Factors Affecting Energy Expenditure and Requirements (original) (raw)
Total energy expenditure (TEE) is the energy expended during oxidation of energy-yielding macronutrients within a 24-hour period. TEE includes three core components: resting metabolic rate, or resting energy expenditure (REE); the thermic effect of food (TEF), also referred to as diet-induced thermogenesis (DIT); and physical activity. REE, generally the largest contribution to TEE, represents the energy needed to support maintenance of normal body functioning and homeostasis. TEF is the increase in energy expenditure associated with the ingestion of food. Physical activity level (PAL) is the energy expenditure above and beyond the basal state and TEF. These three components and their determinants are shown in Figure 4-1. Table 4-1 further describes these and other terms used to indicate various components of energy expenditure. In this report, some terms are used interchangeably because the committee used the original terminology used in each reviewed paper. Additionally, while alternate terms are identified, not all are used in this report.
FIGURE 4-1
Components of energy expenditure and their determinants. NOTE: EER = estimated energy requirement. SOURCE: Adapted from Lam and Ravussin, 2016.
TABLE 4-1
Definitions for the Components of Total Energy Expenditure and Estimated Energy Requirements.
Part of the committee’s task was to review the components of energy expenditure. It was not able to identify relevant, high-quality evidence for every component and therefore focused its discussion on topics for which it found sufficient relevant evidence. The committee’s review of the evidence from systematic reviews related to TEE in general and for specific life-stage conditions such as pregnancy and lactation are discussed at the end of this chapter.
COMPONENTS OF ENERGY EXPENDITURE
Resting Energy Expenditure
Resting energy expenditure (REE) typically accounts for 60 to 70 percent of total energy expenditure (Lam and Ravussin, 2016; Poehlman, 1989). REE varies both within and between individuals and fluctuates over the course of the human life span. As shown in Figure 4-1, REE is affected by several factors, including age, sex, body size and composition, and genetics (which may include the influence of race/ethnicity). The most commonly used method to measure REE is indirect calorimetry using metabolic carts that calculate the minute-by-minute exchange of oxygen consumption (VO2) and carbon dioxide production (VCO2) when an individual is at rest in the fasted state (Compher et al., 2006; Lam and Ravussin, 2016). The values of VO2 and VCO2 are then entered into an equation to calculate 24-hour resting metabolic rate (REE).
Commonly used equations to derive the REE include the Weir equation (Brouwer, 1957; Consolazio et al., 1963) and several empirical predictive equations that have been generated to estimate measured REE, particularly in clinical practice. These include the Harris-Benedict equation (developed in 1919), the Owen equation, the Mifflin St-Jeor equation, and the World Health Organization/Food and Agriculture Organization/United Nations University equation. The ability of estimation equations to predict accurately varies, as error rate is influenced by age, sex, ethnicity, and body mass index (BMI) category (Frankenfield et al., 2005). Accuracy in determining REE is highly important, considering its effect on weight status (Marra et al., 2017).
REVIEW OF EVIDENCE ON THE DETERMINANTS OF REE
Age/Sex Group
A recent analysis of Basal Energy Expenditure (BEE) measured by indirect calorimetry in a large sample of males and females over the life course (n = 2,008) from multiple countries (n = 29) found that BEE increased with the amount of fat-free mass (FFM) in a power law manner, after adjusting for body size, age, and sex (Pontzer et al., 2021). Specifically, size-adjusted BEE was found to increase rapidly in infants up to 15 months of age, with BEE values approximately 50 percent higher than adult values. Size-adjusted BEE then declined slowly until around 20 years of age and remained stable from 20 to 60 years before declining in older adults (Pontzer et al., 2021). The decline in BEE for older adults appears to be related to decreases in fat-free mass, and age-related reduction in organ metabolism.
A systematic review by Schwartz and Doucet (2010) of 90 studies that included 2,996 participants did not find a significant difference in sex for the reduction in REE that occurs with reducing body mass through intentional weight loss. Although there is high interindividual variability in REE, when body mass and composition are controlled in the analysis, it appears that sex has little impact on REE.
Body Size
Body size, a function of weight and height, varies among individuals from all races and ethnicities. Systematic reviews of studies that have determined REE from indirect calorimetry show a linear relationship between increasing BMI and REE. In a systematic review comparing constitutionally thin individuals (BMI ≤ 17.5) with no existing medical conditions (including eating disorders) compared to normal weight individuals, constitutionally thin individuals were found to have a lower REE compared to those of normal weight (Bailly et al., 2021). RMR results in 64 percent of the studies showed a lower RMR in constitutionally thin versus normal BMI control subjects, while 36 percent of studies showed no difference.
Whether a linear relationship between body mass and REE holds true in obesity, particularly class III obesity, is a topic of debate and is frequently challenged by studies using dynamic mathematical modeling (Heymsfield et al., 2019). A systematic review of 20 studies by Kee et al. (2012) showed that REE ranged from 1,800 to 2,600 kcal/d among individuals with morbid obesity, and that REE increased with increasing body mass. While body composition was not reported in all studies in the systematic review, Das et al. (2003) demonstrated that fat mass (FM) contributes significantly to REE variability in individuals with BMI ≥ 50, both before and after weight loss.
A number of systematic reviews examining weight loss show an effect of either adaptive thermogenesis or energy compensation such that REE is reduced more than predicted. These studies found that the reduction in REE varied widely, from 12 to 44 percent less than predicted, which equates to about 220 kcal less per day (Dhurandar et al., 2015; Nunes et al., 2022a,b; Schwartz et al., 2012). One systematic review of seven studies with 361 participants showed that a gradual reduction in body mass (about 0.5 kg/week) resulted in less reduction in REE compared to rapid weight change (about 1.1 kg/week) (Ashtary-Larky et al., 2020).
Body Composition
Assessing body composition is a foundational element of energy metabolism research. The human body contains tissues and organs of varying metabolic activity, with the simplest division of total body mass into two compartments: fat mass (FM) also known as stored fat found in adipose tissue, and fat-free mass (FFM), which includes smooth and skeletal muscle, connective tissue, water, and bone. Although adipose tissue is the main storage site for energy, in the form of triglycerides, it has a low metabolic rate at about 5 kcal/kg compared to 20 kcal/kg for FFM (Javed et al., 2010; Wang et al., 2010). In the systematic review by Bailly et al. (2021), the authors reported that despite very low FFM in constitutionally thin individuals, these individuals have increased metabolic activity when normalized to FFM compared to normal weight individuals, suggesting a highly metabolically active FFM.
Given that FFM is a strong predictor of REE, accounting for 60 to 80 percent of interindividual variance in REE, measurement of REE is often adjusted for FFM by sex as a means of adjusting REE for differences in body size, since body weight alone can explain only about 50 percent of the variance in REE (Gallagher et al., 1996).
More recent investigations consider differences in organ energy expenditure as a component of FFM, which may account for interindividual variability in REE associated with age, sex, and race/ethnicity. Older individuals appear to have a lower REE, however, even after controlling for organ and tissue mass. Thus, age-related changes in body composition, including loss of body water, bone mineral content, FFM, and an increase in the distribution of FM, influence REE.
