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Children's Health and Exercise Research Centre, University of Exeter, Exeter EX1 2LU, United Kingdom
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ABSTRACT |
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The influence of
gender, growth, and maturation on peak
O2 consumption
(
O2 peak)
in 11-13 yr olds were examined by using multilevel regression
modeling. Subjects were 119 boys and 115 girls, aged 11.2 ± 0.4 (SD) yr at the onset of the study. Sexual maturation was
classified according to Tanner's indexes of pubic hair.
O2 peak was
determined annually for 3 yr. The initial model identified body mass
and stature as significant explanatory variables, with an additional
positive effect for age and incremental effects for stage of
maturation. A significant gender difference was apparent with lower
values for girls, and an age-by-gender interaction indicated a
progressive divergence in boys' and girls'
O2 peak. Subsequent
incorporation of the sum of two skinfold thicknesses into the model
negated stature effects, reduced the gender term, and explained much of
the observed maturity effects. The body mass exponent almost doubled,
but the age-by-gender interaction term was consistent with the initial model.
aerobic fitness; growth; maturation; multilevel modeling; gender
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INTRODUCTION |
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AEROBIC FITNESS SERVES as a functional index of the
pulmonary, cardiovascular, and hematologic components of oxygen
delivery and the oxidative mechanisms of the exercising muscles. Peak
oxygen uptake
(
O2 peak), the highest
oxygen uptake elicited during an exercise test to exhaustion, is
recognized as the best single indicator of young people's aerobic
fitness (4). However,
O2 peak is highly
correlated with body size, and, for the effects of chronological age,
maturation, and gender on
O2 peak to be
elucidated, the confounding influence of body size must be accounted
for. Inappropriate analyses have clouded our understanding of growth
and maturational changes in
O2 peak (4, 5).
Although always controversial (32), the expression of
O2 peak in simple ratio
to body mass to account for body size differences has been, and to a
large extent remains (20), the method of choice for normalizing
O2 peak data. However,
the recent literature reflects a resurgence of interest in issues
concerning the validity of ratio scaling and the discussion of
alternative means for controlling for body size differences. There is
accumulating evidence to refute the validity of conventional ratio
methods derived from both convincing theoretical and statistical
arguments and empirical evidence that demonstrates the failure of per
body mass ratios to produce a size-independent exercise variable (4,
5). Scaling techniques based on allometric principles have been shown
to produce size-free performance measures when applied to data derived
from young people, have yielded mass exponents less than the value of
1.0 assumed by the simple ratio method, and in cross-sectional studies
have produced results that challenge conventional interpretations of the growth and maturation of
O2 peak (7,
34).
The application of allometric techniques to the interpretation of
longitudinal data is not straightforward and may provide an incomplete
interpretation of the performance measure under investigation. Two
recent studies (15, 27) have employed an ontogenetic allometric
approach (19), in which individual body mass exponents are calculated
from each subject's longitudinal body
mass-
O2 peak regression
relationship. Individual values may be averaged subsequently to
describe, for example, gender- or maturity-specific group exponents.
This approach has been criticized on the basis that the interpretation
of within-individual and between-group responses requires a
statistically inefficient two-stage process (25). Moreover, as the
longitudinal analysis centers on describing the body
mass-
O2 peak
relationship, limited information is gained regarding the nature or
magnitude of the pattern of change in aerobic fitness.
Two studies have applied one or both of the theoretically proposed mass
exponents of 0.67 and 0.75 (28) to examine the longitudinal tracking of
and age-related changes in
O2 peak (21, 27). Although individual cross-sectional studies in large, homogeneous subject populations have derived mass exponents approximating these
values (1, 7), there is considerable evidence to show that exponents
are highly sample specific (5), often deviating markedly from
theoretical expectations, particularly in small samples. Although
producing results that may better reflect underlying changes, the
application of a theoretical exponent may not provide an accurate
representation of true longitudinal changes within a given subject group.
Few longitudinal studies have considered the influence of covariates
other than body mass despite indications from cross-sectional studies
in both adults and young people that factors such as stature and body
fatness may be significant independent predictors (20, 24). Neither has
the separate influence of age vs. maturity on the growth of
O2 peak been elucidated
comprehensively, in part because of the limitations of traditional
analytic techniques.
