Hostname: page-component-8448b6f56d-mp689 Total loading time: 0 Render date: 2024-04-19T05:42:04.170Z Has data issue: false hasContentIssue false

Dietary patterns throughout childhood and associations with nutrient intakes

Published online by Cambridge University Press:  14 September 2012

Rights & Permissions [Opens in a new window]

Abstract

Objective

To examine how the dietary patterns of children at various time points throughout childhood relate to estimated nutrient intakes.

Design

FFQ at 3, 4, 7 and 9 years of age were completed by mothers. Dietary patterns were identified cross-sectionally using principal component analysis; ‘processed’, ‘health conscious’ and ‘traditional’ patterns were consistently obtained. Correlations between pattern scores and nutrient intakes and proportions of variance in nutrients explained by the patterns were calculated.

Setting

Avon Longitudinal Study of Parents and Children (ALSPAC), Bristol, UK.

Subjects

Children provided data between 3 and 9 years of age (n 8010 to 10 023).

Results

Dietary patterns explained substantial proportions of the variance of the absolute intake for most nutrients (>25 % at 3 years of age, >40 % other ages). After energy adjustment, protein, fibre, K, Mg, Fe, Zn, folate, thiamin and vitamin B6 continued to be well explained. Strong correlations were observed between the ‘processed’ pattern and macronutrients including energy (r = 0·481–0·619), total fat (r = 0·529–0·662) and total sugar (r = 0·475–0·693). However correlations with most micronutrients were reversed after energy adjustment, suggesting that the ‘processed’ pattern is energy-dense but nutrient-poor. The ‘health conscious’ and ‘traditional’ patterns were strongly positively correlated with protein, fibre and most micronutrients, whether energy adjusted or not. Higher scores on these patterns were associated with a better nutrient profile.

Conclusions

Dietary patterns explain a reasonable amount of the variation in the nutrient content of diets. Higher scores on the ‘health conscious’ and ‘traditional’ dietary patterns were related to better nutrient profiles; conversely, with higher scores on the ‘processed’ pattern the nutrient profile was poorer.

Type
Epidemiology
Copyright
Copyright © University of Bristol 2012 

Diet has been associated with many health conditions such as CHD, obesity, diabetes and some types of cancer(Reference Dietz15). Substantial evidence also indicates that diet is important throughout childhood and adolescence, as it has been shown that dietary habits established during childhood are likely to track into adulthood(Reference Mikkila, Rasanen and Raitakari6). It is therefore important to examine diet several times during childhood.

Various epidemiological studies that have examined diet and health relationships have concentrated primarily on either individual nutrients and/or foods(Reference Craig, McNeill and Macdiarmid7). These traditional methods have provided valuable evidence but have several methodological limitations; the high inter-correlations that exist between nutrients mean that the effects of a single nutrient may be hard to detect(Reference Hu8) or distinguish from other nutrients. More recently, the focus has shifted towards exploring the whole diet to assess these relationships using dietary patterns. Individuals do not eat nutrients in isolation; they eat a variety of foods, consisting of a combination of nutrients, and the interaction of these nutrients can make it difficult to explore the individual effect of each nutrient(Reference Michels and Schulze9). Therefore, it is not just the absence or presence of a particular food, but the variety and combination of foods in the diet that are important for optimal health(Reference North and Emmett10)). Principal component analysis (PCA) is the most commonly used method to describe overall dietary patterns, using the correlations that exist between the foods eaten in combination. Such a method gives a summary of the foods/drinks consumed and therefore has the potential to provide a better indicator of disease risk(Reference Hu8). It aims to better understand the complexities of diet and examine the associations between nutrition and health, in contrast to the traditional nutrient-based method(Reference Jacques and Tucker11). Using PCA a score is obtained for each pattern which can be used to explore the relationships between the dietary patterns and either nutrient intakes or health outcomes(Reference Craig, McNeill and Macdiarmid7, Reference Hu8). Using dietary patterns in causal analyses has the potential to be more informative than focusing on individual nutrients or foods, and should inform the development of public health initiatives(Reference Cutler, Flood and Hannan12) and be easier to translate into messages relevant to the day-to-day lives of individuals(Reference Mikkila, Rasanen and Raitakari13).

Research examining the associations between dietary patterns and nutrient intakes is limited. Previous work within the Avon Longitudinal Study of Parents and Children (ALSPAC) has examined such relationships in pregnant women and shown that scores on the ‘health conscious’ and ‘traditional’ patterns were positively related to all nutrients, while the ‘processed’ pattern was negatively associated with most nutrients except for energy, fats and sugar, all of which increased with higher scores(Reference Northstone, Emmett and Rogers14). These relationships have not previously been investigated in children. Thus, the aim of the present study was to use FFQ data to examine dietary patterns, derived from PCA, for children (of the women previously described) when aged 3, 4, 7 and 9 years and relate these to estimated nutrient intakes, using a well-characterised birth cohort study.

