Substrate utilization during submaximal exercise in children with a severely obese parent
© Eaves et al; licensee BioMed Central Ltd. 2012
Received: 15 February 2012
Accepted: 9 May 2012
Published: 9 May 2012
We have reported a reduction in fatty acid oxidation (FAO) at the whole-body level and in skeletal muscle in severely obese (BMI ≥ 40 kg/m2) individuals; this defect is retained in cell culture suggesting an inherent component. The purpose of the current study was to determine if an impairment in whole-body fatty acid oxidation (FAO) was also evident in children with a severely obese parent.
Substrate utilization during submaximal exercise (cycle ergometer) was determined in children ages 8–12 y with a severely obese parent (OP, n = 13) or two lean/non-obese (BMI range of 18 to 28 kg/m2) parents (LP, n = 13). A subgroup of subjects (n = 3/group) performed 4 weeks of exercise training with substrate utilization measured after the intervention.
The children did not differ in age (LP vs. OP, respectively) (10.7 ± 0.5 vs. 10.2 ± 0.5 y), BMI percentile (65.3 ± 5.2 vs. 75.9 ± 7), Tanner Stage (1.4 ± 0.2 vs. 1.5 ± 0.2), VO2peak (40.3 ± 2.7 vs. 35.6 ± 2.6 ml/kg/min) or physical activity levels (accelerometer). At the same absolute workload of 15 W (~38% VO2peak), RER was significantly (P ≤ 0.05) lower in LP vs. OP (0.83 ± 0.02 vs. 0.87 ± 0.01) which was reflected in a reduced reliance on FAO for energy production in the OP group (58.6 ± 5.1 vs. 43.1 ± 4.0% of energy needs during exercise from FAO). At a higher exercise intensity (~65% VO2peak) there were no differences in substrate utilization between LP and OP. After exercise training RER tended to decrease (P = 0.06) at the 15 W workload, suggesting an increased reliance on FAO regardless of group.
These findings suggest that the decrement in FAO with severe obesity has an inherent component that may be overcome with exercise training.
KeywordsBariatric surgery Class III obesity Exercise Fat oxidation Skeletal muscle
In the United States, the incidence of severe or class III obesity (BMI ≥ 40 kg/m2) is increasing at a rate 2 to 3 times faster than lower range obesity . The severely obese condition has a profound effect on health care; while a BMI of 35 to 40 kg/m2 was associated with a 50% increase in health care expenditures, a BMI of ≥ 40 kg/m2 doubled health care costs above those of normal weight . In relation to the underlying etiology of this disease, our research group has consistently found that fatty acid oxidation (FAO) is impaired at the whole body level [3, 4] and specifically in skeletal muscle [5–7] with severe obesity. This decrement in FAO may contribute to the development of the severely obese state, as it has been reported that individuals who exhibit a lower rate of fat oxidation are prone to weight gain . The impairment in FAO is still evident after the pronounced weight loss induced by gastric bypass surgery [3–5] and remains intact in muscle cell cultures raised from severely obese donors [9, 10] both of which suggest a resilient trait. Exercise training, however, rescued FAO in previously severely obese individuals who exhibited this initial deficit .
It is difficult to determine whether the depressed FAO seen with severe obesity is a cause or a consequence of the disease. Parental obesity increases the risk of becoming an obese adult by more than two-fold regardless whether the child is obese or nonobese . It has also been reported that normal weight subjects with a family history of obesity display reduced lipid oxidation implying a genetic contribution . However, FAO in the offspring of specifically severely obese individuals has, to our knowledge, not been examined. The purpose of the present study was to determine if the reduction in FAO seen in adults with severe obesity was also evident in children with at least one severely obese parent and if exercise training could correct this condition. We have previously been able to detect the reduction in FAO with severe obesity using a submaximal exercise protocol ; we thus utilized this non-invasive approach to examine whole-body FAO in children.
