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ORIGINAL ARTICLE
Prevalence of metabolic syndrome and its association withobesity indices in a Chinese populationYun HUANG,1* Zhiyun ZHAO,1* Xiaoying LI,1,2 Jiguang WANG,3 Min XU,1 Yufang BI,1
Weiqing WANG,1 Jianmin LIU1 and Guang NING1,2
1Shanghai Clinical Center for Endocrine and Metabolic Diseases, Shanghai Institute of Endocrinology and Metabolism, 2Shanghai Key
Laboratory of Endocrine Tumors; 3Centre for Epidemiological Studies and Clinical Trials, E Institute of Shanghai University, Rui-Jin Hospital,
Shanghai Jiao-Tong University School of Medicine, Shanghai, China
Introduction
The past two decades have witnessed rapid urbaniza-
tion in China. The transition from a rural to urban-
ized lifestyle, especially in terms of dietary habits, has
inevitably led to an increase in the prevalence of
obesity-related diseases, such as diabetes, hyper-
tension, and metabolic syndrome. A survey (InterASIA
survey) conducted in 2000–2001 reported that the
prevalence of metabolic syndrome in China was 9.8%
in men and 17.8% in women.1 Other surveys have
assessed the prevalence of metabolic syndrome in
rural or urban areas in other countries.2,3 These sur-
veys have consistently found that the prevalence of
metabolic syndrome is much higher in urban than
rural areas. However, with the spread of urbanization,
Correspondence
Guang Ning, Department of Endocrinology
and Metabolism, Rui-Jin Hospital, Shanghai
Jiao-Tong University School of Medicine,
Rui-Jin 2nd Road, Shanghai 200025, China.
Tel: +86 21 6437 0045 ext. 665344
Fax: +86 21 64373514
Email: [email protected]
*These two authors contributed equally to
this study.
Received 25 July 2008; revised 27 October
2008; accepted 11 November 2008.
doi: 10.1111/j.1753-0407.2008.00006.x
Abstract
Background: To investigate the prevalence of metabolic syndrome in an
urbanizing community in Qingpu, a suburb of Shanghai, and to determine
which obesity indices, including body mass index, waist circumference
(WC), and waist:hip (WHpR), and waist:height (WHtR) ratios, are most
closely associated with metabolic syndrome.
Methods: We conducted a cross-sectional health survey of 1634 individuals
(age 15–87 years) in the Jinhulu community located in Qingpu. The
National Cholesterol Education Program Expert Panel on Detection, Eval-
uation, and Treatment of High Blood Cholesterol in Adults (NCEP ATP
III) criteria were used to define metabolic syndrome, with central obesity
defined according to Asia–Pacific (APC) region criteria.
Results: The age-standardized prevalence of metabolic syndrome was 3.6%
in men and 7.2% in women. Using the criterion of central obesity in the
APC, the age-standardized prevalence of metabolic syndrome increased to
8.3% in men and 10.9% in women. Regardless of age, WHtR consistently
showed a higher odd ratios (OR) after adjustment for confounding factors
of 2.17 (95% confidence interval [CI] 1.12–4.20; P ¼ 0.022) in subjects
<52 years of age and 1.92 (95% CI 1.18–3.11; P ¼ 0.008) in those
‡52 years of age. In men, the WHtR was the only significant predictor
(OR 2.42; 95% CI 1.15–5.08; P ¼ 0.02) of metabolic syndrome after
adjustment, whereas in women WHtR (OR 1.87; 95% CI 1.37–2.85; P ¼0.0088) was slightly inferior to WHpR and WC.
Conclusion: Metabolic syndrome is prevalent in an urbanizing rural area in
Qingpu. Of the anthropometric parameters commonly used to identify meta-
bolic syndrome, WHtR may be the best.
Keywords: metabolic syndrome, obesity indices, prevalence.
Journal of Diabetes 1 (2009) 57–64
ª 2009 Ruijin Hospital and Blackwell Publishing Asia Pty Ltd 57
the prevalence of metabolic syndrome is increasing in
China.