Methods

Participants

Participants were children participating in ALSPAC (www.alspac.bris.ac.uk), an ongoing longitudinal cohort study designed to investigate the health and development of children. The study has been described in more detail elsewhere(Reference Golding, Pembrey and Jones15). Briefly, pregnant women were eligible if they had an expected delivery date between April 1991 and December 1992 and were resident in the former Avon Health Authority in South West England. This established a cohort of 14 541 women resulting in 13 988 children (alive at 12 months), with 548 new participants recruited at age 7 years (total children 14 536). The primary source of data collection was via parental self-completion questionnaires. At recruitment the ALSPAC cohort was compared with the 1991 National Census data for mothers with infants aged 1 year resident in the area; they were similar except for a slight shortfall in those living in rented accommodation, single-parent families and ethnic minorities.

Ethical approval for the study was obtained from the ALSPAC Law and Ethics Committee and the Local Research Ethic Committees.

Dietary assessment

Dietary assessments were made using parent-completed FFQ throughout childhood when the children were aged 3·2, 4·5, 6·8 and 8·6 years, but for ease these time points will be referred to as 3, 4, 7 and 9 years, respectively. Each questionnaire contained a series of questions enquiring about the frequency of consumption of a wide range of food and drinks. These FFQ were modified from an original FFQ used to assess maternal diet at 32 weeks of pregnancy and shown to provide mean nutrient intakes(Reference Rogers, Emmett and Golding16) that were similar to those obtained in the UK National Diet and Nutritional Survey for women at that time(17). Over time the original FFQ was modified to include additional foods and drinks (with slight variations at each age) in the light of food record data collected from a sub-sample of ALSPAC children. Modifications included separate categories from age 4 years for vegetarian pies, coated white fish, coated chicken/turkey and tuna. These foods had previously been incorporated in other groups. School dinners (7 and 9 years only) were asked about separately and included in the nutrient analysis, but not the PCA.

The majority of the questions asked how many times the child consumed each food item ‘nowadays’ and the parent was asked to tick one of the following options: (i) ‘never or rarely’; (ii) ‘once in 2 weeks’; (iii) ‘one to three times per week’; (iv) ‘four to seven times per week’; or (v) ‘more than once a day’. In addition, more detailed questions were asked about daily intakes of basic foods such as bread (the type and number of slices per day), tea and coffee (the number of cups). The type of milk (full-fat, semi-skimmed, others), bread (white, wholemeal, others) and spread (butter, margarine, others) usually consumed was also recorded. Standard portion sizes, modified according to the age of the child, were assumed throughout the questionnaires. Food records were used to give information on likely portion sizes and to inform the selection of foods to include in each food group(Reference Emmett, Rogers and Symes18, Reference Glynn, Emmett and Rogers19). Portion sizes were also informed by an analysis of weighed dietary intakes for similar aged children from the National Diet and Nutrition Survey(Reference Gregory and Lowe20Reference Wrieden, Longbottom and Adamson22).

The weekly frequencies of intake assumed for each of the options in the FFQ were as follows: i = 0, ii = 0·5, iii = 2, iv = 5·5 and v = 10 times/week. All items were standardised by subtracting the mean and dividing by the standard deviation for each variable. Some items were combined before the PCA, as they contributed to the same food group, e.g. ‘Fish’ in the PCA includes white fish, oily fish, shellfish and tuna. The final number of combined foods/food groups included in the PCA was thirty-four, thirty-five, forty-one and forty-one at 3, 4, 7 and 9 years, respectively.

Daily nutrient intakes were estimated from the FFQ using the fifth edition of McCance & Widdowson's The Composition of Food (Reference Holland, Welch and Unwin23) and supplements(Reference Chan, Brown and Buss24Reference Holland, Unwin and Buss29). Additional up-to-date nutrient information was obtained from the National Diet and Nutrition Survey database and manufacturers’ information(Reference Rogers, Emmett and Golding16).

Statistical analysis

PCA with varimax rotation(Reference Gorsuch30, Reference Kline31) was performed separately at each time point on the standardised food items and has been described in detail elsewhere(Reference North and Emmett10, Reference Northstone and Emmett32, Reference Northstone and Emmett33). Briefly, PCA reduces the data by forming linear combinations of the original observed variables; thereby grouping together correlated variables, which in turn identifies any underlying dimensions in the data. The coefficients defining these linear combinations are called ‘factor loadings’ and are the correlations of each food item with that component. The number of components that best represented the data at each time point was chosen primarily on the basis of the scree plot(Reference Cattell34) and the interpretability of the factor loadings was also considered.

A score for each child was created for each component identified at each time point. These were calculated by multiplying the factor loadings by the corresponding standardised value for each food and summing across the food types. Each score has a mean of 0 (and a standard deviation of 1) and a higher score indicates that a child's diet is closer to that dietary pattern. Children were excluded from each PCA if they had more than ten items missing from the respective questionnaire. If ten or fewer items were missing, the assumption was made that the child did not consume those items and were given a value of 0. Foods with loadings above 0·3 on a component were considered to have a strong association with that component and were deemed to be most informative in describing the dietary patterns. Labels were assigned to each component at each time point; these do not perfectly describe each underlying pattern, but were helpful in the reporting and the discussion of the results.

