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ORIGINAL RESEARCH COMMUNICATIONS |
1 From the Division of Epidemiology and Public Health, Institute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan (W-HP, W-TY, and C-JY); the Division of Nutritional Sciences, Institute of Agricultural Chemistry, National Taiwan University, Taipei, Taiwan (W-HP); the Graduate Institute of Epidemiology, College of Public Health, National Taiwan University, Taipei, Taiwan (W-HP, C-JY, and W-CL); the National Center for Health Statistics, Centers for Disease Control and Prevention, Hyattsville, MD (KMF); and the Division of Health Policy, National Health Research Institute, Taipei, Taiwan (H-YC).
2 Supported by grants DOH-83-FS-41, DOH-84-FS-11, DOH-85-FS-11, and DOH-86-FS-11 from the Department of Health, Republic of China. 3 Address reprint requests to W-H Pan, Institute of Biomedical Sciences, Academia Sinica, Taipei 115-29, Taiwan. E-mail: pan{at}ibms.sinica.edu.tw.
| ABSTRACT |
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Objective: The goal was to compare relations between BMI and metabolic comorbidity among Asians and US whites and blacks.
Methods: We compared the prevalence rate, sensitivity, specificity, predictive values, and impact fraction of comorbidities at each BMI level and the BMI-comorbidity relations across ethnic groups by using data from the third National Health and Nutrition Examination Survey and the Nutrition and Health Survey in Taiwan (19931996).
Results: For most BMI values, the prevalences of hypertension, diabetes, and hyperuricemia were higher for Taiwanese than for US whites. In addition, increments of BMI corresponded to higher odds ratios in Taiwanese than in US whites for hypertriglyceridemia (P = 0.01) and hypertension (P = 0.075). BMI-comorbidity relations were stronger in Taiwanese than in US blacks for all comorbidities studied. BMIs of 22.5, 26, and 27.5 were the cutoffs with the highest sum of positive and negative predictive value for Taiwanese, US white, and US black men, respectively. The same order was observed for women. For BMIs >27, >85% of Taiwanese, 66% of whites, and 55% of blacks had at least one of the studied comorbidities. However, a cutoff close to the median of the studied population was often found by maximizing sensitivity and specificity. Reducing BMI from >25 to <25 in persons in the United States could eliminate 13% of the obesity comorbidity studied. The corresponding cutoff in Taiwan is slightly <24.
Conclusion: These data suggest a possible need to set lower BMI cutoffs for Asians, but where to draw the line is a complex issue.
Key Words: BMI definitions obesity overweight ethnicity Asians diabetes mellitus hypertension hyperuricemia dyslipidemia
| INTRODUCTION |
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In early 1999, a recommendation was made to set criteria for Asians defining overweight as a BMI (in kg/m2) of
23 and obesity as a BMI of
25 on the basis of the scanty data for Asians (8) that were available at that time. Taiwan recently adopted BMIs of 24 and 27 as the cutoffs for overweight and obesity, respectively. Whether to have separate definitions of overweight and obesity for minorities in multiethnic countries such as the United States is a related and even more complicated issue. Comparative studies are needed to delineate the differences in BMI-disease relations between minority race ethnic groups and whites, because the World Health Organization definitions for overweight and obesity were established by using data primarily from whites. In particular, the rationales and the implications for selecting BMI cutoffs to define overweight and obesity for nonwhite populations should be carefully laid out.