Multilevel regression modeling (18) is a statistical technique that enables a flexible and sensitive interpretation of longitudinal data while avoiding many of the pitfalls associated with the analyses described above. In contrast to traditional analytic approaches, multilevel modeling not only describes the underlying population mean response but also recognizes and describes variation around the group mean. Furthermore, both the number of observations per individual and the temporal spacing of the observations may vary within a multilevel analysis as individual growth trajectories are modeled.
In a reanalysis of the data from a longitudinal study of
O2 peak in young elite
athletes (12), Nevill et al. (25) used an allometric approach within a
multilevel regression analysis to demonstrate age and, in boys,
maturational, influences on
O2 peak that were over
and above those explained by the overall increase in body size.
Unfortunately, the participation of boys and girls in different sports
precluded a detailed examination of differential growth between the
genders. The present study sought to extend our understanding of the
development of aerobic fitness by using a multilevel regression
modeling approach to interpret chronological age-, gender-, and
maturity-associated changes in
O2 peak in a healthy,
untrained population of subjects tested for three consecutive years,
commencing at a mean age of 11.2 yr.
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METHODS |
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Subjects.
All of the children in year 6 (age
10-11 yr) of the 15 state schools in the city of Exeter, United
Kingdom, were invited to participate in a longitudinal study of
physical activity patterns, physiological responses to exercise, and
body composition. Some 745 children (70% of those eligible)
volunteered, and written consent was obtained from both the children
and their parents and/or guardians. The project received ethical
approval from the Exeter District Health Authority Ethical Committee.
In an attempt to detect sample bias, the stature and body mass of the
volunteers were compared with the stature and body mass of those who
declined to participate. No significant difference
(P > 0.05) was detected in either
gender. Twenty-five percent of the eligible children in each school
were randomly selected from those who volunteered. Previous
publications have described the
O2 peak of boys and girls who were prepubertal in the first year of the project (1) and
analyzed cross-sectional changes in
O2 peak by maturity group by using data from the second year of the project (7). The
present study involves a longitudinal analysis of the development of
O2 peak during the
first 3 yr of the study. The subject sample thus comprises those young
people who satisfactorily completed the
O2 peak test and
associated anthropometric measures and for whom maturity assessments
were available. Subject numbers for year
1 are n = 119 boys, n = 115 girls;
year 2,
n = 94 boys, n = 88 girls; and
year 3,
n = 93 boys,
n = 81 girls. There were no
significant differences (P > 0.05)
between those who failed to return for a subsequent test occasion and
the rest of the group on key measures including stature, body mass,
skinfold thicknesses, hemoglobin concentration, and
O2 peak.
Experimental methods. Age was computed from date of birth and date of examination. Anthropometric apparatus was calibrated according to the manufacturers' instructions. Stature was measured by using a Holtain stadiometer (Holtain, Crymych, Dyfed, UK), body mass was determined by using Avery beam balance scales (Avery, Birmingham, UK), and skinfold thickness over the triceps and subscapular regions was measured by using Holtain skinfold calipers (Holtain) according to the techniques described by Weiner and Lourie (33). Sexual maturity was visually assessed by using Tanner's indexes for pubic hair development (31). Anthropometric and maturity measures were taken once on each measurement occasion due to time and ethical restrictions. However, the same trained research team made the anthropometric measures and the same trained research nurse made the maturity assessments throughout the duration of the study. Blood hemoglobin concentration was determined from duplicate fingertip blood samples. Blood samples were immediately assayed by using a HemoCue Photometer (Clandon Scientific, Farnborough, UK), which was calibrated against a control cuvette before each measurement.
The children had visited the laboratory on several occasions and were habituated to both the general environment and the experimental procedures. After a 3-min warm-up at 1.67 m/s (6 km/h),
O2 peak was
determined during an incremental treadmill running test on a motorized
treadmill (Woodway, Cranlea Medical, Birmingham, UK). Belt speed was
increased to 1.94 m/s (7 km/h, year
1) or 2.22 m/s (8 km/h, years
2 and 3) for the
initial stage and then increased by 0.28 m/s (1 km/h) for each 3-min
stage until a speed of 2.78 m/s (10 km/h) was reached. Subsequently,
belt speed was held constant, and the gradient was increased by 2.5%
each stage for further increments. A 1-min rest period separated the
exercise stages. The test was continued to voluntary exhaustion. If the
young person showed signs of intense exertion (hyperpnea, facial
flushing, unsteady gait, sweating) and if his or her heart rate had
reached a value within 5% of age-predicted maximum or the respiratory exchange ratio was at least 1.0, the
O2 peak attained was
accepted as a maximal index. All subjects included in this paper
satisfied these criteria on all test occasions.
