all other methods except DXA and
BIA,,,. The child equation of Deurenberg et al. (1990) originated from girls aged 13-25
years, and from boys aged 1 6 2 5 years. The inclusion of age and sex (zero for girls) is
thought to adjust for variations in FFM hydration, distribution between intra- and
extracellular water and decreasing amounts of electrolytes in the tissues during maturation.
The present results suggest that the Deurenberg et al. (1990) equation ‘overadjusted’ for
effects of maturation in lean subjects, in particular.
Recently, Webster & Ban (1993) compared four different BIA equations to assess BF %
in female athletes aged 12-17 years. They found that an equation specific for children gave
higher values (25.2 YO)than the three other equations (17.5, 202 and 22.7 YO).
Three other
zyxwv
BODY COMPOSITION I N Y O U N G WOMEN
zyxw
zyxw
zy
801
comparisons between BIA from RJL Systems and the criterion (UWW) support our
findings on overprediction of BF% in lean women (Graves et ul. 1987; Gray et ul. 1990;
Pritchard et al. 1993).
zyx
zy
zyxwvut
zy
CONCLUSIONS
In the present study we compared two laboratory methods (VWWand DXA) and four
field methods (two skinfold and two BIA equations) to assess BF% against the 3C model
(fat, fat-free soft tissue, bone) in young, predominantly athletic women, with BF YOvalues
ranging from 13.5 to 31.3. We review our study with the following conclusions: (1) on
average, the difference between UWW and the 3C model was small. Compared with the 3C
model, DXA and both BIA equations clearly overestimated, and both skinfold equations
underestimated, BF%. Based on a signi6cant mean difference from the 3C model and a
large SEE, we do not regard DXA as superior to skinfolds or BIA to assess BF YO; (2) the
difference between the 3C model and three alternatives (VWW, skinfolds,, and BIA,,,)
correlated negatively with BF% (mean of the alternative and the 3C model). This
association induced an overestimation of BF% in the lean subjects (BIALuK),an
underestimation of BF % in normal-weight subjects (skinfolds,,),
or both (UWW).
Consequently, the use of these alternative methods instead of the 3C model would reduce
the obtained range of BF%. The discrepancy between the remaining alternatives (DXA,
skinfolds,,, and BIALUK)and the 3C model was independent of BF %.
The technical assistance of Ulla Hakala, Kirsti Malmivuo, Virpi Nieminen and Kirsi
Turtonen is highly appreciated.
zy
zyxw
zyxw
REFERENCES
Altman, D. G. & Bland, J. M. (1983). Measurement in medicine: the analysis of method comparison studies.
Statistician 32, 307-3 17.
Brozek, J., Grande, F., Anderson, J. T.& Kemp, A. (1963). Densitometricanalysis of body composition: revision
of some quantitative assumptions. Annals of the New York Academy ofSciences 110, 113-140.
Bunt, J. C., Going, S.C., Lohman, T. G., Heinrich, C. H., Perry, C. D. & Pamenter, R. W. (1990). Variation in
bone mineral content and estimated body fat in young adult females. Medicine and Science in Sports and
Exercise 22, 564569.
Clark, R. R., Kuta, J. M. & Sullivan, J. C. (1993). Prediction of percent body fat in adult males using dual energy
X-ray absorptiometry, skinfolds, and hydrostatic weighing. Medicine and Science in Sports and Exercise 25,
528-535.
Deurenberg, P., Kusters, C. S. L. & Smith, H.E. (1990). Assessment of body composition by bioelectrical
impedance in children and young adults is strongly age-dependent. European Journal of Clinical Nutrition 44,
261-268.
Durnin, J. V. G. A. & Womersley, J. (1974). Body fat assessed from total body density and its estimation from
skinfold thickness: measurements on 481 men and women aged from 16 to 72 years. British Journalof Nutrition
32, 77-97.
Eaton, A. W., Israel, R. G., OBrien, K. F., Hortobagyi, T.& McCammon, M. R. (1993). Comparison of four
methods to assess body cornposition in women. European Journal of Clinical Nutrition 41, 35s-360.
Friedl, K. E., DeLuca, J. P.,Marchitelli, L. J. & Vogel, J. A. (1992). Reliability of body-fat estimations from a
four-compartment model by using density, body water, and bone mineral measurements. American Journal of
Clinical Nutrition 55, 164-170.
Gardner, M. J. & Altman, D. B. (1989). Statistics With Conjdence- Conjdence Intervals and Statistical
Guidelines. London : British Medical Journal Publications.