All component scores were approximately normally distributed. Spearman's correlation coefficients were calculated to measure the associations between the dietary pattern scores identified at each time point and the respective nutrient intakes. Additionally, partial correlation coefficients were calculated, adjusting for energy intake, and thus represented the associations between dietary patterns and relative nutrient intakes. Energy adjustment was conducted because energy is highly correlated with most other nutrients and related to body size(Reference Willett, Howe and Kushi35), thus it may obscure underlying relationships with nutrients. The nutrient density of an individual food is the ratio of its nutrient content to total energy content. Nutrient-dense foods provide substantial amounts of micronutrients with relative low energy content(36); thus an overall diet that has a high micronutrient content after energy adjustment is more nutrient-dense and has a better nutrient profile. The proportion of variance explained by the dietary pattern scores was obtained for both absolute and energy-adjusted nutrient intakes by summing the squares of the correlations with each dietary pattern for each nutrient at each time point. All statistical analyses were performed using the statistical software package SPSS for Windows, version 12·0.

Results

Response rates

A total of 10 133, 9722, 9515 and 8331 questionnaires were returned at age 3, 4, 7 and 9 years, respectively, with 10 023, 9550, 8286 and 8010 having sufficient dietary data available at the respective ages for inclusion in the PCA. Three principal components – ‘processed’ (high-fat/sugar processed foods, e.g. sausages, burgers, coated poultry, crisps, biscuits, sweets, chocolate and ice cream); ‘health conscious’ (vegetarian-style foods, salad, rice, pasta, fruit and fish); and ‘traditional’ (meat, potato and vegetables) – were consistently identified to best describe the dietary patterns of the children at the four time points throughout childhood(Reference North and Emmett10, Reference Northstone and Emmett32, Reference Northstone and Emmett33). Note that at 9 years of age the ‘health conscious’ pattern was slightly different; meat and meat products had high negative loadings on this pattern and the name ‘health conscious/vegetarian’ was applied to reflect this change(Reference Northstone and Emmett33).

Correlations with energy

The ‘processed’ pattern scores showed the highest correlations with energy intake at all ages (r = 0·481–0·616; Table 1) with the ‘health conscious’ patterns showing the lowest correlations (r = 0·034–0·306; Table 2) and the ‘traditional’ pattern intermediate (r = 0·219–0·490; Table 3).

Table 1 Correlation coefficients between ‘processed’ dietary pattern scores across the ages and corresponding weekly absolute nutrient intakes and partial correlation coefficients between dietary pattern scores and weekly nutrient intakes adjusting for energy intake: children aged 3–9 years (n 8010 to 10 023), Avon Longitudinal Study of Parents and Children (ALSPAC), Bristol, UK

All P < 0·0001.

Table 2 Correlation coefficients between ‘health conscious’* dietary pattern scores across the ages and corresponding weekly absolute nutrient intakes and partial correlation coefficients between dietary pattern scores and weekly nutrient intakes adjusting for energy intake: children aged 3–9 years (n 8010 to 10 023), Avon Longitudinal Study of Parents and Children (ALSPAC), Bristol, UK

All P < 0·0001.

*‘Health conscious/vegetarian’ at the age of 9 years.

Table 3 Correlation coefficients between ‘traditional’ dietary pattern scores across the ages and corresponding weekly absolute nutrient intakes and partial correlation coefficients between dietary pattern scores and weekly nutrient intakes adjusting for energy intake: children aged 3–9 years (n 8010 to 10 023), Avon Longitudinal Study of Parents and Children (ALSPAC), Bristol, UK

All P < 0·0001.

Associations between the ‘processed’ pattern and nutrient intakes

Table 1 presents the correlations between the ‘processed’ dietary pattern scores and estimated nutrient intakes, both absolute and energy-adjusted, across the age groups. There were reasonably consistent correlations across the ages between this pattern and nutrient intakes. Strong positive correlations were observed between this dietary pattern and intakes of MUFA (r = 0·588–0·708), SFA (r = 0·468–0·574) and sugar (r = 0·475–0·693) across all four time points that were attenuated but not removed by energy adjustment. At all ages, the majority of correlations with protein, fibre and micronutrients were reversed after energy adjustment. Thus higher scores on the ‘processed’ pattern were associated with poorer protein, fibre and micronutrient profile. The highest adjusted correlations were indeed negative and seen for Mg, thiamin, niacin, Zn and fibre intake and the ‘processed’ dietary pattern score at each age (r ranging from −0·539 to −0·399).

