Hostname: page-component-848d4c4894-x24gv Total loading time: 0 Render date: 2024-05-02T18:43:01.305Z Has data issue: false hasContentIssue false

Development and internal validation of the SMILE-FSS: a Free Sugars Screener for Australian children aged 2 and 5 years

Published online by Cambridge University Press:  31 October 2023

Lucinda K Bell*
Affiliation:
Caring Futures Institute, College of Nursing and Health Sciences, Flinders University, Adelaide 5001, Australia
Shalem Leemaqz
Affiliation:
South Australian Health and Medical Research Institute, Adelaide, SA, Australia
Gemma Devenish-Coleman
Affiliation:
School of Population Health, Curtin University, Perth, WA 6102, Australia
Loc G Do
Affiliation:
School of Dentistry, The University of Queensland, Brisbane, QLD, 4072 Australia
Diep Ha
Affiliation:
School of Dentistry, The University of Queensland, Brisbane, QLD, 4072 Australia
Jane A Scott
Affiliation:
School of Population Health, Curtin University, Perth, WA 6102, Australia
Rebecca K Golley
Affiliation:
Caring Futures Institute, College of Nursing and Health Sciences, Flinders University, Adelaide 5001, Australia
*
*Corresponding author: Email lucy.bell@flinders.edu.au
Rights & Permissions [Opens in a new window]

Abstract

Objective:

To develop and internally validate a Free Sugars Screener (FSS) for Australian children aged 2 and 5 years.

Design:

Using data collected from a ninety-nine-item (2-year-olds) and ninety-eight-item (5-year-olds) FFQ in the Study of Mothers’ and Infants’ Life Events affecting oral health (SMILE-FFQ), a regression-based prediction modelling approach was employed to identify a subset of items that accurately estimate total free sugars intake (FSI). The predictors were grams of free sugars (FSg) for individual items in the SMILE-FFQ and child’s age and sex. The outcome variable was total FSI per person. To internally validate the SMILE-FSS items, the estimated FSg was converted to percent energy from free sugars (%EFS) for comparison to the WHO free sugars guideline categories (< 5 %, 5–< 10 % and ≥ 10 %EFS) using cross-classification analysis.

Setting:

Australia.

Participants:

858 and 652 2- and 5-year-old children, respectively, with complete dietary (< 5 % missing) and sociodemographic data.

Results:

Twenty-two and twenty-six items were important in predicting FSI at 2 and 5 years, respectively. Items were similar between ages with more discretionary beverage items (e.g. sugar-sweetened beverages) at 5 years. %EFS was overestimated by 4·4 % and 2·6 %. Most children (75 % and 82 %) were categorised into the same WHO free sugars category with most (87 % and 95 %) correctly identified as having < 10 %EFS in line with the WHO recommendation.

Conclusions:

The SMILE-FSS has good internal validity and can be used in research and practice to estimate young Australian children’s FSI and compare to the WHO free sugars guidelines to identify those ‘at risk’.

Type
Research Paper
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited.
Copyright
© The Author(s), 2023. Published by Cambridge University Press on behalf of The Nutrition Society

High consumption of dietary sugars is a major public health concern, having a negative impact on oral health(1) and contributing to an increased risk of chronic diseases such as obesity(Reference Delli Bovi, Di Michele and Laino2). Excessive intakes of added sugars is of particular concern in children(Reference Vos, Kaar and Welsh3), with approximately one-quarter of Australian children having overweight or obesity(4) and one-third having caries by the age of 5 years(Reference Ha, Roberts-Thomson, Arrow, Doc and Spencer5). Frequent exposure to added sugars in the first years of life may reinforce the innate preference that infants have for sweet foods(Reference Fidler Mis, Braegger and Bronsky6) with taste preferences persisting throughout life and influencing dietary patterns in adulthood(Reference Birch, Savage and Ventura7). It is therefore important to understand patterns of sugars intakes in early life to inform early prevention efforts to reduce dental caries and overweight prevalence in children(8,9) .

Dietary free sugars, defined as sugar added to foods and beverages by the manufacturer, cook or consumer plus those naturally present in honey, syrups, and fruit juices, are the most important risk factor for dental caries(1,Reference Mahboobi, Pakdaman and Yazdani10,Reference Moynihan11) and can contribute to excess energy intake with little nutritional benefit(Reference Crowe, O’Sullivan and Cassetti12). The WHO recommends that less than 10 % of total energy intake come from free sugars, with a conditional recommendation to reduce intake to less than 5 % of energy intake for additional health benefits(1). However, recent analysis of data from the Australian Study of Mothers’ and Infants’ Life Events affecting oral health (SMILE) birth cohort has shown that some children (2·4 %) as young as 1 year old were exceeding the < 10 % energy from free sugars (EFS) recommendation (23 % exceeding < 5 %EFS recommendation)(Reference Devenish, Ytterstad and Begley13), increasing to over a third at 2 years (38 % exceeding < 10 %EFS and 71 % exceeding < 5 %EFS)(Reference Devenish, Golley and Mukhtar14), with similar findings at 5 years (37 %exceeding < 10 %EFS and 75 % exceeding < 5 %EFS, unpublished results). Thus, there is an urgent need to address excess intakes of free sugars in early childhood.

Accurate measurement of free sugars intakes (FSI) in early childhood supports the monitoring of population intakes to inform policy, the evaluation of interventions in practice and at scale, and for screening intakes within the primary healthcare setting to identify ‘at risk’ children requiring referral and intervention(Reference Byrne, Bell and Taylor15,Reference Golley, Bell and Hendrie16) . However, an ongoing limitation in research and practice is the lack of consistency and precision in the assessment of dental-specific dietary factors, leading to a call within the WHO Sugars Intake Guidelines for studies with improved dietary assessment methodology(1). In response to this, the SMILE-FFQ was developed(Reference Devenish, Mukhtar and Begley17). The SMILE-FFQ is a dental-specific, semi-quantitative eighty-nine-item FFQ (generating a list of ninety-nine foods) designed to capture the leading dietary contributories to dental caries risk in toddlers aged 18–30 months(Reference Devenish, Mukhtar and Begley17). Although the SMILE-FFQ was determined to be a valid tool for assessing FSI of Australian toddlers using parental proxy report(Reference Devenish, Mukhtar and Begley17), the length limits its use in both the research and practice settings.