Metabolic syndrome is recognized as a constella-
tion of several metabolic abnormalities, including cen-
tral obesity, impaired glucose tolerance, high blood
pressure, and dyslipidemia, of which central obesity
appears to be the underlying risk factor.4 Many stud-
ies have demonstrated that intra-abdominal fat (IAF)
accumulation is an independent predictor of meta-
bolic risk and cardiovascular disease.5,6 According to
the International Diabetes Federation (IDF) defi-
nition of metabolic syndrome,7 central obesity is
regarded as a mandatory criterion. The commonly
used measures for central obesity include waist cir-
cumference (WC), the waist:hip ratio (WHpR), and
the waist:height ratio (WHtR). However, body mass
index (BMI) is still the most widely used measure to
evaluate overweight and obesity. Although many
studies have tried to clarify the correlation between
measures of obesity and the components of metabolic
syndrome, it is still not known whether BMI, WC,
WHpR, and WHtR have similar predictive effects in
age groups below and above middle age.8–17 In the
present study, we investigated the prevalence of meta-
bolic syndrome and compared various obesity indices
in the Jinhulu community, located in the Qingpu
region of Shanghai, which is undergoing rapid urban-
ization.
Methods
Study population
The community in the present study, Jinhulu from the
Qingpu district, is a suburban area located in west
Shanghai in which marked socioeconomic change has
occurred over the past two decades. Urbanization,
Westernization, and improvements in living standards
have led to substantial changes in dietary habits and
lifestyles. In 2006, most residents had moved away
from traditional farming to work in the industrial or
public service sectors, with the economic income from
farming in this area being 2.8%. Correspondingly, only
2.8% of residents made their living from farming.
Thus, this area has already developed into a highly
urbanized rural district.
The present study was conducted over the period
2004–2005 and included residents from the Jinhulu
community who were between 15 and 87 years of age.
Of the 2330 subjects who gave written informed con-
sent to participate in the study, only 1720 ended up
taking part (73.8% participation rate). These 1720 sub-
jects underwent physical examination and were issued
with standard questionnaires18 to obtain information
regarding demographic characteristics and detailed
lifestyle and medical histories. The Ethics Committee
of Ruijin Hospital and Shanghai Jiaotong University
Medical School approved the study.
Blood pressure was measured in seated subjects after
10 min rest in the non-dominant arm to the nearest
2 mmHg using a mercury sphygmomanometer. Five
consecutive measurements were taken at 1 min inter-
vals and the mean of the five measurements was used.
Weight and height were determined in subjects wearing
light clothing and no shoes. Body mass index (BMI)
was calculated as weight divided by height (kg ⁄m2).
Waist circumference was measured at the umbilical
level, whereas hip circumference was measured at the
level of maximum extension of the buttocks.
Fasting blood samples were obtained for the deter-
mination of plasma glucose, insulin, and serum lipids.
Subjects without a validated history of diabetes under-
went a 75 g oral glucose tolerance test. Plasma glucose
was measured using the glucose oxidase method, serum
lipids were measured using an automated biochemical
instrument (Beckman CX-7 Biochemical Autoanalyser;
Beckman, Brea, CA, USA), and serum insulin was
measured by radioimmunoassay (Sangon, Shanghai,
China). Eighty-six subjects were excluded from final
analysis because of a lack of blood glucose or serum
lipid values.
Metabolic syndrome was defined according to the
criteria of the National Cholesterol Education Pro-
gram Expert Panel on Detection, Evaluation, and
Treatment of High Blood Cholesterol in Adults
(NCEP ATP III)19 as the presence of three or more of
the following risk factors: (i) central obesity (WC
>102 cm in men or >88 cm in women); (ii) elevated
blood pressure (‡130 ⁄ 85 mmHg); (iii) elevated fast-
ing plasma glucose (FPG) concentration (FPG
‡6.1 mmol ⁄L); (iv) elevated triglyceride (TG) levels
(fasting TG>1.70 mmol ⁄L); and (v) decreased high-
density lipoprotein–cholesterol (HDL-C) levels (HDL-C
<1.0 mmol ⁄L in men or <1.3 mmol ⁄L in women).
Subjects who were being treated with antihypertensive
or antidiabetic medication also met the criteria for
hypertension or hyperglycemia. Because the NCEP
ATP III criteria for central obesity may not be appro-
priate for the current population because Asians gener-
ally tend to have leaner figures, we adopted modified
the NCEP ATP III criteria based on the Asia–Pacific
region criterion (APC) of central obesity7 (WC ‡90 cm
in men and ‡80 cm in women). In our analysis of the
relationship between anthropometric variables and
metabolic syndrome, we did not include central obesity
in the diagnosis because WC was one of the indices of
obesity investigated.10
Metabolic syndrome and obesity indices Y. HUANG et al.
