Abstract

Background

Although South Asians experience cardiovascular disease (CVD) and risk factors at an early age, the distribution of CVD risks across the socioeconomic spectrum remains unclear.

Methods

We analysed the 2011 Centre for Cardiometabolic Risk Reduction in South Asia survey data including 16,288 non-pregnant adults (≥20 years) that are representative of Chennai and Delhi, India, and Karachi, Pakistan. Socioeconomic status (SES) was defined by highest education (primary schooling, high/secondary schooling, college graduate or greater); wealth tertiles (low, middle, high household assets) and occupation (not working outside home, semi/unskilled, skilled, white-collar work). We estimated age and sex-standardized prevalence of behavioural (daily fruit/vegetables; tobacco use), weight (body mass index; waist-to-height ratio) and metabolic risk factors (diabetes, hypertension, hypercholesterolaemia; hypo-HDL; and hypertriglyceridaemia) by each SES category.

Results

Across cities, 61.2% and 16.1% completed secondary and college educations, respectively; 52.8% reported not working, 22.9% were unskilled; 21.3% were skilled and 3.1% were white-collar workers. For behavioural risk factors, low fruit/vegetable intake, smoked and smokeless tobacco use were more prevalent in lowest education, wealthy and occupation (for men only) groups compared to higher SES counterparts, while weight-related risks (body mass index 25.0–29.9 and ≥30 kg/m2; waist-to-height ratio ≥0.5) were more common in higher educated and wealthy groups, and technical/professional men. For metabolic risks, a higher prevalence of diabetes, hypertension and dyslipidaemias was observed in more educated and affluent groups, with unclear patterns across occupation groups.

Conclusions

SES-CVD patterns are heterogeneous, suggesting customized interventions for different SES groups may be warranted. Different behavioural, weight, and metabolic risk factor prevalence patterns across SES indicators may signal on-going epidemiological transition in South Asia.

Key questions

  1. What is already known about this subject?

    • In South Asia, cardiovascular disease (CVD) and risk factors are highly prevalent and disease events occur at a younger age.

    • Most epidemiological studies examining the distribution of cardiovascular risks across socioeconomic status (SES) strata have been confined to a single locality or country, have not had representative populations, and have classified SES on the basis of a single indicator (e.g. education or income).

    • Existing studies are mixed in terms of whether CVD risk factors are more or less common among the lowest SES groups. 2. What does this study add?

    • Recent data which are representative of three major cities from two different countries in South Asia.

    • Use of multiple SES indicators to characterize the complexity of SES more comprehensively.

    • Since high proportions of people have undiagnosed risk factors, use of multiple objectively collected CVD risk factors permits readers a more accurate and overarching view of CVD risk in urban South Asia.

Background

South Asia is one of the world’s most densely populated regions and is fast becoming an epicentre of atherosclerotic cardiovascular diseases (CVD). Between 1990 and 2010, healthy years lost due to ischemic heart disease and stroke increased by 73% and 54% in the region, outpacing global increases of 30% and 21%, respectively.1 Moreover, South Asians (people from India, Pakistan, Bangladesh, Nepal, Sri Lanka) experience first myocardial infarction (MI) almost 10 years younger compared to people from other countries; this is largely explained by younger onset of preventable CVD risk factors.2

CVDs impose high direct (e.g. health expenditures) and indirect costs (e.g. lost productivity) on households, potentially stifling micro and macro-economic development.3 Since South Asia’s population pyramid is relatively young by world standards4 and is experiencing rapid economic transitions and burgeoning chronic disease burdens, this raises concerns about CVDs contributing to widening socioeconomic status (SES) differences.5 While data from high-income countries now show consistent patterns (low socioeconomic groups experiencing higher CVD risk factors, events and mortality),6 these patterns were reversed in the first half of the 20th century.7,8 Studies from South Asia in the most recent two decades show conflicting SES–CVD relationships,9,10 which may indicate on-going epidemiological and socioeconomic transitions. Most studies examining these relationships in South Asia have used single SES measures, even though SES is multi-dimensional, reflecting human, social and material capital; opportunities; and access to resources.11 Furthermore, current literature is dominated by studies from India,10,1215 with few data originating in other South Asian countries; and few studies report data from representative populations.14,16

We examined relationships between different SES indicators and the prevalence of objectively measured (not just self-reported) CVD risk factors collected from representative population samples living in three mega-cities in South Asia: typical north Indian (Delhi), south Indian (Chennai) and Pakistani (Karachi) metropolises. These recent data will aid priority-setting and intervention development amid rapid sociodemographic transitions in the region.

Methods

Study population

We analysed cross-sectional survey data collected in 2011 from the baseline of the Centre for Cardiometabolic Risk Reduction in South Asia (CARRS) Study cohort.17 The study used multi-stage cluster random sampling to recruit 16,288 non-pregnant adults aged ≥20 years that are representative of Chennai and Delhi (India) and Karachi (Pakistan). All participants (or their next of kin or caregivers) provided written informed consent prior to enrolment. Data were collected through household interviews in local languages and standardized clinical examinations and fasting blood sample collection either at home (Karachi) or at local camps (Chennai, Delhi). For the three cities together, response rates were 94.7% for questionnaire completion and 84.3% for bio-specimens. Missing observations for each CVD risk factor are reported in Appendix 1.

