No retraction, correction or concern found when last checked on Oct 23, 2026.
Socioeconomic Inequalities in Non-Communicable Diseases Prevalence in India: Disparities between Self-Reported Diagnoses and Standardized Measures
Sukumar Vellakkal, S. V. Subramanian, Christopher Millett and 3 more
PLoS ONE · 2013
doi:10.1371/journal.pone.0068219
Abstract
Background. Whether non-communicable diseases (NCDs) are diseases of poverty or affluence in low-and-middle income countries has been vigorously debated. Most analyses of NCDs have used self-reported data, which is biased by differential access to healthcare services between groups of different socioeconomic status (SES). We sought to compare self-reported diagnoses versus standardised measures of NCD prevalence across SES groups in India.
Methods. We calculated age-adjusted prevalence rates of common NCDs from the Study on Global Ageing and Adult Health, a nationally representative cross-sectional survey. We compared self-reported diagnoses to standardized measures of disease for five NCDs. We calculated wealth-related and education-related disparities in NCD prevalence by calculating concentration index (C), which ranges from −1 to +1 (concentration of disease among lower and higher SES groups, respectively).
Findings. NCD prevalence was higher (range 5.2 to 19.1%) for standardised measures than self-reported diagnoses (range 3.1 to 9.4%). Several NCDs were particularly concentrated among higher SES groups according to self-reported diagnoses (Csrd) but were concentrated either among lower SES groups or showed no strong socioeconomic gradient using standardized measures (Csm): age-standardised wealth-related C: angina Csrd 0.02 vs. Csm −0.17; asthma and lung diseases Csrd −0.05 vs. Csm −0.04 (age-standardised education-related Csrd 0.04 vs. Csm −0.05); vision problems Csrd 0.07 vs. Csm −0.05; depression Csrd 0.07 vs. Csm −0.13. Indicating similar trends of standardized measures detecting more cases among low SES, concentration of hypertension declined among higher SES (Csrd 0.19 vs. Csm 0.03).
Conclusions. The socio-economic patterning of NCD prevalence differs markedly when assessed by standardized criteria versus self-reported diagnoses. NCDs in India are not necessarily diseases of affluence but also of poverty, indicating likely under-diagnosis and under-reporting of diseases among the poor. Standardized measures should be used, wherever feasible, to estimate the true prevalence of NCDs.
Full text
From PubMed Central, U.S. National Library of Medicine, as current on Oct 23, 2026. Paragraph numbers are ours, so an answer can point at one.
Introduction
Non-communicable disease (NCDs) are increasingly dominating health care needs in low and middle income countries (LMICs) with their importance gaining increased policy recognition over the past decade,,,. NCDs such as heart disease, stroke, diabetes, cancer and chronic respiratory diseases are by far the leading causes of mortality representing 60% of all deaths globally - with 80% occurring in LMICs,,,.
Among LMICs, India is considered a particularly important nation to study the emerging burden of NCDs. India is projected to experience more deaths from NCDs than any other country over the next decade, due to the size of population and worsening risk factor profile, associated with recent dramatic economic growth,,,,,. The country has deep and entrenched social and economic disparities, with affordable healthcare being beyond the reach of large sections of society,,. Further, India has emerging data sources with which to study NCD risk factors, and can serve as a policy leader on NCD control for other LMICs,.
The epidemiologic transition from a predominance of infectious diseases to NCDs is thought to arise initially in the better-off sections of a population due to their more rapid acquisition of life-styles related to economic development. For example, while coronary heart disease mortality in England and Wales was initially concentrated among the wealthy, this pattern apparently reversed over two to three decades, although the veracity of these data is contested.
The epidemiological evidence on the socioeconomic status (SES) related patterning of NCDs remains limited in LMICs. Indian data drawn from the National Sample Survey Office (NSSO) 2004 found that prevalence of NCDs was highest among higher-income groups when based on self reported statistics. The positive association between income and the prevalence of disease at the national level was also observed in the self-reported diabetes from the National Family Health Survey-3. Conversely, evidence from a study in Chennai, which used biochemical measures for diagnosis, revealed the prevalence of diabetes and cardio-metabolic risk factors rapidly increased in low income groups over a ten year period, such that they ‘caught up’ to those of middle income groups. Furthermore, a recent study using more objective indicators confirmed greater prevalence of cardiovascular diseases risk factors among the low SES groups in India. An important question is whether these contrasting findings are due to artefact, largely arising from different measurement approaches. And, are reported socioeconomic inequalities in NCDs biased by differential access to healthcare services between groups of different SES in India?