Periods of underfeeding are typically accompanied by compensatory metabolic responses and losses of FFM during episodes of energy deficit, which generally result in reduced energy expenditure. Taken together, metabolic responses to decreased energy intake and weight loss are part of a complex and dynamic energy balance system in which changes to individual components can lead to interrelated compensatory responses (Casanova et al., 2019).
Genetic Traits: Race and Ethnicity
Self-reported race is the only legal basis for racial categorization (Cooper, 1994), and nutrition research almost exclusively uses self-reported race and ethnicity to describe participants and population groups engaged in research. In the public health context, planners use conventional racial or ethnic population characteristics as a proxy for planning programs, facilitating program accessibility, and targeting public health messages. The understanding and use of the concepts of race and ethnicity have evolved over the years.
Currently, the social and political construct that is race/ethnicity is thought to reflect differential distribution of resources, including the availability of high-quality foods, housing, education, transportation, and access to health care, leading to significant inequities among certain population groups (Cooper, 2013; White et al., 2020). These upstream factors influencing health equity are commonly referred to as social determinants of health (WHO, 2022).
In this case, race and ethnicity are not modifiable factors but rather act as proxies for other determinants that can be changed to improve health. About 10 percent of the U.S. population identified as multiracial in the 2020 census, up almost 300 percent from 2010 (Jones et al., 2021). In addition, more than 15 percent identified as “some other race either alone or in combination,” a description that is exclusive of the five categories listed in the census survey: White, Black/African American, American Indian/Alaskan Native, Asian, or Native Hawaiian/Other Pacific Islander. The evidence quantifying the effect of race and/or ethnicity on energy expenditure remains inconclusive despite a relatively robust examination in the scientific literature. The vast majority of studies over the past 20 years have focused on the comparison of REE between Black and White individuals, most with an aim of elucidating documented differences in overweight and obesity between these racial groups.
A preponderance of studies, as shown in Appendix J, Table J-5, reported a significantly lower REE among Black compared to White adults, even after adjustment for body composition, meaning FFM and FM (Adzika Nsatimba et al., 2016; Most et al., 2018; Olivier et al., 2016; Reneau et al., 2019; Spaeth et al., 2015). The same pattern was observed among studies of prepubescent children and adolescents (Bandini et al., 2002; McDuffie et al., 2004; Pretorius et al., 2021; Sun et al., 2001; Tershakovec et al., 2002). Of the 19 studies reporting lower adjusted REE for Black adults, the range of mean differences was 50 to 250 kcal/d with the median of mean differences about 120 kcal/d; for children, the range of mean differences was 36 to 120 kcal/d and the median was 77 kcal/d. The observed differences in REE tended to be attenuated, however, for studies in which REE was adjusted for truncal lean mass, meaning highly metabolically active organ mass, and/or appendicular lean body mass (the sum of the lean muscle mass of the upper and lower extremities adjusted for height) (Byrne et al., 2003; Gallagher et al., 1997, 2006; Hunter et al., 2000; Javed et al., 2010; Jones et al., 2004).
Few studies have examined the effect of race/ethnicity on TEE in either adults or children. In studies among adults, seven reported a significantly lower TEE in Blacks (median of mean differences about 138 kcal/d) (Blanc et al., 2004; DeLany et al., 2014; Dugas et al., 2009; Lam et al., 2014; Most et al., 2018; Walsh et al., 2004; Weinsier et al., 2000), and four reported no statistical differences after adjustment for body composition (Hunter et al., 2000; Katzmaryk et al., 2018; Kushner et al., 1995; Lovejoy et al., 2001). Studies of children reported similar results; two studies reported lower TEE among Blacks (mean difference of 86 kcal/day) (Bandini et al., 2002; DeLany et al., 2002), and two reported no statistically significant difference (Goran et al., 1998; Sun et al., 1998). Attempts to understand the mechanisms responsible for the lower observed REE (and to a lesser extent, TEE) among Blacks compared to Whites in the United States suggest regional body composition differences, i.e., high metabolically active truncal organ mass or low metabolically active appendicular skeletal muscle mass, as one potential explanation for the lack of significant differences (Gallagher et al., 1997).
The relatively few studies that have compared REE or TEE in race/ethnic groups other than Blacks and Whites generally reported no statistically significant differences between groups. Groups examined include adult Hispanics (Deemer et al., 2010), Pima Indians (Christin et al., 1993; Fontveille et al., 1994; Saad et al., 1991), Maori and Pacific Islanders (Rush et al., 1997), Asians (Song et al., 2016; Wouters-Adriaens and Westerterp, 2008), and South Asian Indians (Soares et al., 1998; Song et al., 2016). A few studies also examined energy expenditure among children: Pima Indians (Fontveille et al., 1992), Hispanics (Dugas et al., 2008), Mohawks (Goran et al., 1995, 1998), and Maori and Pacific Islanders (Rush et al., 2003). See Appendix J, Table J-5 for additional details.
Attempts to understand the mechanisms responsible for the lower observed REE (and to a lesser extent, TEE) among Blacks compared to Whites in the United States point to regional body composition differences—meaning highly metabolically active truncal organ mass or low metabolically active appendicular skeletal muscle mass—as one potential explanation (Gallagher et al., 1997). Differences in mitochondrial function (Toledo et al., 2018) and mitochondrial DNA haplotypes (Tranah et al., 2011) may also contribute to differences in energy expenditure between population groups.
Using ancestry informative markers among the participants of a substudy of the U.S.-based Health, Aging and Body Composition Study, investigators reported a significant association between proportion of European genetic admixture among Black participants and REE adjusted for body composition (Manini et al., 2011). Each percent of European admixture was associated with a 1.6 kcal/day higher adjusted REE in these older adults. If confirmed in additional studies, this finding may help explain the variability across studies reporting differences in energy expenditure between Black and White individuals. For context, multiple studies have reported wide variability in the degree of West African and European admixture among self-identified Blacks or African Americans in the United States. The mean European admixture among self-identified Blacks in any given study ranges from about 15 to 25 percent (Klimentidis et al., 2016; Parra et al., 1998; Worsham et al., 2011); however, the range of European admixture can be as wide as 0 to 70 percent (Al-Alem et al., 2014; Manini et al., 2011).
Thermic Effect of Food
Factors that influence TEF include age, physical activity, and a meal’s energy content, composition (i.e., quantity and type of carbohydrate, protein, and fat content of a meal), and size (Calcagno et al., 2019). The TEF, which has been shown to comprise approximately 10 percent of daily energy expenditure, includes obligatory thermogenesis. Obligatory thermogenesis is accounted for by the energy cost of absorption and transport of nutrients, and synthesis of carbohydrate, protein, and fat in tissues (Saito et al., 2020).
Review of Evidence on the Determinants of TEF
Physical Activity
A review by Calcagno and colleagues (2019) identified one study that examined the effect of physical activity on TEF. The study showed that in both younger and older men, those who were active had an approximately 45 percent higher TEF than those who were inactive. Further evidence from a study of active females suggests that consumption of a meal in combination with a short period of moderate to vigorous physical activity (MVPA) results in a greater total energy expenditure than similar activity performed in a fasted state (Binns et al., 2015).
