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ABSTRACT: BACKGROUND: A routine pediatric clinical assessment of body composition is increasingly recommended but has long been hampered by the following 2 factors: a lack of appropriate techniques and a lack of reference data with which to interpret individual measurements. Several techniques have become available, but reference data are needed. OBJECTIVE: We aimed to provide body-composition reference data for use in clinical practice and research. DESIGN: Body composition was measured by using a gold standard 4-component model, along with various widely used reference and bedside methods, in a large, representative sample of British children aged from 4 to ≥20 y. Measurements were made of anthropometric variables (weight, height, 4 skinfold thicknesses, and waist girth), dual-energy X-ray absorptiometry, body density, bioelectrical impedance, and total body water, and 4-component fat and fat-free masses were calculated. Reference charts and SD scores (SDSs) were constructed for each outcome by using the lambda-mu-sigma method. The same outcomes were generated for the fat-free mass index and fat mass index. RESULTS: Body-composition growth charts and SDSs for 5-20 y were based on a final sample of 533 individuals. Correlations between SDSs by using different techniques were ≥0.68 for adiposity outcomes and ≥0.80 for fat-free mass outcomes. CONCLUSIONS: These comprehensive reference data for pediatric body composition can be used across a variety of techniques. Together with advances in measurement technologies, the data should greatly enhance the ability of clinicians to assess and monitor body composition in routine clinical practice and should facilitate the use of body-composition measurements in research studies.
American Journal of Clinical Nutrition 10/2012; · 6.67 Impact Factor
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ABSTRACT: Malnutrition is an indicator of a poor prognosis in patients with cystic fibrosis (CF). Previous body-composition (BC) studies in children with CF used 2-component models (2CMs) to assess fat mass (FM) and fat-free mass (FFM), but to our knowledge no study has used the gold-standard 4-component model (4CM), which allows for a more accurate evaluation of the nature of both elements.
We measured BC by using the 4CM in 6-12-y-old children with CF to 1) compare findings with those of healthy, matched control children and reference data; 2) relate BC to lung spirometry [forced expired volume in 1 s (FEV₁)]; and 3) compare findings with those from more commonly used 2CM techniques.
One hundred clinically stable children with CF (57% girls) aged 6-12 y were measured by using the 4CM. Children with CF underwent spirometry (FEV₁).
Girls with CF had significantly less FM than did healthy girls, even after adjustment for height and pubertal status; boys with CF had higher body mass index SD scores than did healthy boys. FM in girls was positively associated with the FEV₁ percentage predicted. The 2CM FM was significantly different from the 4CM FM, with differences dependent on sex and condition, although most techniques identified a relation between FM and FEV₁ in girls.
Although shorter than healthy children, boys with CF were heavier and had a BC within the normal range; however, girls with CF had lower FM than did healthy girls, and this was associated with poorer lung function. Given the worse prognosis in girls, this finding merits more attention. The reliability of 2CM techniques varied with sex and health status.
American Journal of Clinical Nutrition 10/2010; 92(6):1332-43. · 6.67 Impact Factor
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ABSTRACT: Hydrometry and densitometry are widely used to assess pediatric body composition due to their ease of application. The accuracy of these techniques depends on the validity of age- and sex-specific constant values for lean tissue hydration or density. Empirical data on these constants, and their variability between individuals, are lacking.
The objectives were to measure lean tissue hydration and density in a large sample of children and adolescents and to derive prediction equations.
Body composition was measured in 533 healthy individuals (91% white) aged 4-23 y by using the 4-component model. Age- and sex-specific median values for hydration and density were obtained by using the LMS (lambda, mu, sigma) method. Regression analysis was used to generate prediction equations on the basis of age, sex, and body mass index SD score (BMI SDS). Values were compared with those in previously published predictions.
Age-associated changes in density and hydration differed between the sexes. Compared with our empirical values, use of published values resulted in a mean bias of 2.1% fat (P < 0.0001). Age, sex, and BMI SDS were all significant predictors of lean tissue hydration and density. With adjustment for age and sex, hydration was higher, and density lower, in higher-BMI SDS individuals.