Epidemiological studies of NCDs using self-reported measures might underestimate prevalence in low SES groups as wealthier groups have relatively more access to healthcare in poor countries. More specifically, detection biases can significantly affect the rate of diagnosis between SES groups as socially disadvantaged individuals with less education and living in places with poor medical and health facilities fail to perceive and report the presence of illness and thus fail to seek healthcare, in addition to several organizational and social or cultural and financial barriers that limit the access to healthcare services,,,. Thus, use of more standardized measures may better estimate the true prevalence of NCDs.
Here, we use Indian data from the Study on Global Ageing and Adult Health to assess socio-economic differences in NCD prevalence. We developed a standardized measure of NCD prevalence by utilizing various standardized criteria available and then compared standardised diagnostic measures (hereafter termed standardized measures) with self-reported diagnoses to examine the extent to which socio-economic inequality in NCD prevalence documented in previous studies may be due to artefact and differential access to healthcare services between groups of different SES.
Data and Methods
We used individual level, cross-sectional data (Wave 1: version 1.1.0) from the Study on Global AGEing and Adult Health (SAGE), initiated by the World Health Organisation (WHO) (hereafter WHO SAGE survey) and conducted in India during April-August 2007. The survey was designed to generate a nationally representative sample, thus, the states selected covered diverse geographic locations and varying levels of development in India,,, and comprised of Maharashtra (west), Karnataka (south), West Bengal (east), Assam (north east), Rajasthan (north) and Uttar Pradesh (central). Sampling methods were based on the design developed for the World Health Survey, 2002 where a probability sampling strategy was employed using multi-stage, stratified, random cluster samples. The primary sampling units were stratified by region and location (urban/rural) and, within each stratum, enumeration areas were selected. Details are available on the SAGE website (www.who.int/healthinfo/systems/sage).
The households selected in a state were distributed among its rural and urban areas in proportion to their state population. The WHO SAGE aimed to generate nationally representative samples of persons aged 50+ years with comparison samples of younger adults aged 18–49 years. Only one individual aged 18–49 years was invited to complete the individual interview per household, whereas all individuals aged 50+ were invited. A total of 10424 households were surveyed with information being collected on individual health modules from 12198 individual respondents giving an overall household level response rate of 87% and an individual level response rate of 65%. Of these, 5048 and 7150 individuals were aged 18–49 years and 50+ years, respectively. A weighting scheme was devised to construct a sample with nationally-representative characteristics by including sample selection and a post-stratification factor. The survey instrument was conducted using an interviewer-administered questionnaire in the native language of the respondent using local, commonly understood terms. A total of five languages with back translation to English were used in the survey to ensure accuracy and comparability. Proxy respondents were identified for selected individuals who were unable to complete the interview.
Ethical clearance was obtained from research review boards local to each participating SAGE site (several of which are linked to universities), in addition to the WHO Ethical Review Committee. Informed consent was obtained from each respondent prior to interview.
Major NCDs
Five major NCDs (under two broad categories) were identified using respondent self-reported diagnoses and standardized measures: i) Cardiovascular diseases: angina, and hypertension, and ii) Non- cardiovascular- diseases: chronic lung diseases (emphysema, bronchitis, chronic obstructive pulmonary disease) and asthma, vision problems and depression (mental disorders). The measure of both self-report of diagnoses and standardized measures of these NCDs were used.
Table 1 shows the descriptions of the relevant survey questions for self-reports of diagnosed cases as well as the criteria used for developing standardized measures for the identification of the NCDs. For self-reported diagnosed cases, participants were asked whether they had ever been diagnosed with each condition. This measure would estimate prevalence of specific NCD among only those who i) perceived presence of NCDs or their symptoms (either by people themselves or through family members or other members of society etc), and ii) reported such cases for diagnoses. At the same time, this measure excludes those cases that were undiagnosed irrespective of whether or not people had perceived the presence of NCDs.