Short dietary questionnaires or screeners, typically completed in less than 15 min(18), provide an alternative to longer FFQ in settings where brief tools are needed(Reference Byrne, Bell and Taylor15,Reference Golley, Bell and Hendrie16) . Short questionnaires can be administered quickly in a variety of formats, tailored to outcomes of interest, are associated with a low respondent burden, and allow for easy comparison of intake against guidelines to provide a quick assessment of ‘risk’(Reference Byrne, Bell and Taylor15,Reference Golley, Bell and Hendrie16) . Although short questionnaires have been developed and validated in Australian children for assessing various aspects of diet, predominately dietary intake and diet quality(Reference Byrne, Bell and Taylor15,Reference Golley, Bell and Hendrie16,Reference Bell, Golley and Magarey19) , none specifically assess FSI. Short dental-specific questionnaires that assess FSI of young children and that allow for comparison against the WHO free sugars guidelines are therefore required.

Thus, the aim of this study was to develop and internally validate a short-form Free Sugars Screener (FSS) for Australian children aged 2 and 5years using data derived from the long-form SMILE-FFQ. The objectives were to: (1) identify a subset of SMILE-FFQ questions that accurately estimate FSI from the complete set of survey questions, (2) internally validate the items by comparing measured FSI with predicted FSI and (3) internally validate the items by classifying participants’ FSI into the WHO free sugars guidelines categories (< 5 %, 5–< 10 % and ≥ 10 %EFS)(1) and comparing measured categorisation with predicted categorisation.

Methods

The Study of Mothers’ and Infants’ Life Events affecting oral health

SMILE is a birth cohort study conducted in Adelaide, South Australia. The objectives, methods and cohort profile have been described elsewhere(Reference Do, Ha and Bell20,Reference Do, Scott and Thomson21) . Briefly, 2147 mothers and 2181 newborns were recruited from the three major maternity hospitals in Adelaide between July 2013 and August 2014. All new mothers with sufficient English competency and with no intention of moving out of the greater Adelaide area within the following year were invited to participate. Mothers in hospitals that service lower socio-economic areas were oversampled to compensate for anticipated higher attrition rates(Reference Do, Scott and Thomson21). Participants were invited to complete questionnaires on dental and dietary habits at recruitment, when their child reached 3 and 6 months of age, and again at 1, 2, and 5 years of age. This included the SMILE-FFQ, administered at 2 and 5 years of age. The SMILE study was approved by the Southern Adelaide Clinical Human Research Ethics Committee (HREC/50.13, approval date: 28 Feb 2013) and the South Australian Women and Children Health Network (HREC/13/WCHN/69, approval date: 7 August 2013).

Data collection

The SMILE-FFQ

Development and validation of the SMILE-FFQ has been described in detail elsewhere(Reference Devenish, Mukhtar and Begley17). Briefly, the eighty-nine-item SMILE-FFQ was constructed to capture dietary factors associated with dental caries risk in children aged 1–3 years. This included major food and beverage sources of total and free sugars and dental-protective foods such as milk products(Reference Devenish, Mukhtar and Begley17). Participants report the frequency (from ‘never or rarely’ to ‘3 or more times per day’) and quantity of consumption for each food item in the questionnaire. Portion size options were tailored to the food in question and described using a combination of household measures (teaspoon, tablespoon and cup) and common portion sizes (piece, tub and pouch), each with a corresponding weight (g) and/or volume (ml). Four supplementary questions within the SMILE-FFQ split the coding of six food items into sixteen items so that the eighty-nine-item FFQ generates a list of ninety-nine foods. For example, in the SMILE-FFQ, a supplementary question ‘If your child eats yoghurt, do you choose reduced fat versions?’ is used to split four yogurt line items differentiated by flavour into eight foods, subdivided by both flavour and fat type (see online supplementary material, Supplemental Table S1). The SMILE-FFQ was validated against repeat 24 h recalls in an external cohort of toddlers aged 18–30 months, performing similarly at ranking individuals’ total and FSI, with a tendency to underestimate intakes in participants with lower reported 24 h recall values and overestimate intakes in those with higher reported values(Reference Devenish, Mukhtar and Begley17), highlighting its suitability for observational studies wanting to use ranked total and FSI.

Minor adjustments were made to the SMILE-FFQ ahead of data collection when children were approximately 5 years of age. Checks were undertaken to ensure: (1) the item response wording was appropriate for the target age group, (2) the portion sizes listed reflected current supermarket products for older children and (3) the portion sizes listed were distributed around the median intakes of 4–8-year-old Australians(Reference van der Bend, Bucher and Schumacher22). Examples of wording changes included changing ‘infant formula’ to ‘junior formula’, removing ‘baby jars’ and ‘sippee cups’ from the portion size descriptors for some items, and removing the smallest portion size response option for some questions. No changes were made to the frequency response options. One item was added (coffee, e.g. ready-to-drink coffee beverages such as iced coffee, as coffee is a source of fluoride(Reference Alejandro-Vega, Suarez-Marichal and Niebla-Canelo23)) and two items removed (infant fruit purees and infant vegetable purees due to not being age-appropriate), resulting in eighty-eight items. As above, the additional four supplementary questions are used to split the coding of six food items into sixteen items, generating a list of ninety-eight foods at 5 years.

Sociodemographic data

Sociodemographic data were collected from mothers at recruitment via self-completed questionnaires. These included measures of maternal age, country of birth and educational attainment, in addition to household income, number of children at home and whether their child lived in a one- or two-parent household (Table 1). Mothers’ pre-pregnancy BMI (kg/m2) was calculated from self-reported height and weight and classified into weight status categories (healthy weight < 25 kg/m2, overweight 25–29·9 kg/m2 and obesity ≥ 30 kg/m2)(24). Postcode was used to derive a measure of socio-economic status using the Index of Relative Socio-Economic Advantage and Disadvantage (IRSAD)(25), one of the four Socio-Economic Indexes for Areas (SEIFA) indices that ranks areas across Australia on a continuum of social disadvantage to advantage(Reference Do, Ha and Bell20). Child age was calculated from date of birth and date of completion of the SMILE-FFQ at both 2 and 5 years of age.

