Hostname: page-component-586b7cd67f-2plfb Total loading time: 0 Render date: 2024-11-22T20:20:00.993Z Has data issue: false hasContentIssue false

The relative importance of socioeconomic indicators in explaining differences in BMI and waist:hip ratio, and the mediating effect of work control, dietary patterns and physical activity

Published online by Cambridge University Press:  21 May 2010

Marte Råberg Kjøllesdal*
Affiliation:
Department of Nutrition, Institute for Basic Medical Sciences, University of Oslo, PB 1046 Blindern, 0316Oslo, Norway
Gerd Holmboe-Ottesen
Affiliation:
Department of General Practice and Community Medicine, Institute of Health and Society, University of Oslo, PB 1130 Blindern, 0318Oslo, Norway
Annhild Mosdøl
Affiliation:
Section for Health, Nutrition and Management, Akershus University College, PB 423, 2001Lillestrøm, Norway
Margareta Wandel
Affiliation:
Department of Nutrition, Institute for Basic Medical Sciences, University of Oslo, PB 1046 Blindern, 0316Oslo, Norway
*
*Corresponding author: M. Råberg Kjøllesdal, email [email protected]
Rights & Permissions [Opens in a new window]

Abstract

Socioeconomic differences in overweight are well documented, but most studies have only used one or two indicators of socioeconomic position (SEP). The aim of the present study was to explore the relative importance of indicators of SEP (occupation, education and income) in explaining variation in BMI and waist:hip ratio (WHR), and the mediating effect of work control and lifestyle factors (dietary patterns, smoking and physical activity). The Oslo Health Study, a cross-sectional study, was carried out in 2000–1, Oslo, Norway. Our sample included 9235 adult working Oslo citizens, who attended a health examination and filled in two complementary FFQ with < 20 % missing responses to food items. Four dietary patterns were identified through factor analysis, and were named ‘modern’, ‘Western’, ‘traditional’ and ‘sweet’. In multivariate models, BMI and WHR were inversely associated with education (P < 0·001/P < 0·001) and occupation (P = 0·002/P < 0·001), whereas there were no significant associations with income or the work control. The ‘modern’ (P < 0·001) and the ‘sweet’ (P < 0·001) dietary patterns and physical activity level (P < 0·001) were inversely associated, while the ‘Western’ dietary pattern (P < 0·001) was positively associated with both BMI and WHR. These lifestyle factors could not fully explain the socioeconomic differences in BMI or WHR. However, together with socioeconomic factors, they explained more of the variation in WHR among men (21 %) than among women (7 %).

Type
Full Papers
Copyright
Copyright © The Authors 2010

The increasing prevalence of overweight and obesity has become a major health challenge worldwide(1). Obesity is associated with increased incidence of several chronic diseases, such as CVD, type 2 diabetes and some cancers(Reference Bogers, Bemelmans and Hoogenveen2Reference Qian and Fan6), and the increased risk seems to be particularly associated with central obesity(Reference Walker, Rimm and Ascherio7, Reference Lakka, Lakka and Tuomilehto8). Thus, combating the rise in obesity is a key to disease prevention. The prevalence of overweight and obesity and increase in body weight show socioeconomic differences in developed countries, with less favourable outcomes in the lowest socioeconomic groups(Reference Molarius, Seidell and Sans9Reference Sobal and Stunkard12). However, most of the studies have explored only one or two of the most widely used indicators of socioeconomic position (SEP): education, income and occupation. These indicators are related, but reflect different aspects of the association between SEP and health. Education represents an individual's knowledge-related assets, and is a strong predictor of occupation and income(Reference Galobardes, Lynch and Smith13). Income reflects material circumstances which may form the basis for a health-promoting environment and access to health care(Reference Galobardes, Lynch and Smith13). Occupation is a predictor of social relations and different privileges and facilities(Reference Galobardes, Lynch and Smith13). Psychosocial working conditions are found to vary with occupation(Reference Karasek, Brisson and Kawakami14). Employees with lower SEP are more likely to experience job insecurity, lower work control and heavier work strain than others(Reference Siegrist and Marmot15). Previous research suggests that low work control and work strain are associated with overweight(Reference Lallukka, Lahelma and Rahkonen16Reference Hellerstedt and Jeffery19), possibly due to elevated cortisol levels over time(Reference Kunz-Ebrecht, Kirschbaum and Steptoe20, Reference Rosmond and Bjorntorp21). However, the evidence regarding the association between work control and weight is unclear(Reference Reed, LaCroix and Karasek22, Reference Brisson, Larocque and Moisan23).

Change in body weight is a function of dietary intake and physical activity patterns. Dietary pattern analysis has become a commonly used method to study diet–disease relationships, as it aims at characterising and examining health effects of the overall diet rather than of single food items or nutrients(Reference Hu24). Several studies have shown that the distributions of dietary patterns vary with SEP, and that higher SEP tends to be associated with healthier dietary patterns(Reference Engeset, Alsaker and Ciampi25Reference Tseng and DeVellis28). A few studies have investigated the relationship between overweight, SEP and single dietary indicators(Reference Wamala, Wolk and Orth-Gomer18, Reference Martikainen and Marmot29, Reference Purslow, Young and Wareham30), but few have explored the overall diet, using dietary pattern analyses(Reference Kesse-Guyot, Bertrais and Peneau27, Reference Ball, Mishra and Crawford31).

