ABSTRACT
Meal timing is suggested to influence the obesity risk in children. Our aim was to analyse the effect of energy and nutrient distributions at eating occasions (EO), including breakfast, lunch, supper, and snacks, on the BMI z-score (zBMI) during childhood in 729 healthy children. BMI and three-day dietary protocols were obtained at 3, 4, 5, 6, and 8 years of age, and dietary data were analysed as the percentage of the mean total energy intake (TEI; %E). Intakes at EOs were transformed via an isometric log-ratio transformation and added as exposure variables to linear mixed-effects models. Stratified analyses by country and recategorization of EOs by adding intake from snacks to respective meals for further analyses were performed. The exclusion of subjects with less than three observations and the exclusion of subjects who skipped one EO or consumed 5% energy or less at one EO were examined in sensitivity analyses. Around 23% of the children were overweight at a given time point. Overweight and normal-weight children showed different distributions of dietary intakes over the day; overweight children consumed higher intakes at lunch and lower intakes of snacks. However, no significant effects of timing of EOs on zBMI were found in regression analyses.
Subject(s)
Overweight , Pediatric Obesity , Child , Humans , Body Mass Index , Data Analysis , Eating , Energy Intake , Feeding Behavior , Meals , Pediatric Obesity/epidemiology , SnacksABSTRACT
There is accumulating evidence that early protein intake is related with weight gain in childhood. However, the evidence is mostly limited to the first year of life, whereas the high-weight-gain-velocity period extends up to about 2 years of age. We aimed to investigate whether protein intake during the second year of life is associated with higher weight gain and obesity risk later in childhood. We conducted a systematic review with searches in both PubMed®/MEDLINE® and the Cochrane Central Register of Controlled Trials. Ten studies that assessed a total of 46,170 children were identified. We found moderate-quality evidence of an association of protein intake during the second year of life with fat mass at 2 years and at 7 years. Effects on other outcomes such as body mass index (BMI), obesity risk, or adiposity rebound onset were inconclusive due to both heterogeneity and low evidence. We conclude that higher protein intakes during the second year of life are likely to increase fatness in childhood, but there is limited evidence regarding the association with other outcomes such as body mass index or change in adiposity rebound onset. Further well-designed and adequately powered clinical trials are needed since this issue has considerable public health relevance.
Subject(s)
Child Nutritional Physiological Phenomena , Dietary Proteins/adverse effects , Obesity/epidemiology , Weight Gain , Adipose Tissue , Adiposity , Body Mass Index , Body Weight , Child , Child, Preschool , Clinical Trials as Topic , Dietary Proteins/administration & dosage , Female , Humans , Infant , Infant Nutritional Physiological Phenomena , Male , Obesity/etiology , Overweight/epidemiology , Pediatric Obesity/epidemiology , Pediatric Obesity/etiology , Risk FactorsABSTRACT
BACKGROUND & AIMS: The aim was to generate a predictive equation to assess body composition (BC) in children with obesity using bioimpedance (BIA), and avoid bias produced by different density levels of fat free mass (FFM) in this population. METHODS: This was a cross-sectional validation study using baseline data from a randomized intervention trial to treat childhood obesity. Participants were 8 to 14y (n = 315), underwent assessments on anthropometry and BC through Air Displacement Plethysmography (ADP), Dual X-Ray Absorptiometry and BIA. They were divided into a training (n = 249) and a testing subset (n = 66). In addition, the testing subset underwent a total body water assessment using deuterium dilution, and thus obtained results for the 4-compartment model (4C). A new equation to estimate FFM was created from the BIA outputs by comparison to a validated model of ADP adjusted by FFM density in the training subset. The equation was validated against 4C in the testing subset. As reference, the outputs from the BIA device were also compared to 4C. RESULTS: The predictive equation reduced the bias from the BIA outputs from 14.1% (95%CI: 12.7, 15.4) to 4.6% (95%CI: 3.8, 5.4) for FFM and from 18.4% (95%CI: 16.9, 19.9) to 6.4% (95% CI: 5.3, 7.4) for FM. Bland-Altman plots revealed that the new equation significantly improved the agreement with 4C; furthermore, the observed trend to increase the degree of bias with increasing FM and FFM also disappeared. CONCLUSION: The new predictive equation increases the precision of BC assessment using BIA in children with obesity.
