International Journal of Obesity (1998) 22, 878±884 ß 1998 Stockton Press All rights reserved 0307±0565/98 $12.00 http://www.stockton-press.co.uk/ijo Gender differences in fat mass of 5±7-year old children M Mast1, I KoÈrtzinger1, E KoÈnig2 and MJ MuÈller1 1 Institut fuÈr HumanernaÈhrung und Lebensmittelkunde, Christian-Albrechts-UniversitaÈt zu Kiel and 2SchulaÈrztlicher Dienst der Stadt Kiel, Kiel, Germany OBJECTIVE: Studying gender differences in fat mass and distribution in a homogeneous group of children. DESIGN: Crosssectional study. SUBJECTS: 610 children aged 5 ± 7 y in Kiel, Germany. METHODS: Anthropometric measures, bioelectrical impedance analysis (BIA). RESULTS: Although boys had increased body weights (P<0.05), body mass indexes (BMI's) (P<0.001) and waist=hip ratios (WHRs) (P<0.001), the %fat mass as assessed by BIA (P<0.05) was increased in girls. Although the increased BMI in boys was independent of the percentile used, gender differences (that is, lower values for boys than for girls at the same age) in WHR, the sum of four skinfolds and %fat were seen up to the 90th percentile. By contrast, above the 90th percentile there were no differences in skinfold thickness and %fat between boys and girls. Studying 42 BMImatched pairs (boys and girls) also showed that the %fat estimated by BIA (P<0.001) was increased in girls. Plotting the average of %fat as obtained from skinfold- and BAI-measurements against the difference between data obtained by the use of the two methods shows that BIA %fat overestimates skinfold %fat at low or normal percent fat mass (that is, up to 20%) in both genders. By contrast, at increased fat mass, BIA %fat seems to underestimate skinfold %fat in both genders. CONCLUSIONS: Gender differences in fat mass and fat distribution are obvious in children aged 5 ± 7 y. These differences are independent of gender differences in body weight. However, the nutritional state has an in¯uence and gender differences cannot be detected in overweight and obese children. Our data also suggest that a childrenspeci®c formula used to calculate %fat from skinfold measurements is inappropriate. Keywords: fat mass; fat distribution; obesity; children; bioelectrical impedance; skinfold measurements Introduction Gender differences in fat mass are generally considered to become manifest after puberty. Before puberty boys and girls have similar average heights, weights and body mass indices (BMI).1 However three recent papers using detailed body composition analysis in children, found differences in fat mass between prepubertal boys and girls.2 ± 4 Using dual-energy X-ray absorptiometry (DEXA) or bioelectrical impedance analysis (BIA) in 403 healthy Dutch children and adolescents (age 4±20 y), percentage body fat (%fat) was higher in girls than in boys at all ages.2 In another study on 40 children aged 3±8 y, DEXA-measurements gave strong evidence for gender differences in fat mass: the percentage body fat was 13.5% vs 20.4% in boys and girls, respectively.3 In a third study, Correspondence: Prof Dr MJ MuÈller, Institut fuÈr HumanernaÈhrung und Lebensmittelkunde, Christian-AlbrechtsUniversitaÈt zu Kiel, DuÈsternbrooker Weg 17 ± 19, 24105 Kiel, Germany. E-mail: [email protected] Received 26 November 1997; revised 2 April 1998; accepted 23 April 1998 DEXA-derived fat mass was signi®cantly increased in a total of 31 African±American and eight Caucasian girls aged 5±10 y when compared to boys.4 All these data were contrary to the results of previous studies, where DEXA5 or DEXA plus anthropometry6 had been used:In the ®rst study, 48 perpubertal individuals did not show gender differences in fat mass, which became manifest in peri- and postpubertal subjects.5 This ®nding was supported by another crossectional study on 265 subjects aged 4±26 y6 Before