Objectives To ascertain the extent of socioeconomic and health condition inequalities in people with diagnosed and undiagnosed diabetes and impaired glucose regulation (IGR) in random samples of the general population in England, as earlier diagnosis of diabetes and treatment of people with IGR can reduce adverse sequelae of diabetes. Various screening instruments were compared to identify IGR, in addition to undiagnosed diabetes.
Design 5, annual cross-sectional health examination surveys; data adjusted for complex survey design.
Setting Random selection of private homes across England, new sample annually 2009–2013.
Participants 5, nationally representative random samples of the general, free-living population: ≥1 adult interviewed in 24 254 of 36 889 eligible addresses selected. 18 399 adults had a valid glycated haemoglobin (HbA1c) measurement and answered the diabetes questions.
Main outcome measures Diagnosed diabetes, undiagnosed diabetes (HbA1c ≥48 mmol/mol), IGR (HbA1c 42–47 mmol/mol).
Results Overall, 11% of the population had IGR, 2% undiagnosed and 6% diagnosed diabetes. Age-standardised prevalence was highest among Asian (19% (95% CI 16% to 23%), 3% (2% to 5%) and 12% (9% to 16%) respectively) and black participants (17% (13% to 21%), 2% (1% to 4%) and 14% (9% to 20%) respectively). These were also higher among people with lower income, less education, lower occupational class and greater deprivation. Education (OR 1.49 (95% CI 1.27 to 1.74) for no qualifications vs degree or higher) and income (1.35 (1.12 to 1.62) for lowest vs highest income quintile) remained significantly associated with IGR or undiagnosed diabetes on multivariate regression. The greatest odds of IGR or undiagnosed diabetes were with increasing age over 34 years (eg, OR 18.69 (11.53 to 30.28) aged 65–74 vs 16–24). Other significant associations were ethnic group (Asian (3.91 (3.02 to 5.05)), African-American (2.34 (1.62 to 3.38)) or ‘other’ (2.04 (1.07 to 3.88)) vs Caucasian); sex (OR 1.32(1.19 to 1.46) for men vs women); body mass index (3.54 (2.52 to 4.96) for morbidly obese vs not overweight); and waist circumference (2.00 (1.67 to 2.38) for very high vs low).
Conclusions Social inequalities in hyperglycaemia exist, additional to well-known demographic and anthropometric risk factors for diabetes and IGR.
- PUBLIC HEALTH
- SOCIAL MEDICINE
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Strengths and limitations of this study
This study uses a nationally representative sample of the free-living English population, with 18 399 participants, and non-response weighting.
The combination of (self-reported) diagnosis and objectively measured glycated haemoglobin allowed identification of those with undiagnosed diabetes or impaired glucose regulation.
Socioeconomic as well as health-related covariates were used to show a wide range of associations with diabetes and impaired glucose regulation.
A weakness of the study is the single point of data collection, making direction of effect sometimes hard to ascertain.
Despite the large sample, some subsample groups were small, and had correspondingly wider CIs, for example, undiagnosed diabetics (n=331), African-American (n=351), mixed (n=182) and other ethnic groups (n=122).
Diabetes is a condition that can result in significant morbidity and mortality,1 exacerbated by the latent period of several years during which diabetes is asymptomatic and may therefore remain undiagnosed.2 During this time, people are at risk of the complications of diabetes but being undiagnosed, they do not receive treatment to reduce the risks of cardiovascular or other diabetes-related diseases: at the time of diagnosis, up to 50% of people with diabetes already have microvascular and macrovascular complications.3 ,4 Early glycaemic control can reduce complications,5 so targeted testing for diabetes is advocated by Diabetes UK6 and the American Diabetes Association (ADA).7 In 2012, the National Institute for Health and Care Excellence (NICE) published guidelines recommending targeted screening to identify undiagnosed diabetes in asymptomatic populations.8
Recently, a further high-risk category has been recognised: people with impaired glucose metabolism but with blood glucose levels below the diabetic range, referred to in this paper as having impaired glucose regulation (IGR). Different definitions of IGR exist but an International Expert Committee on the role of glycated haemoglobin (HbA1c) in diagnosing diabetes suggested that people with HbA1c of 42–47 mmol/mol (6.0–6.5%)9 should be included in this group. NICE adopted this recommendation in its 2012 guidance.8 Studies have shown an annual progression rate from IGR to diabetes of 5–10%10 ,11 and that treatment can prevent or delay progression to both diabetes12–15 and its complications.16 ,17 For these reasons, NICE recommends treating people with IGR, primarily with intensive lifestyle interventions but with metformin and orlistat where lifestyle changes fail or are inappropriate.8 These guidelines have not yet been incorporated into the Quality and Outcomes Framework (QOF) for general practitioners (GPs).