58 ª 2009 Ruijin Hospital and Blackwell Publishing Asia Pty Ltd
Statistical analysis
Statistical analyses were performed using sas 8.1 (SAS
Institute, Cary, NC, USA). Continuous variables are
presented as the mean±SD or geometrical mean with
95% confidence intervals (CI) in parentheses. Fasting
TG and insulin levels were transformed logarithmically
before comparison owing to non-normal distribution.
Means of continuous variables between groups were
compared using Student’s t-test. Percentages between
groups were compared using the chi-squared test.
Multiple linear regression models were used to identify
the association between indices of obesity and the
components of metabolic syndrome. Logistic regres-
sion was used to assess the confounder-adjusted odds
ratio (OR) of having metabolic syndrome by gender-
specific quartiles of obesity indices. In model 1, age,
education level, smoking (yes ⁄no) and drinking
(yes ⁄no) status, and a family history of type 2 diabetes
and hypertension were the factors adjusted. In model
2, BMI was further adjusted for WC, WHpR and
WHtR based on model 1, while WHtR was further
adjusted for BMI. Age was stratified into six groups
(15–29, 30–39, 40–49, 50–59, 60–69, and ‡70 years) to
estimate the prevalence of metabolic syndrome in each
age group.
Results
Characteristics of the study population
The mean age of the Qingpu population was 52±
15 years. Subjects >50 years of age made up 56.9%
of the study population. Compared with women, men
had a significantly higher WC, WHpR, systolic and dia-
stolic blood pressure (SBP and DBP, respectively), and
TG concentration, but smaller WHtR, lower 2 h post-
loading plasma glucose, and lower HDL-C concentra-
tions. Moreover, more men were current smokers and
drinkers (P < 0.05 for all comparisons; Table 1).
Prevalence and the components of the metabolic
syndrome
Based on NCEP ATP III criteria, the prevalence of
metabolic syndrome in the study population was 8.4%
(5.6% adjusted for sex and age), with a prevalence of
5.3% in men (3.6% adjusted for age) and 10.4% in
women (7.2% adjusted for age). Using APC criteria,
the overall prevalence of metabolic syndrome in the
study population increased markedly to 13.5% (9.6%
adjusted for sex and age), with a prevalence of 11.0%
in men (8.3% adjusted for age) and 15.3% in women
(10.9% adjusted for age). For almost all age groups,
the prevalence of metabolic syndrome was significantly
higher in women than in men. In addition, the preva-
lence of metabolic syndrome increased with age, reach-
ing a peak at 60–69 years in women (cf. 50–59 years in
men). The incidence of metabolic syndrome started to
decrease in men at 60–69 years of age and in women
at ‡70 years of age (Fig. 1).
Of the disorders associated with metabolic syn-
drome, hypertension was the most frequently encoun-
tered, being present in 43.8% of men and in 40.4% of
women. However, the prevalence of hypertension and
high FPG levels did not differ significantly between
men and women. When compared with men, there was
a higher prevalence of low HDL-C levels and central
obesity in women and a lower prevalence of high TG
levels (P < 0.0001; Table 2).
However, according to NCEP ATP III criteria, the
prevalence of central obesity in men and women was
only 1.2% and 12.8%, respectively (Table 2). This sug-
gests that the NCEP ATP III criteria for central obes-
ity may not be appropriate for the current population
Table 1 Characteristics of the study population
Men
(n = 657)
Women
(n = 977) P-value
Age (years) 53 ± 15 51 ± 15 NS
Waist circumference
(cm)
81.0 ± 9.4 77.0 ± 9.2 <0.0001
Waist:hip ratio 0.86 ± 0.06 0.83 ± 0.06 <0.0001
Waist:height ratio 0.49 ± 0.05 0.50 ± 0.06 0.0009
BMI (kg ⁄ m2) 23.0 ± 3.2 22.7 ± 3.3 NS
Percentage
body fat
23.0 ± 6.2 31.7 ± 7.3 <0.0001
SBP (mmHg) 127 ± 20 125 ± 21 0.04
DBP (mmHg) 78 ± 10 75 ± 10 <0.0001
FPG (mmol ⁄ L) 5.26 ± 1.08 5.28 ± 1.22 NS
2hPPG (mmol ⁄ L) 5.98 ± 2.46 6.53 ± 2.91 <0.0001
Fasting insulin
(mU ⁄ L)
5.64 (5.33–5.98) 6.02 (5.74–6.31) NS
Triglycerides
(mmol ⁄ L)
1.20 (1.16–1.25) 1.08 (1.05–1.12) <0.0001
Total cholesterol
(mmol ⁄ L)
4.48 ± 0.98 4.58 ± 1.03 NS
HDL-C (mmol ⁄ L) 1.47 ± 0.34 1.52 ± 0.32 0.02
LDL-C (mmol ⁄ L) 2.77 ± 0.80 2.83 ± 0.85 NS
Current smoker (%) 53.3 0.3 <0.0001
Current alcohol
consumption (%)
40.5 1.0 <0.0001
Normal data are given as the mean ± SD; skewed data are
given as the geometric mean with 95% confidence intervals in
parentheses.