the age of 10 y, values were similar for both genders. DEXA is a novel technique, which offers the potential of precise measurements of soft tissue composition,7,8 for example, the coef®cient of variation for the in vivo (DEXA-) assessment of fat mass was reported to be 2.52%.3 However, the precision of measures of fat mass, differ between different DEXA-absorptiometers and values between 1.9± 6.9% were reported, suggesting inter-machine differences.7,8 In addition, signi®cant differences between the machines by the same manufacturer were found, despite high standards of quality control within an individual machine: the intra-machine differences in the estimation of fat mass may reach about 3 kg.7 Gender and fat mass in young children M Mast et al Since different DEXA-machines have been used in the studies cited above,2 ± 5 methodological problems limit the comparison between studies and may explain some of the observed discrepancies. Interestingly, Bioelectrical impedance analysis BIA2 or anthropometry5 have been used in combination with DEXA in two of the studies. There was a close correlation between DEXA and BIA (r 0.88) and the mean difference in percentage fat mass as assessed by the two methods was only 5%.2 Higher values were found by BIA than DEXA. The percentage body fat (%fat) as estimated by DEXA, also correlated with skinfold measurements (r 0.82).5 Comparing fat measurements of DEXA with anthropometry, showed no differences between the means for male subjects, but a difference of about 3 kg (that is, DEXA overestimated skinfold measurements) was found for the female subjects.5 Thus, despite differences in absolute values, BIA or anthropometry seem to support DEXA-measurements. Taken together, some discrepancies exist regarding gender differences in fat mass of prepubertal children. Some of the discrepancies may result from methodological problems. Other problems come from the different study designs, for example, none of the above mentioned studies took into account different body weights or the percentiles of the different parameters measured. In addition, all the studies used children from a wide age range, thus, conclusions regarding speci®c age groups are not possible. In Kiel, we had the opportunity to analyse the data of the 1996 cohort of the `Kiel Obesity Prevention Study' (KOPS) to determine whether gender differences in fat mass, as assessed by ®eld measures of body composition, are present in healthy prepubertal children aged 5± 7 y. We used BIA, as well as anthropometric measurements, because KOPS is a large epidemiological trial. It was designed to reduce the prevalence of obesity in children and adolescents in order to decrease obesity and obesity-related diseases in later life.9 ± 11 In KOPS, about 600±1000 children aged 5± 7 y were=are assessed every year for a total of six years. These children are followed until puberty. An integrated intervention program was designed and structured for obese children, non-obese children with obese parents, families with obese children or children at risk of to becoming obese, and their teachers. The aim of the intervention is to encourage the attractiveness of a healthy lifestyle, as well as to increasing personal autonomy. Faced with the discrepancies of the above mentioned results, observed in the fat mass of prepubertal children, we took the opportunity to analyze our 1996 data. These data were used to determine whether gender differences in fat mass, as assessed by ®eld measures of body composition, are present in healthy prepubertal children aged 5±7 y. The 1996 cohort of KOPS, consists of 610 children aged 5±7 y. The nutritional data were analyzed with respect to the different percentiles of body weight. Regarding nutri- tional measures our data show that in children aged 5± 7 y, gender