Associations between the ‘health conscious’ pattern and nutrient intakes

The micronutrients rather than the macronutrients (except protein and fibre) were more strongly correlated with the ‘health conscious’ pattern, with the strength of the correlations lowest in the 9-year-olds (Table 2). Energy adjustment did not greatly attenuate the correlations between this pattern and protein, fibre or most micronutrients (e.g. the correlation with fibre at 3 years attenuated to 0·419 from 0·485 and at 7 years it attenuated to 0·475 from 0·537). However, correlations with some macronutrients were reversed; notably total fat, MUFA and SFA. In general higher scores on the ‘health conscious’ pattern were associated with a better protein, fibre and micronutrient profile. The highest adjusted correlations between the ‘health conscious’ pattern and various nutrients were seen at 3 years of age, but these were much lower by 9 years of age. For example, Mg reduced from 0·484 to 0·230; fibre from 0·419 to 0·203; vitamin C from 0·464 to 0·154; and folate from 0·420 to 0·082.

Associations between the ‘traditional’ pattern and nutrient intakes

Table 3 shows the correlations between the ‘traditional’ dietary pattern scores and nutrient intakes across the ages. The ‘traditional’ pattern showed fairly consistent correlations with most nutrients, with a tendency for coefficients to increase with age (e.g. for carotene from 0·515 to 0·600 and for folate from 0·325 to 0·480). More than half of the nutrients examined at age 9 years were highly correlated with this pattern including protein, fibre, K, Mg, Fe, Zn, folate, carotene, thiamin, niacin and vitamin B6. These remained robust to energy adjustment. Correlations with some macronutrients were reversed after energy adjustment, such as with carbohydrate, sugar and all types of fat. The highest adjusted correlations were consistently seen for protein (r = 0·554–0·646), carotene (r = 0·515–0·613), K (r = 0·413–0·519) and Zn (r = 0·409–0·598). Higher scores on the ‘traditional’ pattern were consistently associated with greater protein, fibre and micronutrient density in the diet.

Proportion of variance

Table 4 indicates the proportion of the variance of each nutrient explained by the combined dietary patterns at each age. A reasonable proportion of the absolute intake of all macronutrients including fibre was explained by the dietary patterns at all ages. However, only fibre and protein were well explained after energy adjustment (37–54 %). For some micronutrients the dietary patterns explained a reasonable proportion of the variance at all ages, whether energy-adjusted or not; these were K, Mg, Fe, Zn, folate, thiamin and vitamin B6 (ranging from 25 % to 86 %). The other micronutrients were not so well explained particularly after energy adjustment.

Table 4 Proportion of variance (%) explained for each nutrient by age at which dietary patterns were assessed: children aged 3–9 years (n 8010 to 10 023), Avon Longitudinal Study of Parents and Children (ALSPAC), Bristol, UK

Discussion

The present study examining dietary data obtained from children at 3, 4, 7 and 9 years of age identified three consistent dietary patterns: ‘processed’, ‘health conscious’ and ‘traditional’. These patterns taken together explained a high proportion of the variance in absolute intakes of energy, fibre and twenty-one nutrients at each age. However after energy adjustment only protein, fibre, K, Mg, Fe, Zn, folate, thiamin and vitamin B6 were well explained by the patterns (ranging from 25 to 86 %). Both the ‘health conscious’ and ‘traditional’ dietary patterns were positively associated with a better protein, fibre and micronutrient profile. On the other hand, high scores on the ‘processed’ pattern were associated with a worse protein, fibre and micronutrient profile at all ages. To our knowledge, the present study is the first one to explore the relationship between dietary patterns using PCA and nutrients at multiple time points throughout childhood.

The fact that the dietary patterns were able to explain a large proportion of the variance of many nutrients adds credibility to the use of these types of pattern to summarise diet. In the present study nine of the twenty-four nutrients were particularly well explained, with a quarter to a half of their variance explained at each age, whether energy-adjusted or not. These were protein, fibre, K, Mg, Fe, folate, Zn, thiamin and vitamin B6. These are all vital nutrients and Zn, Fe and fibre have been shown to be marginal in the diets of children. Zn is required for growth, development and cognitive function(Reference Salgueiro, Zubillaga and Lysionek37); Fe is also essential for cognitive functioning and low levels are an indication of poor nutrition(Reference De Benoist, McLean and Egli38); while fibre is needed for digestion, helps control appetite and is important in determining obesity risk(Reference Johnson, Mander and Jones39).

Clear positive correlations, which were fairly robust to energy adjustment, were evident between the scores on the ‘processed’ pattern and intakes of MUFA, SFA and sugar at all ages. Furthermore, intakes of almost all of the micronutrients as well as fibre and protein were negatively correlated with this pattern after energy adjustment. This result is not surprising given that high scores on the ‘processed’ pattern are associated with high consumption of high-fat/sugar, nutrient-poor processed foods such as chips, pizza, meat pies, sausages and burgers, as well as crisps, biscuits, sweets, chocolate and ice creams. This pattern, characterised by an elevated intake of both fat and sugar, is likely to contribute to the increasing prevalence of childhood obesity(Reference Bray, Paeratakul and Popkin40) and may play an important role in high blood pressure; a risk factor for CVD(Reference He and MacGregor41). The fact that the correlations of this pattern with energy were very strong and those with micronutrients were reversed after energy adjustment suggests that it is a marker for an energy-dense, nutrient-poor diet.