Socioeconomic inequalities in health and risk factors are well known,18 as is Hart's19 inverse care law, that those at highest need are least likely to receive healthcare. Rising obesity levels, which are socially patterned,20 have been paralleled by the increasing prevalence of type 2 diabetes;21 ,22 information regarding trends in diagnosed diabetes is available from QOF and the National Diabetes Audit.23 ,24 These databases provide information about patients, so may not accurately reflect diabetes in the general population. In particular, they do not tell us about IGR or undiagnosed diabetes, nor do they provide information about social inequalities.
Nationally representative information about those with undiagnosed diabetes and IGR is required to understand, manage and reduce the potential impact of diabetes on population health. A recent report used Health Survey for England (HSE) data to count and characterise people with non-diabetic hyperglycaemia (IGR) and assess the relative utility of four risk scores.25 We hypothesised that more deprived groups are likely to have higher prevalence of IGR and undiagnosed diabetes, both for absolute prevalence and as a proportion of all cases of diabetes. The objectives of this study were to: determine the prevalence, and trends in prevalence, of diagnosed and undiagnosed diabetes and IGR in nationally representative data from the HSE; examine socioeconomic and ethnic inequalities in IGR and undiagnosed and diagnosed diabetes; and examine the health status and biomarkers for cardiovascular disease risk in people with these conditions. We also examined the summary performance characteristics of various current screening strategies.
The HSE26 is an annual, cross-sectional, general population survey of individuals living in private households in England, randomly selected by address. Data collection occurs throughout the year. The first stage is a health interview, including questions about diagnosed conditions, self-rated health, and measured height and weight. The second is a nurse visit, including further physical measurements, recording prescribed medication and taking biological samples. All adults in selected households are eligible for interview; all interviewed participants are eligible for the nurse visit and biological sampling. Most years, around 8000 adults have an interview and around 6000 a nurse visit; all data collection occurs in the participants’ own home.
For this analysis, survey data between 2009 and 2013 (during which time core questions and measurements remained comparable) were included, to ensure subsamples (particularly people with undiagnosed diabetes) were as large as possible. Research ethics approval was obtained from the relevant National Health Service (NHS) National Research Ethics Service (NRES) committees prior to starting each year's survey.
In total, 36 889 eligible households (occupied private residences) were identified, of which at least one adult was interviewed in 24 254 (66%) cooperating households. All 44 747 adults (aged 16+) in cooperating households were eligible for interview, nurse visit and blood sample: 38 761 (87%) were interviewed, 26 216 (59%) saw a nurse and 19 578 (44%) gave a blood sample. Non-response was due to non-contacts, refusals or inability to give informed consent (due to mental capacity or language difficulties) at the individual interview or nurse stage. Blood samples were not available because of refusal, unsuccessful attempts to take blood or medical reasons for ineligibility (including pregnancy, anticoagulants or recent fits).