Meal Energy Content, Composition, and Size
The main determinant of TEF is energy and macronutrient composition of the meal, of which proteins have the highest thermogenic response. DIT values are approximately 0 to 3 percent for fat, 5 to 10 percent for carbohydrate, 20 to 30 percent for protein, and 10 to 30 percent for alcohol (Westerterp, 2004).
A systematic review that examined differences in the effects on DIT of meals consumed after fasting conducted mixed model meta-regression analyses that included only energy intake and DIT. It showed that for every 24 kcal increase in energy intake, DIT increased by 0.26 kcal/day (Quatela et al., 2016).
In a systematic review that included 15 studies, 9 showed a significant effect of the type of fatty acids on DIT. Three studies described a DIT increment with the use of polyunsaturated fatty acid, two reported a greater DIT as a result of the use of medium chain fatty acids, and four reported differences with the use of specific foods or oils. Specifically, postprandial fat oxidation and postprandial energy expenditure were greater with the use of alpha linolenic acid–enriched diacylglycerol compared to triacylglycerol. However, no conclusion could be drawn when only the fatty acid composition of the diet was evaluated for DIT (Cisneros et al., 2019).
Park et al., examined dietary factors affecting DIT in studies that included individuals with obesity. In this systematic review of studies published from 2009 to 2019, only two studies of very small sample sizes showed no differences in DIT between obese and lean individuals with varying carbohydrate and protein composition of isocaloric meals (Park et al., 2020). This finding is in contrast to an older review by de Jonge and Bray (1997), which reported that in 29 studies of age-matched individuals, 22 reported a reduction in DIT for individuals with obesity compared to lean individuals. Thus, the issue of the obese state due to insulin resistance being associated with lower DIT remains undecided. The variability in how DIT is measured and the complex interaction of human behaviors including physical activity makes it difficult to estimate DIT accurately and compare results across studies.
Physical Activity Level
Physical activity is the most variable energy component. Energy expenditure from activity is the energy required for the body to move (i.e., perform muscular work) during non-exercise activity thermogeneis (e.g., fidgeting, maintaining posture, and activities of daily living) and voluntary (e.g., exercise, sports) activity. It varies greatly as a proportion of TEE and has been shown to range from a low of 15 percent for sedentary individuals up to 50 percent of TEE for physically active individuals (Livingstone et al., 1991; Ravussin et al., 1986).
Determinants of PAEE include age, sex, body size and composition, movement economy, exercise training, and genetic traits, all of which interact and can result in energy adaptations. Resources such as the Compendium of Physical Activities can provide estimates of an individual’s energy expenditure for specific activities (Ainsworth et al., 2011; Butte et al., 2018).
Review of Evidence on the Determinants of PAL
Age/Sex
PAL varies across the life span. Researchers can obtain precise measures of intraindividual or interindividual differences in PAL using doubly labeled water (DLW), indirect calorimetry, and room calorimetry. Because DLW is used only for measuring free-living TEE and may be cost-prohibitive, researchers often use estimates of physical activity from questionnaires or device-based measures. Questionnaires tend to have a high degree of error because they rely on individual recall and quantification of activity level (see Chapter 6 for further discussion of methodologies). Device-based measures (e.g., ActiGraph; GeneActive, Apple Watch, and Fitbit) use sensors such as accelerometers to capture an individual’s movement and are considered to provide a better estimate of typical activity patterns than questionnaires, but they lack details about the type of activity performed. Furthermore, a lack of consensus on intensity criteria along with variation in device wear location make it challenging to quantify time in intensity categories and comparing estimates across studies (Watson et al., 2014).
Craigie et al. (2011) conducted a systematic review of literature on tracking physical activity and dietary intake from childhood to adulthood. Three studies in this review, which included over 2,000 participants, found that tracking of physical activity from adolescence into adulthood was stronger among males than females. Between 44 and 59 percent of males maintained physical activity during the 5- to 8-year follow-up.
Tanaka et al. (2014) examined longitudinal changes in overall sedentary behavior and how those changes were associated with adiposity in children and adolescents. This systematic review included 7,238 children and adolescents and found that during a 1- to 10-year follow-up among 3- to 13-year-olds, sedentary behavior increased with age, by approximately 30 minutes of additional daily sedentary behavior per year. Little evidence was available to demonstrate any influence of changes in sedentary behavior on changes in adiposity.
Body Size and Composition
A systematic review by Carneiro et al. (2016) examined differences in activity-based energy expenditure in individuals with and without obesity. All four studies included in the analysis reported that individuals with obesity had higher absolute activity energy expenditure than those without obesity. After adjustment for FFM or body weight, two studies showed no difference between the two population groups. The conclusion of the review was that activity energy expenditure was not different in individuals with obesity; rather, they have altered activity patterns and greater amounts of sedentary time, resulting in overall lower activity energy expenditure values. However, higher REE in those with obesity that was reported in most studies could be caused by not adjusting for body composition.
Carneiro et al. (2016) also examined differences in daily energy expenditure between those with and those without obesity. In the three studies included in the systematic review, absolute daily energy expenditure was higher in the group with obesity (approximately 2,690 kcal/d) than in those without obesity (approximately 2,380 kcal/d). Similar to the findings on activity energy expenditure, the difference between the two groups disappeared after adjusting for FFM and body weight.
Movement Economy and Exercise Training
Movement economy is the oxygen cost to perform a given submaximal task. The more trained an individual is, the better their economy (i.e., the oxygen cost or energy expenditure will be lower) (Barnes and Kilding, 2015). This principle also relates to motor coordination, which is a measure of the ability to coordinate muscle activation in multiple body parts to perform a given task. Motor coordination is still developing in children and youth, thus their movement economy is typically poorer (i.e., the energy cost of an activity such as walking is higher) than an adult’s. Children’s motor coordination improves along with movement economy as skill development proceeds. In adults, training improves movement economy.
OTHER CONSIDERATIONS
Carbohydrate Restriction
There has been great interest in understanding the effect of a restricted carbohydrate diet on TEE to explain the heterogeneity found in weight loss clinical trials. The rationale for examining this relationship is the hypothesis that with moderate restriction of carbohydrate over a longer period of time, a shift in the metabolic pathway can occur from carbohydrate oxidation to fat oxidation without bringing on a ketosis condition, thereby subsequently reducing TEE through several mechanisms including a reduction in voluntary physical activity energy expenditure. Ludwig et al. (2021) conducted an updated systematic review with a meta-analysis of previous work by Hall and Guo (2017) and added trials conducted since 2016 up through March 2020. Carbohydrate restriction was allowed to vary in the trials, but study duration was dichotomized at greater than or less than 2 weeks. In studies with short-term carbohydrate restriction (<2.5 weeks), the systematic review found that a lower carbohydrate diet did result in reduced TEE. However, when a restricted carbohydrate diet was maintained for more than 2.5 weeks, TEE increased by approximately 50 kcal/day for every 10 percent decrease in carbohydrate as a percentage of energy intake. The stratification by study duration accounted for the most variability in TEE (R2 = 57.2 percent). The method used to measure TEE, whether whole-room calorimetry or DLW, did not significantly add to the heterogeneity. A conclusion of this work is that shorter versus longer duration of carbohydrate restriction studies are not examining the same physiological states, which may explain the pattern of weight loss seen in clinical trials and thus, not indicative of the success of these short-term trials to treat obesity.
