© 2005 American Public Health Association DOI: 10.2105/AJPH.2003.035592
All of the authors are at the Department of Social Medicine, University of Bristol, Bristol, England. Correspondence: Requests for reprints should be sent to Debbie A. Lawlor, Department of Social Medicine, University of Bristol, Canynge Hall, Whiteladies Road, Bristol BS8 2PR, England (e-mail: d.a.lawlor{at}bristol.ac.uk).
Objectives. We sought to determine whether residential area deprivation, over and above the effect of life-course socioeconomic status or position (SEP), is associated with coronary heart disease. Methods. We conducted a cross-sectional analysis of 4286 women aged 60 to 79 years from 457 British electoral wards. Results. After adjustment for age and 10 indicators of individual life-course SEP, the odds of coronary heart disease was 27% greater among those living in wards with a deprivation score above the median compared with those living in a ward with a deprivation score equal to or below the median (odds ratio=1.27; 95% confidence interval=1.02, 1.57). Conclusions. Adverse area-level socioeconomic characteristics, over and above individual life-course SEP, are associated with increased coronary heart disease.
The idea that where one lives is important for ones health is not new.1 However, there is debate regarding whether the characteristics of where people live (contextual effects) have an important influence on health independent of the characteristics of the people living in these areas (compositional effects).2,3 The relevance of this issue is that if variations in health between areas can be entirely explained by the personal characteristics of the inhabitants of these areas, policymakers need act only on improving the circumstances of individuals. Conversely, the demonstration of independent area-level effects would emphasize the need to focus interventions on features of the areas where people live, not just on the individuals living there. This is important because the widening gap between the rich and the poor appears to be mirrored by a growing divergence of their residential environments, such that affluent people are increasingly living and interacting with other affluent people in affluent areas, whereas the poor increasingly live and interact with other poor people in more economically and socially deprived areas.4 The occurrence of coronary heart disease (CHD) varies geographically,57 and CHD is strongly influenced by individual socioeconomic status or position (SEP).8,9 Six studies have examined the effect of socioeconomic context on CHD by determining the effect of residential area deprivation, having adjusted for individual measures of SEP, and all 6 found moderate effects.1015 However, only 3 studies10,14,15 adjusted for more than 1 individual measure of SEP. In such studies, it is likely that adjustment for only 1 or 2 indicators of an individuals SEP fails to capture the full complexity of their experience over the life course, leading to residual confounding by individual SEP rather than true contextual effects.3,1619 Among studies assessing the contextual effects of SEP on all-cause mortality, the only study to adjust for individual SEP in childhood and adulthood found little remaining area-level effect,20 suggesting that for all-cause mortality at least there may be no contextual effect over and above individual effects.3 None of the studies assessing the association between socioeconomic context and CHD have adjusted for individual measures of SEP from across the life course. The aims of this study were to assess the association between individual life-course SEP and adult residential area deprivation and to determine whether area socioeconomic deprivation, over and above the effect of individual life-course SEP, is associated with prevalent CHD in women.
Study Participants Data from the British Womens Heart and Health Study were used; full details of the selection of participants and measurements have been reported previously.2123 Women aged 60 to 79 years were randomly selected from general practitioner lists in 23 British towns. A total of 4286 women (60% of the 7166 invited) participated, and baseline data (self-completed questionnaire, research nurse interview, physical examination, and primary care medical record review) were collected between April 1999 and March 2001. Local ethics committee approvals were obtained.
Outcome and Exposure Assessment Details of the longest held occupation of the participants father and husband and her own longest held occupation were requested in the self-completed questionnaire. Adult social class was derived from the longest held occupation of the participants husband for married women and the participants own longest held occupation for single women. Childhood social class was derived from the longest held occupation of the participants father. Social class was categorized into 1 of 6 social classes (social class I [professional], II [intermediate], IIInm [skilled non-manual], IIIm [skilled manual], IV [partially skilled manual], and to V [unskilled manual occupations].26 Other indicators of childhood SEP were self-reported childhood household amenities (living in a house with a bathroom, living in a house with a hot water supply, and sharing a bedroom), family access to a car as a child, and age at leaving full-time education. Other indicators of adult SEP were housing status (social housing, private rented, owner-occupied, and other), car ownership, and pension arrangements (state only, state and occupational, state and personal, and other). Full details of all anthropometric measures and measurements of lipids, blood pressure, insulin resistance (measured using the homeostasis model assessment), diabetes status, and lung function have been previously reported.21,22 Smoking was categorized as never, ex, and current smoker (including those who had given up smoking). Participants were asked to indicate their usual duration of activity in hours per week for several types of activities27 and were categorized into 1 of 3 categories of either moderate or vigorous physical activity: less than 1 hour (inactive), 1 to 2 hours, or greater than 2 hours per week.
