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American Journal of Clinical Nutrition, Vol. 83, No. 4, 859-863, April 2006
© 2006 American Society for Nutrition


ORIGINAL RESEARCH COMMUNICATION

Estimating the effects of energy imbalance on changes in body weight in children 1,2,3

Boyd A Swinburn, Damien Jolley, Peter J Kremer, Arline D Salbe and Eric Ravussin

1 From the Schools of Exercise and Nutrition Sciences (BAS and PJK) and of Health and Social Development (DJ), Deakin University, Burwood, Australia; the National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Phoenix, AZ (ADS); and Pennington Biomedical Research Center, Baton Rouge, LA (ER)

2 Supported by Deakin University, the Pennington Biomedical Research Center, and the National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health.

3 Reprints not available. Address correspondence to BA Swinburn, School of Exercise and Nutrition Sciences, Deakin University, 221 Burwood Highway, Burwood, Victoria 3125, Australia. E-mail: boyd.swinburn{at}deakin.edu.au.


    ABSTRACT
 TOP
 ABSTRACT
 INTRODUCTION
 SUBJECTS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
Background: Estimating changes in weight from changes in energy balance is important for predicting the effect of obesity prevention interventions.

Objective: The objective was to develop and validate an equation for predicting the mean weight of a population of children in response to a change in total energy intake (TEI) or total energy expenditure (TEE).

Design: In 963 children with a mean (±SD) age of 8.1 ± 2.8 y (range: 4–18 y) and weight of 31.5 ± 17.6 kg, TEE was measured by using doubly labeled water. Log weight (dependent variable) and log TEE (independent variable) were analyzed in a linear regression model with height, age, and sex as covariates. It was assumed that points of dynamic balance, called "settling points," occur for populations wherein energy is in balance (TEE = TEI), weight is stable (ignoring growth), and energy flux (EnFlux) equals TEE.

Results: TEE (or EnFlux) explained 74% of the variance in weight. The unstandardized regression coefficient was 0.45 (95% CI: 0.38, 0.51; R2 = 0.86) after including covariates. Conversion into proportional changes (time1 to time2) gave the equation (weight2/weight1) = (EnFlux2/EnFlux1)0.45. In 3 longitudinal studies (n = 212; mean follow-up of 3.4 y), the equation predicted the mean follow-up measured weight to within 0.5%.

Conclusions: The relation of EnFlux with weight was positive, which implied that a high TEI (rather than low physical activity and low TEE) was the main determinant of high body weight. Two populations of children with a 10% difference in mean EnFlux would have a 4.5% difference in mean weight.

Key Words: Energy intake • energy expenditure • energy balance • weight change • children


    INTRODUCTION
 TOP
 ABSTRACT
 INTRODUCTION
 SUBJECTS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
The prevalence of childhood obesity is high and is on the increase in many countries (1), which has led to questions about identifying the most effective interventions at a population level. Unfortunately, there are few population intervention studies with anthropometric outcomes (2), and, therefore, evidence-based decisions about the most effective and cost-effective interventions in which to invest will have to rely on modeled estimates (3).

Such modeling needs a logic pathway of the relations between input and outcome variables and a series of coefficients for each relation, so that quantitative changes can be estimated. An example of a logic pathway linking interventions that change patterns of eating and physical activity or inactivity to outcomes of changes in overweight and obesity prevalence is shown in Figure 1Go. This study focused on the component of the pathway that links changes in energy balance to changes in body weight.


Figure 1
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FIGURE 1.. A logic pathway for modeling changes ({Delta}) in eating and physical activity patterns to changes in weight, body mass index (BMI; in kg/m2), and prevalence of overweight and obesity.

 
Modeling the effects of energy imbalance on individual weight changes is complex (4-7), and simpler methods are needed. Hill et al (8) took the approach of back-extrapolating from changes in mean population weight with an assumed 50% efficiency of converting excess energy into storage. They derived a very small value (median: {approx}125 kJ/d) for the progressive, daily positive energy imbalance needed to explain the population weight gain in adults over time—a concept they called the "energy gap." However, Butte and Ellis (9) presented data in children suggesting that this energy gap was substantially higher than the predictions of Hill et al (8). Another option for estimating these energy gaps is the use of the concept of comparing one point of dynamic balance, or "settling point" (10)—ie, the steady state in which energy intake (EI), energy expenditure (EE), and body weight are all in equilibrium—with another settling point that has a higher or lower balance of intake, expenditure, and weight.