Experimental design and research subjects
The purpose of this study was to compare substrate utilization during submaximal exercise in prepubescent children (8 to 12 y) with at least one severely obese (BMI ≥ 40 kg/m2) parent versus children with two non-obese parents (BMI ≤ 28.0 kg/m2). A subgroup of children from each group was also examined after a 4-week endurance-oriented exercise program to determine if substrate utilization could be altered.
Children with a severely obese parent (OP) were recruited by contacting individuals who were either contemplating or had recently undergone gastric bypass or lap banding surgery to treat severe obesity. As the majority of patients undergoing weight loss surgery in our clinics are women, all of the mothers of the children were severely obese. The children with a severely obese mother who had undergone surgery were born > 5 years prior to the procedure. Medical records were checked to ensure that the parent exhibited class III obesity prior to the surgery. Children with lean/non-obese parents (LP) were recruited by flyers, newspaper advertisements, and by contacting individuals who had participated in previous studies. To be placed in the LP group, both biological parents had to possess a BMI that placed them in the normal or non-obese category (BMI between 18.5 and 28.0 kg/m2), been stable at this BMI for ≥ 1 y, and could not have been previously severely obese. The children in each group were matched for age, gender, and race. Children were excluded if they were on any type of medication or had a medical condition that altered metabolism, limited their ability to exercise, or posed a risk for exercise. Children were also excluded if they regularly participated in an organized sport or physical activity. All procedures were approved by the University and Medical Center Institutional Review Board at East Carolina University. Written informed consent was obtained from the parent and either written or verbal assent from the child.
Initial screening involved at least one biological parent and the child. Questionnaires to determine Tanner stage for the child  and both the child and parents’ physical activity patterns  were completed by a parent. Height and weight were measured; if only one parent was present, height and weight were obtained for the other via self-report. Minimum waist circumference was measured in the children, and seated and standing height used to determine peak height velocity as an index of biological maturity [15, 16]. A DEXA scan determined body composition. During the initial visit the child briefly rode the cycle ergometer wearing the head gear, mouth piece, and nose clips used for the maximal and submaximal exercise tests. The child was given the option of wearing an ActiGraph GT1M accelerometer (ActiGraph, Pensacola FL, USA) for one week to provide information on physical activity . Instructions were given about wearing the accelerometer as well as a log sheet to record when the child put on and took off the instrument.
Maximal exercise test
A maximal exercise test was done on a Lode Corval cycle ergometer (Lode BV, Groningen, The Netherlands) and maximal oxygen consumption assessed using indirect calorimetry (ParvoMedics True Max 2400 Metabolic cart, Sandy, UT, USA). The maximal exercise protocol was based on work by Arngrimsson, Sveinsson, and Johannsson  which examined 9 and 15 year old adolescents. Initial workload and the stepwise increments were 20 W if body mass was less than or equal to 30 kg or 25 W if body mass was above 30 kg; workload increased every third minute until voluntary exhaustion or a pedal rate of 60 rpm could not be maintained. Criteria for a valid test included achieving a heart rate ≥ 195 bpm, RER ≥ 1.0, or a plateau in VO2 despite increasing workload . A second maximal exercise test was performed ≥ 4 days after the initial test.
Instructions for the submaximal exercise test stressed the importance of arriving in the laboratory in the morning after an overnight fast. The submaximal exercise protocol was based upon a previous study in our laboratory examining substrate utilization with severe obesity . Children exercised for 10 min at identical absolute (15 W) and relative (~65% VO2peak) workloads in order to account for possible differences in cardiovascular fitness. The workloads were selected as they could be relatively easily maintained and relied on a mixture of substrates for energy production . The order of the workloads was counterbalanced and the child given a 10 to 15 minute rest between each. The average of the final three minutes of submaximal exercise was used to determine substrate utilization .