Standardized measures for angina was derived from WHO-Rose angina questionnaire. The WHO-Rose angina questionnaire has been widely used in epidemiological studies and some studies found that using a shortened version of the WHO-Rose angina questionnaire is adequate,. The WHO-Rose angina questionnaire has been validated among south Asian population. Recently, the full version of questionnaire has been validated among the Bangladesh population (who have similar socioeconomic and cultural characteristics as of Indian population) by comparing with cardiologists’ diagnoses and found that the WHO-Rose angina questionnaire had 53% sensitivity and 89% specificity. The standardised measure used for hypertension was blood pressure measurement and then we used the systolic blood pressure and diastolic blood pressure cut-offs per WHO criteria for hypertension in adults 18 years and older,. Results from spirometry (lung function) test was used as standardised measure for asthma and lung diseases and we followed the criteria suggested by the Global Initiative for Obstructive Lung Disease (GOLD) for identifying obstructive diseases that would include asthma, COPD, chronic bronchitis and emphysema. Prevalence of vision problems were estimated using the Tumbling E LogMAR chart,. Finally, standard criteria of ‘moderate depression’ was derived from the ICD-10 classification of mental and behavioural disorders.
Socio-economic and demographic variables used in our analysis include: age, gender, education, caste/tribe, geographical location and economic status. Except age, all the other included variables were defined as categorical (dummy) variables and the classification are as follows: Gender as male and female; Education as five categories: ‘No formal education’, ‘Less than primary school’ ‘Primary school completed’, ‘High/secondary school’, and ‘College/university education’, Caste and tribe as Scheduled caste (SC)/scheduled tribes (ST), No caste/tribe, and Other caste/tribe; Location as census defined urban or rural; Economic status as asset score quintiles: (first (lowest), and fifth (highest) quintile). A validated asset (wealth) score index, as originally reported in WHO SAGE data set, was derived using WHO standard approach to estimating permanent income from survey data on household ownership of durable goods, neighbourhood and dwelling characteristics, and access to water, sanitation, electricity.
Statistical Analysis
Age-adjusted prevalence rates were calculated for self-reported diagnoses and standardized measures of diseases using an age weighting. We used the concentration index of inequality to quantify the magnitude of socio-economic disparities in NCD prevalence between groups. A variety of methods, ranging from simplest to sophisticated, are available to measure the socio-economic inequalities in health, including range, Gini coefficient (and associated Lorenz curve), Pseudo Gini coefficient (and associated pseudo Lorenz curve), index of dissimilarity, slope index of inequality (and the relative index of inequality- a derived measure from the slope index of inequality), and concentration index,. The measure of range, which considers the differences between the top and bottom socioeconomic groups is considered as the simplest inequality measure reflecting the socio-economic dimension to inequalities in health, however, it does not reflect the population distribution and is not sensitive to changes in the distribution of the population across socioeconomic groups. On the other hand, the Gini coefficient, the pseudo-Gini coefficient and the index of dissimilarity reflect population distribution and sensitive to changes in the distribution of the of the population across socioeconomic groups but do not reflect the socio-economic dimension to inequalities in health. The concentration index, a generalisation of the Gini coefficient, and the slope index (and relative index) of inequality are likely to present an accurate picture of economic inequalities in health by reflecting both the socioeconomic dimension to inequalities in health and the experiences of the entire population, and also being sensitive to changes in the distribution of the population across socioeconomic groups,,,. There is little to choose between the concentration index and slope index (and relative index) of inequality because the slope index is equal to the generalized concentration index divided by the variance of the relative rank variable (relative rank in the socioeconomic distribution) and the relative index of inequality is equal to the concentration index divided by twice the variance of the relative rank. Recently, the concentration index has been increasingly used to characterize socio-economic disparities in health in an objective manner,,,,,.
Concentration index (C) was computed as twice the (weighted) covariance of the health variable (‘ill-health’ in the present study) and a person’s relative rank in terms of economic status, divided by the variable mean, according to equation below,,.where is the sample size, hi is the ill-health of the ith individual, µ is the (weighted) mean of the ill-health, Ri is the fractional rank of the ith individual in terms of the index of household economic status. The value of the concentration index can vary between −1 and +1. However, when the health variable whose inequality is being investigated is binary, the minimum and maximum possible values of the concentration index are equal to μ−1 and 1−μ, respectively, where μ is the mean of the variable in question. A negative value implies that a variable is concentrated among the lower SES while the opposite is true (i.e. concentrated among the better-off) for positive values. When there is no inequality, the concentration index will be zero.