Subject(s)
Body Composition , Electric Impedance , Indicator Dilution Techniques/statistics & numerical data , Pediatric Obesity/diagnosis , Plethysmography/statistics & numerical data , Absorptiometry, Photon , Adolescent , Anthropometry , Body Water , Child , Cross-Sectional Studies , Female , Humans , Male , Predictive Value of Tests , Randomized Controlled Trials as Topic , Reproducibility of ResultsABSTRACT
BACKGROUND & AIMS: Assessment of Fat Mass (FM) and fat-free mass (FFM) using Air-displacement plethysmography (ADP) technique assumes constant density of FFM (DFFM) by age and sex. It has been recently shown that DFFM further varies according to body mass index (BMI), meaning that ADP body composition assessments of children with obesity could be biased if DFFM is assumed to be constant. The aim of this study was to validate the use of the calculations of DFFM (rather than constant density of the FFM) to improve accuracy of body composition assessment in children with obesity. METHODS: cross-sectional validation study in 66 children with obesity (aged 8-14 years) where ADP assessments of body composition assuming constant density (FFMBODPOD and FMBODPOD) were compared to those where DFFM was adjusted in relation to BMI (FFMadjusted and FMadjusted), and both compared to the gold standard reference, the 4-component model (FFM4C and FM4C). RESULTS: FFMBODPOD was overestimated by 1.50 kg (95%CI -0.68 kg, 3.63 kg) while FFMadjusted was 0.71 kg (-1.08 kg, 2.51 kg) (percentage differences compared to FFM4C were 4.9% (±2.9%) and 2.8% (±2.1%), respectively (p < 0.001)). Consistently, FM was underestimated by both methods, representing a mean difference between methods of 4.0% (±2.9%) and 6.8% (±3.8%), respectively, when compared to the reference method. The agreement and reliability of body composition assessments were improved when adjusted using calculations (adjusted models) rather than assuming constant DFFM. CONCLUSIONS: The use of constant values for fat-free mass properties may increase bias when assessing body composition (FM and FFM) in children with obesity by two-component techniques such as ADP. Using adjusted corrections as proposed in the present work may reduce the bias by half.
Subject(s)
Adipose Tissue/diagnostic imaging , Anthropometry/methods , Body Composition , Pediatric Obesity/diagnostic imaging , Plethysmography/methods , Adolescent , Bias , Body Mass Index , Child , Cluster Analysis , Cross-Sectional Studies , Female , Humans , Male , Randomized Controlled Trials as Topic , Reproducibility of ResultsABSTRACT
The primary aim of the Obemat2.0 trial was to evaluate the efficacy of a multicomponent motivational program for the treatment of childhood obesity, coordinated between primary care and hospital specialized services, compared to the usual intervention performed in primary care. This was a cluster randomized clinical trial conducted in Spain, with two intervention arms: motivational intervention group vs. usual care group (as control), including 167 participants in each. The motivational intervention consisted of motivational interviewing, educational materials, use of an eHealth physical activity monitor and three group-based sessions. The primary outcome was body mass index (BMI) z score increments before and after the 12 (+3) months of intervention. Secondary outcomes (pre-post intervention) were: adherence to treatment, waist circumference (cm), fat mass index (z score), fat free mass index (z score), total body water (kg), bone mineral density (z score), blood lipids profile, glucose metabolism, and psychosocial problems. Other assessments (pre and post-intervention) were: sociodemographic information, physical activity, sedentary activity, neuropsychological testing, perception of body image, quality of the diet, food frequency consumption and foods available at home. The results of this clinical trial could open a window of opportunity to support professionals at the primary care to treat childhood obesity. The clinicaltrials.gov identifier was NCT02889406.