There is a general agreement that the way societies are organised can impact health(Reference Mackenbach, Marmot and Siegrist32). Social democratic welfare state models are characterised by egalitarian institutional features producing egalitarian outcomes. They are expected to have on average good health and small differences in health between different socioeconomic groups(Reference Mackenbach, Marmot and Siegrist32). However, the results obtained from studies on health inequalities in such countries are inconsistent. Whether such a state model can serve as a positive example of how health is depending on organisation of society, and which factors are the most influential in determining health and health inequalities, is still unclear(Reference Mackenbach, Marmot and Siegrist32). In the present paper, we have used data obtained from the Oslo Health Study to explore the relative importance of three indicators of SEP (education, income and occupation) in explaining the variation in BMI and waist:hip ratio (WHR), and the possible mediating effect of work control and lifestyle variables (dietary patterns, smoking and physical activity) in a welfare society such as Norway. We have hypothesised that all the three indicators of SEP are inversely related to BMI and WHR, with education being the most important. Furthermore, we assume that work control can to a large extent mediate the differences in BMI and WHR related to occupation, while the lifestyle factors can explain a significant proportion of the variation associated with all the three indicators of SEP.

Experimental methods

Design

The Oslo Health Study was conducted in 2000–1 by the National Institute of Public Health, the Oslo City Council and the University of Oslo. An invitation to participate in the health survey was sent to all men and women born in the following years: 1924, 1925, 1940, 1941, 1955, 1960 and 1970, who had been residing in Oslo on 31 December 1999. Those moving into Oslo between this date and 3 March 2000 were invited as part of the follow-up reminder. A health examination was conducted at a central screening station, and it included anthropometric measurements. The participants received a questionnaire with the letter of invitation by mail, and received another two questionnaires at the screening station, which they completed at home and returned in a prepaid envelope. The study is described in detail at http://www.fhi.no/hubro-en.

The present study was conducted according to the guidelines laid down in the Declaration of Helsinki, approved by the Norwegian Data Inspectorate and cleared by the Regional Committee for Medical Research Ethics. Written informed consent was obtained from all the subjects/patients.

Sample

Since the present study included variables related to work, only people of working age (30–60 years, the birth cohorts from 1940, 1941, 1955, 1960 or 1970) were selected. This is also an age range were most had completed their education. Of 34 151 invited persons, 15 186 underwent the health examination, and/or answered at least one of the questionnaires. The overall attendance rate was 44·5 %, and varied from 55·4 % among the oldest participants to 36·1 % among the youngest participants. For this analysis, 19 % were excluded because they had not returned both questionnaires containing food frequency questions, and a further 8 % were excluded due to ≥ 20 % missing responses to the food frequency items. The excluded participants were less likely than those included to be females (P < 0·001), born in 1940/41 (P < 0·001), and from the highest educational group (P < 0·001). However, the two groups were similar in income distribution. Participants of non-Western origin (687 persons) were excluded due to expected ethnic differences in the distribution of body fat(Reference Deurenberg-Yap, Schmidt and van Staveren33) and in dietary patterns (M Råberg Kjøllesdal, G Holmboe-Ottesen and M Wandel, 2009, unpublished results). Those with no reported work (1154 persons) were also excluded. There were no significant differences in BMI or WHR between those with and without reported work (data not shown). The sample without work had a larger proportion in the lowest educational group than the others (P = 0·019). The findings were similar regarding income groups (P < 0·001). The total number of persons included in the analyses was 9235.

Anthropometry

Body weight (in kg, one decimal) and height (in cm, one decimal) were measured using an electronic height and weight scale, with the participants wearing light clothing without shoes. BMI (kg/m2) was calculated based on weight and height. Both waist and hip circumferences were measured using a measuring tape made of steel. Waist circumference was measured at the umbilicus to the nearest centimetre with the subject standing and breathing normally. In obese individuals, waist circumference was defined as the midpoint between the iliac crest and lower margin of ribs. Hip circumference was measured as the maximum circumference around the buttocks. Waist and hip circumferences were used to calculate the WHR using the formula: waist circumference (cm)/hip circumference (cm).

Food frequency questions

The questionnaires contained questions about eighty-two food-related items (sixty-eight food items, thirteen drink categories and two categories of supplements). The questions covered intake of bread (slices per day for three categories), bread spreads (no portion size, response categories: ‘seldom/never’, ‘1–2 times/week’, ‘3–4 times/week’, ‘5–7 times/week’ and ‘several times/d’), dinner dishes, sauces/dressings, cakes/sweets, fats (no portion size, response categories: ‘seldom/never’, ‘1–3 times/month’, ‘1–2 times/week’, ‘3–4 times/week’ and ‘5–7 times/week’), fruit, vegetables (no portion size, response categories: ‘seldom/never’, ‘1–3 times/month’,‘1–3 times/week’, ‘4–6 times/week’, ‘1–2 times/d’ and ‘ ≥ 3 times/d’), and milk, fruit juice and soft drinks (in glasses, response categories: ‘seldom/never’, ‘1–6 times/week’, ‘1 time/d’, ‘2–3 times/d’ and ‘ ≥ 4 times/d’). The food frequency questions have earlier been validated against intake of the matching food/food group based on a 14 d diet diary(Reference Mosdøl34). The Spearman rank correlation coefficients between responses to the FFQ items and corresponding intake over 14 d were in the range of 0·3–0·7 for the items included in the food pattern analyses. All items were recoded into times/week before being included into the factor analysis. Missing values (2·3 % of values) for the food items were replaced with the lowest value (‘seldom/never’). Sixty-seven non-overlapping food items from the food frequency questions were included in the factor analysis.

Socioeconomic and demographic factors

Education was recoded from the number of years into three groups according to the Norwegian education system: ‘ ≤  high school’ ( ≤ 12 years), ‘lower college/university’ (13–16 years) and ‘higher college/university’ ( ≥ 17 years). Personal annual income was recorded in eight categories, and recoded into three groups: ‘0–200 000 Norwegian Krone (NOK)’ (0–25 000 €), ‘200 000–300 000 NOK’ (25 000–38 000 €) and ‘>300 000 NOK’ (>38 000 €). The occupational groups were constructed after the Erikson–Goldthorpe scheme with seven categories(Reference Erikson35), which are as follows:

  1. (I) Higher grade professionals, administrators and officials; managers in large industrial establishments and large proprietors.