The objective of the present study was to compare the relation of BMI to several obesity-related metabolic disorders in different ethnic groups. The data for Taiwanese Asians came from the Nutrition and Health Survey in Taiwan (NAHSIT), which was carried out during 19931996 (9). The data for US non-Hispanic whites and non-Hispanic blacks came from the third National Health and Nutrition Examination Survey (NHANES III), which was carried out in the United States during 19881994. Issues on how to define overweight and obesity for Asians and across ethnic groups were examined by using information on the relative risk, sensitivity, specificity, predictive values, and impact fraction for the selected metabolic disorders at different BMI cutoffs.
| SUBJECTS AND METHODS |
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4 y selected through a multistage, complex sampling design. Details on the design and operation of the survey have been published elsewhere (9). A sample of 9961 participants was obtained through door-to-door interviews, which corresponds to a 74% response rate. Of these, 4956 were adults aged
20 y, of whom 52.2% (2585) had complete clinical data of interest for this study. Blood pressure was measured by trained technicians using standard sphygmomanometers at each participant's home after the participant had rested for
5 min. An appropriately sized cuff was used for each participant. Two blood pressure measurements were made 30 s apart with the arm at the level of the heart. If the 2 measurements were >10 mm Hg apart, a third measurement was made. The 2 closest blood pressure values were averaged to obtain mean blood pressure. Other clinical data were obtained from a physical examination carried out in temporary clinics set up in the neighborhood of the survey sites. Anthropometric measurements were carried out after the subjects had removed their shoes and heavy clothes. The subjects were asked to wear an examination gown if their apparel was not appropriate for taking measurements. Body weight was measured to the nearest 0.1 kg, and body height was measured to the nearest 1 mm. BMI was calculated from measured weight and height as weight (kg)/height (m2). Fasting whole blood glucose was measured immediately after the blood drawing by the glucose oxidase method with use of a glucose analyzer (model 23A; YSI, Yellow Springs, OH) in blood samples collected into sodium fluoride tubes. Fasting serum uric acid, triacylglycerol, and cholesterol values were measured with a Hitachi 747 analyzer (Hitachi, Tokyo) within 1 mo of the blood draw in collaboration with the clinical chemistry laboratory of the affiliated hospital of National Taiwan University Medical School.
Third National Health and Nutrition Examination Survey
NHANES III (19881994) is the seventh in a series of health examination surveys conducted by the National Center for Health Statistics of the Centers for Disease Control and Prevention. With the use of a complex, multistage sampling design, the survey aimed to provide estimates of the health and nutritional status of the civilian noninstitutionalized population of the United States aged
2 mo. Details of the survey design and questionnaires are published in the NHANES III Plan and Operation reference manual (10). A complete description of the survey and laboratory procedures is also available (11). In this articles, the terms white and black will be used to refer to non-Hispanic whites and non-Hispanic blacks, respectively.
Definitions for selected metabolic disorders
The same definitions were applied to data collected at baseline in both surveys. Hypertension was defined as use of an antihypertensive medication, having a systolic blood pressure
140 mm Hg, or having a diastolic blood pressure
90 mm Hg. Diabetes mellitus was defined as use of insulin or hypoglycemic agents, having a fasting plasma glucose concentration
7.0 mmol/L (NHANES III), or having a fasting whole blood glucose concentration
6.1 mmol/L (NAHSIT) (12). Hypercholesterolemia was defined as use of cholesterol-lowering medication or having a serum cholesterol concentration
6.21 mmol/L. Hypertriglyceridemia was defined as a serum triacylglycerol concentration
2.26 mmol/L. Hyperuricemia was defined as a serum uric acid concentration
392.6 µmol/L (women) or
458 µmol/L (men).
Statistical analysis
All analyses were carried out with SUDAAN version 7.5 (Research Triangle Institute, Research Triangle Park, NC), which was used to account for the effect of the complex sampling design in statistical testing and in deriving means and SEs. Missing values were handled separately in the analysis for each metabolic disorder. The sample sizes are listed in Table 1
. For comparison across populations by BMI, the survey respondents were grouped into 6 BMI categories: 1619.9, 2021.9, 2223.9, 2425.9, 2629.9, and 3039.9; BMI values <16 or
40 were excluded. For other analyses, all BMI data were included. In comparing the prevalence of hypertension, diabetes, hyperuricemia, and dyslipidemia between populations, the data were standardized by age and sex to the 1980 US population, and design effectadjusted SEs were computed. Two-sample t tests were then used to compare the rates either for overall comparison or for comparison at each BMI group. In comparing the distribution of age, sex, and BMI across populations, a chi-square test was used. P values
0.05 were used to indicate statistical significance in general, but a Bonferroni-corrected P value of 0.017 was used for the situation of 3 pairwise multiple comparisons.