Subject(s)
Motivational Interviewing/methods , Patient Education as Topic/methods , Pediatric Obesity/therapy , Psychotherapy, Group/methods , Telemedicine/methods , Adolescent , Body Mass Index , Child , Cluster Analysis , Diet/methods , Diet/psychology , Exercise/psychology , Female , Humans , Male , Pediatric Obesity/psychology , Spain , Treatment Adherence and Compliance , Treatment Outcome , Waist CircumferenceABSTRACT
BackgroundIntestinal microbiota of breast-fed infants is plenty of beneficial bifidobacteria. We aimed to determine whether an infant formula supplemented with probiotic Bifidobacterium longum subsp. infantis CECT7210 (B. infantis IM1) is effective at reducing diarrhea incidence in healthy term infants.MethodsDouble-blinded, randomized, multicenter, controlled clinical trial, where formula-fed infants (<3 months) received an infant formula supplemented (Probiotic) or not (Control) with 107 cfu/g of B. infantis IM1 over 12 weeks. Diarrheas, growth, digestive symptoms, stool bifidobacteria, and microbiota were assessed.ResultsIn all, 97 (Control) and 93 (Probiotic) infants were randomized, and 78 (Control) and 73 (Probiotic) completed the 12 week-follow-up. In the overall study period, a median of 0.29±1.07 and 0.05±0.28 diarrhea events/infant was observed in the Control and Probiotic groups, respectively (P=0.059). This trend to less diarrhea episodes in the Probiotic group reached statistical significance at 8 weeks (0.12±0.47 vs. 0.0±0.0 events/infant, P=0.047). Constipation incidence was higher (odds ratio (OR) 2.67 (1.09-6.50)) and stool frequency lower (2.0±1.0 vs. 2.6±1.3 stools/day, P=0.038) in the Control group after 4 weeks. No differences were found at other time points nor in other digestive symptoms, growth, or formula intake.ConclusionA B. infantis IM1-supplemented infant formula may reduce diarrhea episodes, being safe, well tolerated, and associated with lower constipation prevalence.
Subject(s)
Bifidobacterium longum , Diarrhea/prevention & control , Infant Formula , Probiotics/therapeutic use , Anthropometry , Constipation/prevention & control , Double-Blind Method , Feces/microbiology , Female , Flatulence , Humans , Immune System , Infant , Infant, Newborn , Male , Microbiota , Milk, Human/microbiology , Patient SafetyABSTRACT
BACKGROUND: Constipation is a common disorder in children. OBJECTIVE: The objective of this study is to assess the beneficial effects of a daily supplementation with Orafti® inulin-type fructans in 2-5 year old constipated children. METHODS: Double-blind, randomised, placebo-controlled parallel group trial where constipated children received two doses of 2 g Orafti® inulin-type fructans (OF:IN) or placebo (maltodextrin) for 6 weeks. Primary outcome was stool consistency. Secondary outcomes were stool frequency and gastrointestinal symptoms. RESULTS: Twenty-two children were included, 17 completed the study protocol (nine and eight for the control and the OF:IN group, respectively). Results showed that Orafti® inulin-type fructans supplemented children had softer stools (p = .003). The longitudinal analysis showed no significant changes in controls, whereas supplemented children increased their stool consistency from 2.2 to 2.6 on the modified Bristol scale for children (five items instead of seven) (p = .040). CONCLUSIONS: Prebiotic inulin-type fructans supplementation improves stool consistency in constipated 2-5-year old children. Clinicaltrials.gov, with number NCT02863848.