Throughout the test expired gases were monitored continuously by using
an Oxycon Sigma on-line gas-analysis system (Cranlea Medical), which
was calibrated before each test by using gases of verified
concentration. Heart rate was monitored by using an electrocardiograph
(Rigel, Morden, UK).
Statistical methods.
Descriptive statistics (means and SDs) for anthropometric variables,
blood hemoglobin concentration, and
O2 peak were computed for subjects on the first test occasion. Gender differences within each
year of the study were calculated by using analysis of variance.
O2 peak
(gender and maturity), adjusted for differences in anthropometric measures and age, were investigated by using the multilevel modeling program MLwiN (17). Multilevel modeling is an extension of multiple regression, which is appropriate for analyzing hierarchically structured data. In longitudinal data sets the hierarchy can be seen as
the repeated-measurement occasions (defined as level
1 units), grouped within the individual subject
(defined as the level 2 unit).
Multilevel modeling is preferable to traditional analytic approaches
(e.g., repeated-measures analysis of variance) for longitudinal data
as, in addition to describing the population mean response, this method
recognizes and describes variation around the mean at both levels. For
example, at level 2, individuals are
allowed to have their own growth rates, which vary randomly around the underlying population response and, at level
1, each individual's observed measurements may vary
around his or her own growth trajectory. Furthermore, in contrast to
traditional methods that require a complete longitudinal data set, both
the number of observations per individual and the temporal spacing of
the observations may vary within a multilevel analysis as individual
growth trajectories can be modeled.
In this study a multiplicative, allometric approach was adopted on the
basis of the model proposed by Nevill and associates (25) as follows
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(which varied
randomly at level 1). Subscripts
i and
j denote random variation at
levels 1 and
2, respectively. The variable
"age" was centered around the group mean age of 12.0 yr.
This model can be linearized by logarithmic transformation and
multilevel regression analysis on
loge(y)
used to solve for the unknown parameters. Once transformed, the
equation above becomes
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O2 peak differed for
boys and girls. Age was also allowed to vary randomly at
level 1 to investigate
within-individual variation around the individual growth trajectory.
The need to allow each individual his or her own mass exponent was
examined by letting body mass vary at level
2.
As demonstrated for cross-sectional data (34), this multiplicative,
allometric modeling approach has been shown to be theoretically and
statistically superior for longitudinal analyses (25) to an additive,
polynomial model (12) as the former accommodates the skewness and
heteroscedasticity that often characterize size-related exercise
performance data (34).
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RESULTS |
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The subjects' physical characteristics in each year of the study are
presented in Table 1. There were no
significant (P > 0.05) gender
differences in age, body mass, stature, or hemoglobin concentration at
any point of measurement. Boys had significantly higher
(P < 0.001)
O2 peak than did girls
on each measurement occasion. The sum of skinfolds for boys was
significantly lower (P < 0.05) than
that for girls on the first two measurement occasions.
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The results of the initial modeling of
O2 peak over the three
measurement occasions are presented in Table
2. In this model, mass and
stature proved to be significant covariates with exponents of 0.48 ± (SE) 0.03 and 0.81 ± 0.12, respectively. There was
a significant positive effect for age that was larger for boys than girls, as indicated by the significant age-by-gender interaction term
that would be deducted from the age term for the girls. A small but
significant term for age squared was also identified for both genders,
although girls'
O2 peak was
shown to be significantly lower than that for boys' as reflected by
the negative term for gender (
0.15 ± 0.01). In addition to
these anthropometric, age, and gender effects, there was an incremental
effect of maturation that was consistent for boys and girls. The
maturity-by-gender effects investigated are not included in Table 2 as
they were nonsignificant throughout all models.