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Sensitivity, specificity, and positive and negative predictive values (13) relative to each of the selected conditions (hypertension, diabetes, hypercholesterolemia, hypertriglyceridemia, and hyperuricemia) were calculated every one-half unit of BMI from 20 to 30. A t test was used to compare the difference in predictive values as described previously.
The impact fraction was calculated by using data on the BMI distribution and on the risk ratios for each population. Logistic regression models that included linear and quadratic terms for BMI as a continuous variable were used to generate monotonic risk ratio estimates. The impact fraction (14, 15) for a selected cutoff was calculated as the excess prevalence of the condition associated with BMIs greater than the selected cutoff divided by the total prevalence of the condition. This is an estimate of the fraction of cases that could be removed if persons with BMI values above the cutoff were shifted to below the cutoff. In the impact fraction calculation, a subject was considered as a case if he or she had one or more of the selected metabolic conditions. In calculating sensitivity, specificity, predictive values, and the impact fraction of having at least one disorder, data with missing values for any variable were deleted.
| RESULTS |
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Age- and sex-standardized prevalence estimates by BMI
For most of the high-BMI groups, the age- and sex-standardized prevalence rates of hypertension and hyperuricemia for Taiwanese were higher than those for US whites (Figure 1
). The higher the BMI value, the greater the prevalence difference. In the BMI range of 3040, the differences between the Taiwanese and the other groups in the prevalences of hypertension and hyperuricemia were >20 percentage points. In low-BMI groups, the Taiwanese had lower prevalences of hypertension than did the US blacks, but the prevalence rates increased faster with BMI for the Taiwanese than for the US blacks.
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Odds ratios per unit change in BMI for selected metabolic conditions
The odds ratios for each of the selected conditions were calculated for each increment of BMI (Table 2
). Increments of BMI corresponded to significantly higher odds ratios in the Taiwanese than in the US blacks for all 5 metabolic conditions studied. When the Taiwanese and the US whites were compared, significance and borderline significance were shown for hypertriglyceridemia and hypertension, respectively.
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22.5, 26.0, and 27.5 for Taiwanese, US white, and US black men, respectively. For Taiwanese, US white, and US black women, these BMI cutoffs were
24.8, 28.5, and somewhere >30, respectively.
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13%. The corresponding BMI cutoff in the Taiwanese for a 13% impact fraction was slightly <24.
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| DISCUSSION |
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It has been known for some time that, after control for BMI, Asians have a higher prevalence of hypertension than do whites (16, 17), which indicates a greater effect of factors other than obesity, either genetic or environmental. An extraordinarily high prevalence of hyperuricemia in Taiwan has only recently emerged (9, 18, 19). The extent of the change in the prevalence of hyperuricemia indicates the interplay of genes and environment. The high incidence (20, 21), prevalence (22-26), and mortality (27) of diabetes mellitus and undiagnosed diabetes mellitus (28) have been well documented in recent years in Taiwanese. Short statue and central obesity (28) are among the risk factors. Consistent with the above literature, our results indicate that Taiwanese (or Asians) may respond more severely in either an absolute or a relative sense to the same degree of BMI elevation than do US whites or US blacks regarding the component disorders of the metabolic syndrome.
Studies have shown that given the same level of BMI, Chinese and many other Asian groups have a higher percentage of body fat than do whites (29, 30). Intrauterine malnutrition (31, 32), recent lifestyle associated with low physical activity and a low-fiber diet (33), and genetic differences are among the potential etiologic factors of this phenomenon. The issue of how to define overweight and obesity in Asians and minority groups is not easily resolved by examining the relations between BMI and related disorders. In our study and in those of others (8, 34), there was no clear threshold in the BMI-comorbidity relations that would readily allow selection of a BMI cutoff. It is most likely that body fat, in interaction with age, sex, and other risk factors, increases the risk of metabolic disorders. We should know more about these interactions to simplify the strategy of defining obesity.
