American Journal of Clinical Nutrition, Vol. 85, No. 4, 1121-1126,
April 2007
© 2007 American Society for Nutrition
ORIGINAL RESEARCH COMMUNICATION |
Body mass index and serum leptin concentration independently estimate percentage body fat in older adults1,2,3
Constance E Ruhl,
Tamara B Harris,
Jingzhong Ding,
Bret H Goodpaster,
Alka M Kanaya,
Stephen B Kritchevsky,
Eleanor M Simonsick,
Frances A Tylavsky,
James E Everhart for the Health ABC Study
1 From Social & Scientific Systems Inc, Silver Spring, MD (CER); the Laboratory of Epidemiology, Demography, and Biometry, Intramural Research Program (TBH), and the Clinical Research Branch (EMS), National Institute of Aging, Bethesda, MD; the Department of Internal Medicine, Geriatric Division (JD), and the Section on Gerontology and Geriatric Medicine (SBK), J Paul Sticht Center, Wake Forest University School of Medicine, Winston-Salem, NC; the Division of Endocrinology and Metabolism, University of Pittsburgh Department of Medicine, Pittsburgh, PA (BHG); the Department of Medicine, University of California, San Francisco, San Francisco, CA (AMK); the Department of Preventive Medicine, University of Tennessee, Memphis, TN (FAT); and the National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Department of Health and Human Services, Bethesda, MD (JEE)
2 The Health, Aging, and Body Composition Study was funded in part by the Intramural Research program of the NIH, National Institute on Aging, and by the National Institute on Aging contract numbers N01-AG-6-2106, N01-AG-6-2101, and N01-AG-6-2103. The current work was supported by a contract from the National Institute of Diabetes and Digestive and Kidney Diseases (no. NO1-DK-1-2478).
3 Address reprint requests to CE Ruhl, Social & Scientific Systems Inc, 8757 Georgia Avenue, 12th floor, Silver Spring, MD 20910. E-mail: cruhl{at}s-3.com.
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ABSTRACT
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Background:Because serum concentrations of leptin, a hormone produced by adipocytes, can be relatively reliably and inexpensively measured, it may be considered complementary to, or even a substitute for, body mass index (BMI) as a measure of adiposity.
Objective:We examined the ability of BMI and leptin concentrations, separately and together, to estimate total percentage fat in older adults.
Design:Total percentage fat measured by dual-energy X-ray absorptiometry and fasting serum leptin concentrations were measured in 2911 well-functioning 70–79-y-old participants (42% black, 51% women) in the Health, Aging, and Body Composition Study.
Results:Mean (±SD) total percentage fat was 29.2 ±5.0% in men and 40.5 ± 5.7% in women, and the geometric mean (±SD) serum leptin concentration was 5.6 ± 2.5 ng/mL in the men and 16.4 ± 2.3 ng/mL in the women. Among men, total percentage fat was strongly associated with both BMI (R2 = 0.56) and leptin (R2 = 0.57) in separate linear regression analyses and in a combined linear regression analysis (R2 = 0.68). Similarly, among women, total percentage fat was associated with both BMI (R2 = 0.65) and leptin (R2 = 0.54) separately and in combination (model R2 = 0.71). Independent relations of BMI and leptin with total percentage fat were also found among both black and white participants. With the population divided into quintiles according to percentage fat, BMI and serum leptin correctly classified 49% of men and 50% of women in the correct quintile.
Conclusions:Among older adults, total percentage fat was better estimated by using both serum leptin concentrations and BMI than by using either alone. However, their performance does not suggest that they can substitute for more accurate measures.
Key Words: Leptin • body composition • anthropometry • dual-energy X-ray absorptiometry • race • epidemiology • Health • Aging • and Body Composition Study • Health ABC
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INTRODUCTION
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Obesity is defined as excess body fat. Body mass index (BMI) is nearly universally used as a measure for obesity in large studies that examine the association of obesity with morbidity and mortality—yet it does not discriminate between fat and lean body mass. The percentage variation of percentage body fat, as measured by hydrodensitometry, that can be explained by BMI (R2) has ranged from 0.50 to 0.68 in men and from 0.58 to 0.74 in women (1-7). Because techniques that can discriminate between fat mass and fat-free mass, such as dual-energy X-ray absorptiometry (DXA), are generally not feasible among large populations, an accurate, reliable measure of total body fat that can be easily determined in clinical care and population studies is needed. One such possible measure is leptin, which is produced by adipocytes and whose serum concentration appears to reflect total body fat (8-10). Because leptin can be relatively reliably and inexpensively measured, it may be considered complementary to, or even a substitute for, BMI as a measure of adiposity. However, we are unaware of any full-scale studies of the relative value of BMI and leptin in estimating body fat. We examined these issues in a large cohort of healthy, elderly blacks and whites from the Health, Aging, and Body Composition (Health ABC) Study.