differences exist. They are seen in normal weight children, but are camou¯aged by overweight and obesity. Methods Subjects Between January±June 1996 610 healthy children (316 boys and 294 girls) in different parts of the town of Kiel, North Germany, were randomly sampled and examined in 16 of the 29 primary schools. Nutritional data (age, gender, body weight and height), as well as sociodemographic data, suggest that our study population is representative of the total population of children in Kiel aged 5±7 y. The procedures had been explained to all parents. The 610 children represent 30.6% of the total population examined by the school physicians. All parents had given their informed written consent. The assessment of the nutritional state included bodyweight and height, skinfold measurements (triceps, biceps, abdominal, suprailiac, subscapular), measurements of waist, hip and mid-arm circumferences and a BIA. The study was approved by the local ethical committee. Body composition We decided to use anthropometric and BIA-measurements in our study for two reasons. First, anthropometric measurements are used because there is already a considerable data base in Schleswig-Holstein which can be compared with our data. Second, BIA is used because it can be applied in epidemiological studies (see National Health and Nutrition Examination Survey (NHANES)) and may provide more accurate data when compared with anthropometric data. Since BIA and DEXA data also showed a very close correlation in children,2 we feel justi®ed in taking BIA data as a measure of %fat mass in children. We were not allowed to take DEXA measurements for a subgroup of children, for ethical reasons (that is, radiation exposure). Anthropometry Data were assessed for weight and height of the children, as part of the medical school test. Weight was measured to the nearest 0.1 kg on a calibrated balance-beam scale with subjects wearing light underwear on and height was estimated to the nearest 0.5 cm. All other anthropometric measurements were performed by trained observers, according to standard techniques.12 Skinfold thickness was determined to the nearest 0.2 mm at the right biceps (BSF), triceps (TSF), subscapular (SSF) and suprailiac (SIF) sites, with a lafayette skinfold caliper, (Model 01127, Lafayette Instrument Company, Indiana 47903) calibrated to exert a constant pressure of 879 Gender and fat mass in young children M Mast et al 880 10 g=mm2. The coef®cients of variation forrepeated (n 3) measurements of BSF, TSF, SSF and SIF in 10 children aged 5±7 y were 6.0%, 1.9%, 4.0% and 4.3%, respectively. Fat mass (FM) was determined by age- and gender-speci®c formulas, according to Lohmann,13 involving weight and the log-transformed sum of BSF, TSF, SSF, and SIF skinfolds for subjects aged<12.0 y. FM[kg] weight*((5.28/D)74.86), where (D body density). D, boys [g/ml] 1.16907 0.0788*(log (sum of four skinfolds)) D, girls [g/ml] 1.206370.0999* (log (sum of four skinfolds)) Fat free mass (FFM) was calculated as the difference between weight and body fat. Waist circumference was measured midway between the lower rib margin and the iliac crest. Hip circumference was measured at the point yielding the maximum circumference over the buttocks. The WHR was calculated to obtain an index for the pattern of body fat distribution. groups): group 1: BMI<25. percentile, group 2: BMI between 25±75 percentile, group 3: BMI>75 percentile; and group 4: all BMI matched pairs). In addition to the standard procedure, a Bland and Altman plot17 was used to compare the difference between the two methods with the mean values. A positive difference indicated a relative overestimation of %fat mass, whereas a negative difference suggested a relative underestimation of %fat mass. Results Figure 1A and B, show the association