Table 1 Characteristics of mother–child dyads in the samples with complete dietary and sociodemographic data at 2 and 5 yearsa

a Data are presented as n (%) unless otherwise stated.

b Age and sex-specific BMI z-scores were calculated for children and classified into weight status categories (healthy weight ≥ –2 and ≤ +2 sd, overweight > +2 and ≤ +3 sd, and obesity > +3) using the WHO reference(26).

c Weight status categories equivalent to BMI (kg/m2); healthy weight < 25 kg/m2, overweight 25–29·9 kg/m2 and obesity ≥ 30 kg/m2.

d Missing data n 118 at 2 years.

Child anthropometric data

Child weight and height data were collected at the 2- and 5-year physical examinations using standardised methodology and equipment, including calibrated electronic scales and medical stadiometers(27). Age and sex-specific BMI z-scores were calculated for children and classified into weight status categories (healthy weight ≥ –2 and ≤ +2 sd, overweight > +2 and ≤ +3 sd, and obesity > +3) using the WHO reference(26).

Development of the SMILE Free Sugars Screener

Data source and variables

The SMILE Free Sugars Screener (SMILE-FSS), a short-form version of the SMILE-FFQ, was developed using data obtained from completion of the SMILE-FFQ at 2 and 5 years of the SMILE study. Data reduction techniques were employed to identify a subset of items that accurately estimate FSI in Australian children aged 2 and 5 years, derived from the long-form SMILE-FFQ. The predictor variable was measured FSI in grams calculated for each questionnaire item of the long-form SMILE-FFQ based on quantity and frequency response options. The outcome variable was total usual FSI derived from the long-form SMILE-FFQ calculated per person. A specific number of items was not identified as the target, however, to substantially reduce participant burden, fewer than 50, and ideally about 20–30 items was anticipated, consistent with other short screeners(Reference Bell, Golley and Magarey28Reference Magarey, Golley and Spurrier33).

Data cleaning and preparation

On return of the completed SMILE-FFQ at 2 and 5 years, data were cleaned and questionnaires with more than 5 % of line items left blank were excluded(Reference Devenish, Mukhtar and Begley17). Microsoft Access version 15 (Microsoft Corporation, 2013) was used to link the questionnaire responses to an accompanying database developed specifically for the SMILE study which contained lookup tables of free sugars amounts (g) for the foods, quantity options and frequencies (per d) listed in the SMILE-FFQ(Reference Devenish, Mukhtar and Begley17). This database linked FFQ responses to nutrient values for total sugars and free sugars using the AUSNUT 2011–2013 food consumption database(34), from which total usual FSI in grams per d was calculated. Implausible FSI intakes were excluded, defined as values greater than 3 sd above the mean for both total and free sugars(Reference Devenish, Mukhtar and Begley17).

Statistical analysis

To identify a subset of FFQ items that can reasonably estimate total FSI of each child calculated from the complete set of survey questions, a regularised regression-based prediction modelling approach was employed at both 2 and 5 years. Participants with complete dietary (< 5 % missing FFQ data) and complete sociodemographic data were included (i.e. ‘complete-case analysis’). The predictors included grams of free sugars for each food in the SMILE-FFQ and child’s age and sex. Child’s weight and height were also included as predictors in the 5-year regression model to improve model fit, although not at 2 years due to the number of missing values (n 279, 26·7 %). A sensitivity analysis was performed with height and weight included at 2 years, and height and weight excluded at 5 years, to assess the consistency of variables selected.

Survey items (herein referred to as predictors) with near-zero variance (e.g. foods such as porridge, milk and milk alternatives, fruit (fresh, tinned and puree), cheese and custard, and drinks such as tea, coffee, cordial, vegetable juice and water), defined as less than 10 % unique values or the ratio of most common values is greater than 19, were removed prior to analyses (i.e. survey items which were rarely consumed and made limited contribution to grams of FSI (FSg) in participants) (see online supplementary material, Supplemental Table S2). A 10-fold cross-validation was performed, in which the sample was randomly split into a training (70 %) and testing (30 %) sample with the testing sample reserved for use only in the final internal validation step. In the first step of the analysis, we used regularised linear regression with Elastic Net (a combination of L1 Lasso and L2 Ridge) to select variables which are ‘important’ in predicting the outcome (i.e. total usual FSI per person). Lasso and Ridge regression works by estimating the regression parameters under a constraint which shrinks the estimates towards zero with the aim of reducing prediction variance (determined by the minimum root mean square error (RMSE)) and in the process ‘removes’ (i.e. shrinks to zero) unimportant predictors. The optimal model was chosen on the basis of minimum differences between training and testing RMSE across cross-validation runs.

To internally validate the items in the optimal model, the predicted FSg was converted to %EFS for comparison to the WHO free sugars guidelines categories (< 5 %, 5–< 10 % and ≥ 10 %EFS)(1). However, as the SMILE-FFQ was not designed to capture total energy intake, Estimated Energy Requirements (EER) were used as an alternative for calculating the percentage of EER coming from FSI. The method for calculating EER at 2 years has been described previously(Reference Devenish, Golley and Mukhtar14). That is, EER was determined from age and weight data using the Australian Nutrient Reference Values(35) equation for children aged 13–35 months. At 5 years, the equation for children aged 3–8 year was used and EER determined from child age, weight and height data and applying a standard physical activity level of 1·6 (‘light activity’) due to a lack of physical activity data for the current sample. The percent of EER coming from FSI was then calculated using the following equation: %EERFreeSug = [(Sugars_g × 16·7) ÷ EER_kJ] × 100). The measured and predicted %EFS were then compared using the RMSE, and participants in the testing sample categorised into the WHO categories (< 5 %EFS, 5–< 10 %EFS and ≥ 10 %EFS)(1) and compared descriptively. Sensitivity analysis was also conducted to compared the measured and predicted FSg in the optimal model using the testing sample at 2 and 5 years.

Results

Population studied

Of the 2181 mothers–infant dyads recruited for the SMILE study, 1043/1195 and 716/825 SMILE-FFQs were returned complete (< 5 % missing) and plausible at 2 and 5 years, respectively (Fig. 1). Complete-case analysis was conducted on 885/1043 (2 years) and 652/716 (5 years). Sample characteristics are presented in Table 1. At the 2-year data collection wave, the mean age of children was 2·1 years (sd ± 0·1 years, range 1·9–3·2 years), with sex almost evenly split (females 47 % and males 53 %) and most being from a two-parent household (94 %). The majority of mothers (mean age 30·5 ± 5 years) were born in Australia, New Zealand or UK (78 %), with pre-pregnancy BMI less than 25 kg/m2 (54 %), and were university educated or higher (57 %). Similarly, nearly half of the children at the 5-year data collection wave (mean age 5·3 ± 0·4 years, range 4·7–6·5 years) were female (45 %) and approximately two-thirds from two-parent households (65 %). The majority of mothers were born in Australia, New Zealand or UK (74 %), with a pre-pregnancy BMI less than 25 kg/m2 (48 %), and were university educated or higher (61 %).