The analytic sample comprised 18 399 adults who had a valid HbA1c measurement and answered the diabetes questions. The mean age was 51.3 years (SE 0.13); 45% were male; 53% were in households headed by managerial/professional or intermediate occupations. Four per cent had missing occupation data, 15% missing income, 8% missing body mass index (BMI), 2% missing waist circumference and <1% missing ethnicity. Missing data for these were included as separate categories, to enable inclusion of all participants. In total, 14 529 participants were normoglycaemic, 2400 had IGR, 331 had undiagnosed diabetes and 1139 diagnosed diabetes. Restricting the sample to those without diagnosed diabetes yielded 17 260 participants.
Diabetes and IGR definitions
Participants were grouped according to their HbA1c result and their answers to questions on diagnosed diabetes. Those who reported that their doctor had diagnosed them with diabetes (except only when pregnant), as well as those taking medication prescribed only for diabetes, were categorised as ‘doctor-diagnosed diabetes’. Those not diagnosed with diabetes were categorised as ‘undiagnosed diabetes’ if HbA1c was ≥48 mmol/mol (>6.5%), IGR if 42–47 mmol/mol (6.0–6.5%) and normoglycaemic if <42 mmol/mol (<6.0%).
Demographics and socioeconomic position
Age was grouped from 16 to 24 years to 75+ in 10 years age groups. Ethnicity was self-assigned from a list of the 2001 or 2011 Census categories; categories used were Caucasian, mixed, Asian, African-American and other. Equivalised household income, adjusted for the number of adults and children in the household, was divided into quintiles within each survey year. Highest educational qualification was categorised as degree or equivalent; ‘A’ levels/NVQ3 or other higher qualifications below degree level; other; and none.27 Occupational data were grouped into the five-category National Statistics-Socio-Economic Classification (NS-SEC).28 Area deprivation (the Index of Multiple Deprivation IMD 2007 for HSE 2009 and 2010, and IMD 2010 for HSE 2011–2013) was divided into survey year-specific quintiles.29 All data were self-reported except for area deprivation, which was assigned from the participant's postcode.
BMI was calculated from height and weight measured by the trained interviewers. Waist circumference was measured by the trained nurses. BMI was first categorised as underweight (<18.5 kg/m2), desirable (18.5 to <25 kg/m2), overweight (25 to <30 kg/m2), obese I (30 to <35 kg/m2), obese II (35 to <40 kg/m2) and morbidly obese (≥40 kg/m2). A second categorisation used WHO thresholds for Asian participants30 (<18, 18 to <23, 23 to <27.5, ≥27.5 kg/m2), reflecting their greater risk of diabetes at lower BMI levels. We subdivided the obese categories into 27.5 to <32.5, 32.5 to <37.5 and ≥37.5 kg/m2. Third, black participants were also categorised using those lower thresholds, as recommended by NICE in 2013.31 Similarly, waist circumference was first categorised as low (<94 cm in men, <80 cm in women), high (men 94–102 cm, women 80–88 cm) and very high (men >102 cm, women >88 cm). Second, an ethnic group-specific classification was used, where the threshold for low was <90 cm in Asian and black men but was unchanged for other men and for all women. Third, sex-independent international thresholds were used that are more stringent for men: low <88 cm, high ≥88 cm in both men and women. Finally, the NICE risk categorisation using both BMI and waist circumference was also used.32
Other health measures
Self-rated general health was based on the answer to a standard question about participants’ health in general. Responses of very good and good were combined, as were very bad and bad. Nurses measured blood pressure three times after a 5 min rest, using an automated device, the Omron HEM 307, with 1 min intervals between each measurement. Categories of blood pressure used information on medication prescribed for blood pressure control as well as the mean of the second and third measurements, limited to participants who had not eaten, smoked, drunk alcohol or exercised in the previous 30 min. In 2009 and 2010, a spot urine was collected for laboratory measurement of albumin:creatinine ratio (ACR). Microalbuminuria was defined as ACR 2.5–30 mg/mmol in men and 3.5–30 mg/mmol in women and macroalbuminuria as ACR >30 mg/mmol in either sex. In each year, blood samples were taken for serum total and high-density lipoprotein (HDL) cholesterol as well as the EDTA sample for HbA1c. Urine and blood samples were posted to the Newcastle University Hospitals laboratory, Newcastle-upon-Tyne, for assay. All measurements used standard protocols which have been reported elsewhere, along with laboratory methods and quality assurance.33 ,34
Analyses and statistics
Weighting and complex survey design
Data were weighted for probability of address selection (smaller regions were oversampled31), dwelling unit selection (only one dwelling unit selected per address) and household selection (only one household selected per dwelling unit). In addition, the weights were calibrated for household non-response, and individual non-response to interview, nurse visit or blood sample. The HSE is designed to be representative of people living in private households: non-response weighting is used to correct for differential response compared with known demographics from the census (age, sex, household makeup, strategic health authority and social class of household reference person), and differential response to each stage of the survey. Since the analysis was limited to those with blood samples, the ‘blood weights’ were used.