BMI, body mass index; SBP, systolic blood pressure; DBP,
diastolic blood pressure; FPG, fasting plasma glucose; 2hPPG, 2 h
post-loading plasma glucose; HDL-C, high-density lipoprotein–
cholesterol; LDL-C, low-density lipoprotein–cholesterol.
Y. HUANG et al. Metabolic syndrome and obesity indices
ª 2009 Ruijin Hospital and Blackwell Publishing Asia Pty Ltd 59
owing to the generally leaner figures of Asian popula-
tions. Consequently, we used the APC criterion for
central obesity. Adopting the APC criterion, the preva-
lence of central obesity increased markedly to 18.4%
and 37.4% in men and women, respectively. The over-
all prevalence of metabolic syndrome also increased
markedly to 13.5% (9.6% adjusted for sex and age),
with a prevalence of 11.0% in men (8.3% adjusted for
age) and 15.3% in women (10.9% adjusted for age).
The prevalence of metabolic syndrome differed signifi-
cantly between men and women using either criteria
(P ¼ 0.0003 using NCEP ATP III criteria; P = 0.013
using modified ATPIII criteria).
Association between obesity indices and metabolic
syndrome
Using multiple linear regression, we found that BMI,
WC, WHpR, and WHtR were all significantly related to
the disorders of metabolic syndrome, although the mag-
nitude of the associations varied (Table 3). Of all these
indices examined, somewhat stronger correlations were
observed for WHtR with SBP and TG, for WC with
DBP, for WHpR with FPG, and for BMI with HDL-C.
Multiple logistic regressions were performed to
determine which index was independently associated
with metabolic syndrome. Because of the effects of
aging on fat distribution, we stratified individuals into
two groups according to the mean age (52 years) of
the overall population (Fig. 2a,b). In the group
<52 years of age (Fig. 2a), all obesity indices were sig-
nificantly associated with metabolic syndrome (P<
0.0001), with WHtR exhibiting the highest OR for
metabolic syndrome in model 1 (OR 3.00; 95% CI:
1.91–4.73). In model 2, after further adjustment for
BMI or WHtR, the relationship between metabolic
syndrome and BMI disappeared, whereas the domi-
nant predictive role of WHtR remained significant
(OR 2.17; 95% CI 1.12–4.20; P ¼ 0.022). Similar
results (Fig. 2b) were found after adjustment for con-
founding factors in subjects <52 years of age, with
WHtR presenting the highest OR (1.92, 95% CI 1.18–
3.11; P ¼ 0.008) in this group also.
Given the different distribution of body fat between
men and women, sex-specific OR for metabolic syn-
drome for the different obesity indices were also ana-
lyzed (Fig. 2c). In model 1, all obesity indices were
significantly associated with metabolic syndrome in men
and women (all P < 0.0001). However, WHtR had the
highest OR for metabolic syndrome in men (3.17; 95%
CI 1.89–5.32), whereas WHpR had a slightly higher OR
than WHtR in women (2.43 [95% CI 1.77–3.32] vs 2.41
[95% CI 1.77–3.27], respectively). However, in model 2,
WHtR was the only index that remained significant
(OR 2.46; 95% CI 1.11–4.95) in men (Fig. 2c). In
women (Fig. 2d), the magnitude of the association was
Figure 1 Prevalence of metabolic syndrome according to modified
National Cholesterol Education Program Expert Panel on Detection,
Evaluation, and Treatment of High Blood Cholesterol in Adults
(NCEP ATP III) criteria in men ( ) and women (s) in different age
groups. The prevalence of metabolic syndrome increased with
aging (Pfor trend = 0.39 in men; Pfor trend < 0.0001 in women).