A few studies have used the approach of maximizing the sum of sensitivity and specificity. Ko et al (8) suggested using a BMI of 23 to define overweight in screening for diabetes, hypertension, dyslipidemia, and albuminuria. However, we found that the BMI distributions of the diseased and the healthy in our populations overlapped considerably (data not shown). Therefore, depending on the population studied, this approach will pick up a value close to the BMI median of that given population and designate around one-half of the population as overweight. It seems that the concept of balancing sensitivity and specificity in this setting of complex etiology is not as straightforward and applicable as in the case of clinical diagnostics.
Positive predictive value is a function of the prevalence of a given disorder. For any single metabolic disorder in the present study, and particularly for young adults, the positive predictive value was relatively low (data not shown). However, when several disorders were examined together, the positive predictive values for having one or more become reasonably good. Of every 10 subjects defined as overweight or obese by having a BMI
24, 6-7 had one or more of the studied conditions. On the other hand, of every 10 subjects defined as not overweight by having a BMI <24, 3-4 still had one of the conditions. In general, the performance of BMI in screening the studied disorders ranked the best for the Taiwanese, next best for the US whites, and the poorest for the US blacks if one screened by using the BMI cutoffs that balanced positive and negative predictive value. Around 69% of Taiwanese and 6365% of US whites could be accurately classified as having or not having the disorders included in this study. However, estimates of predictive values do not provide absolute guidance as to whether BMI cutoffs should be lower for Asians and, if so, how much lower. The choice of the best cutoff depends in part on the prevalence and the cost of the selected conditions, which may vary over time and with the kind of disorders studied. In addition, whether the best cutoff is the one with equivalent proportions of false positive and false negative values is also a complex issue.
The impact fraction of any given BMI corresponds to the percentage of persons that will be removed from the original diseased population if their BMIs are lowered to below the cutoff. Because the percentage of persons with a high BMI is much less in Taiwan than in the United States, the impact fraction is also much less. A BMI cutoff slightly <24 is required to achieve the same impact fraction (13%) that US whites can obtain at a BMI of 25. Nonetheless, one needs to know more about the cost-effectiveness of BMI reduction to truly understand its impact.
One major limitation of the present study is that the comparability of 2 surveys is not easy to assess, although each followed stringent protocols. In addition, we did not address the issue of confounding factors such as smoking and drinking habits, physical activity, socioeconomic status, and menopausal status, because these issues are not only complex but also may not be satisfactorily addressed as a result of the differences in culture and questionnaire designs. However, the effect of these related systematic errors, if any, should not affect the results of relative risk per unit change of BMI, which was based on comparisons within surveys.
In conclusion, the results for odds ratios, predictive value, and impact fraction tend to support the use of lower BMI cutoffs for Taiwanese (or Asians). However, there is no easy way to determine how low the cutoffs should be. The BMI with equivalent positive and negative predictive value may be a realistic cutoff for defining overweight. After all, the major purpose of a cutoff is for screening. However, the impact (or cost) of false-positive and false-negative screening should be weighed when predictive value data are used. Another possibility is to take a pragmatic approach and consider the proportion of the population for which a country (or a society) can afford interventions. In Taiwan, one-quarter of the population has a BMI >25, one-third has a BMI >24, and one-half has a BMI >23. Consideration of national resources and of any possible negative impacts can help to determine which BMI cutoff to choose in terms of defining overweight. At the same time, a population approach to reduce overall BMI and waist circumference can be simultaneously implemented. Careful examination of the relations between body fat accumulation and distribution and BMI across ethnic groups is essential for disentangling this problem of defining obesity.
| ACKNOWLEDGMENTS |
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