The chemical maturation of lean tissue is not a linear process and proceeds differently in males and females. Previously published reference values are inaccurate and induce clinically significant bias in percentage fat. New empirical reference values are provided for use in pediatric hydrometry and densitometry. Further research that extends to cover nonwhite ethnic groups is needed.
American Journal of Clinical Nutrition 03/2010; 91(3):610-8. · 6.67 Impact Factor
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ABSTRACT: Decrease in fat mass (FM) is a one of the aims of pediatric obesity treatment; however, measurement techniques suitable for routine clinical assessment are lacking. The objective of this study was to validate whole-body bioelectrical impedance analysis (BIA; TANITA BC-418MA) against the three-component (3C) model of body composition in obese children and adolescents, and to test the accuracy of our new equations in an independent sample studied longitudinally. A total of 77 white obese subjects (30 males) aged 5-22 years, BMI-standard deviation score (SDS) 1.6-3.9, had measurements of weight, height (HT), body volume, total body water (TBW), and impedance (Z). FM and fat-free mass (FFM) were calculated using the 3C model or predicted from TANITA. FFM was predicted from HT(2)/Z. This equation was then evaluated in 17 other obese children (5 males) aged 9-13 years. Compared to the 3C model, TANITA manufacturer's equations overestimated FFM by 2.7 kg (P < 0.001). We derived a new equation: FFM = -2.211 + 1.115 (HT(2)/Z), with r(2) of 0.96, standard error of the estimate 2.3 kg. Use of this equation in the independent sample showed no significant bias in FM or FFM (mean bias 0.5 +/- 2.4 kg; P = 0.4), and no significant bias in change in FM or FFM (mean bias 0.2 +/- 1.8 kg; P = 0.7), accounting for 58% (P < 0.001) and 55% (P = 0.001) of the change in FM and FFM, respectively. Our derived BIA equation, shown to be reliable for longitudinal assessment in white obese children, will aid routine clinical monitoring of body composition in this population.
Obesity 04/2009; 17(12):2245-50. · 4.28 Impact Factor
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ABSTRACT: Preterm infants are at risk of metabolic bone disease due to inadequate mineral intake with unknown consequences for later bone health.
To test the hypotheses that (1) early diet programs peak bone mass and bone turnover; (2) human milk has a beneficial effect on these outcomes; (3) preterm subjects have reduced peak bone mass compared to population reference data.
20 year follow-up of 202 subjects (43% male; 24% of survivors) who were born preterm and randomized to: (i) preterm formula versus banked breast milk or (ii) preterm versus term formula; as sole diet or supplement to maternal milk. Outcome measures were (i) anthropometry; (ii) hip, lumbar spine (LS) and whole body (WB) bone mineral content (BMC) and bone area (BA) measured using DXA; (iii) bone turnover markers.
Infant dietary randomization group did not influence peak bone mass or turnover. The proportion of human milk in the diet was significantly positively associated with WBBA and BMC. Subjects receiving >90% human milk had significantly higher WBBA (by 3.5%, p=0.01) and BMC (by 4.8%, p=0.03) than those receiving <10%. Compared to population data, subjects had significantly lower height SDS (-0.41 (SD 1.05)), higher BMI SDS (0.31 (1.33)) and lower LSBMD SDS (-0.29 (1.16)); height and bone mass deficits were greatest in those born SGA with birthweight <1250 g (height SDS -0.81 (0.95), LSBMD SDS -0.61 (1.3)).
Infant dietary randomization group did not affect peak bone mass or turnover suggesting the observed reduced final height and LS bone mass, most marked in growth restricted subjects with the lowest birthweight, may not be related to sub-optimal early nutrition. The higher WB bone mass associated with human milk intake, despite its low nutrient content, may reflect non-nutritive factors in breast milk. These findings may have implications for later osteoporosis risk and require further investigation.
Bone 04/2009; 45(1):142-9. · 4.02 Impact Factor
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ABSTRACT: Many components of clinical management are tailored to metabolic variables, such as fat-free mass, fat mass, resting metabolic rate (RMR), and body surface area. However, these traits are difficult to measure in routine care and are typically predicted from simple anthropometric or bedside body-composition measurements. Many prediction equations have been published, but validation studies have shown that these equations tend to have limited accuracy in individuals and many have significant average bias.