Pregnancy and Lactation
Many metabolic and physiological changes that influence energy requirements occur during the life stages of pregnancy and lactation. Previous derivations of requirements for pregnancy were based on theoretical energy costs associated with the products of conception (e.g., the fetus, placenta, maternal breast and uterine tissue, and maternal fat). For lactation, requirements have been based on the energy costs associated with producing a specific volume of breast milk for the infant, accounting for the mobilization of maternal fat stores from pregnancy to provide additional energy resources during the postpartum period. Butte and King (2005) comprehensively examined these energy costs and how their estimates have changed over time.
Previous estimates of the energy costs of pregnancy (which considered FM and FFM accretion associated with the products of conception) may have led to overestimation of energy requirements during this life stage. A recent systematic review and meta-analysis provides evidence of wide variability in TEE and in REE and other energy expenditure components during pregnancy (Savard et al., 2021). The data support the notion that REE and TEE increase over the course of pregnancy, with greater increases observed when baseline measurement included a preconception time point. Median increases in TEE were 6.2 percent (144 kcal), 7.1 percent (170 kcal), and 12.0 percent (290 kcal) between early and mid-, mid- and late, and early and late pregnancy, respectively. Most of the included studies enrolled normal weight, Caucasian women, however, and had small sample sizes. The two studies that stratified results by prepregnancy BMI showed smaller increases in TEE for women with overweight and obesity. Most studies did not stratify by adequacy of gestational weight gain. Therefore, the constant physiological adaptation during pregnancy (such as gradual reductions in physical activity expenditure and in DIT) imply that the energy cost of pregnancy should be lower than the costs published by the Institute of Medicine (IOM, 2002/2005).
For lactation, a systematic review that examined volumes and the energy content of breast milk showed a weighted mean milk transfer of 779 g/day at 3 to 4 months, 826 g/day at 5 to 6 months, and 894 g/day at 6 months. Among nine studies, no marked increase in milk transfers were reported during the 2- to 5-month period. The weighted mean metabolizable energy content of milk from 25 studies of 777 mother–infant dyads was 2.6 kJ/g (equivalent to 0.62 kcal/g) (Reilly et al., 2005).
Four individual studies on the energy costs of lactation have been conducted since the systematic review mentioned above (see Appendix J for details). Thakkar et al. (2013) measured the energy content of human milk at 65.92 kcal/100 ml starting at 1 month of age and 70.24 kcal/100 ml at 3 months of age. The energy content of human milk produced for male infants was 24 percent higher at 3 months of age than that produced for females. Two additional studies of the same group of mother–infant dyads used DLW to estimate mean milk intake at 923 g/day at 15 weeks and 999 g/day at 25 weeks among exclusively breastfed infants (Nielsen et al., 2011, 2013). Milk energy content was the same for males and females, 2.72 kJ/g at 15 weeks and 2.62 kJ/g at 25 weeks. Significant differences in total energy intakes by sex were observed at 25 weeks: males consumed 2,582 kJ/d and females 2,403 kJ/d at 15 weeks, and males consumed 2,748 kJ/d and females 2,449 kJ/d at 25 weeks.
Pereira et al. (2019) used whole-body calorimetry to measure REE at 3 and 9 months and TEE at 9 months in a sample of approximately 50 mother–infant dyads. Average breast milk volume was 771 g/d at 3 months, equating to a breast milk energy output of 678 kcal/d. Average breast milk volume was 530 g/day at 9 months (in the presence of complementary feeding), equating to 465 kcal/day. REE increased by 3.2 percent from 3 to 9 months. No difference in TEE was observed between lactating and nonlactating women at 9 months.
FINDINGS AND CONCLUSIONS
Determinants of Resting Energy Expenditure
Findings
The committee’s review of the current evidence confirms that REE is the largest contributor to TEE, varies both within and between individuals, and fluctuates over the course of the human life span. The committee found evidence for a linear relationship between increasing body size and REE. The evidence shows that REE adjusted for body size increases rapidly in infants up to 15 months of age and then begins to decline slowly up to age 20, when REE becomes stable to about age 60 years. Evidence reviewed confirmed that the potential impact of sex on REE is related to differences in body mass and composition. The committee found systematic review evidence was lacking on the influence of Class III or morbid obesity on REE. Also lacking was systematic review evidence on the influence of the gut microbiome and organ tissue energy expenditure to explain the variability in REE among individuals.
The committee finds that data stratified by prepregnancy BMI are lacking, especially for women with overweight and obesity. Further, most of the studies examined did not stratify by adequacy of gestational weight gain. Among lactating women, evidence reviewed by the committee showed that REE increased by 3.2 percent from 3 to 9 months postpartum, although no significant differences were observed in TEE between lactating and nonlactating women at 9 months.
The committee finds that the current evidence confirms that physical activity is the most variable energy component, ranging from 15 to 50 percent of TEE. Additionally, physical activity decreases with age and is influenced by previous activity levels. Activity energy expenditure and total daily energy expenditure were shown to differ between individuals with and without obesity in terms of absolute levels, but differences disappeared after adjusting for FFM and body weight. Systematic review evidence on the influence of movement economy and motor coordination, particularly in persons with obesity, remains lacking.
Conclusions
The committee concludes that overall, the evidence to support an interaction between BMI and REE is limited, especially to examine the influence of BMI on REE by age/sex or life stage. Further, the total energy requirements for pregnancy have not been aligned with current recommendations for rates of weight gain. The IOM (2002/2005) energy requirements may have overestimated requirements during pregnancy among women with overweight or obesity.
Race and Ethnicity
Findings
The committee finds that race and ethnicity are not modifiable factors but rather social constructs that act as proxies for other determinants. While studies reported a significant lower REE among Black compared to White adults, regional body composition differences, and differences in mitochondrial function and mitochondrial DNA haplotypes provide potential explanations for these data. Furthermore, using ancestry informative markers may help explain the variability across studies reporting differences in energy expenditure between Black and White individuals.
Conclusions
The committee concludes that a better understanding of whether race/ethnicity reliably and consistently affects energy expenditure or is a social and political construct that serves as a proxy for other determinants affecting energy expenditure such as cultural, environmental, physical activity, and/or behavioral differences, is crucial to both research and public health efforts.