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SUBJECTS AND METHODS
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The Health ABC study is a population-based, longitudinal study of 3075 community-dwelling, nondisabled white and black men and women aged 70–79 y that was begun in 1997. The main goal was to investigate changes in weight and body composition, weight-related health conditions, and incident functional limitations (11). Participants were recruited from a random sample of white Medicare beneficiaries and all age-eligible black community residents residing in designated zip codes in the metropolitan areas of Pittsburgh, PA, and Memphis, TN. The sample was selected to represent well-functioning older persons. Eligible participants reported no difficulty walking one-fourth mile, walking up 10 steps, or performing basic activities of daily living. The study was approved by the Institutional Review Boards at the Universities of Pittsburgh and Tennessee, and all participants provided written, informed consent to participate. The present analysis used cross-sectional data from the baseline examination conducted between 1997 and 1998 on all 2911 participants with data on serum leptin concentration, total percentage fat, and BMI.
Serum leptin concentrations were measured in duplicate by radioimmunoassay on a morning fasting venous blood sample [Sensitive Human Leptin RIA Kit (product no. SHL-81K); Linco Research Inc, St Charles, MO] (12). The minimum detectable concentration of the assay is 0.05 ng/mL. The mean intraassay CV is 5.8% (range: 3.7–7.5%) and the mean interassay CV is 7.4% (range: 3.2–8.9%). The linear range of leptin concentration was 0–99 ng/mL. Six participants with leptin concentrations >99 ng/mL, for whom an accurate value could not be determined by the laboratory, were excluded from analysis.
Total body fat was estimated from DXA (QDR 4500A, with Software Version 8.21 for analysis; Hologic Inc, Waltham, MA) (13). Height was measured to the nearest mm by using a Harpenden stadiometer (Holtain Ltd, Crosswell, Wales, United Kingdom) with the participant barefoot, and weight was measured to the nearest 0.1 kg by using a standard balance beam scale with the participant wearing lightweight clothing. BMI [weight (in kg)/height2 (in m)] was calculated.
Leptin concentration was log 10 transformed to normalize its distribution. Means and SDs for total percentage fat, serum leptin concentration, and BMI were calculated, and means were compared between sex and race subgroups by using analysis of variance. A P value < 0.05 indicated statistical significance. Multiple linear regression analysis was used to calculate the proportion of variation (R2) in percentage fat explained by BMI and leptin individually and jointly. Quadratic terms for BMI and leptin were considered for inclusion in the models and retained if they improved the R2. Analyses were adjusted for age, field center site, and race (in analyses of men and women). Sex-specific models that best predicted percentage fat from BMI and leptin individually and jointly were determined. The models were tested by calculating the proportion of participants for whom they predicted the correct percentile group (as fifths, quarters, or thirds) of the measured percentage fat. The proportions correctly classified were compared between models by using McNemar's test. The effects of sex and measured percentage fat percentile on the ability of BMI and log10 leptin, independently and jointly, to correctly classify participants were evaluated using logistic regression analysis. Because BMI and leptin were correlated (
= 0.56), collinearity in multiple regression models was evaluated by using variance inflation factor and tolerance (14). Substantial collinearity was not found. Analyses were performed by using SAS 9.1 software (15).
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RESULTS
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Total percentage fat, serum leptin concentrations, and BMI were measured in 2911 participants (889 white men, 528 black men, 807 white women, and 687 black women). Mean (±SD) total percentage fat was higher in the women than in the men (40.5 ± 5.7% compared with 29.2 ± 5.0%) and, within sex groups, was higher in the black women and in the white men (Table 1
). Geometric mean leptin concentrations were higher in the women than in the men (16.4 ± 2.3 ng/mL compared with 5.6 ± 2.5 ng/mL) and higher in the black women than in the white women. No significant ethnic differences in leptin concentrations were observed among the men. BMI was higher in the women than in the men and higher in the black than the white women, but it did not differ significantly between black and white men.