Several measures of SES are available but no measure is considered as the gold standard. Standard economic measures of SES use monetary information, such as income or consumption expenditure. However, the collection of accurate income and expenditure data is a demanding task and have limitations that that, in some instances, measuring income can be difficult for the self or transitory employed (e.g. agricultural work), due to accounting issues and seasonality, people may have income and expenditure in kind, and there is possibility of under-reporting of income due to the fear to potential taxation or exclusion from social security programs,,,. Education also has been used another measure of SES. Recently, asset based measures that capture living standards, such as household ownership of durable assets (e.g. TV, car) and infrastructure and housing characteristics (e.g. source of water, sanitation facility) are increasingly being used to measure the SES,. In the present study, we used wealth (asset score index) and education as two distinct indicators of SES, and thus estimated wealth-related concentration index and education-related concentration index in the prevalence of NCDs. The concentration index was estimated with ADePT software that was developed by the World Bank. All other statistical estimations were done with the STATA version 10 (Stata Corp, College Station, Texas).
Prevalence Rate Differences between Self-reports and Standardized Measures
We found significantly lower prevalence rates for all NCDs when a diagnosis was based on self-report of diagnosed cases rather than standardized measures, except asthma and chronic lung diseases (Figure 1). The prevalence rate of hypertension was 9.4% according to self-report of diagnosed cases versus 19.1% using standardized measures. Similarly, the prevalence of angina was 3.1% versus 6.9%, asthma and chronic lung disease prevalence was 5.9% versus 5.2%, vision problems prevalence was 6.1% versus 16.7% and moderate depression prevalence was 3.4% versus 8.5%.
Disparities in NCD Prevalence by Wealth and Education
The age-standardised prevalence rate of the diseases, using both self-report of diagnosed cases and standardized measures, by demographic and socio-economic variables are presented in Table 2 and Figures 2 and 3. Self-reported diagnosed cases of disease prevalence were significantly higher in the most affluent quintile compared with the least affluent quintile. Conversely, disease prevalence measured using standardized measures tended to show either negative or no strong association with wealth. Similar trends were observed for educational level too.
Table 3 shows the wealth-related and the education-related concentration indices (C) of the diseases in terms of i) Unstandardized C, ii) Age-standardised C, and iii) Age and sex standardized C, separately for self-report of diagnosed cases (Csrd) and standardized measures (Csm).
Several NCDs were concentrated among the lower SES groups using standardized measures whereas self-reported diagnosed cases indicated concentration among the higher SES groups, however, with considerable variation in the magnitude, beyond chance as reflected by the confidence intervals (See Table 3). Each of the two cardiovascular diseases has a higher concentration of disease among higher SES groups according to self-reported diagnoses. The age-standardised wealth-related concentration index and education-related concentration index for standardised measures of the prevalence of angina is −0.17 and −0.13, respectively. It means that the prevalence of angina (identified through standardized measures) is concentrated among the poor and the less-educated, which implies that a 17% reduction in the prevalence of angina among the poor and 13% reduction in the prevalence of angina among the less-educated would eradicate the observed disparity in the total prevalence of angina across SES groups. On the other hands, the self-reported diagnoses of angina was concentrated among the rich (wealth-related Csrd 0.02) and the highly-educated (education-related Csrd 0.03). The self-reported diagnosed cases of hypertension is highly concentrated among the higher SES and continue to concentrate among higher SES groups per standardized measures but with considerable attenuation as standardized measures detect relatively more cases of hypertension among low SES (wealth-related Csrd 0.19 vs. Csm 0.03 and education-related Csrd 0.12 vs. Csm 0.01).
The age-standardised concentration index for self-reported diagnoses of asthma and lung diseases (wealth-related Csrd −0.05 vs. Csm −0.04; education-related Csrd 0.04 vs. Csm −0.05), vision problems (wealth-related Csrd 0.07 vs. Csm −0.05; education-related Csrd 0.02 vs. Csm −0.06) and depression (wealth-related Csrd 0.07 vs. Csm −0.13; education-related Csrd 0.06 vs. Csm −0.09) showed positive values of C (i.e. concentration among the affluent/better educated), whereas negative values of C were found for standardized measures (i.e. concentration among the poor/less educated), with exception of asthma and chronic lung diseases showing negative value for wealth-related Csrd but positive value for education-related Csrd.