Table 2 Prevalence of components of metabolic syndrome in men and women
Men Women Total P-value
High blood pressure 288 (43.8) 395 (40.4) 683 (41.8) NS
High fasting glucose 71 (10.8) 92 (9.4) 163 (10.0) NS
Hypertriglyceride 165 (25.1) 166 (17.0) 331 (20.3) <0.0001
Low HDL-C 39 (5.9) 237 (24.3) 276 (16.9) <0.0001
Central obesity
Defined by NCEP ATP III 8 (1.2) 125 (12.8) 133 (8.1) <0.0001
Defined using the ACP criterion 121 (18.4) 365 (37.4) 486 (29.7) <0.0001
Metabolic syndrome
Defined by NCEP ATP III 35 (5.3) 102 (10.4) 137 (8.4) 0.0003
Defined using the ACP criterion 72 (11.0) 149 (15.3) 221 (13.5) 0.013
Data show the number of subjects in each group, with percentages given in parentheses.
NCEP ATP III, National Cholesterol Education Program Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in
Adults; ACP, criterion for Asia–Pacific (APC) region.
Metabolic syndrome and obesity indices Y. HUANG et al.
60 ª 2009 Ruijin Hospital and Blackwell Publishing Asia Pty Ltd
diminished after further adjustments, although the rela-
tionship between all indices of obesity with metabolic
syndrome persisted. The relationship between metabolic
syndrome and both WHpR (OR 1.92; 95% CI 1.34–
2.74; P ¼ 0.0004) and WC (OR 1.93; 95% CI 1.23–3.05;
P ¼ 0.0046) was of a similar magnitude and was closely
followed by that with WHtR (OR 1.87; 95% CI 1.17–
2.98; P ¼ 0.0088).
Discussion
Using NCEP ATP III criteria, three consecutive
national representative surveys in the US showed an
age-adjusted prevalence of metabolic syndrome of
23.7%.7 Many surveys conducted in urban Asian popu-
lations have reported a prevalence of metabolic
syndrome ranging between 7.8% and 31.6%, as defined
by NCEP ATP III criteria.1,2,20–23 The lifestyle in urban
populations is usually sedentary and is associated with
high calorie food intake, which drives the progression
of obesity. A cross-sectional survey conducted in 2005
in east China revealed that 12.7% of men and 10.1%
of women in an urban area, compared with 1.7% of
men and 9.7% of women in a rural area, had metabolic
syndrome.24 The results of the present study, using
NCEP ATP III criteria, revealed a prevalence of meta-
bolic syndrome in an urbanizing area of 5.6% in men
and 10.2% in women. Compared with findings of the
previous survey in east China,24 the prevalence of meta-
bolic syndrome in Qingpu in the present study is higher
than that in rural areas, but lower than that in urban
areas. These results could imply an essential role of
urbanization in the development of metabolic syn-
drome. Hence, it is crucial to take measures to prevent
Table 3 Associations between obesity indices and components of metabolic syndrome
Body mass index Waist circumference Waist:hip ratio Waist:height ratio
b P-value b P-value b P-value b P-value
SBP 0.185 <0.0001 0.209 <0.0001 0.200 <0.0001 0.225 <0.0001
DBP 0.302 <0.0001 0.330 <0.0001 0.284 <0.0001 0.317 <0.0001
FPG 0.121 <0.0001 0.169 <0.0001 0.182 <0.0001 0.163 <0.0001
Log TG 0.353 <0.0001 0.357 <0.0001 0.340 <0.0001 0.374 <0.0001
HDL-C )0.219 <0.0001 )0.212 <0.0001 )0.213 <0.0001 )0.216 <0.0001
Variables in models of multiple linear regressions included age, sex, education levels, smoking and drinking habits, a family history of
diabetes, and hypertension. Values in bold represent the variable that had stronger associations with components of metabolic syndrome.
SBP, systolic blood pressure; DBP, diastolic blood pressure; FPG, fasting plasma glucose; TG, triglycerides; HDL-C, high-density lipoprotein–
cholesterol.
(a) (b)
(c) (d)
Figure 2 Odds ratios (OR) for metabolic
syndrome for one-quartile increase in anthro-
pometric variables in individuals (a) <52 and
(b) >52 years of age, as well as in (c) men
and (d) women (vertical bars show 95%
confidence intervals). ( ), Model 1 (adjusted
for age, education levels, smoking and drink-
ing habits, family history of diabetes, and
hypertension); (d), model 2 (body mass
index [BMI] further adjusted for waist
circumference [WC], waist:hip ratio [WHpR],
and waist:height [WHtR]; WHtR further
adjusted for BMI based on model 1).