Percentage fat was strongly associated with BMI, leptin, and log10 leptin in separate analyses in both the men and the women (Figure 1, Figure 2, Figure 3, and Table 2). A test for interaction on total percentage fat was significant for sex, race, and log10 leptin (P = 0.002) and borderline for sex, race, and BMI (P = 0.090). Two-way interactions were nonsignificant for sex and BMI (P = 0.39) and for sex and race (P = 0.56) and significant for race and BMI (P = 0.014). Because of significant interactions, separate sex-race models are shown. In analyses with BMI and log10 leptin, percentage fat remained independently associated with both in both sexes. As a result, the proportion of variation in percentage fat explained by BMI and log10 leptin jointly was greater among both the men (R2 = 0.68) and the women (R2 = 0.71) than was that explained by BMI and log10 leptin alone (Table 2). Among the men, there was little difference between log10 leptin and BMI in the ability to predict percentage fat. This was true for both blacks and whites. Among the women, BMI appeared to be a better predictor of percentage fat than was log10 leptin among both whites and blacks. BMI and log10 leptin combined had a similar ability to predict percentage fat in the men and women. The combined predictive ability of BMI and log10 leptin was lowest in the white men and highest in the black women but did not vary greatly among sex-ethnicity subgroups (R2 = 0.65–0.72) (Table 2).
To evaluate the linearity of the relations of percentage fat with log10 leptin and BMI and to develop the best fitting predictive equations, the addition of quadratic terms to the models was tested. Inclusion of quadratic terms for BMI to predict percentage fat increased the R2 by 1% in equations for the men and 3–4% in equations for the women. However, in combination with log10 leptin, BMI squared increased the R2 only in equations for women and only by 1%. Inclusion of quadratic terms for log10 leptin had minimal effect on the R2 (Table 2
). The models that best predicted percentage fat from BMI and log10 leptin individually and jointly are shown in Table 3.
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TABLE 3 Coefficients for best-fit linear regression models for percentage fat using BMI, log10 leptin, or both and after control for race, age, and examination site1
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The ability of BMI and log10 leptin to correctly categorize percentage fat by DXA is shown in Table 4 according to quintiles for men and for women. Inclusion of both BMI and log10 leptin increased the proportion correctly classified over using just one measure. Log10 leptin contributed more among the men than the women (P < 0.001), and BMI contributed more among women than the men (P < 0.001). BMI alone classified women with the lowest and highest DXA-measured percentage fat more accurately than for women with percentage fat in the midrange (P = 0.044), whereas there was no significant difference based on percentage fat quintile among the men (P = 0.37; P for sex-percentage fat quintile interaction = 0.042). Log10 leptin alone predicted percentage fat better among the women than among the men (P = 0.047) and better among the participants with lower DXA-measured percentage fat than among those with higher levels (P < 0.001). BMI and log10 leptin combined did not significantly differ in predictive ability by sex (P = 0.74), but predicted percentage fat better at the lowest and highest quintiles than in the middle (P = 0.005). The overall correct classification was 49% among the men and 50% among the women when using the equations in Table 3. As expected, if percentage fat was divided into larger categories, a higher proportion would be correctly classified. With 4 categories (quartiles), the percentage classified correctly was 54% among the men and 58% among the women. With 3 categories (tertiles), the percentage classified correctly was 67% among the men and 68% among the women.
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TABLE 4 Correct quintile categorization of percentage fat among men and women by BMI, log10 leptin, and BMI and log10 leptin regression models1
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DISCUSSION
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In the United States and many other countries, overweight and obesity are problems of epidemic proportion that increase the risk of numerous medical conditions (16, 17). Consequently, accurate and easily measured indicators of body fat are needed to perform comparisons across populations, to monitor trends, and to study the increased health risks of obesity. They may have a place in clinical medicine as well. BMI is a commonly used surrogate for adiposity that is inexpensive and easily measured, but its correlation with body fat is imperfect. The greatest limitation is that BMI does not discriminate between fat and lean body mass. This can be misleading, because the relation between BMI and body fat is dependent on sex, age, race-ethnicity, and fitness level. Women have a higher proportion of body fat than do men with the same BMI. For example, in the current study, white women had lower BMI than did white men but had considerably higher percentage body fat. Percentage body fat increases with age for a given BMI, particularly after middle age and during menopause in women (18, 19). African Americans have a lower percentage body fat than do whites at a given BMI, whereas the reverse is true of many Asian ethnicities (18, 20, 21).