As shown in Figure 4 and Figure 5, the majority of NCDs were concentrated among higher SES groups using self-reports but were concentrated among lower SES groups or showing no strong gradient based on standardized measures, indicating considerable probable under-diagnosis and under-reporting of diseases among lower SES groups.
Discussion
We have demonstrated that the prevalence and socioeconomic disparities in several NCDs among the Indian adult population using nationally representative data depend on whether self-reported diagnoses or standardized measures of NCDs are used. We attempted to incorporate more standardised measures of prevalence of NCDs as self-reported diagnosed cases of NCDs might be poor indicators of the true prevalence of NCDs across various SES groups where people especially from the lower SES and remote place might often fail to perceive and report the illness, and those who were able to perceive might fail to access healthcare due to several constraints. We found that wealth-related and education-related concentration of disease varied with greater concentration among the affluent/educated when using self-reported diagnoses and either among lower SES groups or showed no strong SES gradient when using standardized measures of disease. This may be consistent with observations that NCDs are typically either under-reported or under-diagnosed in LMICs, including India,. These findings provide salient information for the ongoing debate about whether NCDs in LMICs are concentrated among the affluent or among poorer groups as in high income countries. Furthermore, our findings suggest that self-reported NCD prevalence estimates may be highly misleading if used to determine burden of disease or for targeting interventions.
Though our analysis found statistically significant values of age-standardised concentration indices for each of the five NCDs, no sweeping generalisation about the concentration of NCDs among the affluent or the poor should be made. First, the patterns vary depending on the method used to quantify prevalence of NCD. Second, the patterns vary depending on the disease considered. Third, the magnitude of concentration indices for both self-reported diagnoses and standardized measures were not very high. For instance, the education-related concentration index for the standardized measures of asthma and lung disease is −0.05, which means that a mere 5% reduction of the prevalence of asthma and lung diseases among the less-educated would eradicate the observed disparity in its total prevalence.
Previous studies in India have demonstrated the increased risk of cardiovascular disease and cardio-metabolic risk factors in affluent groups,,, and have highlighted the higher levels of tobacco use among poorer groups,, indicating the likelihood of increased cardiovascular disease and other NCDs in the future. Comparisons of socio-economic patterning of NCDs using self-reported diagnoses and standardized measures within the same nationally representative datasets have not previously been reported. Our study indicates that the socio-economic patterning of NCDs found in LMICs may depend on the diagnostic criteria employed. A recent study conducted in rural India found lower rates of screening for elevated blood pressure, blood glucose and cholesterol in lower SES groups. This is consistent with our assertion that the lower self-reported prevalence of NCDs in low SES groups, identified here and elsewhere, may be due to under-diagnosis and under-reporting arising from poorer access to high quality health care.
There are several important caveats and limitations to this study. First, our data do not include younger people (below 18 years). However, this would have limited bearing on findings, except possibly for asthma and lung diseases, as most of the conditions studied largely occur in adults. Second, we used cross-sectional data which prevent us from making causal inferences on factors contributing to disparities in prevalence rate. We cannot capture, using such data, the full longitudinal trends that may differ between socioeconomic groups to evaluate whether an epidemiological transition is occurring. Differences in prevalence rates between self-reported diagnoses and standardized measure may vary in the future, particularly if proposals for universal health care in India are achieved. Third, though this study incorporated standardized measures to identify NCDs to the extent possible, more comprehensive and reliable indicators such as biomarkers of disease and clinical examination are required to validate these results. Some of the standardized measures used in the WHO SAGE study to assess the prevalence of angina and depression, were based on symptom reports, and the reliability of such measures is also limited by lack of comprehensiveness and is also subject to reporting biases. Considerations such as health literacy are important to account for, and may bias our results toward underestimating prevalence rates among the poor, who may have a more difficult time comprehending questions about disease symptomatology. Finally, our study could not include the standardized measure for diabetes, one of the major NCDs that has a prevalence of 3.1% and concentration among the better-off (wealth-related Csrd 0.24; education-related Csrd 0.25) per self-reported diagnoses. Furthermore, stroke and arthritis (with self-reported diagnoses prevalence rate of 1.0% and 9.4%, respectively) were excluded from our analysis as the prevalence measures available from the WHO SAGE survey were not sufficient enough to construct standardised measures of prevalence.