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These fixed estimates describe the population mean response, whereas
the random parameters describe variation around this response at both
level 1 (within individuals) and at
level 2 (between individuals); i.e.,
these parameters reflect the variance that remains unaccounted for by
the fixed part of the model. Within model
1 there was significant random variation at
level 2 for age, reflecting
differential individual growth rates in
O2 peak. Allowing each
individual his or her own mass exponent proved unnecessary as there was
no random variation between individuals around the fixed (mean) parameter.
The independent effect of introducing the sum of two skinfold thicknesses into the model was examined, with the results summarized in Table 2, model 2. The addition of skinfolds to the baseline model rendered the stature and age squared terms nonsignificant and reduced the magnitude of the gender term, whereas the mass exponent was almost doubled to a value of 0.86 ± 0.03. Inclusion of skinfolds also explained much of the observed maturity effects, with the parameter estimates for maturity stages 3-5 almost halved. Furthermore, the addition of this measure of body fatness explained a considerable proportion of the remaining level 2 (between-individuals) variance associated with the constant in model 1; i.e., the estimate was reduced from 0.0042 ± 0.0005 to 0.0029 ± 0.0004.
Blood hemoglobin concentration was introduced as an additional explanatory variable, but a nonsignificant parameter estimate was obtained.
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DISCUSSION |
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The
O2 peak data in
liters per minute are in accordance with the extant literature (4). The
present data, however, offer further insights into the growth of
O2 peak, with
body size appropriately accounted for. The conventional interpretation
of
O2 peak
"corrected" for body mass
(ml · kg
1 · min
1)
is that, during the teen years, boys' values remain remarkably consistent, whereas girls' values progressively decline (4). However,
although it has been argued that there is no need to abandon the use of
the above-mentioned unit of measure to normalize
O2 peak for body size
(29), the recent literature reflects a growing awareness of the
theoretical and statistical limitations of this approach (4, 20).
There is increasing empirical evidence to refute the
assumption that scaling
O2 peak to a mass
exponent of 1.0 produces a size-free variable (1, 7, 21, 34), and
theoretical arguments based on considerations of geometric similarity
or surface law predict that
O2 peak should scale to
mass raised to the power 0.67 (28). Nevertheless, when
O2 peak is modeled in subject groups heterogeneous for factors such as body size and age,
several studies have reported mass exponents close to the power 0.75 (20). The numeric value of an alternative "universal" or
"true" mass exponent for normalizing
O2 peak has therefore been the focus of much debate in exercise science (5), but few studies
have considered the likelihood that the value of the mass exponent is
dependent on not only sample size (4, 5) and homogeneity (20) but also
the effect of other confounding covariates. For example, with stature
included as an additional covariate the value of the mass exponent has
been reduced in several data sets (20, 34). Conversely, inclusion of a
measure of body fatness tends to raise the value of the mass exponent
(21). The present study demonstrates these effects clearly. When, for illustrative purposes, the data in the present study were analyzed with
mass as the sole body size variable, a mass exponent of 0.67 ± (SE)
0.03 was obtained, reflecting the values reported in cross-sectional investigations of these children at prepuberty (1) and 12 yr of age
(7). The value of the mass exponent decreased to 0.48 ± 0.03 with
the addition of stature (model 1)
and increased to 0.86 ± 0.03 when a measure of body fatness was
incorporated (model 2), illustrating
the interdependence of covariates and supporting the view that a lack
of statistical control over known covariates is a factor underlying the
variability in reported mass exponents (20). These findings also
illustrate that it is inappropriate to assume that scaling to either
the traditional per body mass ratio or to one of the theoretical mass
exponents (i.e., 0.67 or 0.75) will control adequately for body size
differences in children and adolescents.
Welsman et al. (34) used log-linear analysis of covariance to partition
out body size from
O2 peak in groups of
preteen and teenage boys and girls and adult men and
women. These data challenged the conventional
interpretation of
O2 peak during growth
by demonstrating that
O2 peak increases
progressively in boys from prepuberty through puberty into adulthood,
whereas in girls increases are observed from prepuberty into puberty
with no significant decline into adulthood (34). Subsequently, the same
group examined the relationship between maturation and
O2 peak, with body mass
controlled by using allometry (7). Twelve-year-old boys and girls were
classified into maturity stages
1-4 (31), and the results demonstrated significant
increases in
O2 peak across maturity stages that were over and above the changes
attributable to increased body mass alone (7). These maturational
effects had been masked in previous cross-sectional studies by the use of the ratio standard
(ml · kg
1 · min
1)
to partition out body-size effects (10, 17). The present study has
sought to further clarify age, growth, and maturity effects on
O2 peak in boys and
girls studied longitudinally by using appropriate multilevel regression
modeling techniques.