Y. HUANG et al. Metabolic syndrome and obesity indices
ª 2009 Ruijin Hospital and Blackwell Publishing Asia Pty Ltd 61
the development of metabolic disorders in rural areas
that are undergoing urbanization.
In the present study, using either NCEP ATP III or
ACP criteria, the prevalence of metabolic syndrome
was significantly higher in women than in men. This
result is in accordance with findings in other Asian
populations.23,25 Of the disorders of metabolic syn-
drome, women had a nearly threefold higher preva-
lence of low HDL-C levels and a higher prevalence of
central obesity according to NCEP ATP III criteria
(¼ twofold higher prevalence of central obesity accord-
ing to the APC criterion) than men. This may explain,
in part, why the prevalence of metabolic syndrome was
significantly higher in women than in men.
Aging has been regarded as an established risk factor
for metabolic syndrome. The NCEP defined the high-
risk age for men and women to be 35–65 and 45–
75 years, respectively.26 In the Qingpu population, the
prevalence of metabolic syndrome also increased with
increasing age, reaching a peak in women at 60–69 years,
compared with 50–59 years in men. Similar results have
been reported for other Asian populations.20
The prevalence of obesity is increasing not only in
Western countries, but also in Asian countries. Com-
pared with Caucasians, Asians have a lower BMI but
a higher prevalence of metabolic risks. In the present
study, the Qingpu population had a prevalence of meta-
bolic syndrome of 8.3% using NCEP ATP III criteria,
but a prevalence of obesity of only 2.02% according to
WHO criteria.27 In some studies, BMI was the most
predictive index of diabetes, hypertension, and cardio-
vascular diseases.9,28,29 However, an increasing number
of studies argue that BMI, as a measure of general
obesity, cannot reflect intra-abdominal fat (IAF) distri-
bution, which is thought to be tied closely to metabolic
risks.5,6 Moreover, other studies have claimed that
BMI cannot distinguish fat from muscle mass; subse-
quently, the risks tended to be overestimated in young
people and underestimated in older people whose mus-
cle mass has been replaced by fat to varying extents.30
In line with previous findings, the results of the present
study also indicate that the association between BMI
and metabolic syndrome is lost after adjustment for
central obesity, regardless of age. In contrast, the
WHtR was consistently and highly correlated with
metabolic syndrome irrespective of age.
Height has been reported to have an independent
and inverse effect on mortality from ischemic heart
disease and stroke.31,32 In the present study, WHtR
exhibited the strongest and most consistent relation-
ship with metabolic syndrome in men, even after
adjustment for BMI. Although slightly inferior to
WHpR and WC, WHtR was still the second best
predictor of metabolic syndrome in women. In Thai
men, WHtR was strongly associated with coronary
heart disease.33 In addition, in a prospective study,
WHtR appeared to be the strongest predictor than any
other obesity index in identifying men with type 2 dia-
betes.12 These findings imply that WHtR may be the
best predictor of cardiovascular risks in men. In partic-
ular, height is inversely correlated with aging and
increases in the accumulation of IAF may be offset by
declines in subcutaneous fat with aging.34 In addition
to aging, taking height into account could also provide
more accurate information on fat distribution. Unlike
WC and WHpR, WHtR exhibited fewer differences
between men and women, as well as between different
ethnic populations.35 Moreover, WHtR has been report-
ed to be an accurate early index for evaluating obesity
and a good predictor of metabolic risks in children
and adolescents.36,37 Notably, urbanization-related
changes in lifestyle will markedly increase the preva-
lence of obesity-related diseases, consequently hasten-
ing the onset of these diseases, especially in children
and young people who are prone to consuming a high-
fat and high-glucose diet. The WHtR can serve as an
effective index to assess fat distribution and cardiovas-
cular risks not only in adults, but also in children and
adolescents.
There are some limitations of the present study.
First, the study was a cross-sectional study and the
number of children and young people included in the
study population was relatively small. The interpreta-
tion of the results requires considerable caution. The
effectiveness of WHtR in predicting metabolic syn-
drome needs further validation in prospective studies.