A subgroup of children performed 4 weeks of supervised physical activity using a program similar to that utilized by Duncan and Howley which increased fat oxidation during moderate intensity exercise . Training was performed 3 days/wk at ~65% of VO2peak for 30 min/session during the first week which progressed to 60 min/session in week 2. Each session began with a warm-up of stretching and walking for 10 min. All training was supervised and consisted of walking on a treadmill, stationary cycling, and recreational activities such as soccer, racquetball, and tag. Participants exercised in groups to provide a social atmosphere. After the 4 weeks of training participants underwent another maximal and submaximal exercise test and height, weight, and minimal waist circumference measured.
Data were compared between LP and OP and before and after training with a between groups and repeated measures ANOVA, respectively. Significant differences were accepted at P ≤ 0.05. Values are expressed as mean ± the standard error (SE).
39.8 ± 1.6
68.6 ± 2.6
165.5 ± 1.4
168.6 ± 2.1
25.0 ± 0.8
45.4 ± 1.2*
Descriptive characteristics of the children
LP (n = 13)
OP (n = 13)
10.7 ± 0.5
10.2 ± 0.5
39.1 ± 2.4
51.3 ± 6.7
146.9 ± 2.8
151.8 ± 4.7
18.2 ± 0.6
21.3 ± 1.7
BMI Z Score
0.455 ± 0.161
1.031 ± 0.287
65.3 ± 5.2
75.9 ± 7.0
21.7 ± 2.2
26.6 ± 3.2
Minimum Waist, cm
53.5 ± 4.9
60.8 ± 7.2
1.4 ± 0.2
1.5 ± 0.2
3.2 ± 0.4
3.4 ± 0.4
Maximal exercise characteristics of the children
40.3 ± 2.7
35.6 ± 2.6
1.5 ± 0.1
1.7 ± 0.2
113.1 ± 10.0
118.0 ± 17.0
Responses to a submaximal exercise workload (15 W)
14.5 ± 0.7
13.2 ± 1.2
0.55 ± 0.02
0.62 ± 0.05
% peak VO2, ml/kg/min
37.4 ± 2.4
38.0 ± 2.7
% peak VO2, L/min
37.5 ± 2.4
38.1 ± 2.7
Heart Rate (beats/min)
113.3 ± 4.3
109.1 ± 3.7
0.83 ± 0.02
0.87 ± 0.01*
Responses to a submaximal exercise workload (65% VO 2 Peak)
25.5 ± 1.8
21.5 ± 1.8
0.98 ± 0.08
1.1 ± 0.14
% peak VO2, ml/kg/min
63.3 ± 2.1
60.0 ± 2.5
% peak VO2, L/min
63.5 ± 2.2
60.7 ± 2.4
Heart Rate (beats/min)
153.3 ± 4.3
143.8 ± 3.6*
0.90 ± 0.01
0.91 ± 0.01
Minutes of activity per day
Total Physical Activity
Exposure to an obesogenic environment (i.e. high food availability, low physical activity) is a critical component contributing to positive energy balance and the development of obesity. However, genetic susceptibility can also play a role as shown by heritability estimates ranging from 40 to 70% for the obese state . An experimental approach used to examine the role of genetics is to study subjects with a familial history of obesity. Using this model, Giacco et al. reported that the lean offspring of overweight parents responded to a high fat meal with a significantly lower incremental increase in fat oxidation compared to offspring from normal weight parents. This impairment in the ability to effectively utilize lipid under conditions eliciting fatty acid oxidation may be a critical component of obesity, as a lower rate of lipid oxidation has been linked to weight gain in both the Pima Indians  and the Baltimore Longitudinal Study on Aging .
Our research group has reported a decrement in FAO at the whole-body level [3, 4] and in skeletal muscle [7, 24] with severe obesity which may predispose these individuals to weigh gain and the severely obese state. The main finding of the present study was that relatively lean children with a severely obese parent (OP) also displayed an impaired rate of FAO during mild physical activity which required predominantly lipid as the source for energy production (Figure 1, Table 3). This difference did not appear to be due to a higher level of obesity in the OP vs. LP group (Table 2, Results) nor differences in cardiovascular fitness (Table 3) and physical activity patterns (Table 6).