The ‘health conscious’ pattern was the least correlated of the three patterns with energy and showed positive relationships with fibre and many micronutrients, such as vitamin C, Mg, Fe and Zn, that were robust to energy adjustment. This result was again not unexpected given that higher pattern scores are related to higher intakes of nutrient-dense foods such as fruit, vegetables, breakfast cereals, fish and pulses. However, these relationships were not as evident in the 9-year data. This could be because the ‘health conscious’ pattern had a slightly different character at this age; in particular, there was a negative association with meat which had not been present at previous ages(Reference Northstone and Emmett33). It is likely that the associations with Fe and Zn would have been weakened by this. On the whole, however, this pattern is a potential marker of increased diet quality with high scores associated with a better micronutrient profile in the diet.

The ‘traditional’ pattern showed fairly consistent correlations that strengthened a little as the children became older. Higher scores on this pattern are primarily associated with higher meat and vegetable intakes, so the robust positive correlations with protein, K, Zn, carotene and niacin are sensible. The reversal of associations with energy-dense macronutrients such as fat, carbohydrate and sugar after energy adjustment and the continued positive relationship with almost all macronutrients suggest that this pattern is also a marker for a diet with a better nutrient profile, and the consumption of foods associated with this pattern, particularly vegetables, needs to be encouraged.

Dietary patterns have, in recent times, become accepted as an alternative or complementary approach to the more traditional methods of assessing the associations between diet and disease(Reference Cutler, Flood and Hannan12). Previous work exploring these associations in relation to estimated nutrient intakes, although still limited, has primarily been in adults(Reference Arkkola, Uusitalo and Kronberg-Kippilae42Reference Schulze, Hoffmann and Kroke45). To our knowledge, only one UK study has examined the associations between dietary patterns and nutrient intakes in children. Patel et al. (2011) obtained three dietary patterns in a sample of 709 children aged 11 years. They showed that the ‘fruit’ pattern was inversely correlated with fat intakes, while the opposite trend was observed for the ‘processed’ pattern. Both vitamins C and E had positive associations with the ‘fruit’ and ‘traditional’ patterns, but an inverse relationship was seen with the ‘processed’ pattern(Reference Patel, Murray and Simpson46). These finding are very similar to those in the current study.

Another study among schoolchildren (aged 6–18 years) in Bahrain used energy and macronutrient intakes to determine dietary patterns (as opposed to food groups); it found a dietary pattern that was associated with high sugar intake, a high percentage of energy from saturated fat and low fibre intake. Children who scored highly on this pattern were more likely to consume sweets, snacks and soft drinks, but less likely to consume milk, fruit and vegetables. The authors suggested that this pattern is likely to contribute to the risk of obesity and other health problems in later life(Reference Gharib and Rasheed47). In recent times in Bahrain, there has been a considerable shift away from traditional foods and towards diets containing high amounts of fat, sugar and red meat(Reference Musaiger48).

The results observed in the current study were consistent with results obtained in pregnant women (the mothers of the children reported here), which found a ‘processed’ pattern that was positively associated with fats and sugar, as well as ‘health conscious’ and ‘traditional’ patterns that both showed positive linear relationships with most nutrients(Reference Northstone, Emmett and Rogers14). Similar results have also been presented in other adult studies(Reference Arkkola, Uusitalo and Kronberg-Kippilae42Reference Schulze, Hoffmann and Kroke45). Arrkola et al. (2008) reported dietary patterns in relation to dietary intakes in 3730 pregnant women and identified seven dietary patterns, with energy intake found to be positively correlated with the ‘healthy’, ‘fast food’, ‘traditional bread’, ‘traditional meat’ and ‘coffee’ patterns. As expected, the ‘fast food’ pattern was associated primarily with carbohydrate, fat and saturated fat, while the ‘healthy’ pattern was positively correlated with vitamin C, folate, Fe, Mg and protein among others. Fibre intake was positively correlated with the ‘traditional bread’ pattern together with protein, carbohydrate, fat, folate and Fe(Reference Arkkola, Uusitalo and Kronberg-Kippilae42). Using data from the European Prospective Investigation into Cancer and Nutrition (EPIC), Schulze et al. (2001) found in both men and women that most of the seven dietary patterns identified were positively associated with energy intake; a strong correlation between the ‘sweets’ pattern and carbohydrate intake, but not fat or protein intake, remained after energy adjustment; the ‘fruit and vegetables’ pattern had a positive relationship with fibre, Fe and vitamin C in both sexes; and the ‘bread and sausage’ pattern in men was associated with salt intake(Reference Schulze, Hoffmann and Kroke45). Results from the current study and others investigating dietary patterns and nutrient intakes have the potential to inform new public health initiatives, as this method of examining dietary patterns as a whole can be more useful than focusing on single foods and/or nutrients(Reference Cutler, Flood and Hannan12). It is evident from the results presented here that the ‘processed’ pattern is the least ideal in terms of nutrient intake and this persists through early to mid-childhood. By encouraging our children to reduce their intake of fats and sugars (thereby scoring lower on the ‘processed’ pattern) we have the potential to improve their nutrient profile and therefore their health. Conversely, by encouraging increased fruit and vegetable intake (thereby moving towards our ‘health conscious’ or ‘traditional’ pattern) nutrient intakes can be improved.