between height and weight of our study population. When compared with girls, boys aged 5±7 y had an increased body Bioelectrical impedance analysis (BIA) Measurement of whole body bioimpedance in children, has been described previously.14,15 The BIA measurements presented here were performed at a single frequency (50 kHz) (Multi-Frequency-Analyzer 2000-M, Data Input GmbH, Frankfurt=M, Germany) with one pair of electrodes appropriately placed on the dorsal surfaces of the right hand and a second pair of electrodes placed on the right foot.15 With the subjects lying in a supine position, measurements were performed while the hands and feet were extended from the side of the trunk. The equation used for children was based on body density and underwater measurements of speci®c gravity, as reported by Houtkooper et al.16 The equation provides an estimate for fat mass (FM) [%] (71.11)*(ht)2/R1.04*wt 15.16, where R is the body's resistance (O), ht is the subject's height (cm), and wt is the subject's body weight (kg). FFM is then calculated as the difference body weight and FM. The coef®cients of variation for repeated (n 3) estimations of R and XC (reactance (O)) in 10 children aged 5±7 y were 1.0 and 2.1%, respectively, resulting in a cv of 1.5% in %fat mass. Statistical analyses All statistical analyses (calculation of percentiles, regression analyses, statistics) were performed using Excel 5.0. The data are presented as mean values and range. Different percentiles of the various measurements were calculated. The basic statistics included the Student t-Test, for comparison between gender groups, correlation analyses for the relation of different assessment methods for fatmass and paired t-Test for comparison between methods in BMI matched groups 42 BMI matched pairs of boys and girls (divided into four Figure 1 Correlation between height and body weight in 610 children aged 5 ± 7 y. (A) boys ( P<0.001) and (B) girls ( P<0.001). Gender and fat mass in young children M Mast et al 881 Table 1 Characteristics of the children Mean (range) Boys (n 316) Age (y) Height [m] Weight [kg] BMI [kg=m2] MAC [cm] WHR TSF [mm] BSF [mm] SIF [mm] SSF [mm] Trunk: extremity skinfold ratio Sum of four skinfolds [mm] FM, A [%] FM, A [kg] FM, BIA [%] FM, BIA [kg] 6.1 1.21 23.6 16.5 18.2 0.89 11.1 6.2 8.7 5.8 0.97 31.7 15.5 3.86 17.9 4.34 (5.0 ± 7.8) (1.00 ± 1.38) (15.0 ± 45.0)* (11.2 ± 32.1)*** (12.0 ± 28.5) (0.74 ± 1.07)*** (2.6 ± 25.3) (1.3 ± 18) (1.6 ± 36.3) (1.3 ± 28.7) (0.35 ± 2.87) (8.8 ± 100.3) (2.7 ± 36.1)*** (0.5 ± 15.1)*** (4.9 ± 34.3)* (1.4 ± 15.4) Girls (n 294) 6.1 1.2 22.8 15.6 18 0.87 11.4 6.3 8.9 6.2 1.00 32.8 13.6 3.24 18.6 4.31 (5.0 ± 7.3) (1.07 ± 1.38) (15.0 ± 40.7) (11.5 ± 24.5) (14.0 ± 24.0) (0.7 ± 1.11) (3.3 ± 27.0) (2.3 ± 18.3) (2.6 ± 37.3) (1.6 ± 31.3) (0.37 ± 2.35) (11.9 ± 111.7) (0.2 ± 41.1) (0.03 ± 16.7) (5.1 ± 29.1) (1.2 ± 11.8) BMI body mass index; MAC mid-arm circumference; WHR waist ± hip ratio; TSF Triceps skinfold thickness; BSF Biceps skinfold thickness; SIF Subrailiacal skinfold thickness; SSF Subscapular skinfold thickness; FM fat mass; FM, A fat mass from Anthropometry; FM, BIA fat mass from bioelectrical impedance analysis (BIA); the data are given as mean values and range. Gender differences were analysed by unpaired ttest: *P<0.05; ***P<0.001. weight, BMI and WHR (Table 1). The sum of four skinfolds tended to be greater in girls, whilst %fat mass calculated from BIA-measurements was increased in girls. Calculating %fat from skinfold measurements according to Lohman13 resulted in a %fat mass, which was different from BIA-data (Table 1). Table 2 shows the different percentiles for body weight, height, BMI, triceps skinfolds, sum of four skinfolds, FM as estimated from anthropometry, as well as from BIA-measurements, and also includes the WHR and