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obesity reviews doi: 10.1111/j.1467-789X.2007.00455.x
1
Institute of Sports Medicine, Peking Summary
University Third Hospital, 2Ba Yi Middle The aim of this paper was to study the effect of long-term supervised exercise-
School, Beijing, China induced weight maintenance on metabolic risk factors and physical fitness in
obese children in early puberty. A total of 49 obese children aged 12–14 years
Address for correspondence: C Chang, were divided into control and exercise groups. The children in the exercise group
Institute of Sports Medicine, Peking University accepted exercise intervention supervised by a professional sports teacher for 9 of
Third Hospital, Beijing 100083, China. E-mail: the 12 months. All participants in both groups received health education once
cuiqingchang@yahoo.com.cn every 3 months. Anthropometry and fasting serum lipids, glucose, insulin and
homeostatic model assessment for insulin resistance (HOMA-IR) were measured
at months 0, 3, 9, 12 of the intervention. Physical fitness was determined before
and after intervention. After the intervention (i) BMI was reduced by 0.6
(P < 0.05) in the exercise group, but increased by 0.5 (P < 0.05) in the control
group, compared with the pre-intervention level at the end of 9-month interven-
tion; (ii) Triglyceride levels in the exercise group significantly decreased by 23.1%
by 3 months (P < 0.05), and by 30.2% after 9 months (P < 0.05), but increased by
50% (P < 0.05) in the control group; high density lipoprotein-cholesterol
(HDL-C) decreased more by 35% (P < 0.05) in the controls than in the exercise
group (P < 0.05); (iii) Fasting serum glucose, insulin level and HOMA-IR
decreased, respectively, by 23.1%, 36.6% and 48.5% in the exercise group at
9 months (P < 0.05), whereas glucose levels increased by 10.9% (P < 0.05) in the
control group; (iv) Exercise performance, such as upper- and lower-limb strength,
flexibility and endurance, were enhanced by 17.9%, 12.3%, 22.3% and 20.4%
(P < 0.01), respectively and (v) At 12 months, i.e. 3 months after terminating the
supervised exercise, serum triglycerides, glucose, insulin and HOMA-IR level all
returned to the pre-intervention level. Supervised decrement exercise can effec-
tively slow the progress of obesity, improve insulin sensitivity and metabolic risk
factors, but once the supervised exercise is stopped, the health benefits weaken or
vanish. The key to helping these obese children is for them to cultivate good
exercise habits which are sustained throughout their lives.
Exercise
M 19 12.5 ⫾ 0.61 166.2 ⫾ 9.33 77.9 ⫾ 14.14 27.7 ⫾ 3.43
F 6 12.8 ⫾ 1.17 161.3 ⫾ 3.33 69.8 ⫾ 7.10 26.9 ⫾ 3.52
M+F 25 12.6 ⫾ 0.76 165.0 ⫾ 8.45 75.8 ⫾ 13.06 27.5 ⫾ 3.39
Control
M 17 12.3 ⫾ 0.77 162.4 ⫾ 6.87 72.8 ⫾ 13.89 27.4 ⫾ 3.58
F 7 12.9 ⫾ 0.38 158.6 ⫾ 3.78 66.0 ⫾ 6.04 26.2 ⫾ 2.26
M+F 24 12.2 ⫾ 0.07 161.5 ⫾ 6.43 71.3 ⫾ 12.75 27.1 ⫾ 3.32
Time (months) Exercise intensity Exercise mode Exercise duration Exercise frequency Exercise period
(min) (days per week) (weeks)
(a) (b)
Exercise Control Exercise Control
84.0
172.0
82.0
170.0
80.0
166.0 76.0
74.0
164.0
72.0
162.0
70.0
160.0 68.0
158.0 66.0
64.0
156.0
0 3 9 12
0 3 9 12
Intervention time (months) Intervention time (months)
(c) (d)
Exercise Control Exercise Control
28.4 93.0
91.0
27.8 90.0
27.6
89.0
27.4
27.2 88.0
27.0 87.0
26.8 86.0
26.6 85.0
26.4 84.0
26.2 0 3 9 12
0 3 9 12
Intervention Time (months)
Intervention time (months)
(e)
35.0 Exercise Control
Body Fat Percentage (%)
34.0
33.0
32.0
31.0
30.0
29.0
28.0
27.0
0 3 9 12
Figure 1 Anthropometric parameters in obese children (n = 25 in the exercise group, n = 24 in the control group) undergoing a 9-month supervised
exercise intervention and a subsequent 3-month post-exercise assessment. (a) Height; (b) Body weight; (c) Body mass index; (d) Waist
circumference; (e) Body fat percentage.