We tested a mathematical approach that assumes that the aggregate of many independent predictions is more accurate than the best single prediction.
Body composition was measured in 196 children aged 4-16 y by using the 4-component model. RMR was measured in 142 adult women. Data on weight, height, age, skinfold thickness, and body impedance were used in published equations to predict body composition (12 equations) or RMR (13 equations). The accuracy of individual compared with aggregate predictions, relative to the reference measurements, was compared by using the Bland and Altman method.
For children's body composition and adult RMR, the aggregate predictions had lower mean biases and lower limits of agreement than did the individual predictions, and the aggregate predictions performed better than did any individual prediction.
Aggregate predictions perform better than single predictions at predicting fat-free mass, fat mass, total body water, and RMR. Our findings indicate that the accuracy of calculating variables such as energy requirements and drug and dialysis dosages can be improved significantly with the use of our mathematical approach.
American Journal of Clinical Nutrition 02/2009; 89(2):491-9. · 6.67 Impact Factor
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ABSTRACT: Higher birth weight is associated with higher body mass index, traditionally interpreted as greater fatness or obesity, in later life. However, its relation with individual body-composition components and fat distribution remains unclear.
We investigated associations between birth weight and later fat mass (FM), fat-free mass (FFM), and fat distribution.
Body composition was assessed by the criterion 4-component model in 391 healthy children [mean (+/-SD) age, 11.7 +/- 4.2 y; 188 boys]. FM and FFM were adjusted for height (FMI = FM/height(2); FFMI = FFM/height(2)) and were expressed as SD scores (SDS). Findings were compared between the 4-component and simpler methods.
Birth weight was positively associated with height in both sexes and was significantly positively associated with FFMI in boys, equivalent to a 0.18 SDS (95% CI: 0.04, 0.32) increase in FFMI per 1 SDS increase in birth weight. These associations were independent of puberty, physical activity, social class, ethnicity, and parental body mass index. Birth weight was not significantly related to percentage fat, FMI, or trunk FMI in either sex. Equivalent analyses using simpler methods showed a trend for a positive relation between birth weight and FMI in boys that became nonsignificant after adjusting for confounders.
FFMI in later life in males is influenced by birth weight, a proxy for prenatal growth, but evidence for fetal programming of later FM or central adiposity is weak. Different body-composition techniques and data interpretation can influence results and should be considered when comparing studies.
American Journal of Clinical Nutrition 11/2008; 88(4):1040-8. · 6.67 Impact Factor
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ABSTRACT: Rapid weight gain in infancy is associated with higher body mass index in later life, but its relation with individual body-composition components remains unclear.
We aimed to investigate associations between weight gain during different periods in infancy and later fat mass (FM) and fat-free mass (FFM).
Body composition was assessed by using the 4-component model, dual-energy X-ray absorptiometry, and anthropometry in 234 healthy UK children and adolescents (105 boys; x +/- SD age: 11.4 +/- 3.8 y). Early growth measurements were prospective in 52 subjects and retrospective in 182. Relative weight gain was calculated as change in SD score (SDS) during different periods.
Relative weight gain from 0 to 3 mo and from 3 to 6 mo showed positive relations with childhood FM, waist circumference, and trunk FM that were equivalent to increases in FMI (FM/height(2)) of 0.24 SDS (95% CI: 0.04, 0.44) and 0.50 SDS (0.25, 0.75) per 1-SDS increase in early weight and that were comparable to the effect of current obesity risk factors. Relative weight gain from 0 to 3 mo was also positively associated with later FFMI (FFM/height(2)). Relative weight gain from 6 to 12 mo was not associated with later body composition. Associations were independent of birth weight, sex, puberty, physical activity, socioeconomic class, ethnicity, and parental body mass index.
In this Western population, greater relative weight gain during early infancy was positively associated with later FM and central fat distribution and with FFM. Rapid weight gain in infancy may be a risk factor for later adiposity. Early infancy may provide an opportunity for interventions aimed at reducing later obesity risk.