the middle arm circumference (MAC). The sum of four skinfolds and the %fat from BIA-measurements, were greater for girls up to the 80th and 90th percentiles, respectively (Table 3). Signi®cant gender differences were observed up to the 80±90th percentile (Table 3). Skinfold and BIA-measurements showed an increased fat mass for girls up to the 80th or 90th percentile, respectively (Table 3). By contrast, overweight boys showed an increased fat mass when compared with overweight girls (Table 3). There was a correlation between the sum of four skinfolds and BIA-derived %fat mass in boys as well as in girls (Figure 2A and B). Calculating %fat from skinfold measurements showed an increased FM in boys at each percentile studied (Table 3). Plotting the average %fat, as obtained by skinfoldand BIA-measurements against the difference between %fat derived from the two methods for boys (Figure 3A) and girls (Figure 3B) shows that BIA %fat overestimates skinfold %fat at low or normal percent fat mass (that is, up to 20%) in both genders (Figure 1A and B). By contrast, at increased values, BIA %fat seems to underestimate skinfold %fat in both genders (Figure 3A and 3B). As (i) body weight affects the calculation of FM and (ii) differs between both genders, we paired a subgroup of 42 BMI-matched pairs (boys and girls). The data are shown in Table 4. Studying the 42 BMImatched pairs (boys and girls) showed that %fat BIA (Table 4) and the sum of the skinfolds (Table 4) were both increased, but only the BIA-values in girls reached statistical signi®cance. Gender differences in BIA %fat were signi®cant at the different BMI-percentiles studied (Table 4). Comparing three pairs at a BMI >90th percentile showed a mean BIA %fat of 22.4 and 19.1% in girls and boys, respectively. By contrast, calculating %fat from skinfold measurement again showed opposite results for boys (Table 4). Discussion Gender differences in FM are evident in children aged 5±7 y (Tables 1±3). These differences are independent of BMI (Table 4). Our study con®rms and extends three recent studies2 ± 4 in a larger sample (that is, 610 children in our study vs 40±403 children). Our study population was homogenous with respect to age (that is, only children aged 5±7 y were studied, whereas children aged 3±20 y were assessed by the other authors. It is evident from our data that gender differences in fat distribution and %fat mass were signi®cant up to the 90th percentile of the nutritional state (Table 3). No differences in %fat mass and fat distribution could be observed in overweight and obese children (Table 3). Thus overweight camou¯ages gender differences in FM and fat distribution. It is tempting to speculate that the relative proportion of overweight children may contribute to the discrepancies between the studies cited above.2 ± 6 It is evident that the different percentiles of the nutritional parameters have to be taken into account in future studies. 17.76 1.12 13.06 15.7 0.77 7 18.2 0.8 3.19 15.84 75.71 2.74 14.86 14.76 76.89 10.81 56.28 18 1.11 13.56 16 0.8 6.3 17.2 1.5 6.91 15.68 72.97 2.82 14.31 14.93 76.05 10.93 55.67 girls 1.8 8.82 16.46 76.43 3.01 14.95 15.64 78.8 11.45 57.68 19 1.13 14.1 16 0.82 7.3 19.5 boys 1.07 5.35 16.64 77.8 3.08 15.55 15.65 78.2 11.45 57.24 19 1.14 13.8 16 0.8 7.7 20.8 girls 10 percentile 2.19 10.69 17.5 80.37 3.29 15.71 16.87 80.67 12.35 59.05 20 1.16 14.61 17 0.84 8.32 21.94 boys 1.75 8.26 17.55 80.47 3.45 16.43 16.21 79.58 11.87 58.25 19.96 1.16 14.34 16.86 0.82 9 24.08 girls 20 percentile 2.34 11.42 17.76 81.49 3.41 16.12 17.14 81.21 12.54 59.44 20.5 1.17 14.9 17 0.85 9 22.97 boys 1.88 9.09 17.99 81.93 3.53 16.83 16.57 80.05 12.13 58.6 20.1 1.17 14.6 17 0.83 9.6 25.1 girls 25 percentile 3.32 14.84 19.35 85.16 3.86 17.5 18.78 82.5 13.75 60.39 22.5 1.21 15.8 18 0.89 10.3 