Using an identical exercise protocol, we previously reported that the rate of FAO during submaximal exercise at workloads eliciting 15 W and 65% VO2peak was reduced in sedentary, severely obese women who lost weight via gastric bypass surgery compared to sedentary, weight-matched controls who were never severely obese . In the present study in children the impairment in FAO was only evident at the milder, 15 W workload (Figure 1; Tables 45) which offers several hypothetical scenarios concerning severe obesity. First, early in life there may be an underlying deficit in the ability to produce energy from lipid that is evident only during conditions which elicit a relatively lower degree of energy demand and thus higher proportion of FAO (i.e. the 15 W workload) (Figure 1, Table 4) which subsequently progresses into a more encompassing condition in adulthood . This progression of the impairment in FAO could involve an underling genetic/epigenetic component which increases its expression and/or environmental influences that accumulate during the development of the severely obese state. Secondly, the children in the present study appeared to spend a substantial amount of time per day performing relatively mild-intensity activities (Table 6). A lower rate of FAO during such activities (Figure 1) could potentially place children with a severely obese parent in a condition of positive lipid balance compared to their counterparts and predispose them to ectopic lipid accumulation. Both of these hypotheses, however, remain to be verified.
Studies examining children with obese parents exhibit equivocal results with some indicating a low capacity for oxidative metabolism  while others report no relationship between indices of FAO and a predisposition to obesity . Part of this discrepancy may be related to the conditions under which FAO was assessed; in the present study we utilized submaximal exercise inasmuch as deficits in the rate-limiting steps of oxidative pathways in skeletal muscle may be potentially easier to detect during conditions of elevated energy demand. Also, in our previous work we only observed a reduction in FAO in the skeletal muscle of severely obese individuals (BMI ≥ 40 kg/m2) and not with lower grade obesity [5, 6]. The degree of obesity of the parents may thus also be a critical factor when examining metabolic characteristics that can predispose children towards weight gain. For example, a propensity for developing severe obesity may involve an epigenetic/genetic component such as a reduction in the capacity for lipid oxidation; with lower-grade obesity the epigenetic/genetic influences may not be present and thus limit the amount of body mass gain.
Although sample size was small, a relatively short course of physical activity/exercise (30–60 min/d, 3 d/wk, 4 wks) still tended to increase the contribution of FAO to total energy needs during submaximal exercise at the 15 W workload in both the LP and OP groups (Figure 2). A similar exercise protocol decreased RER and increased the rate of fat oxidation during submaximal cycling exercise at workloads ranging from approximately 30 to 70% VO2peak . In this study by Duncan and Howley  children trained entirely on a cycle ergometer for 30 min/d, 3 d/wk for 4 weeks as opposed to the more general exercise program utilized in the current study (Methods). This lack of training specificity may be responsible for the absence of change at our higher (~65% VO2peak) workload compared to their findings . However, we attempted to design an exercise program that was enjoyable and potentially clinically relevant for children; the finding of a possible enhancement in FAO thus offers promise for this intervention. In support of the efficacy of exercise, we have reported that FAO in skeletal muscle increased in previously severely obese individuals after only 10 days of endurance-oriented training .
The current study design cannot exclude environmental factors as a possible influence upon FAO. Dietary intake was also not controlled prior to the submaximal testing, although all subjects were examined in the fasted condition. In addition, we cannot discern possible biological mechanisms explaining the reduction in FAO nor the genes involved, both of which are outside the scope of this work. We have, however, reported that a lower capacity for lipid oxidation is retained in muscle cell cultures raised from obese donors which implies a genetic/epigenetic origin [9, 10, 27]; this premise is supported by the current data indicating a decrement in FAO in children with a severely obese parent.