In the current study of older black and white adults, total percentage fat was better estimated by using both log10 serum leptin concentrations and BMI than by using either alone. Independent relations of log10 leptin and BMI with total percentage fat were found across strata of sex and ethnicity. BMI was a better predictor of percentage fat in the women than was log10 leptin, whereas there was no significant difference between the 2 in the men. Because BMI reflects lean mass as well as fat mass, it may have been a less accurate predictor in men who have a higher proportion of lean mass compared with women. The men exhibited greater variation in percentage fat within BMI categories than did the women (data not shown), so the addition of log10 leptin improved specificity in the men and compensated for the lower predictive ability of BMI.
Although the present analysis shows an improved estimate of percentage fat with the use of both BMI and log10 leptin, their performance does not suggest that they can substitute for more accurate measures. By using DXA as the reference and best fit equations that included log10 leptin, BMI, ethnicity, age, and examination site, not more than one-half of the men and women were classified into the correct quintile of percentage body fat (Table 4). Although this is much better than the expected 20% correct classification by chance alone, this degree of accuracy is somewhat disappointing given the relatively narrow age-range. The lower predictive ability at the highest percentage fat quintiles may have resulted in part from flattening of the leptin-percentage fat curves at higher levels of percentage fat (Figure 2A and B). However, we attempted to address this nonlinear relation using log10 transformed leptin in the regression models and by evaluating quadratic terms for log10 leptin and BMI in the models. The flattening of the leptin curves reflects a greater increase in leptin per unit increase in percentage fat at higher levels of percentage fat. This is consistent with leptin resistance that occurs in most obese persons (22, 23). Substituting height and weight, or the reciprocal of BMI, for BMI did not improve the predictive ability (data not shown). Furthermore, the best fitted equations for estimating percentage fat included ethnicity, age, and study site, which suggests that they could not be generalized to other populations. Whether leptin and BMI independently predict percentage fat in younger adults and among other ethnic groups requires further study.
A better estimate of body fat can be obtained with DXA than with BMI or leptin, but DXA is more complex, time consuming, and expensive than is measuring BMI or leptin. DXA has its own limitations as a measure of fat. The estimation of fat depends on the model of the machine used and even varies from machine to machine, although differences between machines tend to be systematic across the range of body weights. Further, very obese persons cannot undergo DXA measurements because of weight limitations for the equipment. The correlation with other criterion measures of body fat is excellent, although the model used in the current study may underestimate total fat (24).
Because obesity is defined as an excess of body fat and is increasingly common in nearly all age groups and in all populations, it is critical that more accurate measures of body fat be developed that can be applied to large populations. With the ever-increasing public health significance of obesity, it is perhaps surprising that few studies have examined measures other than height and weight and a limited number of other anthropometric measures for this purpose. Bioelectrical impedance is a simple, fast, inexpensive, and reproducible method to use in epidemiologic studies; however, its use is limited by the inability to generalize the prediction equations (25). Leptin may yet prove to be one element in such a search for body fat measures for use in population studies, but the results of the current analysis indicate that it performs better when combined with BMI. Longitudinal studies of body composition changes and health outcomes will demonstrate whether leptin has additional clinical utility.
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ACKNOWLEDGMENTS
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The authors thank Danita Holt and the late Anthony Pridgen for programming support.
CER designed and conducted the data analysis and wrote the manuscript. TBH designed and collected data for the Health ABC study, designed the data analysis, edited the manuscript, and gave advice and consultation. JD designed the data analysis and edited the manuscript. BHG designed and collected data for the Health ABC study and gave advice and consultation for the study. AMK edited the manuscript and gave advice and consultation for the study. SBK designed and collected data for the Health ABC study and gave advice and consultation for the study. EMS designed and collected data for the Health ABC study, edited the manuscript, and gave advice and consultation for the study. FAT designed and collected data for the Health ABC study, edited the manuscript, and provided advice and consultation for the study. JEE designed and collected data for the Health ABC study, analyzed the data, edited the manuscript, and provided advice and consultation for the study. None of the authors have a conflict of interest.
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REFERENCES
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|---|
- Allen TH, Peng MT, Chen KP, Huang TF, Chang C, Fang HS. Prediction of blood volume and adiposity in man from body weight and cube of height. Metabolism 1956;5:328–45.[Medline]
- Keys A, Fidanza F, Karvonen MJ, Kimura N, Taylor HL. Indices of relative weight and obesity. J Chronic Dis 1972;25:329–43.[Medline]
- Womersley J, Roche AF, Sievogel RM, Chumlea WC, Webb P. A comparison of the skinfold method with extent of ‘overweight’ and various weight-height relationships in the assessment of obesity: grading body fatness from limited anthropometric data. Br J Nutr 1977;38:271–84.[Medline]
- Roche AF, Sievogel RM, Chumlea WC, Webb P. Grading body fatness from limited anthropometric data. Am J Clin Nutr 1981;34:2831–8.[Abstract/Free Full Text]
- Revicki DA, Israel RG. Relationship between body mass indices and measures of body adiposity. Am J Public Health 1986;76:992–4.[Abstract/Free Full Text]
- Willett W. Nutritional epidemiology. New York, NY: Oxford, 1990:231–5.