Data were collected by trained field teams using standardized techniques. All sites have accredited laboratories and participated in an external quality assurance scheme that standardized findings to a central laboratory (All India Institute of Medical Sciences (AIIMS)). Further details regarding study design, methods and instruments are published separately.17 The study received approval for human subjects’ research from the ethics committees of the Public Health Foundation of India and AIIMS (Delhi), Madras Diabetes Research Foundation (Chennai), Aga Khan University (Karachi) and Emory University (Atlanta).

Study measures and definitions

We used interview responses to classify participants’ age (20–44 years, 45–64 years, ≥65 years), and sex (male, female).

Exposures: SES indicators

Education level provides a characterization of human and social capital, while wealth reflects material household capital. Income is also a reflection of material worth, but the literature suggests that wealth may be a more reliable indicator than self-reported income in some countries.18 Occupation offers a composite reflection of one’s earning capacity and educational background.

Based on participant responses, we categorized highest education level attained (up to primary schooling, high or secondary schooling, college graduate and higher); monthly income (less than Indian rupees (INR)10,000 (equivalent to US$200), INR10,000–20,000 (US$200–400) and greater than INR20,000 (US$400)); and occupation (not working outside home, semi or unskilled, skilled, white collar). To characterize household wealth, we used principal components analysis that weighted different household amenities (separate cooking room and toilet facilities) and assets (television, refrigerator, washing machine, microwave, mixer-grinder, mobile phone, DVD player, computer, car, motor cycle, bicycle). Components in wealth scores had a Kaiser–Meyer–Olkin (KMO) statistic of 0.62 (the KMO statistic is a measure of sampling adequacy that compares correlations between variables of interest and reports values between 0 and 1: values greater than 0.6 indicate that variables have enough in common to warrant being combined in a principal components analysis); total scores were categorized in tertiles (lowest tertile representing poorest and highest tertile representing wealthiest). For each SES indicator, categories were considered mutually exclusive and collectively exhaustive, such that each person was only classified in a single category based on their highest reported SES level.

Outcomes: cardiovascular risk factors

The INTERHEART and INTERSTROKE studies showed that 80–90% of all coronary and cerebrovascular events, respectively, could be attributed to tobacco use, hypertension, diabetes, dyslipidaemia, physical inactivity, excess body weight, alcohol, poor diet and psychosocial stresses.19,20 For this study, measurement and definitions of each behavioural (diet, tobacco use), weight-related (body mass index (BMI), central adiposity), and metabolic CVD risk factor (diabetes, hypertension, dyslipidaemia) are described below.

Behavioural risk factors were assessed by questionnaires. Using a modified food frequency questionnaire, we estimated proportions reporting low fruit and vegetable consumption (less than two servings/day). Self-reported current tobacco use was classified as smoked (e.g. cigarettes, bidis) and smokeless tobacco (e.g. chewed).21

For weight-related risks, we calculated BMI (weight/height squared (kg/m2)) and reported Asia-specific and international overweight and obesity categories (23.0–24.9 (Asian overweight), 25.0–29.9 (international overweight), ≥30.0 kg/m2 (international obesity)). Central adiposity was defined as a waist-to-height ratio (WHtR) of 0.5 or greater; this is considered a stronger predictor of CVD than waist circumference alone.22

Trained staff took two blood pressure (BP) readings after participants sat at rest for 5 min using an electronic sphygmomanometer (Omron Dalian Company, Liaoning, China). A third measurement was taken if the difference between the first two systolic or diastolic measurements was more than 10 mmHg or 5 mmHg, respectively. For analysis, we used the mean of the first two measurements, or the second and third measurements if a third measurement was obtained. Hypertension was defined by self-report or measured BP of 140/90 mmHg or greater. Venous fasting plasma glucose (FPG) was estimated using hexokinase/kinetic methods while glycated haemoglobin (HbA1c) was estimated using high-performance liquid chromatography (NGSP standardized). Diabetes was defined by self-report, FPG of 126 mg/dl or greater, or HbA1c of 6.5% or greater. Total cholesterol (enzymatic colorimetric cholesterol oxidase peroxidase), high-density lipoprotein cholesterol (HDL; direct), and triglycerides (enzymatic methods) were measured using Roche/Boehringer-Mannheim Diagnostics. Low-density lipoprotein (LDL) cholesterol was calculated using Friedewald’s formula in Delhi and Chennai, and measured directly in Karachi.23 Dyslipidaemia was defined separately: hypercholesterolaemia (self-report, total cholesterol ≥200 mg/dl, or LDL ≥130 mg/dl); low HDL (<40 mg/dl (men) or <50 mg/dl (women)); and hypertriglyceridaemia (≥150 mg/dl).

Statistical analysis

We used Stata (version 12 SE; StataCorp, TX, USA) for data analysis with appropriate sampling weights. We used multiple imputation to account for missing outcomes (shown in Appendix 1). For all variables, separate data sheets were created using chained equations and missing CVD risk factors were predicted using all other available variables. Ten imputed datasets were generated and weighted estimates were pooled.