Children with a severely obese (BMI ≥ 40 kg/m2) parent exhibited a significantly higher RER and a reduced reliance on lipid oxidation during submaximal exercise at a mild workload (15 W or ~38% VO2peak) compared to children with two non-obese parents. This finding is supportive of earlier data suggestive of a genetic or epigenetic component for the reduction in FAO in adults with severe obesity [3, 9, 10]. With a relatively short course of endurance-oriented exercise training (4 weeks) FAO tended to increase at the 15 W workload, indicating the potential effectiveness of exercise for prevention/intervention.
Funding for this work was provided by a grant from the National Institutes of Health (DK 056112, JAH).
- Sturm R: Increases in morbid obesity in the USA: 2000–2005. Public Health. 2007, 121: 492-496.View ArticleGoogle Scholar
- Andreyeva T, Sturm R, Ringel JS: Moderate and severe obesity have large differences in health care costs. Obes Res. 2004, 12: 1936-1943.View ArticleGoogle Scholar
- Thyfault JP, Kraus RM, Hickner RC, Howell AW, Wolfe RR, Dohm GL: Impaired plasma fatty acid oxidation in extremely obese women. Am J Physiol Endocrinol Metab. 2004, 287: E1076-E1081.View ArticleGoogle Scholar
- Guesbeck NR, Hickey MS, MacDonald KG, Pories WJ, Harper I, Ravussin E, Dohm GL, Houmard JA: Substrate utilization during exercise in formerly morbidly obese women. J Appl Physiol. 2001, 90: 1007-1012.Google Scholar
- Berggren JR, Boyle KE, Chapman WH, Houmard JA: Skeletal muscle lipid oxidation and obesity: influence of weight loss and exercise. Am J Physiol Endocrinol Metab. 2008, 294: E726-E732.View ArticleGoogle Scholar
- Hulver MW, Berggren JR, Cortright RN, Dudek RW, Thompson RP, Pories WJ, MacDonald KG, Cline GW, Shulman GI, Dohm GL, Houmard JA: Skeletal muscle lipid metabolism with obesity. Am J Physiol Endocrinol Metab. 2003, 284: E741-E747.View ArticleGoogle Scholar
- Kim JY, Hickner RC, Cortright RL, Dohm GL, Houmard JA: Lipid oxidation is reduced in obese human skeletal muscle. Am J Physiol Endocrinol Metab. 2000, 279: E1039-E1044.Google Scholar
- Zurlo F, Lillioja S, Esposito-Del Puente A, Nyomba BL, Raz I, Saad MF, Swinburn BA, Knowler WC, Bogardus C, Ravussin E: Low ratio of fat to carbohydrate oxidation as predictor of weight gain: study of 24-h RQ. Am J Physiol. 1990, 259: E650-E657.Google Scholar
- Hulver MW, Berggren JR, Carper MJ, Miyazaki M, Ntambi JM, Hoffman EP, Thyfault JP, Stevens R, Dohm GL, Houmard JA, Muoio DM: Elevated stearoyl-CoA desaturase-1 expression in skeletal muscle contributes to abnormal fatty acid partitioning in obese humans. Cell Metab. 2005, 2: 251-261.View ArticleGoogle Scholar
- Consitt LA, Bell JA, Koves TR, Muoio DM, Hulver MW, Haynie KR, Dohm GL, Houmard JA: Peroxisome proliferator-activated receptor-gamma coactivator-1alpha overexpression increases lipid oxidation in myocytes from extremely obese individuals. Diabetes. 2010, 59: 1407-1415.View ArticleGoogle Scholar
- Whitaker RC, Wright JA, Pepe MS, Seidel KD, Dietz WH: Predicting obesity in young adulthood from childhood and parental obesity. N Engl J Med. 1997, 337: 869-873.View ArticleGoogle Scholar