The HSE uses a stratified clustered sample design, and should not be treated as a simple random sample. The strata variables supplied with each annual data set are not identifiable and therefore identical strata cannot be combined across years, so government office region was used as an alternative. Clusters/primary sampling units were used as archived but recoded to avoid duplicated identifiers across years (eg, cluster 1 in 2009 was a different location to cluster 1 in 2010).
Data were analysed using IBM SPSS V.20 (with complex survey design module), with all significance tests taking account of the complex survey design (stratification and clustering) and weighting. Differences between groups are mentioned as being ‘significant’ in this paper if p<0.05. Prevalence of diagnosed and undiagnosed diabetes, and IGR are presented as crude proportions of participants (weighted for non-response, and accounting for complex survey design), and age-standardised and sex-standardised (reweighted to give each occupation, income, deprivation and ethnic group the same age and sex profile as the general population).
Logistic regression models were created, limited to participants without diagnosed diabetes. The two outcomes were (1) IGR or undiagnosed diabetes, and (2) undiagnosed diabetes. An outcome of IGR alone was not used as any testing for IGR in clinical practice would also aim to detect undiagnosed cases of diabetes. Explanatory variables considered were demographic (age group, sex, ethnic group), socioeconomic factors and anthropometry. The main six-category obesity variable and three-category waist circumference were not collinear, with a correlation of 0.162, so both were included in the initial model. Missing data for the explanatory variables were included as separate categories, to enable inclusion of all participants. Income quintiles, educational qualifications, NS-SEC occupational category and area deprivation quintiles were used to assess socioeconomic inequalities. Of these, only income quintiles and educational qualifications were included in the final regression models, as these were the only variables which improved the fit of the model with the addition of each socioeconomic variable. Income and educational qualifications had a correlation of 0.101.
The current health status and biomarkers of cardiovascular risk of participants with IGR and undiagnosed or diagnosed diabetes were also compared with those of normoglycaemic participants, both as crude and age-standardised and sex-standardised proportions.
We also used our data to evaluate the effectiveness of screening using different categories for BMI and/or waist circumference, criteria for NHS Health Checks35 (inviting people aged 40–75 or aged 25 and above from certain ethnicities) and the Diabetes UK/Leicester risk score tool (but excluding family history of diabetes)36 ,37 as the criteria for screening to identify IGR and undiagnosed diabetes. We calculated the sensitivity, specificity, positive predictive value and negative predictive value for the various criteria in this general population sample.
The STROBE checklist was used when writing this manuscript. The raw data are available to download from the UK Data Service.
Social inequalities in diabetes and IGR
There were marked socioeconomic gradients in prevalence of IGR and undiagnosed and diagnosed diabetes. For area deprivation, inequalities in IGR (table 1) were masked in the crude rates (see online supplementary table S1) due to confounding by age. Inequalities in IGR by income and education were attenuated by age/sex standardisation but remained marked, with rates of 10% (95% CI 8% to 11%) in the lowest and 14% (12% to 15%) in the highest income quintile and 10% (9% to 11%) for those with ‘A’ level/NVQ3 or higher educational qualifications and 14% (13% to 16%) for those with no qualifications (table 1). The occupational classification showed higher IGR rates in participants in semiroutine occupations or lower supervisory/technical occupations than in other groups.