The purposes of this study were to use EE data from studies that have used the doubly labeled water technique in children and adolescents to quantify the relation between EE and body weight, to convert this quantified relation into an equation that predicts the body weight settling points for populations as a function of the EI and EE at which energy balance is achieved, and to validate this equation against longitudinal studies in which EE was measured on 2 occasions.


    SUBJECTS AND METHODS
 TOP
 ABSTRACT
 INTRODUCTION
 SUBJECTS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
Subjects
Data from studies that measured EE by using the doubly labeled water technique (11) in normal children and adolescents aged 4–18 y were obtained from 7 centers—4 in the United States (data mostly available in 12) and 1 each in Brazil (nonstunted children only; 13), Australia (14), and New Zealand (15). The inclusion of several centers in the database meant that differences in methods, ages, and ethnicities would be spread across the dataset and would help to reduce study bias. Body weight, height, daily total EE (TEE), sex, age, ethnicity, and study center were the variables included in the analysis. Body weight was the dependent variable of interest, TEE was the major predictor variable of interest, and the other variables were included as covariates. Three centers were able to provide individual data for children who underwent follow-up measurements of TEE several years after baseline, and we used these data to compare the measured weight at follow-up against the weight predicted from our equation.

Written informed consent was obtained from the parents or guardians of all of the children. Ethical approval was obtained from each of the participating institutions.

Assumptions
We made 2 assumptions in converting this cross-sectional relation into a generalizable coefficient that could be used for predicting differences in body weight, given differences in EI and EE. First, we assumed that, on average across the study population, the TEE was equivalent to total EI (TEI). Over the period in which the TEE measurements were made (usually {approx}1–2 wk), there will have been a small mismatch between the average TEE and TEI because of the children's growth in that period, but this mismatch is on the order of 2% (16), and we ignored it for the purposes of this study. Second, we assumed that, if the population is in energy balance, then the average energy flux (EnFlux) under those equilibrium conditions is the amount of daily energy in and out while the subject is in energy balance (EnFlux = TEE = TEI), and that EnFlux is related to the average body weight of the population. This point of dynamic balance is termed the "settling point" (4) or steady state value for the mean body weight (ignoring the small effects of growth), which corresponds to the mean EnFlux. The terms TEE and TEI are used for showing the raw data, and their equivalent term, EnFlux, is used for the equations and implications.

Statistical analysis
We computed the characteristics of the sample and performed 2 simple regression analyses. First, we regressed TEE or TEI onto body weight. Because the relation between body mass and TEE is known to be exponential across mammalian species (17), we used natural logarithms for weight and TEE or TEI for the second regression. The use of logs reduced the skewness of the weight and TEE or TEI variables and also increased the linearity and reduced the heteroscedasticity of their relation.

We used the term lnEnFlux (= lnTEE = lnTEI) in a hierarchical multiple regression with lnWeight (lnkg) as the dependent variable and lnEFlux (lnkJ/d), height (cm), age (y), and sex (males = 0, females = 1) as the first set of variables. We then assessed the value of including study center, ethnicity, and interaction terms (ie, age x lnEnFlux and sex x lnEnFlux) as variables by examining changes to the adjusted R2 value. Study center and ethnicity were coded in 2 sets of 7 dummy variables each. For the longitudinal analyses, we included the changes in age, height, and EnFlux (= TEE) in the equation to predict changes in weight. We used SPSS software (version 12.0.1; SPSS Inc, Chicago, IL) for all analyses.


    RESULTS
 TOP
 ABSTRACT
 INTRODUCTION
 SUBJECTS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
The characteristics of the total study sample (n = 963) and center-specific samples are shown in Table 1Go. The sample covered a broad range of ages (3.9–18.8 y), weights (13.6–141.2 kg), TEE (2848–24 757 kJ/d), and ethnicities.