- Giacco R, Clemente G, Busiello L, Lasorella G, Rivieccio AM, Rivellese AA, Riccardi G: Insulin sensitivity is increased and fat oxidation after a high-fat meal is reduced in normal-weight healthy men with strong familial predisposition to overweight. Int J Obes Relat Metab Disord. 2004, 28: 342-348.View ArticleGoogle Scholar
- Davison KK, Werder JL, Trost SG, Baker BL, Birch LL: Why are early maturing girls less active? Links between pubertal development, psychological well-being, and physical activity among girls at ages 11 and 13. Soc Sci Med. 2007, 64: 2391-2404.View ArticleGoogle Scholar
- Yore MM, Ham SA, Ainsworth BE, Kruger J, Reis JP, Kohl HW, Macera CA: Reliability and validity of the instrument used in BRFSS to assess physical activity. Med Sci Sports Exerc. 2007, 39: 1267-1274.View ArticleGoogle Scholar
- Drenowatz C, Eisenmann JC, Pfeiffer KA, Wickel EE, Gentile D, Walsh D: Maturity-related differences in physical activity among 10- to 12-year-old girls. Am J Hum Biol. 2010, 22: 18-22.View ArticleGoogle Scholar
- Mirwald RL, Baxter-Jones AD, Bailey DA, Beunen GP: An assessment of maturity from anthropometric measurements. Med Sci Sports Exerc. 2002, 34: 689-694.View ArticleGoogle Scholar
- Rowlands AV: Accelerometer assessment of physical activity in children: an update. Pediatr Exerc Sci. 2007, 19: 252-266.Google Scholar
- Arngrimsson SA, Sveinsson T, Johannsson E: Peak oxygen uptake in children: evaluation of an older prediction method and development of a new one. Pediatr Exerc Sci. 2008, 20: 62-73.Google Scholar
- Duncan GE, Howley ET: Metabolic and perceptual responses to short-term cycle training in children. Pediatr Exerc Sci. 1998, 10: 110-122.Google Scholar
- Pories WJ, Swanson MS, MacDonald KG, Long SB, Morris PG, Brown BM, Barakat HA, DeRamon RA, Israel G, Dolezal JM: Who would have thought it? An operation proves to be the most effective therapy for adult-onset diabetes mellitus. Ann Surg. 1995, 222: 339-350. discussion 350–332View ArticleGoogle Scholar
- Krebs NF, Himes JH, Jacobson D, Nicklas TA, Guilday P, Styne D: Assessment of child and adolescent overweight and obesity. Pediatrics. 2007, 120 (Suppl 4): S193-S228.View ArticleGoogle Scholar
- Herrera BM, Lindgren CM: The genetics of obesity. Curr Diab Rep. 2010, 10: 498-505.View ArticleGoogle Scholar
- Seidell JC, Muller DC, Sorkin JD, Andres R: Fasting respiratory exchange ratio and resting metabolic rate as predictors of weight gain: the Baltimore Longitudinal Study on Aging. Int J Obes Relat Metab Disord. 1992, 16: 667-674.Google Scholar
- Berggren JR, Hulver MW, Dohm GL, Houmard JA: Weight loss and exercise: implications for muscle lipid metabolism and insulin action. Med Sci Sports Exerc. 2004, 36: 1191-1195.View ArticleGoogle Scholar
- Treuth MS, Butte NF, Sorkin JD: Predictors of body fat gain in nonobese girls with a familial predisposition to obesity. Am J Clin Nutr. 2003, 78: 1212-1218.Google Scholar
- Treuth MS, Butte NF, Wong WW: Effects of familial predisposition to obesity on energy expenditure in multiethnic prepubertal girls. Am J Clin Nutr. 2000, 71: 893-900.Google Scholar
- Boyle KE, Zheng D, Anderson EJ, Neufer PD, Houmard JA: Mitochondrial lipid oxidation is impaired in cultured myotubes from obese humans. Int J Obes. 2011, 1-7.Google Scholar
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