3-month intervention and to 0% at 9 months in the exer- to 29.4% over the whole 12-month period in the control
cise group, but increased from 18.2% before intervention group (Fig. 2).
to 25% at 9 months in the control group, i.e. double that of Three months after terminating the supervised exercise,
the exercise group (Fig. 2). The prevalence of high-fasting serum TG, glucose, insulin and HOMA-IR level, as well
serum glucose (ⱖ5.6 mmol L-1) decreased from 23.5% as the prevalence of hypertriglyceridema and hyperglyce-
before intervention to 9% at 3 months and to 0% at mia, all returned to the pre-intervention levels (Table 3,
9 months in the exercise group, but increased from 23.1% Fig. 2).
Table 3 Fasting serum lipids, glucose, insulin levels and HOMA-IR in obese children either in a control group or a group undergoing a 9-month
exercise intervention and then 3 months after terminating the exercise
Triglycerides (mmol L-1) Exercise 1.3 ⫾ 0.67ab 1.0 ⫾ 0.60c 0.9 ⫾ 0.29c 1.5 ⫾ 0.73b
Control 1.0 ⫾ 0.50 1.5 ⫾ 0.67a
Total cholesterol (mmol L-1) Exercise 4.1 ⫾ 0.64 4.19 ⫾ 0.62 3.89 ⫾ 0.53 4.55 ⫾ 0.73
Control 4.3 ⫾ 0.84 4.5 ⫾ 0.72
LDL-C (mmol L-1) Exercise 2.4 ⫾ 0.62 2.7 ⫾ 0.55 2.4 ⫾ 0.52 2.7 ⫾ 0.73
Control 2.7 ⫾ 0.82 3.3 ⫾ 0.81
HDL-C (mmol L-1) Exercise 1.3 ⫾ 0.17 1.3 ⫾ 0.16 1.3 ⫾ 0.18 1.6 ⫾ 0.42*
Control 1.4 ⫾ 0.32 0.9 ⫾ 0.29a
Blood glucose (mmol L-1) Exercise 5.2 ⫾ 1.04a 5.0 ⫾ 0.28a 4.0 ⫾ 0.31b 5.4 ⫾ 0.65a
Control 4.6 ⫾ 0.80 5.1 ⫾ 0.91a
†
Insulin (mU L-1) Exercise 29.2 (8.9–59.1)a 23.7 (7.2–54.1)b 18.5 (7.2–56.4)c 39.7 (12.7–81.5)a
Control 37.6 (24.1–92.5) 43.8 (12.6–99.9)
†
HOMA-IR Exercise 6.8 (1.8–15.6)a 5.2 (1.6–12.5)b 3.5 (1.2–9.6)c 9.8 (2.7–16.1)a
Control 7.5 (4.2–21.4) 10.8 (3.2–27.4)
All data are expressed as mean ⫾ SD unless otherwise noted (n = 24 in exercise group, n = 20 in control group).
The data for each parameter without a common superscript letter are significantly different (P < 0.05), comparing within the same group.
*P < 0.05, compared with control group.
†
Date are expressed as median (min–max).
HDL-C, high density lipoprotein; HOMA-IR, homeostatic model assessment for insulin resistance; LDL-C, low density lipoprotein.