Most longitudinal studies have analyzed age-, growth-, or
maturity-associated changes in
O2 peak by correcting
data for a single body-size indicator within each analysis, usually
body mass (15, 27) or anthropometrically predicted lean body mass (21,
27). However, a more comprehensive understanding of developmental changes in
O2 peak
should ideally investigate simultaneously the influence of other known
covariates. For example, despite valid concerns regarding issues of
collinearity among covariates (11), stature has been shown to be a
significant, independent predictor of
O2 peak in
both adults and young people when incorporated alongside mass in an
allometric analysis (20, 25, 34). This was confirmed in the baseline
model presented here (Table 2, model
1) with a significant exponent for stature of 0.78 ± 0.12.
The addition of the sum of two skinfolds (Table 2, model 2) to the baseline model made the terms for both stature and age squared redundant. Incorporating this measure of body fatness also explained a large proportion of the observed maturity effects, with the magnitude of the effect increasing with progression through maturational stages. A similar effect was observed when the development of mean power obtained during a Wingate Anaerobic Test in 12-13 yr olds from the present population (9) was modeled. In the present study, differences in skinfold thickness also explained part of the gender difference observed in addition to a considerable proportion of the residual between-individual variance (level 2).
Studies investigating age, growth, and maturational changes in the body
mass-
O2 peak
relationship by using ontogenetic allometry (15, 27) have noted extreme
variability in individual mass exponents with, for example, values
ranging from 0.18 to 1.74 in one study (27). The flexibility of the
multilevel modeling procedure used in the present study enables the
underlying mean response to be described while concurrently allowing
individuals to have their own mass exponent. The need for this was
examined by fitting a random component for mass at
level 2 of the analysis (i.e., between
individuals). When this was done, however, the model failed to
converge, indicating that the fixed (mean) parameter adequately
described this population. Individual variation in overall growth rates
was evident, as indicated by the significant random variance
at level 2 associated with the age
term. The variability in overall rates of change in
O2 peak during the 3 yr
of this study is clearly evident from the individual growth
trajectories illustrated in Fig. 1.
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The data from the first year of the study support evidence of gender
differences in
O2 peak
at age 11 yr (4). In fact, a significant gender difference in
O2 peak was
demonstrated even when prepubescent girls
(n = 53) and boys
(n = 111) were compared, and with this
subsample there was no significant gender difference in skinfold
thicknesses (1). Explanations for girls' lower
O2 peak at a
young age are speculative but the lower values may be due to a lower
exercise stroke volume than in boys. Boys have consistently
demonstrated higher stroke volumes than girls at the same submaximal
oxygen uptake or exercise intensity, although differences have been
small and in some cases statistically insignificant (26). Comparative
data at
O2 peak appear
to be limited to one published study (23), which, by using carbon
dioxide rebreathing, reported boys' stroke index to be 15% higher
than those in girls at 9-10 yr of age and 5% higher at 11-12
yr of age. However, recent work by Rowland (26), using Doppler
echocardiography, provides supportive data, with 12-yr-old boys
reported to have 13% higher maximal stroke indexes relative to lean
body mass than similarly aged girls.
The results of the multilevel regression models examined here confirm
previous cross-sectional indications (34) in showing increases in
size-related
O2 peak
that contrast with conventional interpretation of
O2 peak
during growth (4). Furthermore, the significant age-by-gender
interaction term in the present data set indicates a progressive
divergence in boys' and girls' values over the age range examined.
The increasing gender difference in
O2 peak during
childhood and adolescence has been attributed to the greater
accumulation of body fat in relation to body mass in girls, boys'
higher hemoglobin concentration, and girls' lower levels of habitual
physical activity (4).
The addition of the sum of skinfold thicknesses to the baseline model reduced the magnitude of the gender term. This may be reflective of boys' relatively greater increase in muscle mass, which would not only facilitate the use of oxygen during exercise but may also supplement the venous return to the heart and therefore augment stroke volume, through the peripheral muscle pump (6, 26).