REFERENCES
- Adzika Nsatimba PA, Pathak K, Soares MJ. Ethnic differences in resting metabolic rate, respiratory quotient and body temperature: A comparison of Africans and European Australians. European Journal of Nutrition. 2016;55(5):1831–1838. [PubMed: 26206564]
- Ainsworth BE, Haskell WL, Herrmann SD, Meckes N, Bassett DR Jr, Tudor-Locke C, Greer JL, Vezina J, Whitt-Glover MC, Leon AS. 2011 compendium of physical activities: A second update of codes and met values. Medicine and Science in Sports and Exercise. 2011;43(8):1575–1581. [PubMed: 21681120]
- Al-Alem U, Rauscher G, Shah E, Batai K, Mahmoud A, Beisner E, Silva A, Peterson C, Kittles R. Association of genetic ancestry with breast cancer in ethnically diverse women from Chicago. PloS One. 2014;9(11):e112916. [PMC free article: PMC4244099] [PubMed: 25423363]
- Ashtary-Larky D, Bagheri R, Abbasnezhad A, Tinsley GM, Alipour M, Wong A. Effects of gradual weight loss v. rapid weight loss on body composition and RMR: A systematic review and meta-analysis. British Journal of Nutrition. 2020;124(11):1121–1132. [PubMed: 32576318]
- Bailly M, Boscaro A, Pereira B, Feasson L, Boirie Y, Germain N, Galusca B, Courteix D, Thivel D, Verney J. Is constitutional thinness really different from anorexia nervosa? A systematic review and meta-analysis. Reviews in Endocrine and Metabolic Disorders. 2021;22(4):913–971. [PubMed: 33929658]
- Bandini LG, Must A, Spadano JL, Dietz WH. Relation of body composition, parental overweight, pubertal stage, and race-ethnicity to energy expenditure among premenarcheal girls. American Journal of Clinical Nutrition. 2002;76(5):1040–1047. [PubMed: 12399276]
- Binns A, Gray M, Di Brezzo R. Thermic effect of food, exercise, and total energy expenditure in active females. Journal of Science and Medicine in Sport. 2015;18(2):204–208. [PubMed: 24589371]
- Blanc S, Schoeller DA, Bauer D, Danielson ME, Tylavsky F, Simonsick EM, Harris TB, Kritchevsky SB, Everhart JE. Energy requirements in the eighth decade of life. American Journal of Clinical Nutrition. 2004;79(2):303–310. [PubMed: 14749238]
- Brouwer E. On simple formulae for calculating the heat expenditure and the quantities of carbohydrate and fat oxidized in metabolism of men and animals, from gaseous exchange (oxygen intake and carbonic acid output) and urine-n. Acta Physiologica et Pharmacologica Neerlandica. 1957;6:795–802. [PubMed: 13487422]
- Butte NF, Caballero B. Energy needs: Assessment and requirements. In: Ross AC, Caballero B, Cousins RJ, Tucker KL, Ziegler TR, editors. Modern Nutrition in Health and Disease. 11th ed. Baltimore, MD: Lippincott, Williams and Wilkins; 2014.
- Butte NF, King JC. Energy requirements during pregnancy and lactation. Public Health Nutrition. 2005;8(7A):1010–1027. [PubMed: 16277817]
- Butte NF, Watson KB, Ridley K, Zakeri IF, McMurray RG, Pfeiffer KA, Crouter SE, Herrmann SD, Bassett DR, Long A, Berhane Z, Trost SG, Ainsworth BE, Berrigan D, Fulton JE. A youth compendium of physical activities: Activity codes and metabolic intensities. Medicine and Science in Sports and Exercise. 2018;50(2):246–256. [PMC free article: PMC5768467] [PubMed: 28938248]
- Byrne NM, Weinsier RL, Hunter GR, Desmond R, Patterson MA, Darnell BE, Zuckerman PA. Influence of distribution of lean body mass on resting metabolic rate after weight loss and weight regain: Comparison of responses in white and black women. American Journal of Clinical Nutrition. 2003;77(6):1368–1373. [PubMed: 12791611]
- Calcagno M, Kahleova H, Alwarith J, Burgess NN, Flores RA, Busta ML, Barnard ND. The thermic effect of food: A review. Journal of the American College of Nutrition. 2019;38(6):547–551. [PubMed: 31021710]
- Carneiro IP, Elliott SA, Siervo M, Padwal R, Bertoli S, Battezzati A, Prado CM. Is obesity associated with altered energy expenditure? Advances in Nutrition. 2016;7(3):476–487. [PMC free article: PMC4863259] [PubMed: 27184275]
- Casanova N, Beaulieu K, Finlayson G, Hopkins M. Metabolic adaptations during negative energy balance and their potential impact on appetite and food intake. Proceedings of the Nutrition Society. 2019;78(3):279–289. [PubMed: 30777142]
- Christin L, O’Connell M, Bogardus C, Danforth E Jr, Ravussin E. Norepinephrine turnover and energy expenditure in Pima Indian and white men. Metabolism: Clinical and Experimental. 1993;42(6):723–729. [PubMed: 8510516]
- Cisneros LCV, Moreno AGM, Lopez-Espinoza A, Espinoza-Gallardo AC. Effect of the fatty acid composition of meals on postprandial energy expenditure: A systematic review. Revista da Associacao Medica Brasileira (1992). 2019;65(7):1022–1031. [PubMed: 31389518]
- Compher C, Frankenfield D, Keim N, Roth-Yousey L. Evidence Analysis Working Group. Best practice methods to apply to measurement of resting metabolic rate in adults: A systematic review. Journal of the American Dietetic Association. 2006;106(6):881–903. [PubMed: 16720129]
- Consolazio CF, Johnson RE, Pecora LJ. Physiological measurements of metabolic functions in man. New York: McGraw-Hill; 1963. [PubMed: 13811589]
- Cooper RS. A case study in the use of race and ethnicity in public health surveillance. Public Health Reports. 1994;109(1):46–52. [PMC free article: PMC1402241] [PubMed: 8303014]
- Craigie AM, Lake AA, Kelly SA, Adamson AJ, Mathers JC. Tracking of obesity-related behaviours from childhood to adulthood: A systematic review. Maturitas. 2011;70(3):266–284. [PubMed: 21920682]
- Das SK, Roberts SB, McCrory MA, Hsu LK, Shikora SA, Kehayias JJ, Dallal GE, Saltzman E. Long-term changes in energy expenditure and body composition after massive weight loss induced by gastric bypass surgery. American Journal of Clinical Nutrition. 2003;78(1):22–30. [PubMed: 12816767]
- Deemer SE, King GA, Dorgo S, Vella CA, Tomaka JW, Thompson DL. Relationship of leptin, resting metabolic rate, and body composition in premenopausal Hispanic and non-Hispanic white women. Endocrine Research. 2010;35(3):95–105. [PMC free article: PMC4635679] [PubMed: 20712423]
- de Jonge L, Bray GA. The thermic effect of food and obesity: A critical review. Obesity Research. 1997;5(6):622–631. [PubMed: 9449148]
- DeLany JP, Bray GA, Harsha DW, Volaufova J. Energy expenditure in preadolescent African American and white boys and girls: The Baton Rouge Children’s Study. American Journal of Clinical Nutrition. 2002;75(4):705–713. [PubMed: 11916757]
- DeLany JP, Jakicic JM, Lowery JB, Hames KC, Kelley DE, Goodpaster BH. African American women exhibit similar adherence to intervention but lose less weight due to lower energy requirements. International Journal of Obesity (2005). 2014;38(9):1147–1152. [PubMed: 24352292]