28.5 boys 2.86 12.84 19.4 87.16 4.03 18.48 18.44 81.52 13.5 59.67 22.5 1.21 15.5 18 0.87 11 30.2 girls 50 percentile 4.31 18.51 21.59 88.68 4.62 18.79 21.06 83.88 15.42 61.4 25.4 1.24 17.4 19 0.93 12.92 35.5 boys 4.13 18.07 21.16 90.91 4.84 19.95 20.02 83.17 14.65 60.88 24.5 1.24 16.38 19 0.91 13.33 38.9 girls 75 percentile 4.79 19.63 22 89.31 4.85 19.33 21.59 84.29 15.8 61.7 26 1.25 17.93 19.5 0.93 14 37.98 boys 4.56 19.53 21.41 91.74 5.02 20.42 20.36 83.57 14.9 61.17 25 1.25 16.76 19 0.92 14.12 41.71 girls 80 percentile 6.91 23.57 23.54 91.18 6.02 21.2 23.8 85.05 17.42 62.26 29.8 1.28 19.8 20.2 0.95 15.3 48.3 boys 5.82 22.2 22.34 94.65 5.88 21.8 21.87 84.45 16.01 61.82 27 1.27 17.8 20 0.95 15 47.3 girls 90 percentile 8.57 27.03 25.08 93.09 7.97 23.95 26.23 85.69 19.2 62.73 32.8 1.3 22.2 22.5 0.97 17.6 59.4 boys 7.04 24.29 23.76 96.81 6.7 23.11 22.95 85.14 16.8 62.32 29.7 1.29 18.6 21.1 0.97 16.3 52.2 girls 95 percentile 882 boys 18.6 1.14*** 13.5 15.6 0.79 19.7*** girls boys girls boys 21.4 1.2 15 17.4 0.85 27.6*** girls 25 to 50 percentile 21.6* 1.19 15.4*** 17.3 0.83*** 0.81 0.84*** 0.83 0.87*** 20.8 22.5*** 22.5 24.7*** 25.9 girls 20 to 25 percentile 19.1 19.2** 20.4*** 20 1.15 1.15 1.17 1.17 14.4*** 14.1 14.8*** 14.5 boys 10 to 20 percentile girls boys 18.2 21.5** 20.2*** 20 31.0*** 1.3 20.6*** 22.8*** 0.96 52.7** boys 28.5 1.28 18.2 21.5 0.96 49.4 girls 90 to 95 percentile girls 1 73.7 28.5 25.4 0.99 65.1 37.7*** 33 1.34 1.32 24.7*** 20.4 boys >95 percentile 20.7 25.0*** 23.3 30.5 21.0*** 22.2 22.2 27.5* 26.2 1.26*** 17.2 19 0.93 44.2* girls 80 to 90 percentile 27.7*** 1.27 18.7*** 19.1 0.94*** 40.0*** 42.7 girls 25.9*** 25 1.25 1.25 17.7*** 16.6 boys 75 to 80 percentile 0.91*** 0.89 31.7 34.1*** 36.4 23.9 23.7 1.23 1.23 16.4*** 15.9 boys 50 to 75 percentile 5.4*** 1.6 7.9*** 4.4 9.8*** 6.9 11.0*** 8.8 13.3*** 10.9 16.5*** 15.2 18.8 12.6 12.2 14.7 15.3*** 15.3 16.1*** 15.9 16.7*** 16.8 17.9*** 18.1 19.2*** 19.1 16.5 18.8 1.11 1.12 12.5 13.9*** 15.5 0.78* 0.72 0.81*** 15.3 16.3 18.4 17.2* 1.1 13.0* girls 5 to10 percentile Mean values within each percentile band are shown. Gender differences were analysed by unpaired t-Test. *P<0.05; **P<0.01; ***P<0.001; BMI body mass index; WHR waist ± hip ratio; MAC middle arm circumference; FM, A=BIA fat mass from Anthropometry=bioelectrical impedance analysis (BIA). Weight [kg] Height [m] BMI [kg=m2] MAC [cm] WHR Sum of four skinfolds [mm] FM, A [%] FM, BIA [%] boys 0 to 5 percentile Table 3 Body composition in different percentile groups BMI body mass index; MAC mid-arm circumference; WHR waist ± hip ratio; TSF Triceps skinfold thickness; FM fat mass; FM, A fat mass from Anthropometry; FFM fat free mass; TBW total body water; FM, BIA fat mass from bioelectrical impedance analysis (BIA). Weight (kg) Height [m] BMI [kg=m2] MAC [cm] WHR TSF [mm] Sum of four skinfolds [mm] FM, A [kg] FM, A [%] FFM, A [kg] FFM, A [%] FM, BIA [kg] FM, BIA [%] FFM, BIA [kg] FFM, BIA [%] TBW, BIA [l] TBW, BIA [%] boys 05 percentile Table 2 Percentiles of characteristics of the children (316 boys and 294 girls) Gender and fat mass in young children M Mast et al Gender and fat mass in young children M Mast et al Our data also point to some methodological issues. Anthropometric measures and BIA were used in our study to assess FM. Comparing the two methods skinfold thickness and %fat BIA went in parallel (Table 1±4, Figure 2A and B). However, calculating Figure 2 Correlation between %fat mass as derived from bioelectrical impedance analysis (BIA)-measurements and the sum of four skinfolds in 610 children aged 5 ± 7 y (A) boys ( P<0.001) and (B) girls ( P<0.001). %fat from skinfolds according to Lohman,13 led to opposite results (Table 1±4). This was also seen in BMI-matched pairs (Table 4). The discrepancy in %fat, as calculated from skinfold