Second, in the present study, no direct measures of
body composition were performed. WC, WHpR, and
WHtR are somewhat crude surrogate indices of central
obesity; consequently, it is difficult to define the rela-
tionship between surrogate indices and real body fat
distribution.
Acknowledgments
The present study would not have been possible with-
out the participation of the volunteers. This research
was supported by grants from 973 Project (No. 2006
CB 503904), Shanghai Commission for Science and
Technology (No. 04DZ19502), and E-Institute of
Shanghai Universities, Shanghai Education Commis-
sion (No. E03007).
Disclosure
The authors report no conflicts of interest.
Metabolic syndrome and obesity indices Y. HUANG et al.
62 ª 2009 Ruijin Hospital and Blackwell Publishing Asia Pty Ltd
References
1. Gu D, Reynolds K, Wu X et al. Prevalence of the
metabolic syndrome and overweight among adults in
China. Lancet. 2005; 365: 1398–405.
2. Lim S, Jang HC, Lee HK et al. A rural–urban compar-
ison of the characteristics of the metabolic syndrome by
gender in Korea: The Korean Health and Genome
Study (KHGS). J Endocrinol Invest. 2006; 29: 313–9.
3. Fezeu L, Balkau B, Kengne AP et al. Metabolic syn-
drome in a sub-Saharan African setting: Central obesity
may be the key determinant. Atherosclerosis. 2007; 193:
70–6.
4. Carr DB, Utzschneider KM, Hull RL. Intra-abdominal
fat is a major determinant of the National Cholesterol
Education Program Adult Treatment Panel III criteria
for metabolic syndrome. Diabetes. 2004; 53: 2087–94.
5. Hayashi T, Boyko EJ, McNeely MJ et al. Minimum
waist and visceral fat values for identifying Japanese
Americans at risk for the metabolic syndrome. Diabetes
Care. 2007; 30: 120–7.
6. Tong J, Boyko EJ, Utzschneider KM et al. Intra-
abdominal fat accumulation predicts the development
of the metabolic syndrome in non-diabetic Japanese-
Americans. Diabetologia. 2007; 50: 1156–60.
7. Alberti KG, Zimmer P, Shaw J. The metabolic syn-
drome: A new world-wide definition. Lancet. 2005; 366:
1059–62.
8. Stevens J, Couper D, Pankow J. Sensitivity and speci-
ficity of anthropometrics for the prediction of diabetes
in a biracial cohort. Obes Rev. 2001; 9: 696–705.
9. Marshall K, Tulloch R, Robert L et al. Do measures of
body fat distribution provide Information on the risk
of type 2 diabetes in addition to measures of general
obesity? Diabetes Care. 2003; 26: 2556–61.
10. Wannamethee S, Shaper A, Morris R et al. Measures of
adiposity in the identification of metabolic abnormalities
in elderly men. Am J Clin Nutr. 2005; 81: 1313–21.
11. Meisinger C, Doring A, Thorand B et al. Body fat dis-
tribution and risk of type 2 diabetes in the general pop-
ulation: Are there differences between men and women?
The MONICA ⁄KORA Augsburg Cohort Study. Am J
Clin Nutr. 2006; 84: 483–9.
12. Hadaegh F, Zabetian A, Harati H et al. Waist ⁄ heightratio as a better predictor of type 2 diabetes compared
to body mass index in Tehranian adult men: A 3.6-year
prospective study. Exp Clin Endocrinol Diabetes. 2006;
114: 310–5.
13. Schneider HJ, Glaesmer H, Klotsche J. Accuracy of
anthropometric indicators of obesity to predict cardio-
vascular risk. J Clin Endocrinol Metab. 2007; 92: 589–
94.
14. Schneider HJ, Klotsche J, Stalla GK et al. Obesity and
risk of myocardial infarction: the INTERHEART
study. Lancet. 2006; 367: 1052.
15. Al-Shayji IA, Akanji AO. Obesity indices and major
components of metabolic syndrome in young adult
Arab subjects. Ann Nutr Metab. 2004; 48: 1–7.
16. Westphal A, Geisler C, Onur S et al. Value of body fat
mass vs anthropometric obesity indices in the assess-
ment of metabolic risk factors. Int J Obes. 2006; 30:
475–83.
17. Shiun DH, Takashi M. Metabolic syndrome in Japa-
nese men and women with special reference to the
anthropometric criteria for the assessment of obesity:
Proposal to use the waist-to-height ratio. Prev Med.