Graves, J. E., Pollock, M. L. & Sparling, P.B. (1987). Body composition of elite female runners. International
Journal of Sports Medicine 8,96102.
Gray, D. S., Bray, G. A., Bauer, M., Kaplan, K., Gemayel, N., Wood, R., Greenway, F. & Kirk, S. (1990).
Skinfold thickness measurements in obese subjects. American Journal of Clinical Nutrition 51, 571-577.
Harrison, G. G., Buskirk, E. R., Carter, J. E. L., Johnston, F. E., Lohman, T.G., Pollock, M. L., Roche, A. F.
& Wilmore, J. (1991). Skinfold thicknesses and measurement technique. In Anthropometric Standardizarion
802
zyxwvutsr
zyxwv
zyxwvutsrq
zyxwvu
G. M. FOGELHOLM A N D OTHERS
Reference Manual, abridged edition, pp. 55-70 p.G. Lohman, A. F. Roche and R. Martorell, editors].
Champaign, IL: Human Kinetics.
Heymsfield, S. B., Wang, J., Kehayias, J., Heshka, S., Lichtman, S. & Pierson, R. N. Jr (1989). Chemical
determination of human body density in vivo: relevance to hydrodensitometry. American Journal of Clinical
Nutrition 50, 1282-1289.
Jackson, A. S., Pollock, M. L. &Ward, A. (1980). Generalized equations for predicting body density of women.
Medicine and Science in Sports and Exercise 12, 175182.
Lohman, T. G. (1986). Applicability of body composition techniques and constants for children and youth. In
Exercise and Sport Science Reviews, vol. 14, pp. 325357 [K. E. Randolf, editor]. New York: Macmillan.
Lukaski, H. C.,Bolonchuk, W. W., Hall, C. B. & Siders, W. A. (1986). Validation of tetrapolar bioelectric
impedance method to assess human body composition. Journal of Applied Physiology 60, 1327-1332.
Lukaski, H. C., Johnson, P. E., Bolonchuk, W. W. & Lykken, G. I. (1985). Assessment of fat-free mass using
bioelectrical impedance measurements of the human body. American Journal of Clinical Nutrition 41, 810-817.
McNeill, G., Fowler, P. A., Maughan, R. J., McGaw, B. A., Fuller, M. F., Gvozdanovic, D. & Gvozdanovic, S.
(1991). Body fat in lean and overweight women estimated by six methods. British Journal of Nutrition 65,
95-103.
Martin, A. D. & Drinkwater, D. T. (1991). Variability in measures of body fat. Assumptions or technique? Sports
Medicine 11, 277-288.
Mazess, R. B., Barden, H. S., Bisek, J. P. & Hanson, J. (1990). Dual-energy X-ray absorptiometry for total-body
and regional bone-mineral and soft-tissue composition. American Journal of Clinical Nutrition 51, 1106-1 112.
Pritchard, J. E., Nowson, C. A., Strauss, B. J., Carlson, J. S., Kayamakci, B. & Wark, J. D. (1993). Evaluation
of dual energy X-ray absorptiometry as a method of measurement of body fat. European Journal of Clinical
Nutrition 47, 216-228.
Sin, W. E. (1956). The gross composition of the body. In Advances in Biological and Medical Physics, pp. 239-280
[C. A. Tobias and J. H. Lawrence, editors]. New York: Academic Press.
Snead, D. S., Birge, S. & Kohrt, W. M. (1993). Age-related differences in body composition by hydrodensitometry
and dualenergy X-ray absorptiometry. Journal of Applied Physiology 14, 770-775.
Suominen, H. (1993). Bone mineral density and long term exercise. An overview of cross-sectionalathlete studies.
Sports Medicine 16, 316330.
Vogel, J. A. & Friedl, K. E. (1992). Body fat assessment in women. Special considerations. Sports Medicine 13,
245-269.
Wang, J., Heymsfield, S. B., Aulet, M., Thornton, J. C. & Pierson, R. N. Jr (1989). Body fat from body density:
underwater weighing vs. dual-photon absorptiometry. American Journal of Clinical Nutrition 256,E82sE834.
Webster, B. L. & Barr, S. I. (1993). Body composition analysis of female adolescent athletes: comparing six
regression equations. Medicine and Science in Sports and Exercise 25, 648-653.
Wilmore, J. (1992). Body weight and body composition. In Eating, Body Weight and Performance in Athletes, pp.
77-93 [K. D. Brownell, J. Rodin and J. H. Wilmore, editors]. Philadelphia: Lea & Febinger.
zyxwvuts
zyx
zyxwv
zyxw
Printed in Great Britain