This analysis included 16,287 non-pregnant adults aged 20 years and greater after excluding a single transgender participant. We described demographic and socioeconomic profiles of participants from each city and cumulatively. To select SES exposures, we assessed relationships between different ordinal indicators of SES (education, occupation, income, wealth) using Spearman’s correlation and Wald chi-square tests. We noted highest correlation between income and wealth, moderate correlations between education and other SES measures, and lowest correlation between occupation and other SES measures (Appendix 2). Based on these findings and the literature showing low reliability of self-reported income in the region,18 we selected education, wealth and occupation as SES exposures.

For each CVD risk factor by SES category, we calculated prevalence estimates which were age- and sex-standardized to the 2010 South Asia regional population. To achieve, this, we used five-year population projection tables (that account for age, sex, mortality, fertility, and migration) separately for India and Pakistan for 2010, provided by the World Bank.4

We estimated combined three-city CVD risk factor prevalence for education categories and asset tertiles. For occupation, an overwhelming majority of women (85%) accounted for those not working outside the home, which prompted us to stratify estimates by sex. To examine overall CVD risk, we estimated proportions of participants with 1, 2, or ≥3 CVD risk factors out of the following: tobacco exposure (smoked/smokeless), central adiposity (WHtR ≥0.5), diabetes, hypertension, and hypercholesterolemia. We used F tests to assess whether CVD risk factor prevalence monotonically increased or decreased over ordered categories of SES.

We performed a number of sensitivity analyses. To assess influences of missing data, we compared imputed data with crude prevalence from complete case data. To assess how estimates from this young South Asian population compare with other global cities that have different population structures, we calculated prevalence estimates standardized to the 2010 world population.4 Finally, we examined SES-CVD risk factor relationships by city to examine if patterns differ between cities surveyed.

Results

For the three cities combined, 47.7% of respondents were men and 59.1%, 34.0% and 6.9% were in the 20–44, 45–64 and 65 years and older age categories, respectively (Table 1). Of all respondents, 61.2% and 16.1% completed secondary schooling and college degrees, respectively. The majority of respondents (72.5%) reported household incomes less than INR10,000 (US$200). Only 3.1% reported working in white-collar professions, 21.3% and 22.9% were in skilled or unskilled occupations, respectively, and 52.8% reported not working outside the home. Age, income, wealth, education and occupational distributions were different across cities: compared to Chennai and Karachi, Delhi’s population had greater proportions of older, higher income, higher wealth and skilled or white-collar workers.

Table 1.

Sociodemographic profile of Chennai, Delhi and Karachi residents aged ≥20 years, CARRS Study (n = 16,287).

ChennaiDelhiKarachiTotal
N = 6,906N = 5,364N = 4,017N = 16,287
Age, %
 20–44 years63.053.560.159.1
 45–64 years31.838.132.234.0
 ≥65 years5.38.47.76.9
 Mean age (SE)41.7 (0.4)44.1 (1.0)41.7 (1.4)42.3 (0.6)
Sex, %
 Male46.150.147.147.7
 Female53.949.952.952.4
Household Size, %
 ≤215.819.015.016.6
 3 to 573.561.049.262.8
 ≥610.720.035.820.7
 Mean size (SE)4.0 (0.02)4.2 (0.03)4.9 (0.04)4.3 (0.02)
Education, %
 Up to Primary School18.721.530.922.6
 High school/Secondary70.454.554.861.2
 College graduate11.024.014.316.1
 Mean years completed7.5 (0.1)8.7 (0.3)7.1 (0.3)8.0 (0.1)
Household Income, %
 <INR 10,000 (US$200)83.551.382.172.5
 INR 10,000–20,00012.521.515.116.1
 >INR 20,000 (US$400)4.027.22.811.4
Assets Owned, %
 Low46.131.416.833.9
 Medium37.024.347.135.3
 High17.044.336.230.8
Occupation, %
 Not working49.951.060.052.8
 Skilled worker20.624.118.921.3
 Semi- or unskilled28.419.817.722.9
 White collar1.25.23.43.1
ChennaiDelhiKarachiTotal
N = 6,906N = 5,364N = 4,017N = 16,287
Age, %
 20–44 years63.053.560.159.1
 45–64 years31.838.132.234.0
 ≥65 years5.38.47.76.9
 Mean age (SE)41.7 (0.4)44.1 (1.0)41.7 (1.4)42.3 (0.6)
Sex, %
 Male46.150.147.147.7
 Female53.949.952.952.4
Household Size, %
 ≤215.819.015.016.6
 3 to 573.561.049.262.8
 ≥610.720.035.820.7
 Mean size (SE)4.0 (0.02)4.2 (0.03)4.9 (0.04)4.3 (0.02)
Education, %
 Up to Primary School18.721.530.922.6
 High school/Secondary70.454.554.861.2
 College graduate11.024.014.316.1
 Mean years completed7.5 (0.1)8.7 (0.3)7.1 (0.3)8.0 (0.1)
Household Income, %
 <INR 10,000 (US$200)83.551.382.172.5
 INR 10,000–20,00012.521.515.116.1
 >INR 20,000 (US$400)4.027.22.811.4
Assets Owned, %
 Low46.131.416.833.9
 Medium37.024.347.135.3
 High17.044.336.230.8
Occupation, %
 Not working49.951.060.052.8
 Skilled worker20.624.118.921.3
 Semi- or unskilled28.419.817.722.9
 White collar1.25.23.43.1

Abbreviations: CARRS, Centre for cArdiometabolic Risk Reduction in South Asia; SE, standard error; INR, Indian Rupees; US$, United States dollars (exchange rate during period: US$1 = INR50).