2006; 42: 135–9.
18. Wang JG, Staessen JA, Tizzoni L et al. Renal function
in relation to three candidate genes. Am J Kidney Dis.
2001; 38: 1158–1116.
19. Expert Panel on Detection, Evaluation and Treatment
of High Blood Cholesterol in Adults. Executive sum-
mary of the third report of the national cholesterol edu-
cation program (NCEP) expert panel on detection,
evaluation and treatment of high blood cholesterol in
adults (Adult Treatment Panel III). JAMA. 2001; 285:
2486–97.
20. Hidenri A, Akira Y, Yuji M. Prevalence of meta-
bolic syndrome in general Japanese population in 2000.
J Atheroscler Thromb. 2006; 13: 202–8.
21. Thomas GN, Ho SY, Janus ED. The US National
Cholesterol Education Programme Adult Treatment
Panel III (NCEP ATP III) prevalence of the metabolic
syndrome in a Chinese population. Diabetes Res Clin
Pract. 2005; 67: 251–7.
22. Oh JY, Hong YS, Sung YA et al. Prevalence and
factor analysis of metabolic syndrome in an urban
Korean population. Diabetes Care. 2004; 27: 2027–
32.
23. Rajeev G, Prakash CD, Arvind G. Prevalence of meta-
bolic syndrome in an Indian urban population. Int J
Cardiol. 2004; 97: 257–61.
24. Weng X, Liu Y, Ma J et al. An urban-rural compari-
son of the prevalence of the metabolic syndrome
in Eastern China. Public Health Nutr. 2007; 10: 131–
6.
25. Park HS, Kim SM, Lee JS. Prevalence and trends of
metabolic syndrome in Korea: Korean National Health
and Nutrition Survey 1998–2001. Diabetes Obes Metab.
2007; 9: 50–8.
26. Ford ES, Giles WH, Dietz WH. Prevalence of the
metabolic syndrome among US adults: Finding from
the third National Health and Nutrition Examination
Survey. JAMA. 2002; 287: 356–9.
27. World Health Organization. Obesity: Preventing and
managing the global epidemic. Report of a WHO consul-
tation. World Health Organ Tech Rep. 2000; 894: 1–253.
28. Lu M, Ye W, Adami HO et al. Prospective study of
body size and risk for stroke amongst women below
age 60. J Intern Med. 2006; 260: 442–50.
Y. HUANG et al. Metabolic syndrome and obesity indices
ª 2009 Ruijin Hospital and Blackwell Publishing Asia Pty Ltd 63
29. He Y, Jiang B, Wang J et al. Body mass index versus the
metabolic syndrome in relation to cardiovascular risk in
the Chinese elderly. Diabetes Care. 2007; 30: 2128–34.
30. Willett WC, Dietz WH, Colditz GA. Guidelines for
healthy weight. N Engl J Med. 1999; 341: 427–34.
31. Hozawa A, Murakami Y, Okamura T et al. Relation of
adult height with stroke mortality in Japan: NIPPON
DATA80. Stroke. 2007; 38: 22–6.
32. Williams SR, Jones E, Bell W. Body habitus and coro-
nary heart disease in men. A review with reference to
methods of body habitus assessment. Eur Heart J.
1997; 18: 376–93.
33. Wichai A, Varapat P, Crystal MY et al. Abdominal
obesity and coronary heart disease in Thai men. Int J
Obes. 2007; 15: 1036–42.
34. Hsieh SD, Yoshinaga H, Muto T. Waist-to-height
ratio, a simple and practical index for assessing central
fat distribution and metabolic risk in Japanese men and
women. Int J Obes. 2003; 27: 610–6.
35. Patel S, Unwin N, Bhopal R et al. A comparison of proxy
measures of abdominal obesity in Chinese, European
and South Asian adults. Diabet Med. 1999; 16: 853–
60.
36. Weili Y, He B, Yao H et al. Waist-to-height ratio is an
accurate and easier index for evaluating obesity in chil-
dren and adolescents. Obesity. 2007; 15: 748–52.
37. Kahn HS, Imperatore G, Cheng YJ. A population-
based comparison of BMI percentiles and waist-
to-height ratio for identifying cardiovascular risk in
youth. J Pediatr. 2005; 146: 482–8.
Metabolic syndrome and obesity indices Y. HUANG et al.
64 ª 2009 Ruijin Hospital and Blackwell Publishing Asia Pty Ltd