The strengths of the current study are its large sample size and its longitudinal design, which allowed dietary patterns and nutrient intakes to be examined in the same children throughout childhood. However, there are several limitations. First, it was conducted in one geographic area of England and so results may not be applicable throughout the UK. However, the cohort was reasonably representative of the UK population at recruitment. Second, dietary intakes were obtained using an unquantified FFQ which is a less accurate method of dietary assessment than using weighed dietary records(Reference Bingham, Gill and Welch49). Nevertheless, FFQ have been shown to provide a reasonable measure of diet in large cohorts(Reference Willett and Stampfer50) and may in fact estimate intakes of less commonly eaten foods more accurately than dietary records. We chose to examine the data cross-sectionally at each time point as the dietary patterns changed slightly at each age, no doubt due to the children progressing through different life stages from pre-school through to starting school and moving on into middle childhood with different influences being felt. In order to perform longitudinal analysis we would have needed to impose the pattern scores from the diet at 3 years on to the later data, and we felt that this was inappropriate due to the changing circumstances of the children.

Conclusions

We have shown that dietary patterns throughout childhood have similar relationships with estimated nutrient intakes at each age. It is noteworthy that the ‘traditional’ and ‘health conscious’ patterns showed very similar relationships and the ‘traditional’ dietary pattern should not be dismissed as a ‘nutritiously poor’ pattern in studies assessing diet and health outcomes. The construction of dietary patterns can be a useful way of summarising diet which has a credible relationship with important nutrients and with diet quality. Their use in dietary investigation should be helpful in providing evidence of how diet interacts with later health outcomes(Reference Cutler, Flood and Hannan12).

Acknowledgements

Source of funding: This specific research was funded by the World Cancer Research Fund (grant number 2009/23). The UK Medical Research Council, the Wellcome Trust and the University of Bristol provide core support for ALSPAC. Conflict of interest: The authors declare no conflict of interest. Authors’ contribution: P.E. collected the data, K.N. conceived the study design and performed the analyses, V.C. wrote the first draft of the manuscript and all authors approved the final version. This publication is the work of all of the authors and K.N. serves as guarantor for the contents of this paper. Acknowledgements: The authors are extremely grateful to all families who took part in the study, the midwives for their help in recruiting them and the whole ALSPAC team, which includes interviewers, computer and laboratory technicians, clerical workers, research scientists, volunteers, managers, receptionists and nurses.