During puberty there is a marked increase in hemoglobin concentration
and hence oxygen-carrying capacity in boys, whereas girls' values
plateau (16). It might therefore be expected that differences in
hemoglobin levels between boys and girls would be a contributory factor
to the observed gender difference in
O2 peak, and this has
been demonstrated with 14 and 15 yr olds (10). Hemoglobin levels were
determined routinely in the present study at each laboratory visit,
but, when investigated as an additional explanatory variable, a
nonsignificant parameter estimate was obtained with these 11-13 yr
olds. This is not an unexpected finding given the minimal change in
hemoglobin concentration across the 3 yr of observation in both boys
and girls (see Table 1).
Boys have been consistently demonstrated to have higher levels of
habitual physical activity than girls, but the evidence relating
habitual physical activity to
O2 peak is
conflicting (5). In parallel studies the physical activity patterns of the present children were monitored over 3 days, using continuous heart
rate monitoring, and no significant relationships were detected between
O2 peak and heart rate
indicators of level of physical activity in either the first (3) or
second year (8) of the study. In a multilevel regression analysis of
the 3-yr heart rate data,
O2 peak was examined as
an additional explanatory variable, but a nonsignificant parameter
estimate was obtained (2). Habitual physical activity is unlikely to
influence children's and adolescents'
O2 peak
because such activity typically lacks the intensity and duration
sufficient to improve aerobic fitness (5).
In the exercise sciences, maturity is usually assessed by using
indicators of skeletal, somatic, or sexual maturity. Although no single
assessment gives a complete description of the tempo of maturation,
there is a high concordance among the aforementioned indicators (13).
Previous studies have revealed that skeletal age adds little to the
description of physiological variables yielded by chronological age and
body size (30). Beunen and Malina (14) reviewed the literature
concerning
O2 peak and the adolescent growth spurt, commented that the available data should
be interpreted with caution, and concluded that the evidence suggests a
spurt in
O2 peak in
boys that reaches a maximum gain at the time of peak height velocity,
but secure data are insufficient to offer any generalization for girls.
Few longitudinal studies have investigated the influence of maturity,
independent of body size, on
O2 peak. Baxter-Jones
et al. (12) used an additive polynominal model within a multilevel
regression structure. They assessed maturity by using secondary sexual
characteristics (31) and reported that, in athletic boys, there was a
significant increase in
O2 peak toward the end
of puberty that was in direct contrast to the nonsignificant increase
in
O2 peak
found in athletic girls during this time. The authors attributed this
additional increase in
O2 peak partially to
the boys' trained status. Using stature velocity as an indicator of
maturity status and analysis of covariance to control for body mass,
Malina et al. (22) observed similar results with children from a sports
school. In the present study of untrained boys and girls, maturity
positively affected
O2 peak in both
genders, and an additional effect of chronological age indicated the
importance of incorporating both age and maturity into analyses of
O2 peak during growth
and maturation.
In summary, the multilevel modeling approach has revealed age, gender,
and maturity effects, independent of body size, on the
O2 peak of untrained
boys and girls. These effects may have been masked in previous studies
by the inappropriate use of
O2 peak in ratio to
body mass and/or the failure to consider the impact of covariates other
than body mass. Physiological explanations for these effects cannot be
established fully by the present data set, but it appears that gender,
age, and maturity differences in the increase in fat-free mass relative
to body mass are the predominant influences on the differential growth
of boys' and girls'
O2 peak in 11-13
yr olds.
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ACKNOWLEDGEMENTS |
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We gratefully acknowledge the technical assistance of Jenny Frost, Alison Husband, and Sue Vooght.
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FOOTNOTES |
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The work was supported by the British Heart Foundation and the Healthy Heart Research Trust. Alan Nevill is with the School of Human Sciences, Liverpool John Moores University, Liverpool, UK.
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. §1734 solely to indicate this fact.
Address for reprint requests and other correspondence: N. Armstrong, Children's Health and Exercise Research Centre, Univ. of Exeter, Heavitree Rd., Exeter, EX1 2LU, UK (E-mail: N.Armstrong{at}exeter.ac.uk).
Received 27 April 1999; accepted in final form 10 August 1999.
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