American Journal of Clinical Nutrition 07/2008; 87(6):1776-84. · 6.67 Impact Factor
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ABSTRACT: Arm anthropometry is used as a proxy of body composition in clinical and field research but its validity has not been established in children. To address this issue, mid-upper arm circumference (MUAC) and triceps skinfold thickness (TS) were measured in 110 healthy children aged 4.4-13.9 y (55 boys) and 49 cystic fibrosis (CF) patients aged 8.1-13.4 y (22 boys). Reference values were arm and whole-body fat mass (FM) and fat-free mass (FFM) measured by dual x-ray absorptiometry and four-component model, respectively. Arm fat area (AFA), MUAC, and TS correlated well with arm FM (r = 0.84-0.92) and total FM (r = 0.78-0.92). Arm muscle area (AMA) and MUAC correlated well with arm FFM (r = 0.68-0.82) and total FFM (r = 0.60-0.86). After adjusting for age, sex, and height, arm anthropometry correlated strongly with FM but weakly with FFM. AFA, MUAC, and TS explained 67, 63, and 61% of variability in total FM in healthy children and 70, 72, and 63% in CF. AMA and MUAC explained only 24 and 16% of variability in total FFM in healthy children and 33 and 28% in CF. Arm anthropometry is useful for predicting FM and ranking healthy children and patients for fatness. It has poorer success in predicting regional or total FFM.
Pediatric Research 07/2006; 59(6):860-5. · 2.70 Impact Factor
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ABSTRACT: Dual-energy X-ray absorptiometry (DXA) is widely used to assess body composition in research and clinical practice. Several studies have evaluated its accuracy in healthy persons; however, little attention has been directed to the same issue in patients.
The objective was to compare the accuracy of the Lunar Prodigy DXA for body-composition analysis with that of the reference 4-component (4C) model in healthy subjects and in patients with 1 of 3 disease states.
A total of 215 subjects aged 5.0-21.3 y (n = 122 healthy nonobese subjects, n = 55 obese patients, n = 26 cystic fibrosis patients, and n = 12 patients with glycogen storage disease). Fat mass (FM), fat-free mass (FFM), and weight were measured by DXA and the 4C model.
The accuracy of DXA-measured body-composition outcomes differed significantly between groups. Factors independently predicting bias in weight, FM, FFM, and percentage body fat in multivariate models included age, sex, size, and disease state. Biases in FFM were not mirrored by equivalent opposite biases in FM because of confounding biases in weight.
The bias of DXA varies according to the sex, size, fatness, and disease state of the subjects, which indicates that DXA is unreliable for patient case-control studies and for longitudinal studies of persons who undergo significant changes in nutritional status between measurements. A single correction factor cannot adjust for inconsistent biases.
American Journal of Clinical Nutrition 06/2006; 83(5):1047-54. · 6.67 Impact Factor
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ABSTRACT: Changes in body composition are commonly reported in pediatric survivors of acute lymphoblastic leukemia (ALL). However, the effect of ALL and of its treatment on body composition in children in remission from ALL has not been fully examined with the use of a reference method.
We aimed to determine the body composition and composition of fat-free mass (FFM) in children in remission from ALL. We also aimed to compare the effects that prednisolone and dexamethasone had on the body composition of an ALL survivor population.
This cross-sectional study measured height, weight, body volume, total body water, and bone mineral content in 24 children in remission from ALL and 24 age-matched, healthy control subjects. Body composition and FFM composition were evaluated by using the 4-component model.
The mean body mass index and fat mass index were significantly (P = 0.05 for both) higher in the ALL survivors than in age-matched control subjects. The composition of the FFM in the 2 treatment groups was not observed to differ significantly. Examination of the composition of FFM made it evident that children in remission from ALL had both significantly greater hydration (P = 0.001) and lower density (P = 0.0001) of FFM than did the control children.
Children in remission from ALL may develop excess body fat. To measure body composition accurately in an ALL population, the high hydration and low density of FFM in this population should be taken into consideration.
American Journal of Clinical Nutrition 02/2006; 83(1):70-4. · 6.67 Impact Factor