References

1.Dietz, WH (1994) Critical periods in childhood for the development of obesity. Am J Clin Nutr 59, 955959.CrossRefGoogle ScholarPubMed
2.Dietz, WH (2001) The obesity epidemic in young children. BMJ 322, 313314.CrossRefGoogle ScholarPubMed
3.Steyn, NP, Mann, J, Bennett, PHet al. (2004) Diet, nutrition and the prevention of type 2 diabetes. Public Health Nutr 7, 147165.CrossRefGoogle ScholarPubMed
4.World Cancer Research Fund & American Institute for Cancer Research (1997) Food, Nutrition and the Prevention of Cancer: A Global Perspective. Washington, DC: American Institute for Cancer Research.Google Scholar
5.World Health Organization (2003) Diet, Nutrition and the Prevention of Chronic Diseases. Joint WHO/FAO Expert Consultation. WHO Technical Report Series no. 916. Geneva: WHO.Google Scholar
6.Mikkila, V, Rasanen, L, Raitakari, OTet al. (2005) Consistent dietary patterns identified from childhood to adulthood: the Cardiovascular Risk in Young Finns Study. Br J Nutr 93, 923931.CrossRefGoogle ScholarPubMed
7.Craig, LCA, McNeill, G, Macdiarmid, JIet al. (2010) Dietary patterns of school-age children in Scotland: association with socio-economic indicators, physical activity and obesity. Br J Nutr 103, 319334.CrossRefGoogle ScholarPubMed
8.Hu, FB (2002) Dietary pattern analysis: a new direction in nutritional epidemiology. Curr Opin Lipidol 13, 39.CrossRefGoogle ScholarPubMed
9.Michels, KB & Schulze, MB (2005) Can dietary patterns help us detect diet–disease associations? Nutr Res Rev 18, 241248.CrossRefGoogle ScholarPubMed
10.North, K, Emmett, P & the ALSPAC Study Team (2000) Multivariate analysis of diet among three-year-old children and associations with socio-demographic characteristics. Eur J Clin Nutr 54, 7380.CrossRefGoogle ScholarPubMed
11.Jacques, PF & Tucker, KL (2001) Are dietary patterns useful for understanding the role of diet in chronic disease? Am J Clin Nutr 73, 12.CrossRefGoogle ScholarPubMed
12.Cutler, GJ, Flood, A, Hannan, Pet al. (2009) Major patterns of dietary intake in adolescents and their stability over time. J Nutr 139, 323328.CrossRefGoogle ScholarPubMed
13.Mikkila, V, Rasanen, L, Raitakari, OTet al. (2007) Major dietary patterns and cardiovascular risk factors from childhood to adulthood. The Cardiovascular Risk in Young Finns Study. Br J Nutr 98, 218225.CrossRefGoogle ScholarPubMed
14.Northstone, K, Emmett, PM & Rogers, I (2008) Dietary patterns in pregnancy and associations with nutrient intakes. Br J Nutr 99, 406415.CrossRefGoogle ScholarPubMed
15.Golding, J, Pembrey, M, Jones, Ret al. (2001) ALSPAC – The Avon Longitudinal Study of Parents and Children I. Study methodology. Paediatr Perinat Epidemiol 15, 7487.CrossRefGoogle ScholarPubMed
16.Rogers, IS, Emmett, P, Golding, Jet al. (1998) Diet during pregnancy in a population of pregnant women in South West England. Eur J Clin Nutr 52, 246250.CrossRefGoogle Scholar
17.Ministry of Agriculture, Fisheries and Food (1994) The Dietary and Nutritional Survey of British Adults: Further Analysis. London: HMSO.Google Scholar
18.Emmett, PM, Rogers, IS, Symes, Cet al. (2002) Food and nutrient intakes of a population sample of 3-year-old children in the South West of England in 1996. Public Health Nutr 5, 5564.CrossRefGoogle ScholarPubMed
19.Glynn, L, Emmett, P, Rogers, Iet al. (2005) Food and nutrient intakes of a population sample of 7-year-old children in the south-west of England in 1999/2000 – what difference does gender make? J Hum Nutr Diet 18, 719.CrossRefGoogle ScholarPubMed
20.Gregory, J & Lowe, S (2000) National Diet and Nutrition Survey: Young People Aged 4 to 18 Years. vol. 1: Report of the Diet and Nutrition Survey. London: The Stationery Office.Google Scholar
21.Gregory, JR, Collins, DL, Davies, PSWet al. (1995) The National Diet and Nutrition Survey Children Aged 1 1/2 to 4 1/2 Years. vol. I: Report of the Diet and Nutrition Survey. London: HMSO.Google Scholar
22.Wrieden, WL, Longbottom, PJ, Adamson, AJet al. (2008) Estimation of typical food portion sizes for children of different ages in Great Britain. Br J Nutr 99, 13441353.CrossRefGoogle ScholarPubMed
23.Holland, B, Welch, AA, Unwin, IDet al. (1991) McCance & Widdowson's The Composition of Foods, 5th ed. Cambridge: The Royal Society of Chemistry.Google Scholar
24.Chan, W, Brown, J & Buss, DH (1994) Miscellaneous Foods. Fourth Supplement to 5th edition of McCance & Widdowson's The Composition of Foods. Cambridge: The Royal Society of Chemistry.CrossRefGoogle Scholar
25.Chan, W, Brown, J, Church, SMet al. (1996) Meat Products and Dishes. Sixth Supplement to 5th edition of McCance & Widdowson's The Composition of Foods. Cambridge: The Royal Society of Chemistry.CrossRefGoogle Scholar
26.Holland, B, Brown, J & Buss, DH (1993) Fish and Fish Products. Third Supplement to 5th edition of McCance & Widdowson's The Composition of Foods. Cambridge: The Royal Society of Chemistry.CrossRefGoogle Scholar
27.Holland, B, Welch, AA & Buss, DH (1992) Vegetable Dishes. Second Supplement to 5th edition of McCance & Widdowson's The Composition of Foods. Cambridge: The Royal Society of Chemistry.Google Scholar
28.Holland, B, Unwin, ID & Buss, DH (1992) Fruit and Nuts. First Supplement to 5th edition of McCance & Widdowson's The Composition of Foods. Cambridge: The Royal Society of Chemistry.CrossRefGoogle Scholar
29.Holland, B, Unwin, ID & Buss, DH (1991) Vegetables, Herbs and Spices. Fifth Supplement to McCance & Widdowson's The Composition of Foods, 4th ed. Cambridge: The Royal Society of Chemistry.CrossRefGoogle Scholar
30.Gorsuch, RL (1974) Factor Analyses. Philaelphia, PA: W.B. Saunders.Google Scholar
31.Kline, P (1994) An Easy Guide to Factor Analysis. London: Routledge.Google Scholar
32.Northstone, K, Emmett, P & the ALSPAC Study Team (2005) Multivariate analysis of diet in children at four and seven years of age and associations with socio-demographic characteristics. Eur J Clin Nutr 59, 751760.CrossRefGoogle ScholarPubMed
33.Northstone, K & Emmett, P (2008) Are dietary patterns stable throughout early and mid-childhood? Br J Nutr 100, 10691076.CrossRefGoogle ScholarPubMed
34.Cattell, RB (1966) The scree test for the number of factors. Multivariate Behav Res 1, 245276.CrossRefGoogle ScholarPubMed
35.Willett, WC, Howe, GR & Kushi, LH (1997) Adjustment for total energy intake in epidemiologic studies. Am J Clin Nutr 65, 4 Suppl., S1220S1228.CrossRefGoogle ScholarPubMed
36.US Department of Agriculture & US Department of Health and Human Services (2010) Dietary Guidelines for Americans 2010. Washington, DC: US Government Prininting Office.Google Scholar
37.Salgueiro, MJ, Zubillaga, MB, Lysionek, AEet al. (2002) The role of zinc in the growth and development of children. Nutrition 18, 510519.CrossRefGoogle ScholarPubMed
38.De Benoist, B, McLean, E, Egli, Iet al. (2008) Worldwide Prevalence of Anaemia 1993–2005: WHO Global Database on Anaemia. Geneva: WHO.Google Scholar
39.Johnson, L, Mander, AP, Jones, LRet al. (2008) Energy-dense, low-fiber, high-fat dietary pattern is associated with increased fatness in childhood. Am J Clin Nutr 87, 846854.CrossRefGoogle ScholarPubMed
40.Bray, GA, Paeratakul, S & Popkin, BM (2004) Dietary fat and obesity: a review of animal, clinical and epidemiological studies. Physiol Behav 83, 549555.CrossRefGoogle ScholarPubMed
41.He, FJ & MacGregor, GA (2010) Reducing population salt intake worldwide: from evidence to implementation. Prog Cardiovasc Dis 52, 363382.CrossRefGoogle Scholar
42.Arkkola, T, Uusitalo, U, Kronberg-Kippilae, Cet al. (2008) Seven distinct dietary patterns identified among pregnant Finnish women – associations with nutrient intake and sociodemographic factors. Public Health Nutr 11, 176182.CrossRefGoogle ScholarPubMed
43.Crozier, SR, Robinson, SM, Borland, SEet al. (2006) Dietary patterns in the Southampton Women's Survey. Eur J Clin Nutr 60, 13911399.CrossRefGoogle ScholarPubMed
44.Randall, E, Marshall, J, Graham, Set al. (1990) Patterns in food use and their associations with nutrient intakes. Am J Clin Nutr 52, 739745.CrossRefGoogle ScholarPubMed
45.Schulze, MB, Hoffmann, K, Kroke, Aet al. (2001) Dietary patterns and their associations with food and nutrient intake in the European Prospective Investigation into Cancer and Nutrition (EPIC) – Potsdam study. Br J Nutr 85, 363373.CrossRefGoogle ScholarPubMed
46.Patel, S, Murray, CS, Simpson, Aet al. (2011) Dietary patterns of 11-year-old children and associations with nutrient intakes. J Hum Nutr Diet 24, 399400.CrossRefGoogle Scholar
47.Gharib, N & Rasheed, P (2011) Energy and macronutrient intake and dietary pattern among school children in Bahrain: a cross-sectional study. Nutr J 10, 62.CrossRefGoogle ScholarPubMed
48.Musaiger, AO (2000) The state of nutrition in Bahrain. Nutr Health 14, 6374.CrossRefGoogle ScholarPubMed
49.Bingham, SA, Gill, C, Welch, Aet al. (1994) Comparison of dietary assessments methods in nutritional epidemiology: weighed records v. 24 h recalls, food-frequency questionnaires and estimated-diet records. Br J Nutr 72, 619643.CrossRefGoogle ScholarPubMed
50.Willett, W & Stampfer, M (1998) Implications of total energy intake for epidemiologic analysis. In Nutritional Epidemiology, 2nd ed., pp. 273–301 [W Willett, editor]. New York: Oxford University Press.CrossRefGoogle Scholar
Figure 0