Table 1.

Sociodemographic profile of Chennai, Delhi and Karachi residents aged ≥20 years, CARRS Study (n = 16,287).

ChennaiDelhiKarachiTotal
N = 6,906N = 5,364N = 4,017N = 16,287
Age, %
 20–44 years63.053.560.159.1
 45–64 years31.838.132.234.0
 ≥65 years5.38.47.76.9
 Mean age (SE)41.7 (0.4)44.1 (1.0)41.7 (1.4)42.3 (0.6)
Sex, %
 Male46.150.147.147.7
 Female53.949.952.952.4
Household Size, %
 ≤215.819.015.016.6
 3 to 573.561.049.262.8
 ≥610.720.035.820.7
 Mean size (SE)4.0 (0.02)4.2 (0.03)4.9 (0.04)4.3 (0.02)
Education, %
 Up to Primary School18.721.530.922.6
 High school/Secondary70.454.554.861.2
 College graduate11.024.014.316.1
 Mean years completed7.5 (0.1)8.7 (0.3)7.1 (0.3)8.0 (0.1)
Household Income, %
 <INR 10,000 (US$200)83.551.382.172.5
 INR 10,000–20,00012.521.515.116.1
 >INR 20,000 (US$400)4.027.22.811.4
Assets Owned, %
 Low46.131.416.833.9
 Medium37.024.347.135.3
 High17.044.336.230.8
Occupation, %
 Not working49.951.060.052.8
 Skilled worker20.624.118.921.3
 Semi- or unskilled28.419.817.722.9
 White collar1.25.23.43.1
ChennaiDelhiKarachiTotal
N = 6,906N = 5,364N = 4,017N = 16,287
Age, %
 20–44 years63.053.560.159.1
 45–64 years31.838.132.234.0
 ≥65 years5.38.47.76.9
 Mean age (SE)41.7 (0.4)44.1 (1.0)41.7 (1.4)42.3 (0.6)
Sex, %
 Male46.150.147.147.7
 Female53.949.952.952.4
Household Size, %
 ≤215.819.015.016.6
 3 to 573.561.049.262.8
 ≥610.720.035.820.7
 Mean size (SE)4.0 (0.02)4.2 (0.03)4.9 (0.04)4.3 (0.02)
Education, %
 Up to Primary School18.721.530.922.6
 High school/Secondary70.454.554.861.2
 College graduate11.024.014.316.1
 Mean years completed7.5 (0.1)8.7 (0.3)7.1 (0.3)8.0 (0.1)
Household Income, %
 <INR 10,000 (US$200)83.551.382.172.5
 INR 10,000–20,00012.521.515.116.1
 >INR 20,000 (US$400)4.027.22.811.4
Assets Owned, %
 Low46.131.416.833.9
 Medium37.024.347.135.3
 High17.044.336.230.8
Occupation, %
 Not working49.951.060.052.8
 Skilled worker20.624.118.921.3
 Semi- or unskilled28.419.817.722.9
 White collar1.25.23.43.1

Abbreviations: CARRS, Centre for cArdiometabolic Risk Reduction in South Asia; SE, standard error; INR, Indian Rupees; US$, United States dollars (exchange rate during period: US$1 = INR50).

Behavioural risk factors were more common among lower educated and less wealthy individuals (Table 2). From low to high education categories, low fruit/vegetable intake was less prevalent (primary: 68.0% [95% CI 65.6, 70.2] vs. secondary: 60.3% [58.6, 62.0] vs. graduate: 48.0% [45.1, 50.9]; P < 0.001), tobacco smoking was less prevalent (primary: 17.0% [15.5, 18.5] vs. secondary: 12.2% [11.3, 13.0] vs. graduate: 7.0% [5.8, 8.2]; P < 0.001), and smokeless tobacco use was less prevalent (primary: 20.9% [18.7, 23.2] vs. secondary: 13.9% [12.8, 15.1] vs. graduate: 4.8% [3.8, 5.7]; P < 0.001). Similarly, from low to high wealth, low fruit/vegetable intake (low: 68.0% [66.2, 69.8] vs. middle: 61.4% [59.3, 63.5] vs. high: 50.5% [48.4, 52.6]; P < 0.001), tobacco smoking (low: 16.1% [14.9, 17.2] vs. middle: 11.9% [11.1, 12.7] vs. high: 9.3% [8.3, 10.4]; P < 0.001), and smokeless tobacco use (low: 19.3% [17.6, 21.0] vs. middle: 14.3 [12.9, 15.7] vs. high: 6.8% [5.8, 7.8]; P < 0.001) were all less common.

Table 2.

Age and sex-standardized CVD risk factor prevalencea among Chennai, Delhi, and Karachi residents aged ≥20 years by education level and household assets, CARRS Study (n=16,287).