Fig. 1 Participant flow through the study to develop a short-form version of the SMILE-FFQ. SMILE, Study of Mothers’ and Infants’ Life Events affecting oral health

Supplemental Table S3 presents the sample characteristics for the complete-case samples compared to the excluded cases (i.e. those with complete dietary data but incomplete sociodemographic data). Participants excluded were largely similar to the analysed samples at 2 and 5 years; however, children from the analysed sample were slightly younger at 2 years (2·1 ± 0·1 years v. 2·2 ± 0·2 years, p = 0·03) and slightly older at 5 years (5·3 ± 0·4 v. 5·2 ± 0·4 years, p = 0·004). Mothers who provided complete data at 2 years were more likely to be born in Australia/New Zealand/UK (78 % v. 68 %, p = 0·006), while at 5 years they were less likely to be university-educated (61 % v. 75 %, p = 0·04).

Development of the SMILE-FSS

SMILE-FFQ item reduction at 2 years of age

Figure 2 shows the reduction of the 2-year SMILE-FFQ from ninety-nine items to twenty-two items using data from the training sample (n 622). First, the ninety-nine FFQ items were reduced by collapsing twenty-five FFQ items into eight (see online supplementary material, Supplemental Table S1) and subsequently removing sixty items with near-zero variance (see online supplementary material, Supplemental Table S2). A total of twenty-four predictors (twenty-two FFQ items plus child age and sex) were entered into the regularised linear regression prediction model. Table 2 shows the model coefficients after variable shrinkage across ten cross-validation runs. The RMSE across the ten runs was 2275·6 ± 28·2 (%EFS, 4·06 ± 0·26 %). The best model was R8, with an RMSE of 4·4 %EFS, meaning that on average a child’s predicted %EFS was overestimated by 4·4 %.

Fig. 2 Reduction of the ninety-nine-item and ninety-eight-item SMILE-FFQ into the twenty-two-item and twenty-six-item SMILE-FSS at 2 years and 5 years, respectively. SMILE, Study of Mothers’ and Infants’ Life Events affecting oral health

Table 2 Model coefficients after variable shrinkage across ten cross-validation runs of the regularised regression-based prediction model, using the training sample (n 622) at 2 years a

a Bold values indicate coefficients for best model with minimum root mean square error difference between training (2263·86) and testing (2263·59) data.

Of the twenty-four predictors entered into the regression model, all remained after variable shrinkage. The twenty-two items included discretionary items (i.e. those that do not fit into the five food groups due to their high saturated fat and/or added sugars or salt content(36)) such as: icy poles and sorbets; ice creams and frozen yogurts; flavoured breakfast cereals (i.e. chocolate, vanilla or malt-flavoured with added sugar content); snack foods (i.e. potato crisps), sweet biscuits; muesli and cake-type bars; cakes and puddings; sweet breads and pancakes; spreads such as jam and honey; chocolate and lollies; fruit juice (no added sugar); and sugar. Sugar-sweetened beverages (such as soft drinks, cordials and fruit drinks) were not a strong predictor of FSI in the 2-year-old sample. Core (‘healthy’)(36) food items such as custard, nut paste, wheat biscuits and cereal flakes, flavoured yogurts (i.e. fruit flavoured), and plain savoury biscuits also remained as strong predictors of FSI. The secondary analysis showed that for the model including child height and weight (see online supplementary material, Supplemental Table S3), the resultant FFQ items (n 21) were similar, however, without sweet style sauces and marinades, and savoury biscuits and snack foods.

SMILE-FFQ item reduction at 5 years of age

Figure 2 shows the reduction of the 5-year SMILE-FFQ from ninety-eight items to twenty-six items using data from the training sample (n 460). First, the ninety-eight FFQ items were reduced by collapsing twenty-five FFQ items into eight (see online supplementary material, Supplemental Table S1) and removing fifty-one items with near-zero variance (see online supplementary material, Supplemental Table S2). A total of thirty-four items (thirty FFQ items plus child age, sex, weight and height) were entered into the linear regression prediction model. Table 3 shows the model coefficients resulting after variable shrinkage across ten cross-validation runs. The RMSE across the ten runs was 2193·3 ± 37·1 (%EFS, 2·5 ± 0·4 %). The best model was R8, with an RMSE of 2·6 %EFS, meaning that on average a child’s predicted %EFS was overestimated by 2·6 %.

Table 3 Model coefficients after variable shrinkage across ten cross-validation runs of the regularised regression-based prediction model, using the training sample (n 460) at 5 years a

a Bold values indicate coefficients for best model with minimum root mean square error difference between training (2199·41) and testing (2196·15) data.

Of the thirty-four predictors entered into the regression model, twenty-six remained after variable shrinkage. That was, four SMILE-FFQ items (nut paste, wheat biscuits, cereal flakes and mayonnaise) were removed via the regression-based predictive analysis model, in addition to the four child predictors. Items remaining as strong predictors were those as per the 2-year analysis, with additional items including discretionary drinks such as flavoured milk, fruit drink, soft drink and powdered milo/Ovaltine (added to milk drinks) and discretionary foods such as chocolate spreads, sweet-style sauces/marinades, sugar syrups (e.g. maple syrup), and sweet pastries. The sensitivity analysis showed that for the model excluding child height and weight (see online supplementary material, Supplemental Table S4), the resultant FFQ items (n 27) were similar; however, they did not include wheat biscuits, cereal flakes and mayonnaise.

Internal validation of the SMILE-FSS

Comparison of the measured and predicted percent energy from free sugars

Figure 3 shows a scatter plot of the measured v. predicted %EFS, including a unity line which represents perfect calibration (i.e. where predicted = measured), developed using the testing sample (n 263 at 2 years; n 193 at 5 years). The figure indicates that at both 2 and 5 years, the models performed worse at predicting larger values of %EFS. The horizontal and vertical dashed and dotted lines represent the cut points for < 5 %EFS and < 10 %EFS, respectively, and indicate that no participant with a %EFS of less than 5 % was predicted to have a %EFS greater than 10 % or vice versa. Supplemental Fig. S3 shows the scatter plot of the measured v. predicted FSg, also developed using the testing sample (n 263 at 2 years; n 193 at 5 years).