Statistical Analysis Women in the study were randomly selected from 23 towns covering 457 electoral wards from a larger population of all wards in Britain. The data therefore form a natural hierarchy of individuals residing within electoral wards. Multilevel logistic regression was used to obtain estimates of the effects of area deprivation on CHD.28 Because the main exposure of interest is an area-level measure, its effect cannot vary across the areas, and, therefore, multilevel models with varying intercepts but fixed exposure effects were used. To assess the association between area-level socioeconomic characteristics and CHD, a series of multilevel logistic regression models were fitted with area (ward) as the level 2 clusters and individual life-course socioeconomic indicators and potential mediating factors as level 1 covariates. Homeostasis model assessment scores (insulin resistance) and triglyceride levels had positively skewed distributions, but logged values were normally distributed; geometric means were presented and logged values were used in the regression models. With these transformations, residuals were normally distributed in all models. All analyses were undertaken using Stata Version 8.0 (Stata Corp, College Station, Tex).
Missing Data
Nonresponders were slightly older and more likely to have suffered a stroke or to have diabetes but did not differ from responders with respect to myocardial infarction, angina, or cancer prevalence.23 The response proportion was similar across the 23 towns (P= .5 for effect of town on response) and across fifths of Carstairs deprivation score (P= .7 for effect of Carstairs deprivation score on response). Of the 4286 participants, 694 had CHD, yielding a prevalence of 16.2% (95% confidence interval [CI] = 15.1%, 17.3%). Across the 23 towns, the prevalence of CHD varied from 9.4% (95% CI = 5.8%, 14.1%) in Guildford in the south of England to 32.6% (95% CI = 25.0%, 41.0%) in Merthyr Tydfil in Wales. In general, towns in the southeast of England had the lowest prevalences and those in Scotland and Wales had the highest prevalences. Study participants resided in 457 electoral wards. The wards in which the women lived were those in the middle of the distribution of all wards for Britain, with the mean population size of wards in which study participants resided being 6889 (range, 175315 372). The number of women in the study residing in each of the 457 wards ranging from 1 to 112. Fifty-five (12%) of the wards contained just 1 woman from the study and 45 (10%) contained 20 or more participants. Ward-level Carstairs scores for study participants were positively skewed and ranged from 5.13 to 18.68 with a median of 0.11 (interquartile range = 2.222.34).
Table 1
All further analyses were based on the 3626 (85% of study responders) women with complete data on any variable included in any of the multilevel logistic regression models. Compared with women without these data, women with complete data did not differ substantively in their mean age (68.9 vs 69.1 years, P= .50), median ward-level Carstairs score (0.22 vs 0.15, P = .25), and CHD prevalence (16.0% vs 18.5%, P = .68). The intraclass correlation coefficient with age as the only explanatory variable in the CHD multilevel model was 0.07 (P < .001), suggesting that 7% of the variation in age-adjusted CHD was attributable to area effects. This reduced to 0.05 with addition of area-level Carstairs score.
Table 3
Main Findings In this sample of postmenopausal British women, individual measures of SEP from across the life course were associated with area-level socioeconomic characteristics. The odds of prevalent CHD increased with worsening area deprivation. This association was independent of a wide range of individual life-course indicators of SEP, and these findings provide support for the suggestion that socioeconomic context, over and above the socioeconomic characteristics of individuals living in an area (compositional effects), is associated with CHD. This independent area-level effect was attenuated by adjustment for leg length, a biomarker of childhood exposures that affect linear growth and later adult disease,22,29,30 and also by adjustment for adult lifestyle and physiological risk factors. These findings suggest that contextual socioeconomic effects on CHD are in part mediated by more proximal outcomes of childhood exposures and adult lifestyle and physiological risk factors. Area-level socioeconomic context may have a direct effect on lifestyle factors such as diet and physical inactivity in both childhood and adulthood because of a lack of neighborhood healthy food outlets, green spaces, and exercise facilities.2 Smoking may be influenced by peer pressure or the neighborhood culture and the heavy promotion of cigarettes in deprived areas.31,32 Physiological risk factors such as dyslipidemia, hypertension, and insulin resistance are influenced by these lifestyle factors.