Education Level
p-valueAsset Tertiles
p-value
Up to Primary (n = 3604)High/Secondary (n = 9924)Graduate or higher (n = 2759)Low (n = 5431)Medium (n = 5722)High (n = 5134)
Low F&V Intake68.060.348.0<0.00168.061.450.5<0.001
(65.6, 70.2)(58.6, 62.0)(45.1, 50.9)(66.2, 69.8)(59.3, 63.5)(48.4, 52.6)
Smoked Tobacco Use17.012.27.0<0.00116.111.99.3<0.001
(15.5, 18.5)(11.3, 13.0)(5.8, 8.2)(14.9, 17.2)(11.1, 12.7)(8.3, 10.4)
Smokeless Tobacco20.913.94.8<0.00119.314.36.8<0.001
(18.7, 23.2)(12.8, 15.1)(3.8, 5.7)(17.6, 21.0)(12.9, 15.7)(5.8, 7.8)
BMI 23–24.9 kg/m214.214.817.80.03814.515.116.00.130
(11.7, 16.6)(13.8, 15.9)(15.5, 20.2)(13.3, 15.7)(13.9, 16.4)(14.5, 17.5)
BMI 25–29.9 kg/m224.730.634.6<0.00124.231.336.5<0.001
(22.4, 27.1)(29.3, 31.9)(31.9, 37.4)(22.6, 25.8)(29.8, 32.8)(33.4, 38.6)
BMI ≥30 kg/m212.216.016.50.0029.914.920.6<0.001
(10.3, 14.2)(15.1, 16.9)(14.7, 18.4)(8.6, 11.1)(13.7, 16.1)(19.1, 22.0)
WHtR ≥0.559.665.669.7<0.00156.766.273.9<0.001
(56.9, 62.3)(64.4, 66.8)(67.5, 72.0)(54.9, 58.4)(64.6, 67.7)(72.3, 75.5)
Diabetes18.122.122.3<0.00118.321.026.0<0.001
(16.6, 19.6)(21.1, 23.1)(20.6, 24.1)(16.8, 19.8)(19.7, 22.2)(24.5, 27.5)
Hypertension26.930.428.20.41026.630.031.2<0.001
(25.1, 28.8)(29.3, 31.5)(25.9, 30.5)(25.0, 28.2)(28.6, 31.4)(29.8, 32.7)
Hypercholesterolemia40.041.444.30.02540.740.344.50.019
(37.4, 42.7)(40.0, 42.8)(41.9, 46.7)(38.4, 43.2)(38.9, 41.8)(42.7,46.3)
Low HDL58.260.057.80.82060.159.361.50.310
(55.5, 60.9)(58.6, 61.5)(55.1, 60.5)(58.1, 62.1)(57.4, 61.1)(59.4, 63.3)
Hypertriglyceridemia29.131.233.20.01229.731.134.0<0.001
(26.6, 31.6)(30.0, 32.5)(30.8, 35.5)(27.7, 31.6)(29.5, 32.8)(32.3, 35.7)
Education Level
p-valueAsset Tertiles
p-value
Up to Primary (n = 3604)High/Secondary (n = 9924)Graduate or higher (n = 2759)Low (n = 5431)Medium (n = 5722)High (n = 5134)
Low F&V Intake68.060.348.0<0.00168.061.450.5<0.001
(65.6, 70.2)(58.6, 62.0)(45.1, 50.9)(66.2, 69.8)(59.3, 63.5)(48.4, 52.6)
Smoked Tobacco Use17.012.27.0<0.00116.111.99.3<0.001
(15.5, 18.5)(11.3, 13.0)(5.8, 8.2)(14.9, 17.2)(11.1, 12.7)(8.3, 10.4)
Smokeless Tobacco20.913.94.8<0.00119.314.36.8<0.001
(18.7, 23.2)(12.8, 15.1)(3.8, 5.7)(17.6, 21.0)(12.9, 15.7)(5.8, 7.8)
BMI 23–24.9 kg/m214.214.817.80.03814.515.116.00.130
(11.7, 16.6)(13.8, 15.9)(15.5, 20.2)(13.3, 15.7)(13.9, 16.4)(14.5, 17.5)
BMI 25–29.9 kg/m224.730.634.6<0.00124.231.336.5<0.001
(22.4, 27.1)(29.3, 31.9)(31.9, 37.4)(22.6, 25.8)(29.8, 32.8)(33.4, 38.6)
BMI ≥30 kg/m212.216.016.50.0029.914.920.6<0.001
(10.3, 14.2)(15.1, 16.9)(14.7, 18.4)(8.6, 11.1)(13.7, 16.1)(19.1, 22.0)
WHtR ≥0.559.665.669.7<0.00156.766.273.9<0.001
(56.9, 62.3)(64.4, 66.8)(67.5, 72.0)(54.9, 58.4)(64.6, 67.7)(72.3, 75.5)
Diabetes18.122.122.3<0.00118.321.026.0<0.001
(16.6, 19.6)(21.1, 23.1)(20.6, 24.1)(16.8, 19.8)(19.7, 22.2)(24.5, 27.5)
Hypertension26.930.428.20.41026.630.031.2<0.001
(25.1, 28.8)(29.3, 31.5)(25.9, 30.5)(25.0, 28.2)(28.6, 31.4)(29.8, 32.7)
Hypercholesterolemia40.041.444.30.02540.740.344.50.019
(37.4, 42.7)(40.0, 42.8)(41.9, 46.7)(38.4, 43.2)(38.9, 41.8)(42.7,46.3)
Low HDL58.260.057.80.82060.159.361.50.310
(55.5, 60.9)(58.6, 61.5)(55.1, 60.5)(58.1, 62.1)(57.4, 61.1)(59.4, 63.3)
Hypertriglyceridemia29.131.233.20.01229.731.134.0<0.001
(26.6, 31.6)(30.0, 32.5)(30.8, 35.5)(27.7, 31.6)(29.5, 32.8)(32.3, 35.7)