  2. (II) Lower grade professionals, administrators and officials; higher grade technicians; managers in small industrial establishments and supervisors of non-manual employees.

  3. (III) Routine non-manual employees: higher and lower grade.

  4. (IV) Small proprietors, artisans, farmers and smallholders, and other self-employed workers in primary production.

  5. (V) Lower grade technicians and supervisors of manual workers.

  6. (VI) Skilled manual workers.

  7. (VII) Semi- and unskilled manual workers.

The seven occupational groups were collapsed into four categories for use in the regression analyses: higher grade or lower grade professionals (groups I and II); routine non-manual employees (group III); artisans and self-employed workers in primary production (group IV); and manual workers (groups V–VII). Control over own working situation was assessed through a question about being able to make decisions about how to organise work, and was recoded from four categories to 1 = ‘never/seldom’, 2 = ‘most often’ and 3 = ‘always’.

In addition to sex, the following demographic and lifestyle variables were used. Birth cohorts were divided into three categories, labelled according to age at the time the study was carried out: ‘30 years’, ‘40/45 years’ and ‘59/60 years’. Number of children born was controlled for as a continuous variable (women only) due to its possible effects on weight status and especially WHR. Physical activity was assessed through the question ‘can you describe your spare time activity?’, with the answer categories ‘read, watch television, other activities done sitting’, ‘walk, cycle or move in other ways ≥ 4 h/week’, ‘exercise, heavy garden work ≥ 4 h/week’ and ‘competitive sports or heavy exercise several times a week’. The last two categories were merged into one category in the analyses. Smoking was recoded to 0 = ‘no’ (never or former smoker) and 1 = ‘yes’ (current smoker).

Analyses

Data were analysed in SPSS 14.0 (SPSS, Chicago, IL, USA). The dietary patterns were identified using factor analysis with Varimax rotation. A Scree plot was used to decide a four-factor solution, and all factors had an eigenvalue >2. Each food item used to characterise a pattern had factor loadings of 0·35 or more. Labelling of the factors was based on our interpretation of the factor structures. Factor scores were divided into tertiles.

The χ2 and one-way ANOVA tests were used to find differences between men and women and participants in different tertiles of dietary patterns. Multiple linear regressions were carried out to explore the associations between BMI/WHR and SEP, with BMI or WHR, respectively, as the dependent variable. Model 1 included demographic variables (sex, birth cohort and number of children born) as independent variables, model 2 included in addition SEP indicators (education, income and occupation), and model 3 also included work control and lifestyle variables (dietary patterns, physical activity and smoking). The dietary patterns were analysed as linear variables in the regression analyses. The associations between BMI/WHR and the independent variables were also analysed in crude models and adjusted for demographic variables only, but the results are not given in the tables. For the trend tests, the number of years with education and the eight initial response categories for income were used. For the trend analyses of occupational status, the self-employed workers were excluded because they do not fit a hierarchical order. All independent variables were checked for multicollinearity, and there were no problems regarding this. Significance level was set to P < 0·05. It should be kept in mind that because of the large number of observations, statistical tests of significance are quite sensitive.

Results

Characterisation of sample

The distribution of the sample into socioeconomic groups and weight status is given in Table 1. About one-third had lower education and one-third had higher education from university/college (both sexes). More than half of the men and about a quarter of the women had an annual income above 300 000 NOK. Almost two-thirds of the women were employed in routine non-manual work, while close to one-third of the men were employed in the highest occupational group. More men than women had control over how their work was organised always, while almost one-third of the women seldom/never had such control. The largest proportion of persons with complete control over organisation of own work was found among the self-employed workers (women 53·5 % and men 55·4 %), followed by the higher and lower grade professionals (women 18·3 % and men 23·1 %). The highest proportion of participants reporting seldom/never to be able to organise own working situation was recorded among manual workers (women 51·2 % and men 34·5 %; data not shown). About one-quarter of the women and almost half of the men were overweight, and obesity was observed in about 15 % of the men and slightly less among women. Mean BMI was 25·0 kg/m2 (sd 4·28) among women and 26·5 kg/m2 (sd 3·66) among men, and mean WHR was 0·79 (sd 0·07) among women and 0·90 (sd 0·07) among men. Number of children born per woman was on average 1·3 (sd 1·17).

Table 1 Distribution of demographic and socioeconomic groups, control over own working situation and proportion of overweight and obese, by sex

NOK, Norwegian Krone.

* Difference in distribution between women and men.

Characterisation of dietary patterns

We identified four dietary patterns through factor analysis. The ‘modern’ dietary pattern was characterised by high factor loadings for frequent use of vinaigrette, oil for cooking, sour cream, raw vegetables, spaghetti/macaroni/pasta, dishes with chicken and rice (Table 2). The ‘Western’ dietary pattern loaded high on béarnaise sauce, coleslaw, mayonnaise, gravy, hot dog/hamburger, salami, chips, melted butter on dinner dishes, potato salad/mashed potato, red meat and cream-based sauce. The ‘traditional’ diet was characterised by boiled potatoes, dishes with fish, cooked vegetables and fish as sandwich spread, and by negative loadings for chips, spaghetti/macaroni/pasta, crisps and pizza. The ‘sweet’ pattern had high factor loadings for cakes/sweet biscuits, desserts, buns, jam, chocolate/sweets, ice cream, Danish pastry and waffles. These four patterns explained 20 % of the total variance.

Table 2 Results obtained from factor analysis*

*  Factor loadings ≥ 0·35 are presented.

Fig. 1 shows the mean BMI in the tertiles of the different dietary patterns. The ‘modern’ and the ‘sweet’ dietary patterns were inversely associated with BMI, whereas the ‘Western’ and the ‘traditional’ patterns were positively associated.