Our study has important policy implications. As a part of the growing attention to the prevention and management of NCDs in LMICs, early detection of chronic diseases is now part of Indian national policy (National Program for Prevention and Control of Cancer, Diabetes, Cardiovascular Diseases and Stroke-NPCDCS 2010), and similar efforts are being considered in other LMICs. Similar to other NCDs, mental health had so far not been in the policy priorities in India, where scarcity in mental healthcare infrastructure and social stigma in accessing mental health are major concerns, and the findings from this study will inform policy making as the Indian government has recently been considering a national mental health bill. It is important that the potential impact of such programmes on health disparities is assessed during their design, implementation and evaluation. Our findings suggest that use of self-reported diagnoses of NCDs may lead to erroneous conclusions about policy impacts and that more standardized objective diagnostic criteria for NCDs should be used wherever feasible. While policy interest in NCD prevention in LMICs is increasing, many health and development programmes still neglect NCDs on the grounds that they are diseases of affluence. Our findings add to growing evidence that this may no longer be a tenable proposition.
Further research into the mechanisms that may explain discrepancies between self-reported diagnoses and standardized or more objective measures of the prevalence of NCDs is warranted. Moreover, we need further evidence on whether transitions of diseases from affluent to poor groups occurs in LMICs, as its occurrence has been questioned in high income countries. Several theories about the rise in NCDs have assumed that higher income correlates with the increased intake of energy-dense and unhealthy foods that are high in fat, sugars and total calories, as well as increased sedentary lifestyles, which is believed to relate to obesity and heart disease. This theory does not adequately explain our findings.
In summary, we found that self-reported diagnoses prevalence rates of NCDs were concentrated among the affluent while standardized measures of the same NCDs showed them to be concentrated among the poor or show no gradient. This suggests considerable problems of access to healthcare for NCD diagnosis as well as under-reporting of diseases condition among the poor. Strategies to reduce socioeconomic inequalities in NCD prevalence should be further investigated by testing hypotheses that may further explain disparities in risk, disparities in diagnosis, and effective intervention among the highest-prevalence groups. Moreover, disease-wise in-depth investigation of the socio-economic determinants of each chronic diseases is required instead of considering all NCDs in one basket. Health development programmes should consider re-orientating their programmes to include NCDs which are diseases associated with poverty and are impoverishing.
References 75
- 1.
WHO (2005) Preventing chronic diseases: a vital investment: World Health Organization.
Not in our library
- 2.
Adeyi O, Smith O, Robles S (2007) Public policy and the challenge of chronic noncommunicable diseases: World Bank Publications.
Not in our library
- 3.
UN (2011) Political declaration of the High-level Meeting of the General Assembly on the Prevention and Control of Non-communicable Diseases- Draft resolution submitted by the President of the General Assembly.
Not in our library
- 4.
Beaglehole R, Bonita R, Horton R, Adams C, Alleyne G, et al (2011 ) Priority actions for the non-communicable disease crisis. The Lancet 377: 1438–1447.
Not in our library10.1016/s0140-6736(11)60393-0
- 5.
Mathers C, Fat DM, Boerma J (2008) The global burden of disease: 2004 update: World Health Organization.
Not in our library
- 6.
Murray CJL, Lopez AD (1997 ) Mortality by cause for eight regions of the world: Global Burden of Disease Study. The Lancet 349: 1269–1276.
Not in our library10.1016/s0140-6736(96)07493-4
- 7.
Lozano R, Naghavi M, Foreman K, Lim S, Shibuya K, et al (2012 ) Global and regional mortality from 235 causes of death for 20 age groups in 1990 and 2010: a systematic analysis for the Global Burden of Disease Study 2010. Lancet 380: 2095–2128.
Not in our library10.1016/s0140-6736(12)61728-0
- 8.
Lim SS, Vos T, Flaxman AD, Danaei G, Shibuya K, et al (2012 ) A comparative risk assessment of burden of disease and injury attributable to 67 risk factors and risk factor clusters in 21 regions, 1990–2010: a systematic analysis for the Global Burden of Disease Study 2010. Lancet 380: 2224–2260.
Not in our library10.1016/s0140-6736(12)61766-8
- 9.
Jha P, Jacob B, Gajalakshmi V, Gupta PC, Dhingra N, et al (2008 ) A nationally representative case–control study of smoking and death in India. New England Journal of Medicine 358: 1137–1147.
Not in our library10.1056/nejmsa0707719
- 10.