Fig. 3 Scatter plot of measured and predicted %EFS with the unity line (representing perfect calibration), using the testing sample (n 263 at 2 years; n 192 at 5 years). The horizontal and vertical dashed and dotted lines represent the cut-off for < 5 % total energy from free sugars (EFS) and < 10 % total EFS, respectively. EFS, energy from free sugars

Comparison to WHO free sugars guideline categories at 2 years of age

Table 4 shows the cross-classification of measured v. predicted WHO categorisation of %EFS, in which the column-wise percentages in the diagonal equal the proportion of the participants correctly predicted to be in a given category. At 2 years, a total of 74·9 % were classified into the same category and 25·1 % into an adjacent category (15·6 % over classified and 9·5 % under classified). Correct classification was highest for category 3 (≥ 10 %EFS, 84·5 %), followed by category 1 (< 5 %EFS, 75·9 %) and category 2 (5–< 10 %EFS, 63·2 %). In regard to risk identification (see online supplementary material, Supplemental Table S6), more than four out of five children (n 144/166, 87 %) with FSI < 10 %EFS were correctly identified as such, with less than one-quarter (n 22/166, 13 %) misclassified as ‘at risk’ (i.e. ≥ 10 %EFS). Conversely, few children (n 15/263, 6 %) with FSI ≥ 10 %EFS were not identified as such by the SMILE-FSS (i.e. were predicted to have FSI < 10 %EFS).

Table 4 Cross-classification table of measured and predicted WHO free sugars percentage categoriesa, using the testing sample (n 263 at 2 years; n 192 at 5 years)b

a WHO categories: (1) < 5 %EFS, (2) 5–< 10 %EFS and (3) ≥ 10 %EFS.

b Column-wise percentages in the diagonal (in bold) equal the proportion of the participants within each category correctly predicted to be in a given category.

Comparison to WHO free sugars guideline categories at 5 years of age

At 5 years, a total of 82·3 % were classified into the same WHO free sugars guideline category and 17·7 % classified into an adjacent category (11·9 % over classified and 5·8 % under classified) (Table 4). Correct classification was highest for category 3 (≥ 10 %EFS, 89·5 %), followed by category 2 (5–< 10 %EFS, 88·3 %) and category 1 (< 5 %EFS, 56·4 %). In regard to risk identification (see online supplementary material, Supplemental Table S6), nearly all children (n 110/116, 95 %) with FSI < 10 %EFS were correctly identified as such, with few (n 6/116, 5 %) misclassified as ‘at risk’ (i.e. ≥ 10 %EFS). Conversely, few (n 8/192, 4 %) children with FSI ≥ 10 %EFS at 5 years were not identified as such by the SMILE-FSS (i.e. were predicted to have FSI < 10 %EFS).

Discussion

This study employed a regression-based prediction modelling approach to reduce the long-form SMILE-FFQ at 2 and 5 years to a short-form SMILE-FSS. Food items that strongly predicted FSI and were included in the SMILE-FSS (22 and 26 items, respectively) were relatively consistent between age groups, with more discretionary food and beverage items included at 5 years. Internal validation of the SMILE-FSS showed that it performs well in comparison to the long-form SMILE-FFQ at both ages. Most children (75 % and 82 %, respectively) were categorised into the same WHO free sugars category with nearly all children (87 % and 95 %, respectively) correctly identified as having < 10 %EFS in line with the WHO recommendation(1). Overall, the SMILE-FSS was shown to have good internal validity and can be used in future research and practice to estimate total FSI in Australian children aged 2–3 and 5–6 years and compare to the WHO free sugars guidelines to determine those ‘at risk’.

Key predictors of FSI included in the SMILE-FSS were similar at 2 (twenty-two items) and 5 years (twenty-six items) and included discretionary items such as ice cream, sweet biscuits, cakes and puddings, sweet breads and pancakes, sugar-based sauces and spreads, chocolate and lollies. At 5 years (but not 2 years) of age, additional discretionary beverage items such as sugar-sweetened beverages (known as ‘soft drink’ in Australia) and fruit drinks were key predictors of FSI. This is not overly surprising given trends of increasing discretionary beverage intake in the first years of life in Australian children(Reference Byrne, Zhou and Perry37,Reference Cockburn, Lalloo and Schubert38) . For example, a study of Australian children’s beverage intake reported that the proportion of consumers of sweet beverages (including flavoured milk, 100 % juice, fruit drink, cordial and soft drink) increased from approximately one-third (38 %) at 2 years to half at 3·7 (55 %) and 5 (47 %) years(Reference Byrne, Zhou and Perry37). A similar trend was observed in a longitudinal study of beverage consumption in Australian children(Reference Cockburn, Lalloo and Schubert38), whereby soft drink and cordial consumers increased from 1 % in the first year of life to one-quarter (28 %) at 2 years and nearly half (43 %) at 10 years. Discretionary items such as chocolate spreads and sugar syrups were also additional predictors of FSI at 5 years (but not at 2 years), while core items such as nut paste, wheat (cereal) biscuits (e.g. Weet-Bix, Vita Brits, etc), cereal flakes (e.g. Cornflakes, Wheeties, Sultana Bran, Light n Tasty, etc.) were important in predicting FSI at 2 years (but not at 5 years). Together these findings demonstrate a shift from healthy/core foods as key free sugar contributors in the first few years of life towards greater discretionary food contributors in school-aged children, consistent with population trends(39). Overall, consistency and discrepancies in key free sugar contributors between 2 and 5 years are reflective of changes in patterns of consumption as children move from toddlerhood to childhood.