Table 1 Correlation coefficients between ‘processed’ dietary pattern scores across the ages and corresponding weekly absolute nutrient intakes and partial correlation coefficients between dietary pattern scores and weekly nutrient intakes adjusting for energy intake: children aged 3–9 years (n 8010 to 10 023), Avon Longitudinal Study of Parents and Children (ALSPAC), Bristol, UK

Figure 1

Table 2 Correlation coefficients between ‘health conscious’* dietary pattern scores across the ages and corresponding weekly absolute nutrient intakes and partial correlation coefficients between dietary pattern scores and weekly nutrient intakes adjusting for energy intake: children aged 3–9 years (n 8010 to 10 023), Avon Longitudinal Study of Parents and Children (ALSPAC), Bristol, UK

Figure 2

Table 3 Correlation coefficients between ‘traditional’ dietary pattern scores across the ages and corresponding weekly absolute nutrient intakes and partial correlation coefficients between dietary pattern scores and weekly nutrient intakes adjusting for energy intake: children aged 3–9 years (n 8010 to 10 023), Avon Longitudinal Study of Parents and Children (ALSPAC), Bristol, UK

Figure 3

Table 4 Proportion of variance (%) explained for each nutrient by age at which dietary patterns were assessed: children aged 3–9 years (n 8010 to 10 023), Avon Longitudinal Study of Parents and Children (ALSPAC), Bristol, UK