Fig. 1 Mean measured BMI (unadjusted) in each tertile of different dietary patterns. Trend for difference between tertiles: ‘modern’, ‘Western’ and ‘sweet’, P < 0·001; ‘traditional’, P = 0·003. , Lowest; , medium; □, highest.

BMI and waist:hip ratio

Table 3 shows the associations between BMI and the demographic, socioeconomic and mediating factors in three multiple regression models. Men had higher BMI than women, and BMI was higher in the older birth cohorts (model 1). Duration of education and occupational group were inversely associated with BMI when adjusted for each other and for income (model 2), and also when further adjusted for the mediating factors (model 3). Income was positively associated with BMI in the bivariate analyses (P for trend = 0·002), but it was not so when adjusted for demographic factors (model 1) and further for socioeconomic factors (model 2). The explained variance when adding only education to model 1 was 0·07 (data not shown). Adding occupation and income to the model did not change this figure significantly. Work control was significantly associated with BMI when adjusted for demographic factors only (P = 0·021, data not shown), but it was not (P = 0·729) so in a model with the socioeconomic variables included. The four dietary pattern scores, physical activity level and smoking status contributed independently to the variation in BMI in the full model. The ‘modern’, ‘traditional’ and ‘sweet’ dietary patterns were inversely associated with BMI, whereas the ‘Western’ pattern was positively associated.

Table 3 Associations between measured BMI and demographic factors (model 1), socio-economic position (SEP) (model 2) and mediating factors (model 3) in multiple linear regressions

(B values and 95 % confidence intervals)

ref., Reference; NOK, Norwegian Krone.

*  Mean values were significantly different from reference category for each variable (P < 0·001). All the variables included in each model are mutually adjusted.

The models exploring the variation in WHR in relation to demographic, socioeconomic and mediating factors were similar to the analyses of BMI in the magnitude and direction of associations (Table 4). Unlike for BMI, however, the traditional dietary pattern was not significantly associated with WHR. Adding only education to model 1 gave an explained variance of 0·45 (data not shown). This figure increased to 0·46 when adding occupation into the model. Work control was significantly associated with WHR when adjusted for demographic factors (P = 0·027), but it was not so after additional adjustment for socioeconomic factors (P = 0·31).

Table 4 Associations between measured WHR and demographic factors (model 1), socio-economic position (SEP) (model 2) and mediating factors (model 3) in multiple linear regressions

(B values and 95 % confidence intervals)

WHR, waist:hip ratio; ref., Reference; NOK, Norwegian Krone.

*  Mean values were significantly different from reference category for each variable (P < 0·001). All the variables included in each model are mutually adjusted.

The analyses were also repeated stratified by sex, and all the significant associations were similar for each sex separately. However, the R 2 for the full model was 0·07 for WHR among the women and 0·21 among the men. The R 2 for the full model was 0·09 for BMI among the women and 0·10 among the men. In addition, for BMI, the incremental R 2 from model 1 to model 3 was 6 % for women and 8 % for men, whereas the incremental R 2 for WHR was 3 % for women and 8 % for men.

To illustrate what these results would mean in real terms, we calculated the difference in kilogram between persons in different categories of the variables in model 3 (Table 3) using mean height for the sample. Being in the reference categories for all other variables, the difference in kilogram between two persons in the highest and lowest educational groups would be 2·3 kg. If we consider a person in the highest educational, income and occupational groups, compared with a person in the lowest groups, the difference would be 4·0 kg. By running the same analyses with the dietary patterns in tertiles, we calculated that the difference between two persons in the highest and the lowest tertiles of the Western pattern, being similar in all other variables, would be 1·1 kg.

Discussion

The results showed significant socioeconomic differences in BMI and WHR. However, the associations with income were to some extent mediated by occupation and education. Lifestyle factors contributed independently to the variation, but could not alone explain the socioeconomic differences.

The strength of the Oslo Health Study is the large population-based sample from different birth cohorts, with the extensive data collection including food frequency questions, factual and not reported anthropometric measures and questions about working conditions and SEP. An analysis of the non-attendants found a somewhat higher attendance rate among females (OR 1·32) and persons with higher age (OR 2·20 for 59–60 years compared with 30 years), education (OR 1·46 for education from college or university compared with ≤ 9 years) and annual income (OR 1·52 for ≥ 400 000 NOK compared with < 100 000 NOK), but the results were concluded to be viewed as robust(Reference Sogaard, Selmer and Bjertness36). Furthermore, since associations rather than prevalence were the focus of the present study, the low response rate should be of less concern. However, the lower attendance rates among the lower socioeconomic groups, together with a higher likelihood of excluded participants to belong to lower educational and income groups, may have resulted in an underestimation of the socioeconomic differences in weight status. This situation may also have influenced the cutoffs for education, as the number reporting education for ≤ 9 years were too few to make a separate category. Previous research has shown that the association between weight status and education level in Norway is relatively linear down to 9 years of education(37). The occupational groups were adapted from the Erikson–Goldthorpe scheme, and were not aggregated according to numbers in each group. Regarding income, the cutoff for the lowest group was rather low. Thus, the lower attendance in the lower SEP groups is not likely to have impacted the categorisation of occupation and income in the same way as it impacted education. With regard to the dietary patterns, factor analysis is an a posteriori research approach, which means that the results reflect observed rather than optimal dietary patterns. Given the cross-sectional design of the study, causal inference should be done with care. For example, we do not know if the dietary patterns observed cause overweight or if weight status leads people to adopt certain eating habits. Neither can we conclude whether SEP influences body weight, or vice versa.