GoI (2008) Summary statistics of causes of death India. Office of the Registrar General of India, Ministry of Home Affairs, New Delhi.
Not in our library
- 11.
Reddy KS (2002 ) Cardiovascular diseases in the developing countries: dimensions, determinants, dynamics and directions for public health action. Public Health Nutr 5: 231–237.
Not in our library10.1079/phn2001298
- 12.
Majra J, Gur A (2009 ) Poverty, tobacco, and health: an Indian scenario. Journal of Health, Population, and Nutrition 27: 316.
Not in our library10.3329/jhpn.v27i3.3373
- 13.
Patel V, Chatterji S, Chisholm D, Ebrahim S, Gopalakrishna G, et al (2011 ) Chronic diseases and injuries in India. Lancet 377: 413–428.
Not in our library10.1016/s0140-6736(10)61188-9
- 14.
Kinra S, Bowen LJ, Lyngdoh T, Prabhakaran D, Reddy KS, et al (2012 ) Sociodemographic patterning of non-communicable disease risk factors in rural India: a cross sectional study. BMJ 341: c4974.
Not in our library10.1136/bmj.c4974
- 15.
Kurian N (2007 ) Widening economic & social disparities: implications for India. The Indian journal of medical research 126: 374.
Not in our library
- 16.
Deaton A, Dreze J (2002) Poverty and inequality in India: a re-examination. Economic and Political Weekly: 3729–3748.
Not in our library
- 17.
Balarajan Y, Selvaraj S, Subramanian S (2011 ) Health care and equity in India. Lancet 377: 505.
Not in our library10.1016/s0140-6736(10)61894-6
- 18.
Raban MZ, Dandona R, Dandona L (2012 ) Availability of data for monitoring noncommunicable disease risk factors in India. Bull World Health Organ 90: 20–29.
Not in our library10.2471/blt.11.091041
- 19.
WHO (2011) WHO Study on global AGEing and adult health (SAGE), Health statistics and health information systems, World Health Organisation. Available: http://www.who.int/healthinfo/systems/sage/en/index1.html. Accessed 2011 Aug 21.
Not in our library
- 20.
GoI (2010) National Programme for Prevention and Control of Diabetes Cardiovascular Disease and Stroke (NPCDCS) approved, Government of India, Press Information Bureau, Available: http://www.pib.nic.in/newsite/erelease.aspx?relid=63087.Accessed 2012 Dec 26.
Not in our library
- 21.
Reddy KS GP, editors. (2004) Report on tobacco control in India, Ministry of Health and Family Welfare, Government of India, New Delhi. Available: http://mohfw.nic.in/WriteReadData/l892s/911379183TobaccocontroinIndia_10Dec04.pdf. Accessed 2012 Dec 26.
Not in our library
- 22.
Reddy K, Yusuf S (1998 ) Emerging epidemic of cardiovascular disease in developing countries. Circulation 97: 596.
Not in our library10.1161/01.cir.97.6.596
- 23.
Marmot M, Adelstein A, Robinson N, Rose G (1978 ) Changing social-class distribution of heart disease. British Medical Journal 2: 1109.
Not in our library10.1136/bmj.2.6145.1109
- 24.
George DS (1997) Socioeconomic differentials. In: Kuh D, Ben-Shlomo S, editors. A life course approach to chronic disease epidemiology. Oxford: Oxford University Press; 1997. p.242–73.
Not in our library
- 25.
Mahal A, Karan A, Engelgau M (2010) The economic implications of non communicable disease for India. Washington: World Bank.
Not in our library
- 26.
Corsi DJ, Subramanian S (2012) Association between socioeconomic status and self-reported diabetes in India: a cross-sectional multilevel analysis. BMJ open 2.
Not in our library10.1136/bmjopen-2012-000895
- 27.
Deepa M, Anjana RM, Manjula D, Narayan KM, Mohan V (2011 ) Convergence of prevalence rates of diabetes and cardiometabolic risk factors in middle and low income groups in urban India: 10-year follow-up of the Chennai Urban Population Study. J Diabetes Sci Technol 5: 918–927.
Not in our library10.1177/193229681100500415
- 28.
Gupta R, Deedwania PC, Sharma K, Gupta A, Guptha S, et al (2012 ) Association of educational, occupational and socioeconomic status with cardiovascular risk factors in Asian Indians: a cross-sectional study. PLoS One 7: e44098.