Abbreviations: CVD, cardiovascular disease; F&V, fruit and vegetable; BMI, body mass index; WHtR, waist-to-height ratio; HDL, high-density lipoprotein cholesterol.

Definitions:

  • Diabetes (self-report or fasting blood glucose≥126 mg/dl or glycated hemoglobin≥6.5%);

  • Hypertension (self-report or measured blood pressure≥140/90 mmHg);

  • Hypercholesterolemia (self-report or total cholesterol≥200 mg/dl or low-density lipoprotein cholesterol≥130 mg/dl);

  • Low HDL (<40 mg/dl [males] and <50 mg/dl [females]);

  • Hypertriglyceridemia (≥150 mg/dl).

a

With 95% confidence intervals in parentheses.

Table 2.

Age and sex-standardized CVD risk factor prevalencea among Chennai, Delhi, and Karachi residents aged ≥20 years by education level and household assets, CARRS Study (n=16,287).

Education Level
p-valueAsset Tertiles
p-value
Up to Primary (n = 3604)High/Secondary (n = 9924)Graduate or higher (n = 2759)Low (n = 5431)Medium (n = 5722)High (n = 5134)
Low F&V Intake68.060.348.0<0.00168.061.450.5<0.001
(65.6, 70.2)(58.6, 62.0)(45.1, 50.9)(66.2, 69.8)(59.3, 63.5)(48.4, 52.6)
Smoked Tobacco Use17.012.27.0<0.00116.111.99.3<0.001
(15.5, 18.5)(11.3, 13.0)(5.8, 8.2)(14.9, 17.2)(11.1, 12.7)(8.3, 10.4)
Smokeless Tobacco20.913.94.8<0.00119.314.36.8<0.001
(18.7, 23.2)(12.8, 15.1)(3.8, 5.7)(17.6, 21.0)(12.9, 15.7)(5.8, 7.8)
BMI 23–24.9 kg/m214.214.817.80.03814.515.116.00.130
(11.7, 16.6)(13.8, 15.9)(15.5, 20.2)(13.3, 15.7)(13.9, 16.4)(14.5, 17.5)
BMI 25–29.9 kg/m224.730.634.6<0.00124.231.336.5<0.001
(22.4, 27.1)(29.3, 31.9)(31.9, 37.4)(22.6, 25.8)(29.8, 32.8)(33.4, 38.6)
BMI ≥30 kg/m212.216.016.50.0029.914.920.6<0.001
(10.3, 14.2)(15.1, 16.9)(14.7, 18.4)(8.6, 11.1)(13.7, 16.1)(19.1, 22.0)
WHtR ≥0.559.665.669.7<0.00156.766.273.9<0.001
(56.9, 62.3)(64.4, 66.8)(67.5, 72.0)(54.9, 58.4)(64.6, 67.7)(72.3, 75.5)
Diabetes18.122.122.3<0.00118.321.026.0<0.001
(16.6, 19.6)(21.1, 23.1)(20.6, 24.1)(16.8, 19.8)(19.7, 22.2)(24.5, 27.5)
Hypertension26.930.428.20.41026.630.031.2<0.001
(25.1, 28.8)(29.3, 31.5)(25.9, 30.5)(25.0, 28.2)(28.6, 31.4)(29.8, 32.7)
Hypercholesterolemia40.041.444.30.02540.740.344.50.019
(37.4, 42.7)(40.0, 42.8)(41.9, 46.7)(38.4, 43.2)(38.9, 41.8)(42.7,46.3)
Low HDL58.260.057.80.82060.159.361.50.310
(55.5, 60.9)(58.6, 61.5)(55.1, 60.5)(58.1, 62.1)(57.4, 61.1)(59.4, 63.3)
Hypertriglyceridemia29.131.233.20.01229.731.134.0<0.001
(26.6, 31.6)(30.0, 32.5)(30.8, 35.5)(27.7, 31.6)(29.5, 32.8)(32.3, 35.7)
Education Level
p-valueAsset Tertiles
p-value
Up to Primary (n = 3604)High/Secondary (n = 9924)Graduate or higher (n = 2759)Low (n = 5431)Medium (n = 5722)High (n = 5134)
Low F&V Intake68.060.348.0<0.00168.061.450.5<0.001
(65.6, 70.2)(58.6, 62.0)(45.1, 50.9)(66.2, 69.8)(59.3, 63.5)(48.4, 52.6)
Smoked Tobacco Use17.012.27.0<0.00116.111.99.3<0.001
(15.5, 18.5)(11.3, 13.0)(5.8, 8.2)(14.9, 17.2)(11.1, 12.7)(8.3, 10.4)
Smokeless Tobacco20.913.94.8<0.00119.314.36.8<0.001
(18.7, 23.2)(12.8, 15.1)(3.8, 5.7)(17.6, 21.0)(12.9, 15.7)(5.8, 7.8)
BMI 23–24.9 kg/m214.214.817.80.03814.515.116.00.130
(11.7, 16.6)(13.8, 15.9)(15.5, 20.2)(13.3, 15.7)(13.9, 16.4)(14.5, 17.5)
BMI 25–29.9 kg/m224.730.634.6<0.00124.231.336.5<0.001
(22.4, 27.1)(29.3, 31.9)(31.9, 37.4)(22.6, 25.8)(29.8, 32.8)(33.4, 38.6)
BMI ≥30 kg/m212.216.016.50.0029.914.920.6<0.001
(10.3, 14.2)(15.1, 16.9)(14.7, 18.4)(8.6, 11.1)(13.7, 16.1)(19.1, 22.0)
WHtR ≥0.559.665.669.7<0.00156.766.273.9<0.001
(56.9, 62.3)(64.4, 66.8)(67.5, 72.0)(54.9, 58.4)(64.6, 67.7)(72.3, 75.5)
Diabetes18.122.122.3<0.00118.321.026.0<0.001
(16.6, 19.6)(21.1, 23.1)(20.6, 24.1)(16.8, 19.8)(19.7, 22.2)(24.5, 27.5)
Hypertension26.930.428.20.41026.630.031.2<0.001
(25.1, 28.8)(29.3, 31.5)(25.9, 30.5)(25.0, 28.2)(28.6, 31.4)(29.8, 32.7)
Hypercholesterolemia40.041.444.30.02540.740.344.50.019
(37.4, 42.7)(40.0, 42.8)(41.9, 46.7)(38.4, 43.2)(38.9, 41.8)(42.7,46.3)
Low HDL58.260.057.80.82060.159.361.50.310
(55.5, 60.9)(58.6, 61.5)(55.1, 60.5)(58.1, 62.1)(57.4, 61.1)(59.4, 63.3)
Hypertriglyceridemia29.131.233.20.01229.731.134.0<0.001
(26.6, 31.6)(30.0, 32.5)(30.8, 35.5)(27.7, 31.6)(29.5, 32.8)(32.3, 35.7)