and BIA-measure- Figure 3 Altman and Bland22 plot comparing the difference of %fat as derived from anthropometric or bioelectrical impedance analysis (BIA)-measurements and the mean of the results obtained by two methods. The relative bias (BIA minus skinfolds) is plotted against the size of measurement. Each data point represents a single measurement. ( n 610 children; (A) 316 boys, (B) 294 girls). Table 4 Body composition characteristics of children (n 42 body mass index (BMI) matched pairs) BMI matched, <25 percentile girls (n 8) Age (y) BMI (kg=m2) FM, BIA (%) FM, A (%) Sum of 4 skinfolds (mm) 6.0 13.9 18** 11.6 28.7 BMI matched, between 25 and 75 percentile boys (n 8) girls (n 28) boys (n 28) 6.0 13.8 16.5 14.2 28 6.2 15.7 18.2** 11.8 29.6 6.0 15.7 16.9 14.2* 28.2 BMI matched, BMI>75 percentile girls (n 6) 6.4 18.7 22.2* 21.4 46.8 BMI matched boys (n 6) girls (n 42) boys (n 42) 6.2 18.8 18.1 20.9 42 6.2 15.8 18.8*** 13.1 31.9 6.0 15.8 17 15.2* 30.2 Gender differences were analysed by paired t-test: *P<0.05; **P<0.01; ***P<0.001. Data are given as mean values. FM, BIA: fat mass from bioelectrical impedance analysis (BIA); FM, A: fat mass from Anthropometry. 883 Gender and fat mass in young children M Mast et al 884 ments. becomes obvious using a Bland and Altman plot (Figure 3A and B). Our results suggest that the calculation from skinfolds according to Lohman13 underestimate BIA data at low and normal %fat, whereas an overestimation is seen at increased %fat. These differences were seen in boys (Figure 3A) as well as in girls (Figure 3B). When compared to BIA or DEXA, skinfold measurements are generally considered to be less sensitive. Our data provide some evidence that the Lohman-formula used to assess %fat from skinfold measurements13 is inappropriate for children aged 5±7 y. Comparing BIA with DEXA, some authors have proposed that the body-composition data from DEXA could be a reference method and thus could replace underwater weighing (comp. 18). However a recent metanalysis of 54 papers, published between 1985±1996 on the measurement of body composition in adult caucasians, various methods (for example, DEXA and BIA) in comparison with underwater weighing, showed no systematic over- or underestimation of %fat mass by DEXA or BIA and both methods had similar differences in bias.18 In children, there was a close agreement between BIA and DEXA data, and the mean difference in %fat mass as assessed by the two methods was only 5%.2 In addition, the accuracy of BIA-measurements in children (that is, a CU of 1.5%, see Methods) is in the order of DEXA-measurements (comp. Above). Thus, we feel that BIA can be used with some con®dence for adults as well as children. There are only few data on the prevalence of central body obesity in children.19 Although the WHR was shown to be only a poor predictor of intra-abdominal adipose tissue in children19 and adults,20 our data may add some useful information. First, the WHR had a wide variance in children aged 5±7 y (that is, from 0.70±1.11; Table 1). Second, the mean values were increased in boys up to the 90th percentile. Third, no differences were found between overweight and obese boys and girls. As there is ®rm evidence that central body fat in childhood is a risk for hyperlipidaemia or hypertension, for example, in adults,21,22 we are going to follow the subgroup of overweight and obese children with an increased WHR (that is, >90th percentile) in our obesity prevention study (i.e. KOPS). Acknowledgements This work was supported by grants from Verein zur FoÈrderung der Rehabilitationsforschung in SchleswigHolstein e.V., LuÈbeck; Wirtschaftliche Vereinigung Zucker, Bonn; Else KroÈner-Fresenius Stiftung, Bad Homburg; Bad Schwartau Werke, Bad Schwartau; team success, Selent. References 1 Siervogel RM, Roche AF, Guo S, Mukherjee D, Chumlea WC. Patterns of change in weight=stature2 from 2 to 18 years: ®ndings from long-term serial data for children in Fels longitudinal growth study. Int J Obes 1991; 15: 479 ± 485. 