- Dhurandhar EJ, Kaiser KA, Dawson JA, Alcorn AS, Keating KD, Allison DB. Predicting adult weight change in the real world: A systematic review and meta-analysis accounting for compensatory changes in energy intake or expenditure. International Journal of Obesity. 2015;39(8):1181–1187. [PMC free article: PMC4516704] [PubMed: 25323965]
- Dugas LR, Ebersole K, Schoeller D, Yanovski JA, Barquera S, Rivera J, Durazo-Arzivu R, Luke A. Very low levels of energy expenditure among pre-adolescent Mexican-American girls. International Journal of Pediatric Obesity. 2008;3(2):123–126. [PMC free article: PMC2467388] [PubMed: 18465439]
- Dugas LR, Cohen R, Carstens MT, Schoffelen PF, Luke A, Durazo-Arvizu RA, Goedecke JH, Levitt NS, Lambert EV. Total daily energy expenditure in black and white, lean and obese South African women. European Journal of Clinical Nutrition. 2009;63(5):667–673. [PubMed: 18270522]
- Fontvieille AM, Dwyer J, Ravussin E. Resting metabolic rate and body composition of Pima Indian and Caucasian children. International Journal of Obesity and Related Metabolic Disorders. 1992;16(8):535–542. [PubMed: 1326483]
- Fontvieille AM, Rising R, Spraul M, Larson DE, Ravussin E. Relationship between sleep stages and metabolic rate in humans. American Journal of Physiology. 1994;267(5 Pt 1):E732–737. [PubMed: 7977724]
- Frankenfield D, Roth-Yousey L, Compher C. Comparison of predictive equations for resting metabolic rate in healthy nonobese and obese adults: A systematic review. Journal of the American Dietetic Association. 2005;105(5):775–789. [PubMed: 15883556]
- Gallagher D, Visser M, Wang Z, Harris T, Pierson RN Jr, Heymsfield SB. Metabolically active component of fat-free body mass: Influences of age, adiposity, and gender. Metabolism: Clinical and Experimental. 1996;45(8):992–997. [PubMed: 8769358]
- Gallagher D, Visser M, De Meersman RE, Sepulveda D, Baumgartner RN, Pierson RN, Harris T, Heymsfield SB. Appendicular skeletal muscle mass: Effects of age, gender, and ethnicity. Journal of Applied Physiology (1985). 1997;83(1):229–239. [PubMed: 9216968]
- Gallagher D, Albu J, He Q, Heshka S, Boxt L, Krasnow N, Elia M. Small organs with a high metabolic rate explain lower resting energy expenditure in African American than in white adults. American Journal of Clinical Nutrition. 2006;83(5):1062–1067. [PMC free article: PMC1847651] [PubMed: 16685047]
- Goran MI, Kaskoun M, Johnson R, Martinez C, Kelly B, Hood V. Energy expenditure and body fat distribution in Mohawk children. Pediatrics. 1995;95(1):89–95. [PubMed: 7770316]
- Goran MI, Nagy TR, Gower BA, Mazariegos M, Solomons N, Hood V, Johnson R. Influence of sex, seasonality, ethnicity, and geographic location on the components of total energy expenditure in young children: Implications for energy requirements. American Journal of Clinical Nutrition. 1998;68(3):675–682. [PubMed: 9734747]
- Hall KD, Guo J. Obesity energetics: Body weight regulation and the effects of diet composition. Gastroenterology. 2017;152(7):1718–1727.e1713. [PMC free article: PMC5568065] [PubMed: 28193517]
- Heymsfield SB, Thomas DM, Bosy-Westphal A, Muller MJ. The anatomy of resting energy expenditure: Body composition mechanisms. European Journal of Clinical Nutrition. 2019;73(2):166–171. [PMC free article: PMC6410366] [PubMed: 30254244]
- Hunter GR, Weinsier RL, Darnell BE, Zuckerman PA, Goran MI. Racial differences in energy expenditure and aerobic fitness in premenopausal women. American Journal of Clinical Nutrition. 2000;71(2):500–506. [PubMed: 10648264]
- IOM (Institute of Medicine). Dietary Reference Intakes for energy, carbohydrate, fiber, fat, fatty acids, cholesterol, protein, and amino acids. Washington, DC: The National Academies Press; 2002/2005.
- Javed F, He Q, Davidson LE, Thornton JC, Albu J, Boxt L, Krasnow N, Elia M, Kang P, Heshka S, Gallagher D. Brain and high metabolic rate organ mass: Contributions to resting energy expenditure beyond fat-free mass. American Journal of Clinical Nutrition. 2010;91(4):907–912. [PMC free article: PMC2844678] [PubMed: 20164308]
- Jones A Jr, Shen W, St-Onge MP, Gallagher D, Heshka S, Wang Z, Heymsfield SB. Body-composition differences between African American and white women: Relation to resting energy requirements. American Journal of Clinical Nutrition. 2004;79(5):780–786. [PubMed: 15113715]
- Katzmarzyk PT, Most J, Redman LM, Rood J, Ravussin E. Energy expenditure and substrate oxidation in white and African American young adults without obesity. European Journal of Clinical Nutrition. 2018;72(6):920–922. [PMC free article: PMC5990476] [PubMed: 29849180]
- Kee AL, Isenring E, Hickman I, Vivanti A. Resting energy expenditure of morbidly obese patients using indirect calorimetry: A systematic review. Obesity Reviews. 2012;13(9):753–765. [PubMed: 22568725]
- Klimentidis YC, Arora A, Zhou J, Kittles R, Allison DB. The genetic contribution of West-African ancestry to protection against central obesity in African-American men but not women: Results from the ARIC and MESA studies. Frontiers in Genetics. 2016;7:89. [PMC free article: PMC4888933] [PubMed: 27313598]
- Kushner RF, Racette SB, Neil K, Schoeller DA. Measurement of physical activity among black and white obese women. Obesity Research. 1995;3(Suppl 2):261s–265s. [PubMed: 8581785]
- Lam YY, Ravussin E. Analysis of energy metabolism in humans: A review of methodologies. Molecular Metabolism. 2016;5(11):1057–1071. [PMC free article: PMC5081410] [PubMed: 27818932]
- Lam YY, Redman LM, Smith SR, Bray GA, Greenway FL, Johannsen D, Ravussin E. Determinants of sedentary 24-h energy expenditure: Equations for energy prescription and adjustment in a respiratory chamber. American Journal of Clinical Nutrition. 2014;99(4):834–842. [PMC free article: PMC3953881] [PubMed: 24500151]
- Levine JA. Non-exercise activity thermogenesis (NEAT). Best Practice & Research: Clinical Endocrinology & Metabolism. 2002;16(4):679–702. [PubMed: 12468415]
- Livingstone MB, Strain JJ, Prentice AM, Coward WA, Nevin GB, Barker ME, Hickey RJ, McKenna PG, Whitehead RG. Potential contribution of leisure activity to the energy expenditure patterns of sedentary populations. British Journal of Nutrition. 1991;65(2):145–155. [PubMed: 2043600]
- Lovejoy JC, Champagne CM, Smith SR, de Jonge L, Xie H. Ethnic differences in dietary intakes, physical activity, and energy expenditure in middle-aged, premenopausal women: The Healthy Transitions Study. American Journal of Clinical Nutrition. 2001;74(1):90–95. [PubMed: 11451722]
- Ludwig DS, Dickinson SL, Henschel B, Ebbeling CB, Allison DB. Do lower-carbohydrate diets increase total energy expenditure? An updated and reanalyzed meta-analysis of 29 controlled-feeding studies. Journal of Nutrition. 2021;151(3):482–490. [PMC free article: PMC7948201] [PubMed: 33274750]
- Manini TM, Patel KV, Bauer DC, Ziv E, Schoeller DA, Mackey DC, Li R, Newman AB, Nalls M, Zmuda JM, Harris TB. European ancestry and resting metabolic rate in older African Americans. European Journal of Clinical Nutrition. 2011;65(6):663–667. [PMC free article: PMC3915864] [PubMed: 21468093]