Not in our library10.1371/journal.pone.0044098
- 29.
Sen A (2002 ) Health: perception versus observation: Self reported morbidity has severe limitations and can be extremely misleading. BMJ 324: 860–861.
Not in our library10.1136/bmj.324.7342.860
- 30.
Kehoe R, Wu SY, Leske MC, Chylack LT Jr (1994 ) Comparing self-reported and physician-reported medical history. Am J Epidemiol 139: 813–818.
Not in our library10.1093/oxfordjournals.aje.a117078
- 31.
Mackenbach JP, Looman CW, van der Meer JB (1996 ) Differences in the misreporting of chronic conditions, by level of education: the effect on inequalities in prevalence rates. Am J Public Health 86: 706–711.
Not in our library10.2105/ajph.86.5.706
- 32.
Gulliford M, Figueroa-Munoz J, Morgan M, Hughes D, Gibson B, et al (2002 ) What does ‘access to health care’ mean? J Health Serv Res Policy 7: 186–188.
Not in our library10.1258/135581902760082517
- 33.
WHO (2011b) World Health Survey, Health Statistics and Health Information Systems, World Health Organisation, Geneva. Available: http://www.who.int/healthinfo/survey/en/. Accessed 2011 Aug 21.
Not in our library
- 34.
WHO (2011c) Sampling Guidelines for Participating Countries. The World Health Survey, World Health Organisation, Geneva. Available: http://www.who.int/healthinfo/survey/en/. Accessed 2011 Aug 21.
Not in our library
- 35.
Kowal P, Chatterji S, Naidoo N, Biritwum R, Fan W, et al (2012 ) Data resource profile: the World Health Organization Study on global AGEing and adult health (SAGE). Int J Epidemiol 41: 1639–1649.
Not in our library10.1093/ije/dys210
- 36.
Rose GA (1962 ) The diagnosis of ischaemic heart pain and intermittent claudication in field surveys. Bull World Health Organ 27: 645–658.
Not in our library
- 37.
Lampe FC, Whincup PH, Wannamethee SG, Ebrahim S, Walker M, et al (1998 ) Chest pain on questionnaire and prediction of major ischaemic heart disease events in men. Eur Heart J 19: 63–73.
Not in our library10.1053/euhj.1997.0729
- 38.
Lawlor DA, Adamson J, Ebrahim S (2003 ) Performance of the WHO Rose angina questionnaire in post-menopausal women: are all of the questions necessary? J Epidemiol Community Health 57: 538–541.
Not in our library10.1136/jech.57.7.538
- 39.
Fischbacher CM, Bhopal R, Unwin N, White M, Alberti KG (2001 ) The performance of the Rose angina questionnaire in South Asian and European origin populations: a comparative study in Newcastle, UK. Int J Epidemiol 30: 1009–1016.
Not in our library10.1093/ije/30.5.1009
- 40.
Rahman MA, Spurrier N, Mahmood MA, Rahman M, Choudhury SR, et al (2012 ) Rose Angina Questionnaire: Validation with cardiologists’ diagnoses to detect coronary heart disease in Bangladesh. Indian Heart J 65: 30–39.
Not in our library10.1016/j.ihj.2012.09.008
Cited by papers we hold 6
- A systematic review of associations between non-communicable diseases and socioeconomic status within low- and lower-middle-income countries · 2018No notice
- Impact of Noncommunicable Disease Multimorbidity on Healthcare Utilisation and Out-Of-Pocket Expenditures in Middle-Income Countries: Cross Sectional Analysis · 2015No notice
- Multimorbidity and the inequalities of global ageing: a cross-sectional study of 28 countries using the World Health Surveys · 2015No notice
- Averting Obesity and Type 2 Diabetes in India through Sugar-Sweetened Beverage Taxation: An Economic-Epidemiologic Modeling Study · 2014No notice
- Chronic Conditions and Sleep Problems among Adults Aged 50 years or over in Nine Countries: A Multi-Country Study · 2014Corrected
- Non communicable disease multimorbidity and associated health care utilization and expenditures in India: cross-sectional study · 2014No notice
Reads
Read by people on this page
None yet.
Checked or read by AI through naulon
None yet.
A person counts once a day per paper. We keep no cookie and no address: a reader is a hash that changes every day. Any month under five reads shows no number.
Are you an author?
Is this your paper?
Claim it to add your note and be paid when agents cite it. Free.