Study Strengths and Limitations A strength of this study is that it is the first to assess the effect of area SEP on CHD with adjustment for a large range of individual measures of SEP from across the life course. Childhood SEP was associated with adult area of residence deprivation, and adjustment for indicators of childhood SEP in addition to adult indicators resulted in greater attenuation of the area effects, thus supporting the suggestion that contextual effects should be determined by adjustment for individual measures from across the life course.3 We have relied on self-report of characteristics of individual life-course SEP, and there may be some misclassification or recall bias for these covariates.35 Self-report of childhood socioeconomic circumstances in particular may be affected by reporting bias, although recall of the occupation of the head of the household and of educational attainment has been shown to be accurate among middle-aged adults.36,37 It is unlikely that recall inaccuracy of SEP would be affected by CHD status, and, therefore, any misclassification would most likely be nondifferential. This would tend to dilute the effect of individual SEP and therefore in this study may exaggerate the main effect of interestthat of the association between area SEP, having taken individual SEP into account. The inclusion of 10 different measures of individual life-course SEP and the fact that previous studies have shown that self-report of some childhood circumstances is accurate36 should mean that there would be less residual confounding attributable to individual SEP in this study than in previous studies. Because individual SEP is multifactorial, it is possible that some residual confounding by individual-level factors explains the remaining associations of area deprivation with CHD. We have no measures of household income, which is an important indicator of individual-level SEP. However, within our 10 life-course measures, we have occupational social class on 2 occasions, car access on 2 occasions, housing status, pension arrangements, and childhood household amenities, all of which are strong predictors of having material resources. This study is cross-sectional; therefore, 2 potential limitations are reverse causality and survival bias. Reverse causality would suggest that rather than the socioeconomic circumstances of the area in which one lives having an effect on CHD occurrence, the association found in this study is attributable to women with CHD migrating to poorer residential areas. A number of studies have shown that downward social mobility does not explain the association between SEP and health outcomes,9 and our findings are consistent with those of 2 prospective studies of the contextual effect of area socioeconomic circumstances on CHD,13,14 suggesting that reverse causality is unlikely to fully explain our results. Survival bias would be important if large numbers of deaths caused by CHD occurred before the age of 70 years, the mean age of study participants. Mortality resulting from CHD among British women before the age of 70 years is uncommon. For example, in England and Wales in 1999, just 3826 women between the ages of 30 and 69 years died as a result of CHD, for a mortality rate of 2.0 per 100 000 and accounting for just 6% of the total of 59 363 deaths in women in that age group.38 Furthermore, the consistency of findings here with those of prospective studies13,14 suggests that survival bias is unlikely to fully explain our results.
Implications
The British Womens Heart and Health Study is funded by the Department of Health and British Heart Foundation. Debbie A. Lawlor is funded by a UK Department of Health Career Scientist Award. The British Womens Heart and Health Study is codirected by Shah Ebrahim, Peter Whincup, Goya Wannamethee, and Debbie A. Lawlor. We thank Carol Bedford, Alison Emerton, Nicola Frecknall, Karen Jones, Mark Taylor, and Katherine Wornell for collecting and entering data; all of the general practitioners and their staff who have supported data collection; and the women who have participated in the study. Note. The views expressed in this publication are those of the authors and not necessarily those of any of the funding bodies.
Human Participant Protection
Contributors D. A. Lawlor, G. Davey Smith, and S. Ebrahim developed the study aim. S. Ebrahim and D. A. Lawlor manage data collection, storage, and cleaning for the British Womens Heart and Health Study. R. Patel maintains the study database and abstracted data for the deprivation scores. D. A. Lawlor undertook the analysis and coordinated writing of the article. All authors contributed to the final version. Accepted for publication February 19, 2004.
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