2 Boot AM, Bouquet J, de Ridder MAJ, Krenning EP, deMuinck Keizer-Schrama SMPF. Determinants of body composition measured by dual energy X-ray absorptiometry in Dutch children and adolescents. Am J Clin Nutr 1997; 66: 232 ± 238. 3 Taylor RW, Gold E, Manning P, Goulding A. Gender differences in body fat content are present well before puberty. Int. J. Obes 1997; 21: 1082 ± 1084. 4 Nagy TR, Gower BA, Trownbridge CA, Dezenberg C, Shewchuk M, Goran M. Effects of gender, ethnicity, body composition, and fat distribution on serum leptin concentrations in children. J Clin Endo Metab 1997; 82: 2148 ± 2152. 5 Rico H, Revilla M, Villa LF, Hernandez ER, Alvarez de Buergo M, Villa M. Body composition in children and Tanner's stages: A study with Dual-Energy X-ray Absorptiometry. Metabolism 1993; 42: 967 ± 970. 6 Ogle GD, Allen JR, Humphries IRJ, Lu PW, Briody JN, Howard-Giles R, Cowell CT. Body-composition assessment by dual-energy X-ray absorptiometry in subjects aged 4 ± 26 y. Am J Clin Nutr 1995; 61: 746 ± 753. 7 Jebb SA. Measurement of soft tissue by dual-energy X-ray absorptiometry. Br J Nutr 1997; 77: 151 ± 163. 8 Fogelholm M and von Marken Lichtenbelt W. Comparison of body composition methods: a literature analysis. Eur J Clin Nutr 1997; 51: 495 ± 503. 9 Mast M, KoÈrtzinger I, Bartrow A, Hunte V, Neite S, KoÈnig E, MuÈller MJ. Kiel obesity prevention study (KOPS): De®nition of obesity in children. Int J Obes 1997; 21: Suppl. 2, S121. 10 KoÈrtzinger I, Mast M, Bumbe A, Grund A, MuÈller MJ. Schooloriented intervention for the prevention of obesity as part of KOPS (Kiel obesity prevention study). Intern J Obesity 1997; 21 (Suppl. 2): S30. 11 KoÈrtzinger I, Mast M, MuÈller MJ. PraÈvention der Adipositas bei Kindern und Jugendlichen. ErnaÈhrungs-Umschau 1996; 43: 455 ± 460. 12 Lohman TG. Anthropometric Standardization Reference Manual. A division of Human Kinetics Publishers: Champaign, 1988. 13 Lohman TG. Applicability of body-composition techniques and constants for children and youths. In: Pandolph, KB (ed.), Exercise and Sport Sciences Review, Macmillan: New York 1986, pp 325 ± 357. 14 Kushner R. Bioelectrical impedance analysis: A review of principles and applications. J Am Coll Nutr 1992; 11: 199 ± 209. 15 MuÈller MJ, von zur MuÈhlen A, Lautz HU, Schmidt W, Daiber M, HuÈrter P. Energy expenditure in children with type I diabetes: evidence for increased thermogenesis. BMJ 1989; 299: 487 ± 491. 16 Houtkooper LB, Lohmann TG, Going SB, Hall MC. Validity of bioelectrical impedance for body composition assessment in children. J Appl Physiol 1989; 66: 814 ± 821. 17 Bland JM, Altman DG. Statistical methods for assessing agreement between two methods of clinical measurement. Lancet 1986, 307 ± 310. 18 Fogelholm M, van Marken Lichtenbelt W. Comparison of body composition methods: a literature analysis. Eur J Clin Nutr 1997; 51: 495 ± 503. 19 Goran MI, Kaskoun M, Shuman WP. Intra-abdominal adipose tissue in young children. Int J Obesity 1995; 19: 279 ± 283. 20 Van der Koy K, Leenen R, Seidell JC, Deurenberg P, Droop A, Bakker CJG. Waist ± hip ratio is a poor predictor of changes in visceral fat. Am J Clin Nutr 1993; 57: 327 ± 333. 21 Freedman DS, Srinivasan SR, Harsha DW, Webber LS, Berenson GS. Relation of body fat patterning to lipid and lipoprotein concentrations in children and adolescents: the Bogalusa Heart Study. Am J Clin Nutr 1989; 50: 930 ± 939. 22 Shear CL, Freedman DS, Burke GL, Harsha DW, Berenson GS. Body fat patterning and blood pressure in children and young adults. Hypertension 1987; 9: 236 ± 243.
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