Prevalence of doctor-diagnosed diabetes across the 5 years was 6%, undiagnosed diabetes was 2%, and a further 11% had IGR. In general, the characteristics of people with diagnosed diabetes, undiagnosed diabetes and IGR followed similar patterns: each increased with age, overweight, lower socioeconomic position, and were higher among minority ethnic groups than the white population (after age standardisation). There were some differences, for example, while both diagnosed and undiagnosed diabetes were more common among men, age-standardised prevalence of IGR was not different between the sexes (table 1).
Predictors of IGR or undiagnosed diabetes
Among people without diagnosed diabetes, age was the biggest risk factor, with those aged 75 and over having almost 30 times higher odds of IGR/undiagnosed diabetes (table 2). The other important associations, which each had an independent effect, were ethnicity and both general and abdominal obesity. Unlike the prevalence figures, men had a 32% higher odds of IGR than women.
Restricting the outcome to undiagnosed diabetes, similar results were seen: although the sex difference, effects of BMI and waist circumference and associations with lower education were substantially greater, the odds for black people was similar to that for white participants. However, income was no longer significant.
Health status of those with IGR, undiagnosed or diagnosed diabetes
Normoglycaemic people were generally the healthiest. Those with IGR had higher rates than normoglycaemic participants of hypertension, high total cholesterol, low HDL cholesterol, high total:HDL ratio and albuminuria (table 3). Many of these differences remained after adjusting for the different age/sex profile of the groups. The proportion with untreated hypertension was highest among those with undiagnosed diabetes; overall hypertension rates were higher among those with diagnosed or undiagnosed diabetes, and lower among normoglycaemic and IGR participants. Those with undiagnosed diabetes were also more likely to have poor levels of HDL cholesterol, and a higher total:HDL cholesterol ratio. Those with diagnosed diabetes were least likely to have high total cholesterol.
Self-rated health showed a marked gradient, with the age-standardised proportion reporting bad or very bad health being low among normoglycaemic and IGR participants and highest in those with diagnosed diabetes.
Screening instruments for IGR and/or undiagnosed diabetes
Among those without diagnosed diabetes, a number of possible screening criteria, using information that should be readily available to individuals or their GPs, were applied. Online supplementary table S2 shows the screening characteristics in this general population sample (excluding those with diagnosed diabetes), along with the proportion of the population so identified for screening. Despite the HSE data not including family history of diabetes, the best measure examined was based on the Diabetes UK/Leicester risk score, finding 69% of people with IGR or undiagnosed diabetes with a specificity of 72% if using ‘moderate risk’ (score 16+).
Our study provides up-to-date information on prevalence and trends in prevalence of diabetes, undiagnosed diabetes and IGR in the general population and social inequalities in these. These survey data show the average prevalence of diagnosed diabetes in adults aged 16+ in England in 2009–2013 was 6%, the same as the prevalence reported by QOF over the 2012/2013 period among those aged 17+.23 As expected, diabetes was more prevalent with increasing age and obesity as well as among males, people of black and Asian ethnicities and those in lower socioeconomic positions. Around a quarter of people with diabetes are still undiagnosed. Consistent with previous work,38–42 HSE participants with IGR have health characteristics between those with normoglycaemia and with diabetes, supporting the idea of a continuum of disease.43 ,44 We also showed that low socioeconomic status, known to be associated with diabetes,45 ,46 is also associated with IGR; education was the best marker. The prevalence of people with IGR is lower than expected and appears to be static. There is a graded association of cardiovascular characteristics across the continuum of impaired glucose metabolism; a diagnosis of diabetes appears to have beneficial impacts on risk factor modification. A number of different screening criteria can each identify the majority of those with impaired glucose metabolism but support the use of a validated risk assessment tool as the most sensitive screening method.