(a) (b)
25 exercise control 30 exercise control
25
Prevalence of
Prevalence of high
20
high TG (%)
glucose (%)
20
15
Figure 2 (a) the prevalence of high TG 15
10
(= 1.7 mmol L-1) and (b) high glucose 10
(= 5.6 mmol L-1) in obese children undergoing 5 5
a 9-month exercise intervention and at 0 0
12 months, 3 months after terminating the 0 3 9 12 0 3 9 12
exercise. Intervention time (months) Intervention time (months)
Throwing a heavy ball Standing jump Times of sit-and-up Time for a 50-m 800/1000-m
(cm) (cm) per minute running (s) running time (min)
Pre-intervention 636.4 ⫾ 167.8 162.9 ⫾ 23.5 30.4 ⫾ 11.0 9.49 ⫾ 1.24 6.2 ⫾ 1.7
Post-intervention 750.0 ⫾ 138.3* 183.0 ⫾ 26.5* 36.6 ⫾ 8.6* 9.01 ⫾ 1.02 4.8 ⫾ 0.7*
Difference 113.6 (17.9%) 20.1 (12.3%) 6.2 (20.4%) -0.38 (P = 0.059) -1.4 (22.3%)
continuous 3-day dietary surveys showed the daily energy was modestly reduced by exercise, whereas in the control
intake was not significantly different between the exercise group there was a progressive increase in waist circumfer-
and control groups (8.62 ⫾ 2.41 kJ vs. 8.48 ⫾ 2.48 kJ). ence even when BMI was on average little changed (see
This study supports the evidence that exercise is very Fig. 1). The marked reduction in the prevalence of high-
important in preventing the progression of obesity in fasting serum glucose from 23.5% to 0% is in-keeping with
adolescents. exercise increasing insulin receptor auto-phosphorylation,
The marked improvements in fasting serum TG, HDL-C, glucose transporter 4 expression and glucose transport
glucose and insulin reflect the impact of the estimated (14–16).
improvements in insulin sensitivity. The serum TG was, as The exercise not only improved the measures of obesity
expected, marked and evident within the first 3 months and the metabolic risk factors, but also improved the physi-
with moderate exercise, and remained at the lower level in cal fitness in terms of endurance, strength and flexibility of
the next 6 months, when the exercise level was performance, with the exception of sprinting times. Half of
more modest but still associated with a further decline in our subjects in the exercise group developed the exercise
insulin resistance. Thus, the prevalence of high TG habit and kept on doing regular exercise on their own when
(ⱖ1.7 mmol L-1) decreased from 12.5% to 8.3% initially, the supervision stopped. The other half, however, seemed
but then dropped to 0% after 9 months. The decrease in to need the continued stimulation and supervision, because
insulin resistance may play an important role in reducing they rapidly give up their exercise and went back to their
TG (Table 3). The results indicate that once established inactive lifestyle.
regular but modest exercise can improve dyslipidaemias. The demonstration that the BMI, serum TG, glucose,
The absence of change in serum TC and LDL-C probably insulin and HOMA-IR level all returned to pre-intervention
reflects the fact that in practice, the children’s dietary fat levels after 3 months of stopping the supervised exercise
intake did not change: improvement in serum cholesterol emphasizes the importance of maintaining the level of
levels also needs more exercise and physical activity (2.5– physical activity used in the second phase of our interven-
4.5 h d-1)(9–11). The data, however, suggest that a suitable tion study, and re-emphasizes the need to prevent obesity
ad libitum diet and relatively low amounts of physical and metabolic syndrome in children by helping them to
activity may be more sustainable in this obese population; formulate an active lifestyle and a good habit of exercise, so
prolonged times of exercise may not be required to achieve that the health benefits can be sustained throughout their
significant metabolic benefits. The present study found future lives.
that the serum HDL-C in exercise group was maintained In summary, the results of this study in obese adolescents
despite a reduction in BMI, and showed the characteristic document that supervised weight-limiting exercise in two
slow response to exercise with an increase by 12 months, stages over a 9-months period can effectively slow down
whereas in the control group HDL-C was significantly the progress of obesity, improve insulin sensitivity and
lower – which indicates that regular moderate exercise can the associated factors of metabolic syndrome, as well as
induce progressively accumulating health benefits. enhancing physical fitness. After stopping the supervised
Insulin resistance, considered to be at least partially exercise for 3 months, the health benefits achieved from
modulated by visceral and intramuscular lipid accumula- exercise may weaken or disappear subsequently. Obesity
tion (12), is considered to be an underlying cause for the and physical inactivity are associated with each other not
risk factors of the metabolic syndrome (13). Thus in only in childhood (17), but also more importantly, they are
the present study, where there was a large decrease in often carried over into adulthood and increase the risks
HOMA-IR (48.5%) suggestive of increased insulin sensi- of cardiovascular disease and future chronic diseases. If
tivity, the exercise probably contributed to this insulin sen- sustained, the lifestyle modification achieved in this study
sitivity by reducing both muscle and liver fat accumulation. could help mitigate chronic diseases-related complications
It is therefore not surprising that the waist circumference in the future.