- Gray DS, Fujioka K. Use of relative weight and body mass index for the determination of adiposity. J Clin Epidemiol 1991;44:545–50.[Medline]
- Rosenbaum M, Nicolson M, Hirsch J, et al. Effects of gender, body composition, and menopause on plasma concentrations of leptin. J Clin Endocrinol Metab 1996;81:3424–7.[Abstract]
- Hickey MS, Israel RG, Gardiner SN, et al. Gender differences in serum leptin levels in humans. Biochem Mol Med 1996;59:1–6.[Medline]
- Couillard C, Mauriege P, Prud'homme D, et al. Plasma leptin concentrations: gender differences and associations with metabolic risk factors for cardiovascular disease. Diabetologia 1997;40:1178–84.[Medline]
- Harris TB, Visser M, Everhart J, et al. Waist circumference and sagittal diameter reflect total body fat better than visceral fat in older men and women. The Health, Aging and Body Composition Study. Ann N Y Acad Sci 2000;904:462–73.[Abstract/Free Full Text]
- Ma Z, Gingerich RL, Santiago JV, Klein S, Smith CH, Landt M. Radioimmunoassay of leptin in human plasma. Clin Chem 1996;42:942–6.[Abstract/Free Full Text]
- Tylavsky FA, Fuerst T, Nevitt M, et al. Measurement of changes in soft tissue mass and fat mass with weight change: pencil- versus fan-beam dual-energy X-ray absorptiometry. Health ABC Study. Ann N Y Acad Sci 2000;904:94–7.[Free Full Text]
- Wetherill GB, Duncombe P, Kenward M, Köllerström J, Paul SR, Vowden BJ. Regression analysis with applications. London, United Kingdom: Chapman and Hall, 1986.
- SAS Institute Inc. SAS/STAT 9.1 user's guide. Cary, NC: SAS Institute Inc, 2004.
- Hedley AA, Ogden CL, Johnson CL, Carroll MD, Curtin LR, Flegal KM. Prevalence of overweight and obesity among US children, adolescents, and adults, 1999–2002. JAMA 2004;291:2847–50.[Abstract/Free Full Text]
- Bray GA. Medical consequences of obesity. J Clin Endocrinol Metab 2004;89:2583–9.[Abstract/Free Full Text]
- Prentice AM, Jebb SA. Beyond body mass index. Obes Rev 2001;2:141–7.[Medline]
- Cohn SH. New concepts of body composition. In: Ellis KJ, Yasumura S, Morgan WD, eds. In vivo body composition studies. London, United Kingdom: The Institute of Physical Sciences in Medicine, 1987:1–14.
- Banerji MA, Faridi N, Atluri R, Chaiken RL, Lebovitz HE. Body composition, visceral fat, leptin, and insulin resistance in Asian Indian men. J Clin Endocrinol Metab 1999;84:137–44.[Abstract/Free Full Text]
- Deurenberg P, Yap M, van Staveren WA. Body mass index and percent body fat: a meta analysis among different ethnic groups. Int J Obes Relat Metab Disord 1998;22:1164–71.[Medline]
- Considine RV, Sinha MK, Heiman ML, et al. Serum immunoreactive-leptin concentrations in normal-weight and obese humans. N Engl J Med 1996;334:292–5.[Abstract/Free Full Text]
- Arch JR. Central regulation of energy balance: inputs, outputs and leptin resistance. Proc Nutr Soc 2005;64:39–46.[Medline]
- Tylavsky F, Lohman T, Blunt BA, et al. QDR 4500A DXA overestimates fat-free mass compared with criterion methods. J Appl Physiol 2003;94:959–65.[Abstract/Free Full Text]
- Kuczmarski RJ. Bioelectrical impedance analysis measurements as part of a national nutrition survey. Am J Clin Nutr 1996;64(suppl):453S–8S.[Abstract/Free Full Text]
Received for publication January 2, 2006.
Accepted for publication November 16, 2006.
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ABSTRACT
INTRODUCTION
, n = 528) and white (
, n = 889) men (A) and among well-functioning older black (