Socioeconomic position

Our study confirms previous findings that there are socioeconomic differences in BMI/WHR, with more overweight and obesity in lower socioeconomic groups(Reference Molarius, Seidell and Sans9, Reference Rosmond and Bjorntorp10, Reference Sobal and Stunkard12, Reference Roskam and Kunst38). It also confirms that these socioeconomic inequalities are more strongly associated with education or occupation than with income in Norway(Reference Dahl, Fritzell, Lahelma, Marmot and Siegrist39). However, even if occupation was significantly associated with BMI/WHR, it could not explain variation in BMI/WHR beyond what was explained by education. The strong predictive value of education in occupation, and thereby also in income, may explain the absent or small incremental R 2 when adding the latter two variables to model 1. Income is possibly associated with age, reflecting years in work life, and sex, which may explain the attenuation of the association between income and BMI.

A Spanish study(Reference Martin, Nieto and Ruiz40) analysed the relationship between education, employment status (employed, unemployed, retired, domestic work and student), income and marital status and the presence of overweight using logistic regression. The study found inverse associations between overweight and both education and income. It also found an inverse relationship between overweight and being employed. Our study included only the working population, but a one-way ANOVA test between those with and without a reported work showed no significant difference in BMI between the two groups. However, the group without any reported work may have other characteristics and correlates with BMI that have to be taken into account when considering factors influencing overweight for the whole population.

The variables in model 3 explained more of the variation in WHR than in BMI, but when stratified for sex, the explained variance in WHR was larger than that in BMI only for men. A possible explanation for this finding can be the tendency of central obesity to be more of a problem among men than among women. Furthermore, the incremental R 2 from model 1 to model 3 was larger for men than for women regarding both BMI and WHR, which may be due to a more general awareness about healthy eating and ideal of slimness among women than among men, regardless of SEP.

Control over own working situation

Perceived work control was inversely associated with BMI and WHR when adjusted for demographic factors, but it was not so when adjusted for socioeconomic factors. Overgaard et al. (Reference Overgaard, Gyntelberg and Heitmann41) did a review regarding work control and BMI/central obesity. They found no evidence to conclude that low work control is associated with BMI, and found few and inconsistent associations between work control and central obesity. In the Whitehall II study(Reference Brunner, Chandola and Marmot17), a dose–response relationship between work stress and BMI was found, and also a significant association between work stress and central obesity was found. The measure of work stress in the Whitehall II study was a composite measure of decision latitude, job demands and social support at work, taking into account a wider range of the psychosocial circumstances at work than those that were taken into account in the present study. This was NS while analysing the association between central obesity and decision latitude only(Reference Brunner, Chandola and Marmot17). The diverging results may also be due to the way in which work control had been measured, and other factors were controlled for. In addition to stress hormones(Reference Rosmond and Bjorntorp21), the relationship between BMI/WHR and work control may be mediated by lifestyle factors. Results obtained from a qualitative study of men in three different occupations revealed that control over the work situation could have an impact on both when and what to eat(Reference Wandel and Roos42). In the present study, the significant associations between work control and BMI disappeared when including SEP indicators into the model, suggesting that the effect of work control to some extent is determined by SEP. We also reanalysed the data using the lifestyle factors, demographic factors and work control, but not the SEP variables, as independent variables (data not shown). Both the association between work control and BMI and that between work control and WHR then turned NS. This suggests that the effect of working conditions on BMI/WHR is mediated by lifestyle factors. However, as SEP is also associated with lifestyle(Reference Engeset, Alsaker and Ciampi25, Reference Robinson, Crozier and Borland43, Reference Watt, Carson and Lawlor44), lifestyle may mediate the effect of both SEP and work control on BMI/WHR.

Dietary patterns

The ‘traditional’ dietary pattern was positively associated with BMI in the bivariate analyses (Fig. 1), but it was inversely associated with BMI in the multivariate model (Table 3). This pattern is probably associated with several variables in the multivariate model. Boiled potatoes and cooked vegetables are traditional foods in Norway, and are more likely to be consumed by elderly people. In addition, previous research has shown that these food items are more frequently consumed by those in the lower socioeconomic groups(Reference Wandel, Fagerli and Kjaernes45).

The most unexpected association was the inverse association between a sweet dietary pattern and BMI/WHR. This could be due to the fact that slim subjects are less restricted than overweight persons in eating sweets generally perceived as unhealthy, but this could also be due to more underreporting in general, and selective underreporting of such foods among heavier subjects. A similar sweet dietary pattern has been observed in several studies(Reference Newby and Tucker46), however, with inconsistent associations with weight status. Shi et al. (Reference Shi, Hu and Yuan47) found an inverse association between a sweet dietary pattern and central obesity, and suggested that this may be due to a negative association between this pattern and total energy intake. An inverse association has also been reported by Schulze et al. (Reference Schulze, Hoffmann and Kroke48), whereas others have found no significant association(Reference Newby, Muller and Hallfrisch49).