The main strengths of this study are the analysis of data from nationally representative random samples of the free-living population, rather than limiting analysis to those in the healthcare system with diagnoses or tests of blood glucose levels. Non-response weighting, recommended as the best approach to enhancing representativeness,47 was used, making these data as generalisable as possible for England. Being a general health examination survey, the richness of data about each participant enables wider examination than a diabetes-focused study, hence the breadth of information on socioeconomic position and the range of variables that could be examined. However, all surveys are limited in the extent of the questionnaire; we had no information on family history of diabetes, one component of the Diabetes UK/Leicester risk score tool. A sizeable minority of data were missing for explanatory variables, especially income and BMI. These participants were retained in the analysis, coded as a separate ‘missing’ category. The nature of the study results in other limitations, particularly in how the categories of impaired glucose metabolism were defined. First, to be included in the diagnosed diabetes group, participants needed to self-report a diagnosis or be on diabetic medication. For this reason, a proportion of diagnosed diabetics may have been missed. The effect of this is likely to be small; furthermore, if people do not report that they have diabetes and are not treating their condition, it may be appropriate to consider them as undiagnosed diabetics. Another problem is the use of a single HbA1c test to categorise participants. In practice, symptoms or a confirmatory test would often be used to diagnose diabetes in people with an HbA1c of ≥48 mmol/mol. Applications of such strict definitions might alter the number of patients in each category but any such alteration and its impact are likely to be small at a population level. As discussed, impaired glucose metabolism is a continuum, and although categories are defined for practical reasons, all those with raised HbA1c levels are at risk and could benefit from identification and risk reduction. Although the direction of association cannot be determined in cross-sectional surveys, these are the only ethical way to monitor trends in IGR and undiagnosed diabetes; cohort studies should always release such results to their participants, thus new participants are required for these analyses.
The HSE gives unique information about undiagnosed populations and social inequalities in health, not available in routine data; until recently, prevalence estimates of undiagnosed diabetes and IGR were based on models.6 Unlike the recent Public Health England report,25 we found marked socioeconomic inequalities in IGR. They examined only deprivation quintiles but failed to adjust for confounding by age; we also examined three individual-level markers of socioeconomic position and found similar health inequalities, with education and income remaining significant in a multivariate regression model with IGR or undiagnosed diabetes as the outcome. We found the average prevalence of undiagnosed diabetes in 2009–2013 was 1.6%. Approximately 22% of people with diabetes remain undiagnosed, a higher proportion than the Association of Public Health Observatories (APHO) Diabetes Prevalence Model estimates.6 This proportion has fluctuated over the 5 years, but the prevalence of both undiagnosed diabetes and IGR have not changed appreciably over this time, possibly mirroring the stabilising prevalence of obesity in adults in England.20 It is too soon to assess the impact of 2012 NICE guidance and the introduction of targeted screening for earlier diagnosis.
The average IGR prevalence was 11%, with no discernible trend over our 5 years of data. This contrasts starkly with another recent study using HSE data that suggested an increase in IGR prevalence from 11.6% in 2003 to 35.3% in 2011.48 This is explained by the differences between definitions of IGR. We used an HbA1c range of 42–47 mmol/mol, as recommended by an international expert panel, NICE and Diabetes UK,6 ,8 whereas Mainous et al used a range of 39–47 mmol/mol (5.7–6.4%) as recommended by ADA,7 finding similar 2011 prevalence in the UK as in the USA using the same definition.49 Our own findings, using the same data set for this paper, are that using a definition of 39–47 mmol/mol, IGR was 31.2% (30.4% to 32.1%) 2009–2013, and tended to decrease since 2010 (34%) to 28% in 2013. Overall, the proportion with HbA1c 39 mmol/mol or above was 38.4%, increasing from 2009 (37.7%) to 2011 (41.2%) before decreasing again to 35.9% in 2013.