Subject(s)
Constipation/prevention & control , Fructans/pharmacology , Child, Preschool , Dietary Supplements , Double-Blind Method , Feces/chemistry , Female , Fructans/chemistry , Humans , Male , Pilot ProjectsABSTRACT
OBJECTIVE: To test the reliability and factorial validity of the Child Feeding Questionnaire (CFQ) within a Spanish sample. DESIGN: Cross-sectional study. SETTING: All schools in a Spanish Mediterranean city of about 100,000 inhabitants. PARTICIPANTS: From a potential population of 1,623 children (mean age, 8.5 years), 960 parents (459 fathers and 501 mothers) of 515 children participated (32% response). MAIN OUTCOME MEASURE(S): The Spanish version of the CFQ was completed by both parents. Body mass index of the children was obtained from measured heights and weights. Parents reported their anthropometric and employment data. ANALYSIS: Reliability was assessed using Cronbach α. Factorial validity was examined by Procrustes semi-confirmatory factor and confirmatory factor analyses. RESULTS: Seven major factors with loadings similar to those in the original questionnaire were found: perceived responsibility, perceived parent weight, perceived child weight, concern about child weight (CN), pressure to eat (PE), monitoring, and restriction. Reliability was adequate for each factor and overall CFQ (α = .86). Goodness of fit indexes for confirmatory factor analysis solutions was acceptable. Item loadings ranged from 0.30 to 0.92. The factor of CN was associated with restriction [multivariate coefficient (R(2)) = 0.14; P < .001] and PE (R(2) = 0.36; P< .001). Child's body mass index showed a negative association with PE (R(2) = 0.11; P < .001) and a positive association with CN (R(2) = 0.25; P < .001) and factors related to feeding control (monitoring and restriction, R(2) = 0.04 and R(2) = 0.09, respectively; P < .001). CONCLUSIONS AND IMPLICATIONS: Results support the reliability and validity of the CFQ for a Spanish population, allowing for comparisons across cultures. The CFQ may be useful to identify parental feeding attitudes that can contribute to preventing risky eating behaviors in their children.
Subject(s)
Feeding Behavior , Nutrition Surveys/methods , Nutrition Surveys/standards , Surveys and Questionnaires/standards , Child , Child, Preschool , Cross-Sectional Studies , Female , Humans , Male , Parents , Reproducibility of Results , SpainABSTRACT
AIM: This study investigated the relationship between being overweight or obese and executive function in six- to ten-year-olds. METHODS: The participants were 515 children (250 boys) from schools in Reus, Spain. The initial sample was measured and weighed and assessed with the Children's Color Trail Test. Children classified as overweight, including obese, and their age- and gender-matched controls (n = 221), were assessed in a second phase with the Five Digit Test (FDT) and the Symbol Digit Modalities Test. Logistic regression models were applied to analyse the effect of executive functions on being overweight, including obese. RESULTS: We found that 28.9% of the children were overweight and 7.2% were obese. The FDT showed that inhibition (odds risk of 1.04, range 1.00-1.08, p = 0.04) and flexibility (odds risk of 1.04, range 1.00-1.07, p = 0.02) were significantly associated with overweight, including obesity, regardless of sociodemographic and psychopathological variables. CONCLUSION: These results suggest that children who were overweight or obese had a reduced ability to mobilise the cognitive effort required to inhibit involuntary responses and to switch between different mental operations. A developmental trajectory would provide important insights into the relationship between executive functioning pattern and the risk of being overweight or obese.
Subject(s)
Executive Function , Pediatric Obesity/psychology , Body Mass Index , Child , Female , Humans , Inhibition, Psychological , Logistic Models , Male , Neuropsychological Tests , Prospective StudiesABSTRACT
BACKGROUND: Idiopathic hypercalciuria (IHC), i.e. an elevated urinary calcium excretion without concomitant hypercalcemia, is a common disorder in children and can have a range of urinary clinical presentations and decreased bone mineral density (BMD). AIM: To assess the effect of IHC on bone mineral content in children without urological symptoms. METHODS: Calcium excretion, BMD (by dual-energy X-ray absorptiometry), and anthropometry were assessed in 175 seven-year-old children who were classified as IHC or controls. Calcium intake and physical activity were measured as confounding factors. RESULTS: The prevalence of IHC was 17.7%. Both groups (controls and IHC) showed similar baseline characteristics in terms of their anthropometry, gender distribution, and protein and calcium dietary intakes as well as physical activity scores. Urinary calciuria was independent of the calcium dietary intake and anthropometry. BMD correlated with anthropometry and physical activity but not with calcium dietary intake. IHC children had lower whole-body BMD z-scores compared to controls. The role of IHC in reducing the whole-body BMD z-score was still significant even when anthropometry, physical activity, and calcium intake were included as confounders in multivariate analyses. CONCLUSIONS: The prevalence of IHC in this population of 7-year-old children was about 17%. IHC diagnosis was associated with lower BMD z-scores and osteopenia in 22% of them.