Importantly, in this study, 100 % fruit juice and flavoured milk ((i.e. chocolate/strawberry milk and milkshakes) were key predictors of FSI at 2 and 5 years, respectively, aligning with the downward trend by age group in fruit juice consumption (78 % 2–3 year olds, 59 % in 4–8 year olds)(40) and the upward trend in flavoured milk consumption(Reference Baird, Syrette and Hendrie41). However, although the primary goal of the SMILE-FSS is a reduction in FSI for dental health, and thus identification of free sugar containing items is important, 100 % fruit juice and flavoured milk are considered core beverage items within the Australian Dietary Guidelines(36), providing essential nutrients and contributing to children’s fruit and dairy serves(Reference Fayet-Moore, Cassettari and McConnell42) This is a particularly important consideration for the 5-year-old SMILE FFS with respect to flavoured milk consumption and dairy serve recommendations given that Australian children older than 4 years of age do not reach recommendations for dairy food intake, consuming ≤ 2 servings/d(Reference Baird, Syrette and Hendrie41). Thus, end users of the SMILE-FSS should be cautious not to recommend avoidance of these items but rather balance recommendations to reduce FSI with respect to their nutrient contribution.

Validation of the SMILE-FSS showed that the short-form screener has good internal validity. Although a child’s predicted %EFS was overestimated by 4·4 % in 2–3 year olds and by 2·6 % in 5–6 year olds, the SMILE-FSS correctly classified most children (75 % and 82 %, respectively) into the WHO free sugars guidelines categories (< 5, 5–< 10, ≥ 10 %EFS)(1). Further, nearly all children (87 % and 95 %, respectively) were correctly identified as having < 10 %EFS in line with the WHO free sugars recommendation with few children (6 % at 2 years and 4 % at 5 years) with intakes ≥ 10 %EFS (i.e. ‘at risk’) not identified as such by the SMILE-FSS. In contrast, the proportion of children misclassified as ‘at risk’ (i.e. ≥ 10 %EFS) at 2 (13 %) years was higher than that at 5 years (5 %), although similar studies have shown misclassification levels as high as 25 %(Reference Bell, Golley and Magarey30,Reference Bell, Golley and Mauch31) .Overall, findings show that the SMILE-FSS performs well in identifying children ‘at risk’ (≥ 10 %EFS) and in need of referral and intervention and can be used in future research to estimate total FSI in Australian children aged 2–3 and 5–6 years.

To our knowledge, no other short dietary-related screening tools exist within the dental context to assess FSI in Australian children. A short-form 8–16 item child oral health-related quality-of-life tool has been developed in a sample of New Zealand 11–14-year-old children, while several short diet-related screening tools (7–28 items) that assess food intake(Reference Bell, Golley and Magarey28,Reference Bell, Golley and Magarey30Reference Magarey, Golley and Spurrier33) , diet quality(Reference Hendrie, Viner Smith and Golley29) and or obesity-related behaviours have been developed and validated in Australian children ranging from 12 months to 16 years of age. These include the twenty-eight-item Children’s Dietary Questionnaire (4–16 years)(Reference Magarey, Golley and Spurrier33), the nineteen-item Toddler (ages 12–36 months)(Reference Bell, Golley and Magarey28,Reference Bell, Golley and Magarey30) and Preschooler (3–5 years) Dietary Questionnaires(Reference Bell, Golley and Mauch31), and the 7–15-item Early Prevention of Obesity in Childhood Dietary Questionnaire (EPOCH-DQ). None of these tools were designed to capture the leading dietary contributors to dental caries risk, and thus none specifically assess total and/or FSI from major food and beverages sources in young Australian children. The 2- and 5-year-old versions of the SMILE-FSS therefore add to the small yet increasing number of short tools to assess dietary intakes in young Australian children.

The SMILE-FSS is the first short screening tool to assess FSI across the first years of life that is suitable for dental research and practice, showing good internal validity compared with the longer SMILE-FFQ. The SMILE-FSS was developed in a large sample of children (n 885 at 2 years and n 652 at 5 years) through application of an innovative approach to item selection, a regression-based model utlilising existing data of 2- and 5-year-olds dietary intakes. Other strengths include combining items a priori to ensure the final screener would be fit-for-purpose and the 10-fold cross-validation that was undertaken to determine the best subset of SMILE-FFQ questions that accurately estimate children’s FSI. Child factors (age, sex, height and weight) were added to the model to improve model fit, and sensitivity analyses conducted (with or without height and weight and using both %EFS and FSg to internally validate items in the optimal model) with minimal differences seen between models. Additionally, demographic characteristics of included participants (n 885 at 2 years; n 652 at 5 years) were compared to those excluded (n 158 at 2 years; n 64 at 5 years) with no meaningful differences found. However, despite the extensive analyses undertaken in this study to determine internal validity, the external validity of the SMILE-FSS is unknown. This could be determined through completion of the short-form SMILE-FSS and repeat 24-h recalls (the gold standard in dietary assessment)(Reference Burrows, Martin and Collins43) by the same sample to compare FSI of Australian children derived from the two tools. The SMILE-FSS is also limited by the fact that it was developed and internally validated in discrete samples of Australian children aged 2–3 years and 5–6 years, and thus the applicability to children outside of these age ranges is unknown.

Despite these limitations, the SMILE-FSS fills an important gap in the literature, being highly useful in dental research where dietary assessment resources are limited. However, caution should be taken to ensure that core foods that provide nutritional benefits, such as 100 % fruit juice and flavoured milks, are not restricted to ensure young children’s nutritional intake is not compromised. Further, if the SMILE-FSS is to be used in a population substantially different to the one described here, or the tool is modified in any way, further validation (internal or external) would be required to determine its validity within that context. It also has potential, following further work to translate it into a user-friendly online version, to be utilised within the primary healthcare dental setting to screen children’s FSI and support appropriate intervention (i.e. behaviour change messages for oral health regarding reducing and/or limiting sugar consumption) to reduce caries risk(Reference Daley44). Future research, however, is required to determine the feasibility and acceptability (by dental practitioners and caregivers) of this approach(Reference Daley44).

This study used a regression-based prediction modelling approach to develop and internally validate a short twenty-two-item (2 years) and twenty-six-item (5 years) FSS (the SMILE-FSS) using data derived from a longer (99 and 98 items, respectively) FFQ (the SMILE-FFQ). The SMILE-FSS was shown to have good internal validity, accurately estimating FSI and allowing for good comparison to the WHO free sugars guideline categories to determine those ‘at risk’ (i.e. not meeting the < 10 %EFS WHO recommendation). Food items in the SMILE-FSS at both 2 and 5 years are relatively consistent, with more discretionary foods and beverages featuring in the 5-year-SMILE-FSS. In summary, the SMILE-FSS is a novel, age-appropriate, culturally appropriate tool that can be used in research and practice settings to assess FSI of Australian children aged 2–3 and 5–6 years and provide quick assessment against the WHO free sugars guideline. Future research should determine the acceptability and feasibility of implementing the SMILE-FSS within the primary care dental setting.