Abbreviations: CVD, cardiovascular disease; F&V, fruit and vegetable; BMI, body mass index; WHtR, waist-to-height ratio; HDL, high-density lipoprotein cholesterol.

Definitions:

  • Diabetes (self-report or fasting blood glucose≥126 mg/dl or glycated hemoglobin≥6.5%);

  • Hypertension (self-report or measured blood pressure≥140/90 mmHg);

  • Hypercholesterolemia (self-report or total cholesterol≥200 mg/dl or low-density lipoprotein cholesterol≥130 mg/dl);

  • Low HDL (<40 mg/dl [males] and <50 mg/dl [females]);

  • Hypertriglyceridemia (≥150 mg/dl).

a

With 95% confidence intervals in parentheses.

For weight-related risks, from low to high education levels, we noted higher prevalence of overweight ([BMI 25–29.9 kg/m2] primary: 24.7% [22.4, 27.1] vs. secondary: 30.6% [29.3, 31.9] vs. graduate: 34.6% [31.9, 37.4]; p<0.001) and obesity ([BMI ≥ 30 kg/m2] primary: 12.2% [10.3, 14.2] vs. secondary: 16.0% [15.1, 16.9] vs. graduate: 16.5% [14.7, 18.4]; p=0.002) and central adiposity (primary: 59.6% [56.9, 62.3] vs. secondary: 65.6% [64.4, 66.8] vs. graduate: 69.7% [67.5, 72.0]; p<0.001). From low to high wealth, similarly, we noted higher prevalence of overweight (low: 24.2% [22.6, 25.8] vs. middle: 31.3% [29.8, 32.8] vs. high: 36.5% [33.4, 38.6]; p<0.001) and obesity (low: 9.9% [8.6, 11.1] vs. middle: 14.9% [13.7, 16.1] vs. high: 20.6% [19.1, 22.0]; p<0.001). Higher wealth was also associated with higher prevalence of central adiposity (low: 56.7% [54.9, 58.4] vs. middle: 66.2% [64.6, 67.7] vs. high: 73.9% [72.3, 75.5]; p<0.001).

With higher education, there were graded patterns of higher prevalence of diabetes (primary: 18.1% [16.6, 19.6] vs. secondary: 22.1% [21.1, 23.1] vs. graduate: 22.3% [20.6, 24.1]; p<0.001), hypercholesterolemia (primary: 40.0% [37.4, 42.7] vs. secondary: 41.4% [40.0, 42.8] vs. graduate: 44.3% [41.9, 46.7]; p=0.025), and hypertriglyceridemia (primary: 29.1% [26.6, 31.6] vs. secondary: 31.2% [30.0, 32.5] vs. graduate: 33.2% [30.8, 35.5]; p=0.012). For wealth, similarly, there were clear graded relationships between higher assets and diabetes (low: 18.3% [16.8, 19.8] vs. middle: 21.0% [19.7, 22.2] vs. high: 26.0% [24.5, 27.5]; p<0.001), hypertension (low: 26.6% [25.0, 28.2] vs. middle: 30.0% [28.6, 31.4] vs. high: 31.2% [29.8, 32.7]; p<0.001), hypercholesterolemia (low: 40.7% [38.4, 43.2] vs. middle: 40.3% [38.9, 41.8] vs. high: 44.5% [42.7, 46.3]; p=0.019), and hypertriglyceridemia (low: 29.7% [27.7, 31.6] vs. middle: 31.1% [29.5, 32.8] vs. high: 34.0% [32.3, 35.7]; p<0.001).