The differences between the results for the different thresholds suggest that there is an increasing prevalence of people with an HbA1c of 39–41 mmol/mol but not with an HBA1c of 42–47 mmol/mol. There are two potential explanations for this. First, there may be a lag period and the impact of the increasing prevalence of those with lower range IGR is yet to be felt. The second explanation is that people with lower range IGR do not necessarily develop increasingly deranged glucose metabolism, meaning a change in prevalence of this group would not necessarily be reflected in groups with higher HbA1c levels. If this is the case, it would provide significant support for the use of an HbA1c of 42 mmol/mol as the lower threshold for IGR as per current UK recommendations.
We showed a continued increase in the prevalence of diabetes over the 5 years, consistent with information from other databases.23 ,24 This is unsurprising in the context of rising levels of obesity but provides concerning insight into the potential impact of this serious and costly condition on population health in the future. A large proportion of people with diabetes are still undiagnosed, so do not benefit from the potential advantages that a diagnosis carries. Modelling studies have suggested a benefit in using screening to detect early diabetes.50 ,51 In contrast, recent data from the ADDITION trial52 does not show a reduction in mortality with screening for diabetes. In terms of biomarkers, our data support the assumption that a diagnosis can be beneficial,53 particularly for lipid and blood pressure modification: people who are diagnosed will benefit from QOF and guideline-driven risk factor modification, resulting in a stalling or reduction of cardiovascular risk factor progression despite advancing disease. However, self-reported health was worst in this group.
There is a clear case for identifying IGR as cost-effective interventions exist to prevent or delay diabetes6 ,8 ,54 ,55 for people in this category. Our lower prevalence of IGR implies that interventions to manage this population may be more feasible and less costly than was anticipated based on an earlier study.38 IGR and undiagnosed diabetes are more prevalent in more deprived groups, even after adjusting for demographic factors and obesity. Undiagnosed diabetes as a proportion of all cases is also higher in these groups. It is recognised that individual ‘agentic’ interventions may widen inequalities, as disadvantaged groups are less likely to participate.56 Thus, only if GPs manage to target deprived groups successfully for detection and support with lifestyle modification, this programme could reduce social inequalities in health. Similarly, focusing screening and advice by occupational health departments on employees in lower supervisory and technical and semiroutine occupations could also reduce health inequalities and employee morbidity. Future health examination surveys are needed to monitor continuing trends in changes in national prevalence and social inequalities of IGR and undiagnosed diabetes, as clinical commissioning groups pilot and roll out detection and intervention programmes.
The authors thank our colleagues at UCL and NatCen Social Research, the interviewers and nurses, and the participants in the Health Survey for England series.
This web only file has been produced by the BMJ Publishing Group from an electronic file supplied by the author(s) and has not been edited for content.
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Contributors AM had the original idea; all four authors prepared the analysis plan and interpreted the findings; AM and LNF conducted the analyses; AM and GC wrote the first draft of the manuscript; JSM wrote the second draft; all four authors contributed to subsequent drafts and approved the final version. All authors had full access to all of the data (including statistical reports and tables) in the study and can take responsibility for the integrity of the data and the accuracy of the data analysis.
Funding The Health Survey for England (HSE) 2009–2013 was funded by the Health and Social Care Information Centre. AM, LNF and JSM are funded to conduct the annual HSE but this specific study was not funded.
Disclaimer The funders of the HSE took no part in the decisions to undertake or publish this study, nor in its conduct and writing this paper; the views expressed are those of the authors alone.
Competing interests JSM reports grants from Health and Social Care Information Centre, outside the submitted work.
Ethics approval HSE 2009 was approved by Oxford B Research Ethics Committee (REC), ref. 08/H0605/103; HSE 2010 was approved by Oxford B REC, ref. 09/H0605/73; HSE 2011 and 2012 were approved by Oxford A REC, ref. 10/H0604/56; and HSE 2013 was approved by Oxford A REC, ref. 12/sc/0317.
Provenance and peer review Not commissioned; externally peer reviewed.
Data sharing statement No additional data are available.
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