The positive association between BMI and a Western dietary pattern supports previous findings from studies describing similar patterns loading high on high-fat foods and red and processed meat(Reference Slattery, Boucher and Caan50, Reference Murtaugh, Herrick and Sweeney51). Several previous analyses of dietary patterns have found that prudent or healthy patterns are associated with lower BMI(Reference Murtaugh, Herrick and Sweeney51Reference Hu, Rimm and Stampfer55). Our two patterns labelled ‘modern’ and ‘traditional’ have similarities with these patterns, with high loadings of vegetables(Reference Murtaugh, Herrick and Sweeney51, Reference Quatromoni, Copenhafer and D'Agostino53Reference Hu, Rimm and Stampfer55) and poultry(Reference Quatromoni, Copenhafer and D'Agostino53, Reference Hu, Rimm and Stampfer55) and of vegetables(Reference Murtaugh, Herrick and Sweeney51, Reference Quatromoni, Copenhafer and D'Agostino53Reference Hu, Rimm and Stampfer55), fish(Reference Hu, Rimm and Stampfer55) and less fast food(Reference Newby, Muller and Hallfrisch52), respectively. Some of these studies have found associations with weight status over time; larger increases in BMI were found for those adhering to dietary patterns characterised by high intake of fats, sweets, desserts, meat, mixed dishes and sweetened beverages, and smaller increases were found among those adhering to patterns characterised by high loadings for food items such as fruit, vegetables, and low-fat and high-fibre foods(Reference Newby, Muller and Hallfrisch52, Reference Quatromoni, Copenhafer and D'Agostino53). This indicates that weight change follows lifestyle dietary changes. Furthermore, Newby et al. (Reference Newby, Weismayer and Akesson56) found favourable changes in BMI over time in persons increasing their intake of vegetables and other foods with high loadings in a healthy dietary pattern. However, research regarding associations between dietary patterns and weight status is inconsistent(Reference Togo, Osler and Sorensen57). For example, Kesse-Guyot et al. (Reference Kesse-Guyot, Bertrais and Peneau27) found a prudent diet to be inversely associated with waist circumference, but positively associated with overweight. Newby et al. (Reference Newby, Muller and Hallfrisch52) found a healthy dietary pattern, with similarities to our ‘traditional’ pattern, to be associated with lower waist circumference, which was not observed in the present study.

All dietary patterns in our study were significantly associated with BMI and/or WHR in different ways. Still, they could not, together with physical activity and smoking, fully explain the socioeconomic differences in BMI/WHR. Among civil servants in the Whitehall II study(Reference Martikainen and Marmot29), a larger gain in BMI over time in the lower socioeconomic groups was partly explained by differences in dietary patterns and physical activity. Both the Whitehall II study and the present study confirm that various lifestyle factors, but also other factors and circumstances, are important contributors to socioeconomic inequalities in weight and central obesity. However, our four dietary patterns explained about 20 % of the variation in the diet, and may not fully capture all the important aspects of how diet can be related to the socioeconomic disparities in health. The demographic and socioeconomic factors, together with work control and traditional lifestyle factors, explained more of the variation in WHR than in BMI. WHR has been found to be more strongly associated with the risk of chronic diseases than BMI(Reference Welborn, Dhaliwal and Bennett58, Reference Hu, Xie and Fu59), implying that it can be more useful to focus on the factors associated with WHR in health promotion work.

Conclusions

BMI and WHR are more strongly associated with education and occupation than with income, and the latter was to some extent mediated by the other two measures of SEP. There were no strong associations between work control and BMI/WHR beyond what could be explained by SEP. Traditional lifestyle factors, such as dietary patterns, physical activity and smoking, could not fully explain socioeconomic differences in weight, even if they are independently associated with BMI/WHR. Further research is needed to explore other factors which can explain socioeconomic differences in BMI and WHR.

Acknowledgements

The data collection was done as part of the Oslo Health Study carried out in 2000–1 as a collaboration between the National Institute of Public Health, the Oslo City Council and the University of Oslo. No external funding was used, and no conflict of interest exists for any of the authors. All the authors contributed in the conception and the writing of the article. Statistical analyses were executed by M. R. K.