- Marra M, Cioffi I, Sammarco R, Montagnese C, Naccarato M, Amato V, Contaldo F, Pasanisi F. Prediction and evaluation of resting energy expenditure in a large group of obese outpatients. International Journal of Obesity (2005). 2017;41(5):697–705. [PMC free article: PMC5418562] [PubMed: 28163316]
- McDuffie JR, Adler-Wailes DC, Elberg J, Steinberg EN, Fallon EM, Tershakovec AM, Arslanian SA, Delany JP, Bray GA, Yanovski JA. Prediction equations for resting energy expenditure in overweight and normal-weight black and white children. American Journal of Clinical Nutrition. 2004;80(2):365–373. [PMC free article: PMC2267722] [PubMed: 15277157]
- Most J, Gilmore LA, Altazan AD, St Amant M, Beyl RA, Ravussin E, Redman LM. Propensity for adverse pregnancy outcomes in African-American women may be explained by low energy expenditure in early pregnancy. American Journal of Clinical Nutrition. 2018;107(6):957–964. [PMC free article: PMC6454439] [PubMed: 29767680]
- Nielsen SB, Reilly JJ, Fewtrell MS, Eaton S, Grinham J, Wells JCK. Adequacy of milk intake during exclusive breastfeeding: A longitudinal study. Pediatrics. 2011;128(4):e907–e914. [PubMed: 21930538]
- Nielsen SB, Wells JCK, Fewtrell MS, Eaton S, Grinham J, Reilly JJ. Validation of energy requirement references for exclusively breast-fed infants. British Journal of Nutrition. 2013;109(11):2036–2043. [PubMed: 23148915]
- Nunes CL, Casanova N, Francisco R, Bosy-Westphal A, Hopkins M, Sardinha LB, Silva AM. Does adaptive thermogenesis occur after weight loss in adults? A systematic review. British Journal of Nutrition. 2022a;127(3):451–469. [PubMed: 33762040]
- Nunes CL, Jesus F, Francisco R, Matias CN, Heo M, Heymsfield SB, Bosy-Westphal A, Sardinha LB, Martins P, Minderico CS, Silva AM. Adaptive thermogenesis after moderate weight loss: Magnitude and methodological issues. European Journal of Nutrition. 2022b;61(3):1405–1416. [PubMed: 34839398]
- Olivier N, Wenhold FA, Becker P. Resting energy expenditure of black overweight women in South Africa is lower than of white women. Annals of Nutrition and Metabolism. 2016;69(1):24–30. [PubMed: 27403525]
- Park MY, Kim J, Chung N, Park HY, Hwang H, Han JS, So JM, Lee CH, Park J, Lim K. Dietary factors and eating behaviors affecting diet-induced thermogenesis in obese individuals: A systematic review. Journal of Nutritional Science and Vitaminology. 2020;66(1):1–9. [PubMed: 32115447]
- Parra EJ, Marcini A, Akey J, Martinson J, Batzer MA, Cooper R, Forrester T, Allison DB, Deka R, Ferrell RE, Shriver MD. Estimating African American admixture proportions by use of population-specific alleles. American Journal of Human Genetics. 1998;63(6):1839–1851. [PMC free article: PMC1377655] [PubMed: 9837836]
- Pereira LCR, Purcell SA, Elliott SA, McCargar LJ, Bell RC, Robson PJ, Prado CM. the Enrich Study. The use of whole body calorimetry to compare measured versus predicted energy expenditure in postpartum women. American Journal of Clinical Nutrition. 2019;109(3):554–565. [PMC free article: PMC6408201] [PubMed: 30793166]
- Poehlman ET. A review: Exercise and its influence on resting energy metabolism in man. Medicine and Science in Sports and Exercise. 1989;21(5):515–525. [PubMed: 2691813]
- Pontzer H, Yamada Y, Sagayama H, Ainslie PN, Andersen LF, Anderson LJ, Arab L, Baddou I, Bedu-Addo K, Blaak EE, Blanc S, Bonomi AG, Bouten CVC, Bovet P, Buchowski MS, Butte NF, Camps SG, Close GL, Cooper JA, Cooper R, Das SK, Dugas LR, Ekelund U, Entringer S, Forrester T, Fudge BW, Goris AH, Gurven M, Hambly C, El Hamdouchi A, Hoos MB, Hu S, Joonas N, Joosen AM, Katzmarzyk P, Kempen KP, Kimura M, Kraus WE, Kushner RF, Lambert EV, Leonard WR, Lessan N, Martin C, Medin AC, Meijer EP, Morehen JC, Morton JP, Neuhouser ML, Nicklas TA, Ojiambo RM, Pietiläinen KH, Pitsiladis YP, Plange-Rhule J, Plasqui G, Prentice RL, Rabinovich RA, Racette SB, Raichlen DA, Ravussin E, Reynolds RM, Roberts SB, Schuit AJ, Sjödin AM, Stice E, Urlacher SS, Valenti G, Van Etten LM, Van Mil EA, Wells JCK, Wilson G, Wood BM, Yanovski J, Yoshida T, Zhang X, Murphy-Alford AJ, Loechl C, Luke AH, Rood J, Schoeller DA, Westerterp KR, Wong WW, Speakman JR. Daily energy expenditure through the human life course. Science. 2021;373(6556):808–812. [PMC free article: PMC8370708] [PubMed: 34385400]
- Pretorius A, Wood P, Becker P, Wenhold F. Resting energy expenditure and related factors in 6- to 9-year-old southern African children of diverse population groups. Nutrients. 2021;13(6) [PMC free article: PMC8229942] [PubMed: 34207655]
- Quatela A, Callister R, Patterson A, Macdonald-Wicks L. The energy content and composition of meals consumed after an overnight fast and their effects on diet induced thermogenesis: A systematic review, meta-analyses and meta-regressions. Nutrients. 2016;8(11) [PMC free article: PMC5133058] [PubMed: 27792142]
- 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. Journal of Clinical Investigation. 1986;78(6):1568–1578. [PMC free article: PMC423919] [PubMed: 3782471]
- Reilly JJ, Ashworth S, Wells JCK. Metabolisable energy consumption in the exclusively breast-fed infant aged 3–6 months from the developed world: A systematic review. British Journal of Nutrition. 2005;94(1):56–63. [PubMed: 16115333]
- Reneau J, Obi B, Moosreiner A, Kidambi S. Do we need race-specific resting metabolic rate prediction equations? Nutrition & Diabetes. 2019;9(1):21. [PMC free article: PMC6662665] [PubMed: 31358726]
- Rush EC, Plank LD, Robinson SM. Resting metabolic rate in young Polynesian and Caucasian women. International Journal of Obesity and Related Metabolic Disorders. 1997;21(11):1071–1075. [PubMed: 9368833]
- 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. British Journal of Nutrition. 2003;90(6):1133–1139. [PubMed: 14641973]
- Saad MF, Alger SA, Zurlo F, Young JB, Bogardus C, Ravussin E. Ethnic differences in sympathetic nervous system-mediated energy expenditure. American Journal of Physiology. 1991;261(6 Pt 1):E789–E794. [PubMed: 1685070]
- Saito M, Matsushita M, Yoneshiro T, Okamatsu-Ogura Y. Brown adipose tissue, diet-induced thermogenesis, and thermogenic food ingredients: From mice to men. Frontiers in Endocrinology. 2020;11:222. [PMC free article: PMC7186310] [PubMed: 32373072]
- Savard C, Lebrun A, O’Connor S, Fontaine-Bisson B, Haman F, Morisset AS. Energy expenditure during pregnancy: A systematic review. Nutrition Reviews. 2021;79(4):394–409. [PMC free article: PMC7947828] [PubMed: 32974660]
- Schutz Y, Jequier E. Resting energy expenditure, thermic effect of food, and total energy expenditure. In: Bray GA, Bouchard C, James WPT, editors. Handbook of obesity. New York: Marcel Dekker; 1998.