Subject(s)
Bone Diseases, Developmental/etiology , Bone Diseases, Metabolic/etiology , Hypercalciuria/physiopathology , Absorptiometry, Photon , Bone Density , Calcium/urine , Calcium, Dietary/administration & dosage , Child , Child Development , Child Nutritional Physiological Phenomena , Female , Humans , Hypercalciuria/diagnostic imaging , Hypercalciuria/epidemiology , Hypercalciuria/urine , Male , Motor Activity , Osteogenesis , Prevalence , Prospective Studies , Risk , Severity of Illness Index , Spain/epidemiology , Whole Body ImagingABSTRACT
AIM: Segmental body composition in children was assessed using the bioimpedance analyzer (BIA) TANITA BC-418 and compared with dual-energy X-ray absorptiometry (DXA) values. METHODS: A cross-sectional validation study in which 7-year-old children from the Spanish subsample of the EU Childhood Obesity Project were assessed through anthropometry, BIA and DXA. Main outcome measures were fat and lean masses of the trunk, left arm and left leg (in kg) assessed through BIA direct outputs (BIAoutputs) and DXA. Predictive equations for the composition of each segment were derived from raw impedance and anthropometric measurements; results obtained from these predictive equations (BIAregressions) were also compared to DXA. RESULTS: One hundred seventy-one (84 boys) 7-year-old children were studied. BIAoutputs and DXA results showed small differences for leg lean mass (6.5%) and high differences for trunk fat and trunk lean masses (>30%). BIAregressions results showed differences of about 20% for trunk fat mass, 1.5% for trunk lean mass and 3.7% for leg lean mass compared to DXA. CONCLUSIONS: Segmental body composition measures predicted by internal algorithms of the TANITA BC-418 were not valid for clinical or epidemiological use, except for leg lean mass. The assessment of segmental composition was improved using our own predictive equations combining segmental-specific anthropometric measurements with segmental impedances.
Subject(s)
Absorptiometry, Photon/methods , Body Composition , Pediatric Obesity/epidemiology , Adipose Tissue , Body Mass Index , Child , Cross-Sectional Studies , Electric Impedance , Female , Humans , Linear Models , Male , White PeopleABSTRACT
AIM: To validate the bioimpedance analyzer (BIA) Tanita BC-418 for its clinical and epidemiological use in children compared to dual-energy X-ray absorptiometry (DXA). METHODS: A cross-sectional validation study was performed in 7-year-old children using anthropometry, BIA and DXA. Whole body fat and lean masses were assessed through BIA (BIAoutputs) and DXA. Fat mass index (FMI) was calculated. Predictive equations were derived from raw impedance and anthropometric measures; results obtained from these predictive equations (BIAregressions) were also compared to DXA. RESULTS: 171 children (84 boys) were studied. BIAoutputs and DXA results revealed small differences for lean mass (1%) and moderate differences for fat mass (13%). BIAregressions results showed small differences for both body lean and fat masses (0.21 and 4.62%, respectively). Sensitivity and specificity to correctly classify children >90.8th percentile of FMI was 84.6 (64.3-94.9) and 95.9% (90.8-98.3) for BIAoutputs and 100 (98.1-100.0) and 95.9% (92.3-99.4) for BIAregressions, respectively. CONCLUSIONS: Tanita BC-418 may be valid for epidemiological studies assessing whole body composition. Its measurements may help in the diagnosis and monitoring of childhood overweight and obesity. The validation of predictive equations in specific populations may increase the precision of the technique.