References

1 World Health Organisation (2003) Diet, Nutrition, and the Prevention of Chronic Diseases. Joint WHO/FAO Expert Consultation. WHO Technical Report Series no. 916. Geneva: WHO.Google Scholar
2 Bogers, RP, Bemelmans, WJ, Hoogenveen, RT, et al. (2007) Association of overweight with increased risk of coronary heart disease partly independent of blood pressure and cholesterol levels: a meta-analysis of 21 cohort studies including more than 300 000 persons. Arch Intern Med 167, 17201728.CrossRefGoogle Scholar
3 Hussain, A, Claussen, B, Ramachandran, A, et al. (2007) Prevention of type 2 diabetes: a review. Diabetes Res Clin Pract 7, 317326.CrossRefGoogle Scholar
4 Must, A, Spadano, J, Coakley, E, et al. (1998) The disease burden associated with overweight and obesity. JAMA 282, 15231529.CrossRefGoogle Scholar
5 Dai, Z, Xu, YC & Niu, L (2007) Obesity and colorectal cancer risk: a meta-analysis of cohort studies. World J Gastroenterol 13, 41994206.CrossRefGoogle Scholar
6 Qian, Y & Fan, JG (2005) Obesity, fatty liver and liver cancer. Hepatobiliary Pancreat Dis Int 4, 173177.Google ScholarPubMed
7 Walker, SP, Rimm, EB, Ascherio, A, et al. (1996) Body size and fat distribution as predictors of stroke among US men. Am J Epidemiol 144, 11431150.CrossRefGoogle ScholarPubMed
8 Lakka, HM, Lakka, TA, Tuomilehto, J, et al. (2002) Abdominal obesity is associated with increased risk of acute coronary events in men. Eur Heart J 23, 706713.CrossRefGoogle ScholarPubMed
9 Molarius, A, Seidell, JC, Sans, S, et al. (2000) Educational level, relative body weight, and changes in their association over 10 years: an international perspective from the WHO MONICA Project. Am J Public Health 90, 12601268.Google ScholarPubMed
10 Rosmond, R & Bjorntorp, P (1999) Psychosocial and socio-economic factors in women and their relationship to obesity and regional body fat distribution. Int J Obes Relat Metab Disord 23, 138145.CrossRefGoogle ScholarPubMed
11 Ball, K & Crawford, D (2005) Socioeconomic status and weight change in adults: a review. Soc Sci Med 60, 19872010.CrossRefGoogle ScholarPubMed
12 Sobal, J & Stunkard, AJ (1989) Socioeconomic status and obesity: a review of the literature. Psychol Bull 105, 260275.CrossRefGoogle ScholarPubMed
13 Galobardes, B, Lynch, J & Smith, GD (2007) Measuring socioeconomic position in health research. Br Med Bull 81-82, 2137.CrossRefGoogle ScholarPubMed
14 Karasek, R, Brisson, C, Kawakami, N, et al. (1998) The Job Content Questionnaire (JCQ): an instrument for internationally comparative assessments of psychosocial job characteristics. J Occup Health Psychol 3, 322355.CrossRefGoogle ScholarPubMed
15 Siegrist, J & Marmot, M (2004) Health inequalities and the psychosocial environment – two scientific challenges. Soc Sci Med 58, 14631473.CrossRefGoogle ScholarPubMed
16 Lallukka, T, Lahelma, E, Rahkonen, O, et al. (2008) Associations of job strain and working overtime with adverse health behaviors and obesity: evidence from the Whitehall II Study, Helsinki Health Study, and the Japanese Civil Servants Study. Soc Sci Med 66, 16811698.CrossRefGoogle ScholarPubMed
17 Brunner, EJ, Chandola, T & Marmot, MG (2007) Prospective effect of job strain on general and central obesity in the Whitehall II Study. Am J Epidemiol 165, 828837.CrossRefGoogle ScholarPubMed
18 Wamala, SP, Wolk, A & Orth-Gomer, K (1997) Determinants of obesity in relation to socioeconomic status among middle-aged Swedish women. Prev Med 26, 734744.CrossRefGoogle ScholarPubMed
19 Hellerstedt, WL & Jeffery, RW (1997) The association of job strain and health behaviours in men and women. Int J Epidemiol 26, 575583.CrossRefGoogle ScholarPubMed
20 Kunz-Ebrecht, SR, Kirschbaum, C & Steptoe, A (2004) Work stress, socioeconomic status and neuroendocrine activation over the working day. Soc Sci Med 58, 15231530.CrossRefGoogle ScholarPubMed
21 Rosmond, R & Bjorntorp, P (2000) Occupational status, cortisol secretory pattern, and visceral obesity in middle-aged men. Obes Res 8, 445450.CrossRefGoogle ScholarPubMed
22 Reed, DM, LaCroix, AZ, Karasek, RA, et al. (1989) Occupational strain and the incidence of coronary heart disease. Am J Epidemiol 129, 495502.CrossRefGoogle ScholarPubMed
23 Brisson, C, Larocque, B, Moisan, J, et al. (2000) Psychosocial factors at work, smoking, sedentary behavior, and body mass index: a prevalence study among 6995 white collar workers. J Occup Environ Med 42, 4046.CrossRefGoogle ScholarPubMed
24 Hu, FB (2002) Dietary pattern analysis: a new direction in nutritional epidemiology. Curr Opin Lipidol 13, 39.CrossRefGoogle ScholarPubMed
25 Engeset, D, Alsaker, E, Ciampi, A, et al. (2005) Dietary patterns and lifestyle factors in the Norwegian EPIC cohort: the Norwegian Women and Cancer (NOWAC) study. Eur J Clin Nutr 59, 675684.CrossRefGoogle ScholarPubMed
26 Arkkola, T, Uusitalo, U, Kronberg-Kippila, C, et 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
27 Kesse-Guyot, E, Bertrais, S, Peneau, S, et al. (2009) Dietary patterns and their sociodemographic and behavioural correlates in French middle-aged adults from the SU.VI.MAX cohort. Eur J Clin Nutr 63, 521528.CrossRefGoogle ScholarPubMed
28 Tseng, M & DeVellis, RF (2001) Fundamental dietary patterns and their correlates among US whites. J Am Diet Assoc 101, 929932.CrossRefGoogle ScholarPubMed
29 Martikainen, PT & Marmot, MG (1999) Socioeconomic differences in weight gain and determinants and consequences of coronary risk factors. Am J Clin Nutr 69, 719726.CrossRefGoogle ScholarPubMed
30 Purslow, LR, Young, EH, Wareham, NJ, et al. (2008) Socioeconomic position and risk of short-term weight gain: prospective study of 14,619 middle-aged men and women. BMC Public Health 8, 112.CrossRefGoogle Scholar
31 Ball, K, Mishra, GD & Crawford, D (2003) Social factors and obesity: an investigation of the role of health behaviours. Int J Obes Relat Metab Disord 27, 394403.CrossRefGoogle ScholarPubMed
32 Mackenbach, J (2006) Socio-economic inequalities in health in Western Europe. From description to explanation to intervention. In Social Inequalities in Health: New Evidence and Policy Implications, pp. 223250 [Marmot, MG and Siegrist, J, editors]. Oxford: Oxford University Press.CrossRefGoogle Scholar