- Schwartz A, Doucet E. Relative changes in resting energy expenditure during weight loss: A systematic review. Obesity Reviews. 2010;11(7):531–547. [PubMed: 19761507]
- Schwartz A, Kuk JL, Lamothe G, Doucet E. Greater than predicted decrease in resting energy expenditure and weight loss: Results from a systematic review. Obesity (Silver Spring). 2012;20(11):2307–2310. [PubMed: 22327054]
- Soares MJ, Piers LS, O’Dea K, Shetty PS. No evidence for an ethnic influence on basal metabolism: An examination of data from India and Australia. British Journal of Nutrition. 1998;79(4):333–341. [PubMed: 9624224]
- Song LL, Venkataraman K, Gluckman P, Chong YS, Chee MW, Khoo CM, Leow MK, Lee YS, Tai ES, Khoo EY. Smaller size of high metabolic rate organs explains lower resting energy expenditure in Asian-Indian than Chinese men. International Journal of Obesity (2005). 2016;40(4):633–638. [PubMed: 26568151]
- Spaeth AM, Dinges DF, Goel N. Resting metabolic rate varies by race and by sleep duration. Obesity (Silver Spring). 2015;23(12):2349–2356. [PMC free article: PMC4701627] [PubMed: 26538305]
- Sun M, Gower BA, Nagy TR, Trowbridge CA, Dezenberg C, Goran MI. Total, resting, and activity-related energy expenditures are similar in Caucasian and African-American children. American Journal of Physiology. 1998;274(2):E232–E237. [PubMed: 9486152]
- Sun M, Gower BA, Bartolucci AA, Hunter GR, Figueroa-Colon R, Goran MI. A longitudinal study of resting energy expenditure relative to body composition during puberty in African American and white children. American Journal of Clinical Nutrition. 2001;73(2):308–315. [PubMed: 11157329]
- Tanaka C, Reilly JJ, Huang WY. Longitudinal changes in objectively measured sedentary behaviour and their relationship with adiposity in children and adolescents: Systematic review and evidence appraisal. Obesity Reviews. 2014;15(10):791–803. [PubMed: 24899125]
- Tershakovec AM, Kuppler KM, Zemel B, Stallings VA. Age, sex, ethnicity, body composition, and resting energy expenditure of obese African American and white children and adolescents. American Journal of Clinical Nutrition. 2002;75(5):867–871. [PubMed: 11976160]
- Thakkar SK, Giuffrida F, Cristina CH, De Castro CA, Mukherjee R, Tran LA, Steenhout P, Lee LY, Destaillats F. Dynamics of human milk nutrient composition of women from Singapore with a special focus on lipids. American Journal of Human Biology. 2013;25(6):770–779. [PubMed: 24105777]
- Toledo FGS, Dubé JJ, Goodpaster BH, Stefanovic-Racic M, Coen PM, DeLany JP. Mitochondrial respiration is associated with lower energy expenditure and lower aerobic capacity in African American women. Obesity (Silver Spring). 2018;26(5):903–909. [PMC free article: PMC5918421] [PubMed: 29687648]
- Tranah GJ, Manini TM, Lohman KK, Nalls MA, Kritchevsky S, Newman AB, Harris TB, Miljkovic I, Biffi A, Cummings SR, Liu Y. Mitochondrial DNA variation in human metabolic rate and energy expenditure. Mitochondrion. 2011;11(6):855–861. [PMC free article: PMC3998521] [PubMed: 21586348]
- Walsh MC, Hunter GR, Sirikul B, Gower BA. Comparison of self-reported with objectively assessed energy expenditure in black and white women before and after weight loss. American Journal of Clinical Nutrition. 2004;79(6):1013–1019. [PubMed: 15159231]
- Wang Z, Ying Z, Bosy-Westphal A, Zhang J, Schautz B, Later W, Heymsfield SB, Muller MJ. Specific metabolic rates of major organs and tissues across adulthood: Evaluation by mechanistic model of resting energy expenditure. American Journal of Clinical Nutrition. 2010;92(6):1369–1377. [PMC free article: PMC2980962] [PubMed: 20962155]
- Watson KB, Carlson SA, Carroll DD, Fulton JE. Comparison of accelerometer cut points to estimate physical activity in US adults. Journal of Sports Sciences. 2014;32(7):660–669. [PMC free article: PMC4589136] [PubMed: 24188163]
- Weinsier RL, Hunter GR, Zuckerman PA, Redden DT, Darnell BE, Larson DE, Newcomer BR, Goran MI. Energy expenditure and free-living physical activity in black and white women: Comparison before and after weight loss. American Journal of Clinical Nutrition. 2000;71(5):1138–1146. [PubMed: 10799376]
- White K, Lawrence JA, Tchangalova N, Huang SJ, Cummings JL. Socially-assigned race and health: A scoping review with global implications for population health equity. International Journal for Equity in Health. 2020;19(1):25. [PMC free article: PMC7011480] [PubMed: 32041629]
- Wong WW, Butte NF, Hergenroeder AC, Hill RB, Stuff JE, Smith EO. Are basal metabolic rate prediction equations appropriate for female children and adolescents? Journal of Applied Physiology (1985). 1996;81(6):2407–2414. [PubMed: 9018486]
- Worsham MJ, Divine G, Kittles RA. Race as a social construct in head and neck cancer outcomes. Otolaryngology and Head and Neck Surgery. 2011;144(3):381–389. [PMC free article: PMC3707616] [PubMed: 21493200]
- Wouters-Adriaens MP, Westerterp KR. Low resting energy expenditure in Asians can be attributed to body composition. Obesity (Silver Spring). 2008;16(10):2212–2216. [PubMed: 18719650]