Acknowledgements

The authors wish to acknowledge and thank all participants and research support staff of the Study of Mothers’ and Infants’ life Events (SMILE) affecting oral health.

Financial support

The SMILE birth cohort is funded by Australian National Health and Medical Research Council Grants #1046219 and #1144595. LKB is supported by this grant.

Conflict of interest

None declared.

Authorship

The study was conceived by G. D-C., J. A. S., L. K. B. and R. K. G. with funding obtained by L. G. D., D. H., J. A. S. and R. K. G. G. D-C. conducted the validation of the original SMILE-FFQ, and L. K. B. and G. D-C. led the implementation of the present study with supervision from R. K. G. and J. A. S. S. L. conducted the statistical analyses with contribution from L. K. B., and all authors contributed to the interpretation of results. L. K. B. drafted the manuscript, and all authors have read and approved the final version.

Ethics of human subject participation

This study was conducted according to the guidelines laid down in the Declaration of Helsinki, and all procedures involving research study participants were approved by the Southern Adelaide Clinical Human Research Ethics Committee (HREC/50.13, approval date: 28 Feb 2013) and the South Australian Women and Children Health Network (HREC/13/WCHN/69, approval date: 7 August 2013). Written informed consent was obtained from all subjects/patients.

Supplementary material

For supplementary material accompanying this paper visit https://doi.org/10.1017/S1368980023002380

References

World Health Organization (2017) Sugars and Dental Caries. WHO Technical Information Note. Geneva, Switzerland: WHO.Google Scholar
Delli Bovi, AP, Di Michele, L, Laino, G et al. (2017) Obesity and obesity related diseases, sugar consumption and bad oral health: a fatal epidemic mixtures: the pediatric and odontologist point of view. Transl Med UniSa 16, 1116.Google Scholar
Vos, MB, Kaar, JL, Welsh, JA et al. (2017) Added sugars and cardiovascular disease risk in children: a scientific statement from the American Heart Association. Circulation 135, e1017e1034.Google Scholar
Australian Institute of Health and Welfare (AIHW) (2017) A Picture of Overweight and Obesity in Australia. Canberra, Australia: Australian Institute of Health and Welfare (AIHW).Google Scholar
Ha, D, Roberts-Thomson, K, Arrow, P et al. (2016) Oral health of Australian children: The National Child Oral Health Study. In Children’s Oral Health Status in Australia, 2012–2014, pp. 86152 [Doc, LG & Spencer, AJ, editors]. Adelaide: University of Adelaide Press.Google Scholar
Fidler Mis, N, Braegger, C, Bronsky, J et al. (2017) Sugar in infants, children and adolescents: a position paper of the european society for paediatric gastroenterology, hepatology and nutrition committee on nutrition. J Pediatr Gastroenterol Nutr 65, 681696.Google Scholar
Birch, L, Savage, JS & Ventura, A (2007) Influences on the development of children’s eating behaviours: from infancy to adolescence. Can J Diet Pract Res 68, s1s56.Google Scholar
COAG (Council of Australian Governments) Health Council (2015) Healthy Mouths Healthy Lives - Australia’s National Oral Health Plan 2015–2024. Adelaide: South Australian Dental Service.Google Scholar
World Health Organization (2017) Report of the Commission on Ending Childhood Obesity. Geneva: WHO.Google Scholar
Mahboobi, Z, Pakdaman, A, Yazdani, R et al. (2021) Dietary free sugar and dental caries in children: a systematic review on longitudinal studies. Health Promot Perspect 11, 271280.Google Scholar
Moynihan, P (2016) Sugars and dental caries: evidence for setting a recommended threshold for intake. Adv Nutr 7, 149156.Google Scholar
Crowe, M, O’Sullivan, M, Cassetti, O et al. (2020) Estimation and consumption pattern of free sugar intake in 3-year-old Irish preschool children. Eur J Nutr 59, 20652074.Google Scholar
Devenish, G, Ytterstad, E, Begley, A et al. (2019) Intake, sources, and determinants of free sugars intake in Australian children aged 12–14 months. Matern Child Nutr 15, e12692.Google Scholar
Devenish, G, Golley, RK, Mukhtar, A et al. (2019) Free sugars intake, sources and determinants of high consumption among Australian 2-year-olds in the SMILE cohort. Nutrients 11, 161.Google Scholar
Byrne, R, Bell, L, Taylor, RW et al. (2019) Brief tools to measure obesity-related behaviours in children under 5 years of age: a systematic review. Obes Rev 20, 432447.Google Scholar
Golley, RK, Bell, LK, Hendrie, GA et al. (2017) Validity of short food questionnaire items to measure intake in children and adolescents: a systematic review. J Hum Nutr Diet 30, 3650.Google Scholar
Devenish, G, Mukhtar, A, Begley, A et al. (2017) Development and relative validity of a food frequency questionnaire to assess intakes of total and free sugars in Australian toddlers. Int J Environ Res Public Health 14, 1361.Google Scholar
Dietary Assessment Primer, Screeners at a Glance. National Institutes of Health, National Cancer Institute. https://dietassessmentprimer.cancer.gov/ (accessed June 2022).Google Scholar
Bell, LK, Golley, RK & Magarey, AM (2013) Short tools to assess young children’s dietary intake: a systematic review focusing on application to dietary index research. J Obes 2013, 709626.Google Scholar
Do, LG, Ha, DH, Bell, LK et al. (2020) Study of Mothers’ and Infants’ Life Events Affecting Oral Health (SMILE) birth cohort study: cohort profile. BMJ Open 10, e041185.Google Scholar
Do, LG, Scott, JA, Thomson, WM et al. (2014) Common risk factor approach to address socioeconomic inequality in the oral health of preschool children – a prospective cohort study. BMC Public Health 14, 429.Google Scholar
van der Bend, D, Bucher, T, Schumacher, TL et al. (2017) Trends in food and beverage portion sizes in Australian children; a time-series analysis comparing 2007 and 2011–2012 national data. Children (Basel) 4, 69.Google Scholar
Alejandro-Vega, S, Suarez-Marichal, D, Niebla-Canelo, D et al. (2022) Fluoride exposure from ready-to-drink coffee consumption. Life (Basel) 12, 1615.Google Scholar
World Health Organization (2000) Obesity: Preventing and Managing the Global Epidemic. Report of a WHO Consultation. WHO Technical Report Series. Geneva: WHO.Google Scholar
Australian Bureau of Statistics (2013) Socio-Economic Indexes for Areas (SEIFA) 2011. Canberra, ACT: ABS.Google Scholar
World Health Organization (1995) Weighing and Measuring a Child Training Course on Child Growth Assessment. Geneva, Switzerland: WHO.Google Scholar
World Health Organization (1995) Physical Status: Use and Interpretation of Anthropometry. Geneva, Switzerland: WHO Expert Committee on Physical Status.Google Scholar
Bell, LK, Golley, RK & Magarey, AM (2015) Dietary risk scores of toddlers are associated with nutrient intakes and socio-demographic factors, but not weight status. Nutr Diet 73, 7380.Google Scholar
Hendrie, GA, Viner Smith, E & Golley, RK (2014) The reliability and relative validity of a diet index score for 4–11-year-old children derived from a parent-reported short food survey. Public Health Nutr 17, 14861497.Google Scholar
Bell, LK, Golley, RK & Magarey, AM (2014) A short food-group based dietary questionnaire is reliable and valid for assessing toddlers’ dietary risk in relatively advantaged samples. Br J Nutr 112, 627637.Google Scholar
Bell, LK, Golley, RK, Mauch, C et al. (2018) Validation testing of a short food-group based questionnaire to assess dietary risk in preschoolers aged 3–5 years. Nutr Diet. Published online 23 February 2018. doi: 10.1111/1747-0080.12412.Google Scholar
Grady, A, Fielding, A, Golley, RK et al. (2020) Adaptation, acceptability and feasibility of a Short Food Survey to assess the dietary intake of children during attendance at childcare. Public Health Nutr 23, 14841494.Google Scholar
Magarey, A, Golley, RK, Spurrier, N et al. (2009) Reliability and validity of the Children’s Dietary Questionnaire; a new tool to measure children’s dietary patterns. Int J Pediatr Obes 4, 257265.Google Scholar
Food Standards Australia and New Zealand Determining the Amount of Added Sugars and Free Sugars in Foods Listed in the AUSNUT 2011–2013 Dataset. https://www.foodstandards.gov.au/science/monitoringnutrients/ausnut/foodnutrient/Pages/Determining-the-amount-of-added-sugars-and-free-sugars-in-foods-listed-in-the-AUSNUT-201113-dataset.aspx (accessed February 2018).Google Scholar
National Health and Medical Research Council (2006) Nutrient Reference Values for Australia and New Zealand. Canberra, Australia: NHMRC.Google Scholar
National Health and Medical Research Council (2013) Eat for Health Guidelines. Canberra, Australia: NHMRC.Google Scholar
Byrne, R, Zhou, Y, Perry, R et al. (2018) Beverage intake of Australian children and relationship with intake of fruit, vegetables, milk and body weight at 2, 3.7 and 5 years of age. Nutr Diet 75, 159166.Google Scholar
Cockburn, N, Lalloo, R, Schubert, L et al. (2018) Beverage consumption in Australian children. Eur J Clin Nutr 72, 401409.Google Scholar
Australian Bureau of Statistics (2011) Australian Health Survey: Nutrition First Results – Foods and Nutrients. https://www.abs.gov.au/statistics/health/health-conditions-and-risks/australian-health-survey-nutrition-first-results-foods-and-nutrients/latest-release#discretionary-foods (accessed December 2022).Google Scholar
Australian Bureau of Statistics (2018) Australian Health Survey: Consumption of Food Groups from the Australian Dietary Guidelines, 2011–2012. https://www.abs.gov.au/ausstats/abs@.nsf/Lookup/by%20Subject/4364.0.55.012∼2011-12∼Main%20Features∼Fruit∼15#2 (accessed August 2023).Google Scholar
Baird, DL, Syrette, J, Hendrie, GA et al. (2012) Dairy food intake of Australian children and adolescents 2–16 years of age: 2007 Australian National Children’s Nutrition and Physical Activity Survey. Public Health Nutr 15, 20602073.Google Scholar
Fayet-Moore, F, Cassettari, T, McConnell, A et al. (2019) Australian children and adolescents who were drinkers of plain and flavored milk had the highest intakes of milk, total dairy, and calcium. Nutr Res 66, 6881.Google Scholar
Burrows, TL, Martin, RJ & Collins, CE (2010) A systematic review of the validity of dietary assessment methods in children when compared with the method of doubly labeled water. J Am Diet Assoc 110, 15011510.Google Scholar
Daley, AJ (2022) Time to get our teeth into reducing obesity: should dentists screen and deliver interventions to reduce obesity in the population? Br Dent J 232, 7879.Google Scholar
Figure 0