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TABLE 1. Characteristics of the study population1

 
The positive relation between body weight and TEE or TEI on the arithmetic (R2 = 0.71) and logarithmic (R2 = 0.74) scales is shown in Figure 2Go. At the first step of the hierarchical regression, the model included height, age, and sex with the lnTEE variable (henceforth called lnEnFlux). This model explained 86% of the variance in lnWeight, and the unstandardized regression coefficient for lnEnFlux was 0.45 (95% CI: 0.38, 0.51). lnEnFlux (P < 0.001), height (P < 0.001), age (P = 0.009), and sex (P = 0.031) were all statistically significant. The inclusion of the dummy variables for study center and ethnicity and the interaction terms age x lnEnFlux and sex x lnEnFlux at the second step increased the adjusted R2 to 0.89. Whereas many of the interaction and dummy variables were statistically significant in the full model, they added considerable complexity to the equations given here (see below), and their total added contribution toward explaining the variance in lnWeight was small (3%). For these reasons, they have not been included in the equation transformations below.


Figure 2
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FIGURE 2.. The relation between body weight and total energy expenditure or intake as linear variables (top: r = 0.84) or as log-transformed (ln) variables (bottom: r = 0.86).

 
The following equation is based on the unstandardized coefficients derived from the first regression model:

Formula 1(1)
The antilog of both sides of equation 1 is taken in the following equation:

Formula 2(2)
Equation 2 is transformed into a ratio from time1 to time2 for considering the same population at different time points (sexand constant variables cancel out), as shown in the following equation:

Formula 3(3)
If height and age are considered the same, these variables also cancel out, as shown in the following equation:

Formula 4(4)
which can represent a "what if" scenario for a population: eg, what would be the mean weight of a population with the same age, height, and sex mix if the population were consuming 10% more or 10% less energy? Equation 4 has been plotted for a range of values for percentage differences in EnFlux and body-weight settling points (Figure 3Go). Within the range shown, the slope is not quite linear: a 10% higher EnFlux resulted in a predicted settling point weight 4.36% higher, and a 10% lower EnFlux resulted in a 4.61% lower body weight.


Figure 3
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FIGURE 3.. Estimated differences in the "settling points" for the mean body weight of 3 populations of children or adolescents according to differences in the mean equilibrium energy flux [which equals total energy intake (TEI) or total energy expenditure (TEE) when in energy balance]. The slope of the line is {approx}0.45, which implies that, if population B has a mean equilibrium energy flux that is 10% higher than that of population A, its settling point for mean body weight will be {approx}4.5% higher. Similarly, if population C has a mean equilibrium energy flux that is 10% lower than that of population A, its settling point for mean body weight will be {approx}4.5% lower.

 
To test the validity of the above equations, we used 3 studies (18-20) in which TEE, height, and weight had been measured twice in the same children or adolescents some years apart. The study by Spadano et al (20) measured 24 girls on 3 occasions; we used only the first and last measurements for the current study. The weighted mean follow-up duration for all longitudinal studies was 3.4 y. The characteristics of the 212 subjects with longitudinal data are shown in Table 2Go, which compares the mean observed follow-up body weight with the predicted follow-up weight for each study by using equation 3. For each of the follow-up populations, there were no significant differences between the observed and the predicted final mean weights. For the whole follow-up population, the predicted final mean weight (53.19 kg) was within {approx}250 g (<0.5%) of the observed mean weight (53.44 kg).


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TABLE 2. Characteristics of children with measured weight and total energy expenditure (TEE) on 2 occasions

 

    DISCUSSION
 TOP
 ABSTRACT
 INTRODUCTION
 SUBJECTS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
We have used the cross-sectional relation between TEE and body weight as the basis for predicting the mean weight of a population of children with a given total equilibrium energy flux (where EnFlux = TEE = TEI when in energy balance). The validation of the equation with the use of longitudinal studies was very tight: it predicted the follow-up weight to within {approx}250 g. The equation would predict that, if the whole study population of 963 children was, for example, eating 10% less energy (785 kJ/d or {approx}450 mL of a soft drink), their mean weight would be {approx}4.5% (1.4 kg) lower. If this population was eating the same amounts but was instead far more active (eg, walking 2.5 h more to burn an extra 785 kJ/d; 21), the same reduction in body weight would be expected.