33 Deurenberg-Yap, M, Schmidt, G, van Staveren, WA, et al. (2000) The paradox of low body mass index and high body fat percentage among Chinese, Malays and Indians in Singapore. Int J Obes Relat Metab Disord 24, 10111017.CrossRefGoogle ScholarPubMed
34 Mosdøl, A (2004) Dietary assessment – the weakest link? A dissertation exploring the limitations to questionnaire based methods of dietary assessment. PhD Thesis, University of Oslo.Google Scholar
35 Erikson, R (1992) The Constant Flux: A Study of Class Mobility in Industrial Societies. Oxford: Clarendon Press.Google Scholar
36 Sogaard, AJ, Selmer, R, Bjertness, E, et al. (2004) The Oslo Health Study: the impact of self-selection in a large, population-based survey. Int J Equity Health 3, 3.CrossRefGoogle Scholar
37 The Norwegian Departments (2007) Oppskrift for et sunnere kosthold: handlingsplan for bedre kosthold i befolkningen (2007–2011) (Recipe for a More Healthy Diet. Action Plan for a More Healthy Diet in the Population (2007–2011)). Oslo: The Norwegian Departments.Google Scholar
38 Roskam, AJ & Kunst, AE (2008) The predictive value of different socio-economic indicators for overweight in nine European countries. Public Health Nutr 29, 111.Google Scholar
39 Dahl, E, Fritzell, J, Lahelma, E, et al. (2006) Welfare state regimes and health inequalities. In Social Inequalities in Health: New Evidence and Policy Implications, pp. 193222 [Marmot, MG and Siegrist, J, editors]. Oxford: Oxford University Press.CrossRefGoogle Scholar
40 Martin, AR, Nieto, JM, Ruiz, JP, et al. (2008) Overweight and obesity: the role of education, employment and income in Spanish adults. Appetite 51, 266272.CrossRefGoogle ScholarPubMed
41 Overgaard, D, Gyntelberg, F & Heitmann, BL (2004) Psychological workload and body weight: is there an association? A review of the literature. Occup Med (Lond) 54, 3541.CrossRefGoogle Scholar
42 Wandel, M & Roos, G (2005) Work, food and physical activity. A qualitative study of coping strategies among men in three occupations. Appetite 44, 93102.CrossRefGoogle ScholarPubMed
43 Robinson, SM, Crozier, SR, Borland, SE, et al. (2004) Impact of educational attainment on the quality of young women's diets. Eur J Clin Nutr 58, 11741180.CrossRefGoogle ScholarPubMed
44 Watt, HC, Carson, C, Lawlor, DA, et al. (2009) Influence of life course socioeconomic position on older women's health behaviors: findings from the British Women's Heart and Health Study. Am J Public Health 99, 320327.CrossRefGoogle ScholarPubMed
45 Wandel, M, Fagerli, R & Kjaernes, U (2001) Changes in potato consumption in different stages of life in Norway. Appetite 36, 211223.CrossRefGoogle ScholarPubMed
46 Newby, PK & Tucker, KL (2004) Empirically derived eating patterns using factor or cluster analysis: a review. Nutr Rev 62, 177203.CrossRefGoogle ScholarPubMed
47 Shi, Z, Hu, X, Yuan, B, et al. (2008) Vegetable-rich food pattern is related to obesity in China. Int J Obes (Lond) 32, 975984.CrossRefGoogle ScholarPubMed
48 Schulze, MB, Hoffmann, K, Kroke, A, et al. (2001) Dietary patterns and their association with food and nutrient intake in the European Prospective Investigation into Cancer and Nutrition (EPIC) – Potsdam study. Br J Nutr 85, 363373.CrossRefGoogle ScholarPubMed
49 Newby, PK, Muller, D, Hallfrisch, J, et al. (2004) Food patterns measured by factor analysis and anthropometric changes in adults. Am J Clin Nutr 80, 504513.CrossRefGoogle ScholarPubMed
50 Slattery, ML, Boucher, KM & Caan, BJ (1998) Eating patterns and risk of colon cancer. Am J Epidemiol 148, 416.CrossRefGoogle ScholarPubMed
51 Murtaugh, MA, Herrick, JS, Sweeney, C, et al. (2007) Diet composition and risk of overweight and obesity in women living in the southwestern United States. J Am Diet Assoc 107, 13111321.CrossRefGoogle ScholarPubMed
52 Newby, PK, Muller, D, Hallfrisch, J, et al. (2003) Dietary patterns and changes in body mass index and waist circumference in adults. Am J Clin Nutr 77, 14171425.CrossRefGoogle ScholarPubMed
53 Quatromoni, PA, Copenhafer, DL, D'Agostino, RB, et al. (2002) Dietary patterns predict the development of overweight in women: The Framingham Nutrition Studies. J Am Diet Assoc 102, 12391246.CrossRefGoogle ScholarPubMed
54 Maskarinec, G, Novotny, R & Tasaki, K (2000) Dietary patterns are associated with body mass index in multiethnic women. J Nutr 130, 30683072.CrossRefGoogle ScholarPubMed
55 Hu, FB, Rimm, EB, Stampfer, MJ, et al. (2000) Prospective study of major dietary patterns and risk of coronary heart disease in men. Am J Clin Nutr 72, 912921.CrossRefGoogle ScholarPubMed
56 Newby, PK, Weismayer, C, Akesson, A, et al. (2006) Longitudinal changes in food patterns predict changes in weight and body mass index and the effects are greatest in obese women. J Nutr 136, 25802587.CrossRefGoogle ScholarPubMed
57 Togo, P, Osler, M, Sorensen, TI, et al. (2001) Food intake patterns and body mass index in observational studies. Int J Obes Relat Metab Disord 25, 17411751.CrossRefGoogle ScholarPubMed
58 Welborn, TA, Dhaliwal, SS & Bennett, SA (2003) Waist–hip ratio is the dominant risk factor predicting cardiovascular death in Australia. Med J Aust 179, 580585.CrossRefGoogle ScholarPubMed
59 Hu, D, Xie, J, Fu, P, et al. (2007) Central rather than overall obesity is related to diabetes in the Chinese population: the InterASIA study. Obesity (Silver Spring) 15, 28092816.CrossRefGoogle ScholarPubMed
Figure 0

Table 1 Distribution of demographic and socioeconomic groups, control over own working situation and proportion of overweight and obese, by sex

Figure 1

Table 2 Results obtained from factor analysis*

Figure 2

Fig. 1 Mean measured BMI (unadjusted) in each tertile of different dietary patterns. Trend for difference between tertiles: ‘modern’, ‘Western’ and ‘sweet’, P < 0·001; ‘traditional’, P = 0·003. , Lowest; , medium; □, highest.

Figure 3

Table 3 Associations between measured BMI and demographic factors (model 1), socio-economic position (SEP) (model 2) and mediating factors (model 3) in multiple linear regressions(B values and 95 % confidence intervals)

Figure 4

Table 4 Associations between measured WHR and demographic factors (model 1), socio-economic position (SEP) (model 2) and mediating factors (model 3) in multiple linear regressions(B values and 95 % confidence intervals)