Table 1 Characteristics of mother–child dyads in the samples with complete dietary and sociodemographic data at 2 and 5 yearsa

Figure 1

Fig. 1 Participant flow through the study to develop a short-form version of the SMILE-FFQ. SMILE, Study of Mothers’ and Infants’ Life Events affecting oral health

Figure 2

Fig. 2 Reduction of the ninety-nine-item and ninety-eight-item SMILE-FFQ into the twenty-two-item and twenty-six-item SMILE-FSS at 2 years and 5 years, respectively. SMILE, Study of Mothers’ and Infants’ Life Events affecting oral health

Figure 3

Table 2 Model coefficients after variable shrinkage across ten cross-validation runs of the regularised regression-based prediction model, using the training sample (n 622) at 2 yearsa

Figure 4

Table 3 Model coefficients after variable shrinkage across ten cross-validation runs of the regularised regression-based prediction model, using the training sample (n 460) at 5 yearsa

Figure 5

Fig. 3 Scatter plot of measured and predicted %EFS with the unity line (representing perfect calibration), using the testing sample (n 263 at 2 years; n 192 at 5 years). The horizontal and vertical dashed and dotted lines represent the cut-off for < 5 % total energy from free sugars (EFS) and < 10 % total EFS, respectively. EFS, energy from free sugars

Figure 6

Table 4 Cross-classification table of measured and predicted WHO free sugars percentage categoriesa, using the testing sample (n 263 at 2 years; n 192 at 5 years)b

Supplementary material: File

Bell et al. supplementary material
Download undefined(File)
File 445.7 KB