The first fundamental point of the study is that the relation between body weight and EnFlux (TEE) was strongly positive and not negative. If most of the variation in body weight (once age, height, and sex were taken into account) was due to differences in the physical activity levels of the children, then the relation should have been negative (ie, higher TEE associated with a lower weight). That the overall relation is positive suggests that it is higher TEI that is the major determinant of a higher body weight. In other words, a high TEI drives an increase in body weight, which in turn increases fat-free mass and resting metabolic rate (22, 23) until TEE matches TEI and body weight reaches its new settling point of body weight for that EnFlux. Differences in physical activity levels and body composition, however, undoubtedly explain much of the variation around the positive regression line.

The longitudinal data have provided strong empirical validity for the prediction equation; nevertheless, it is important to examine the assumptions that have been made in the process of deriving this equation. The assumption that TEE data from doubly labeled water studies can be considered the equivalent of TEI and EnFlux data is probably reasonable, because the energy cost of growth over the measurement period of 1–2 wk is small enough (16) to be ignored. Over several years, however, the energy contribution to growth is substantial and, in the case of the longitudinal data, this contribution was accounted for by having height and age in the equation.

Another assumption was the use of "settling points," or states of dynamic equilibrium between EnFlux and body weight. At the individual level, TEI and TEE fluctuate substantially on a daily basis, whereas body weight varies (generally in an upward direction in children) over weeks, months, and years. However, if the mean values for body weight and EnFlux are considered at a population level, many of these individual fluctuations cancel each other out, and, if the measurement "snapshot" is over a short period, then the cost of growth can probably be ignored.

Notwithstanding these cautions, equation 4 can be used to answer questions posed in the logic pathway outlined in Figure 1Go. For example, the difference in median body weights of 10–15-y-old children between 2 national nutrition surveys in Australia in 1985 and 1995 was {approx}8% (range: 45.3–48.9 kg; 24). On the basis of these mean weights, how much more energy were children eating to sustain their higher body weight in 1995 than in 1985? Equation 4 estimates that they were eating 19% more, which compares to the reported increase in TEI of 13% (range: 8266–9345 kJ/d) between the 2 surveys (24). TEI was measured by using a 24-h dietary recall, which is known to underestimate TEI because of underreporting (25). Secular reductions in physical activity (26) may also contribute to this discrepancy.

One way to describe the energy gap between these 2 Australian surveys is in terms of the 19% increase in EI ({approx}1500 kJ/d), which is rather large. Another way is to convert the population weight gain (3.6 kg) into excess energy in storage ({approx}119 MJ at 33 MJ/kg), assuming an energy efficiency of storage ({approx}50%), and then to divide it by the number of days of the study (8). This calculation gives a very small value of {approx}65 kJ excess energy/d (3.6 kg x 33 MJ/kg x 2 ÷ 3650 d = 65 kJ/d).

The reconciliation between the large and small estimates of the energy gap is that the large estimate (1500 kJ/d) is the final energy gap needed to sustain that higher weight (independent of the time needed to achieve that weight), whereas the smaller value (65 kJ/d) is the daily positive energy balance needed every day over 10 y to achieve that higher weight. Unfortunately, this latter approach is often misinterpreted to mean that only small behavioral changes are needed to reverse the obesity epidemic (27-29). The misinterpretation is to equate the initial EI needed to create the positive energy balance on day 1 with the daily positive energy balance needed over a period of 10 y.

One issue not considered in this study is the potential for behavioral compensation or other interaction resulting from a change in behavior such that the full effect of the initial energy change is not carried through to energy imbalance (30, 31). This is depicted in the lefthand side of Figure 1Go. For example, having more time for physical education at school may trigger other changes in physical activity or dietary intake so that the net energy imbalance is lower than expected (32).

In conclusion, we have presented a validated model for estimating the difference in the mean body weights of populations of children who have different equilibrium energy fluxes, which seem to be principally driven by differences in wEI. The equation could be used to model the effect of populationwide obesity prevention interventions on mean body weight and obesity prevalence, but caution is needed in applying such models to individual persons. Modeling the effectiveness of various population interventions should provide public health decision makers with an important interim guide to investment in obesity prevention while they await more empirical weight-change studies in children and adolescents.


    ACKNOWLEDGMENTS
 
We thank the following people who helped with the provision of data for this study: US data—Linda Bandini, James DeLany, Susan Roberts, and Margarita Treuth; Brazilian data—Daniel Hoffman and Ana Sawaya; Australian data—Louise Baur, Peter Davies, and Janice O'Connor; New Zealand data—Elaine Rush. In addition, Aicha Bassile provided research assistance and Nancy Butte provided a valuable critique of the manuscript.

BAS was responsible for the conception of the study, with assistance from ER and DJ; BAS and ER were responsible for sourcing the data; ADS provided much of the original data; PJK and ER analyzed the data; all authors helped interpret the data, and DJ provided statistical interpretations; BAS was the lead writer of the manuscript, and ER provided input; and DJ, PJK, and ADS reviewed the manuscript. None of the authors had a personal or financial conflict of interest.


    REFERENCES
 TOP
 ABSTRACT
 INTRODUCTION
 SUBJECTS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 

  1. Lobstein T, Baur L, Uauy R. Obesity in children and young people: a crisis in public health. Obes Rev 2004; 5(suppl 1): 4-104.
  2. Campbell K, Waters E, O'Meara S, Kelly S, Summerbell C. Interventions for preventing obesity in children. Cochrane Database Syst Rev 2002(2):CD001871.
  3. Swinburn B, Gill T, Kumanyika S. Obesity prevention: a proposed framework for translating evidence into action. Obes Rev 2005; 6: 23-33.[Medline]
  4. Swinburn BA, Ravussin E. Energy and macronutrient metabolism. Baillieres Clin Endocrinol Metab 1994; 8: 527-48.[Medline]
  5. Westerterp KR, Donkers JH, Fredrix EW, Boekhoudt P. Energy intake, physical activity and body weight: a simulation model. Br J Nutr 1995; 73: 337-47.[Medline]
  6. Alpert SS. Growth, thermogenesis, and hyperphagia. Am J Clin Nutr 1990; 52: 784-92.[Abstract/Free Full Text]
  7. Christiansen E, Garby L, Sorensen TI. Quantitative analysis of the energy requirements for development of obesity. J Theor Biol 2005; 234: 99-106.[Medline]
  8. Hill JO, Wyatt HR, Reed GW, Peters JC. Obesity and the environment: where do we go from here? Science 2003; 299: 853-5.[Abstract/Free Full Text]
  9. Butte NF, Ellis KJ. Comment on "Obesity and the environment: where do we go from here?" Science 2003; 301: 598 (letter).
  10. Egger G, Swinburn B. An "ecological" approach to the obesity pandemic. BMJ 1997; 315: 477-80.[Free Full Text]
  11. Schoeller DA, Ravussin E, Schutz Y, Acheson KJ, Baertschi P, Jequier E. Energy expenditure by doubly labeled water: validation in humans and proposed calculation. Am J Physiol 1986; 250(5 Pt 2): R823-30.
  12. Institute of Medicine. Dietary reference intakes for energy, carbohydrate, fiber, fat, fatty acids, cholesterol, protein, and amino acids. Washington DC: Institute of Medicine, 2002.
  13. Hoffman DJ, Sawaya AL, Coward WA, et al. Energy expenditure of stunted and nonstunted boys and girls living in the shantytowns of Sao Paulo, Brazil. Am J Clin Nutr 2000; 72: 1025-31.[Abstract/Free Full Text]
  14. Ball EJ, O'Connor J, Abbott R, et al. Total energy expenditure, body fatness, and physical activity in children aged 6–9 y. Am J Clin Nutr 2001; 74: 524-8.[Abstract/Free Full Text]
  15. Rush EC, Plank LD, Davies PS, Watson P, Wall CR. Body composition and physical activity in New Zealand Maori, Pacific and European children aged 5–14 years. Br J Nutr 2003; 90: 1133-9.[Medline]
  16. Butte NF. Fat intake of children in relation to energy requirements. Am J Clin Nutr 2000; 72(suppl): 1246S-52S.[Abstract/Free Full Text]
  17. White CR, Seymour RS. Mammalian basal metabolic rate is proportional to body mass2/3. Proc Natl Acad Sci U S A 2003; 100: 4046-9.[Abstract/Free Full Text]
  18. DeLany JP, Bray GA, Harsha DW, Volaufova J. Energy expenditure in African American and white boys and girls in a 2-y follow-up of the Baton Rouge Children's Study. Am J Clin Nutr 2004; 79: 268-73.[Abstract/Free Full Text]
  19. Salbe AD, Weyer C, Harper I, Lindsay RS, Ravussin E, Tataranni PA. Assessing risk factors for obesity between childhood and adolescence: II. Energy metabolism and physical activity. Pediatrics 2002; 110(2 Pt 1): 307-14.
  20. Spadano JL, Bandini LG, Must A, Dallal GE, Dietz WH. Longitudinal changes in energy expenditure in girls from late childhood through midadolescence. Am J Clin Nutr 2005; 81: 1102-9.[Abstract/Free Full Text]
  21. Health Promotion Strategy Unit. Active For Life. Physical Activity Patterns & Health Impacts in Victoria. Melbourne, Australia: Public Health & Development Division, Victoria Government Department of Human Services, 1999.
  22. Ravussin E, Lillioja S, Anderson TE, Christin L, Bogardus C. Determinants of 24-hour energy expenditure in man. Methods and results using a respiratory chamber. J Clin Invest 1986; 78: 1568-78.[Medline]
  23. Tataranni PA, Ravussin E. Variability in metabolic rate: biological sites of regulation. Int J Obes Relat Metab Disord 1995; 19(suppl): S102-6.
  24. Cook P, Rutishauser IHE, Seelig M. Comparable data on food and nutrient intake and physical measurements from the 1983, 1985 and 1995 National Nutrition Surveys. Brisbane, Australia: Australian Food and Nutrition Monitoring Unit, 2001.
  25. Bandini LG, Must A, Cyr H, Anderson SE, Spadano JL, Dietz WH. Longitudinal changes in the accuracy of reported energy intake in girls 10–15 y of age. Am J Clin Nutr 2003; 78: 480-4.[Abstract/Free Full Text]
  26. Bauman A, Bellew B, Vita P, Brown W, Owen N. Getting Australia Active: towards better practice for the promotion of physical activity. Melbourne, Australia: National Public Health Partnership, 2002.
  27. Levine JA, Lanningham-Foster LM, McCrady SK, et al. Interindividual variation in posture allocation: possible role in human obesity. Science 2005; 307: 584-6.[Abstract/Free Full Text]
  28. Stubbs CO, Lee AJ. The obesity epidemic: both energy intake and physical activity contribute. Med J Aust 2004; 181: 489-91.[Medline]
  29. Murray R, Frankowski B, Taras H. Are soft drinks a scapegoat for childhood obesity? J Pediatr 2005; 146: 586-90.[Medline]
  30. Melzer K, Kayser B, Saris WH, Pichard C. Effects of physical activity on food intake. Clin Nutr 2005; 21: 885-95. Epub 2005 Jul 21.
  31. Woo R, Garrow JS, Pi-Sunyer FX. Effect of exercise on spontaneous calorie intake in obesity. Am J Clin Nutr 1982; 36: 470-7.[Abstract/Free Full Text]
  32. Mallam KM, Metcalf BS, Kirkby J, Voss LD, Wilkin TJ. Contribution of timetabled physical education to total physical activity in primary school children: cross sectional study. BMJ 2003; 327: 592-3.[Free Full Text]
Received for publication August 29, 2005. Accepted for publication January 6, 2006.




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