Among men, from non-working to white-collar occupations (Table 3), we noted lower prevalence of low fruit and vegetable intake (p<0.001), smoked tobacco (p<0.001), and smokeless tobacco use (p=0.009), with the highest prevalence of each risk among low-skilled workers. The prevalence of overweight (p<0.001), obesity (p=0.019), and central adiposity (p<0.001) were all significantly higher among men in skilled and white-collar occupations. For metabolic risk factors among men, from less-skilled to white-collar occupations, there were significant gradations of higher prevalence of hypercholesterolemia (p<0.001), and hypertriglyceridemia (p=0.006); but not for diabetes and hypertension.

Table 3.

Age and sex-standardized CVD risk factor prevalencea among male and female Chennai, Delhi and Karachi residents aged ≥20 years by occupation, CARRS (n = 16,287).

Male (N = 7760)
p-valueFemale (N = 8527)
p-value
Not Working N = 1369Low skilled N = 2791Skilled N = 3129White Collar N = 471Not Working N = 7283Low skilled N = 666Skilled N = 508White Collar N = 70
Low F&V Intake59.962.453.347.6<0.00162.669.157.057.00.062
(54.6, 65.2)(59.7, 65.2)(50.7, 55.9)(43.3,51.8)(60.4, 64.8)(64.3, 74.0)(52.4, 61.6)(47.2, 66.8)
Smoked Tobacco Use21.229.321.012.6<0.0010.81.42.7
(17.2, 25.3)(27.1, 31.5)(19.1, 22.8)(8.5, 16.7)(0.5, 1.1)(0.6, 2.2)(0.0, 6.2)
Smokeless Tobacco19.028.016.613.50.0096.69.53.2
(14.5, 23.4)(25.2, 30.8)(14.6, 18.7)(8.5, 18.5)(5.7, 7.4)(5.6, 13.4)(1.6, 4.7)
BMI 23–24.9 kg/m214.917.017.515.40.84012.514.916.714.60.613
(11.3, 18.6)(14.9, 19.0)(15.5,19.5)(11.2, 19.5)(11.4, 13.6)(11.2, 18.5)(11.6, 21.7)(4.7, 24.4)
BMI 25–29.9 kg/m226.823.331.839.8<0.00132.726.432.125.70.433
(21.7, 31.9)(21.2, 25.3)(29.3, 34.3)(32.6, 47.0)(31.3, 34.1)(21.7, 31.1)(25.9, 38.4)(13.1, 38.3)
BMI ≥30 kg/m28.75.510.913.10.01922.713.621.833.10.028
(5.3, 12.1)(4.5, 6.6)(9.4, 12.4)(9.4, 16.9)(21.2, 24.1)(10.8, 16.4)(17.2, 26.5)(22.1, 44.1)
WHtR ≥0.558.654.464.871.7<0.00170.557.870.865.40.820
(54.6, 62.7)(51.7, 57.0)(62.5, 67.1)(65.9, 77.5)(69.0, 72.1)(52.5, 63.1)(66.0, 75.6)(58.5, 72.2)
Diabetes22.917.322.822.60.65023.318.720.620.70.580
(18.9, 26.9)(15.6, 18.9)(20.9, 24.6)(17.3, 28.0)(22.1, 24.5)(14.7, 22.7)(17.4, 23.7)(13.3, 28.1)
Hypertension35.527.731.531.50.50028.825.522.124.50.200
(29.8, 41.2)(25.6, 29.8)(29.3, 33.7)(26.4, 36.6)(27.7, 30.0)(20.4, 30.8)(19.2, 25.0)(16.5, 32.6)
Hypercholesterolemia38.940.244.353.4<0.00141.338.139.242.00.830
(35.7, 42.1)(37.6, 42.8)(41.8, 46.8)(48.4, 58.4)(39.6, 42.9)(32.9, 43.4)(34.9, 43.6)(32.4, 51.6)
Low HDL48.448.151.753.50.23069.268.071.473.10.470
(42.7, 54.1)(44.9, 51.3)(48.7, 54.6)(45.1, 61.8)(67.5, 70.9)(61.8, 74.2)(66.8, 76.1)(59.1, 87.2)
Hypertriglyceridemia32.234.440.445.10.00626.223.931.323.10.900
(26.4, 38.1)(31.9, 36.9)(38.2, 42.7)(36.6, 53.7)(24.9, 27.6)(19.0, 28.7)(26.9, 35.7)(12.6, 33.5)
Male (N = 7760)
p-valueFemale (N = 8527)
p-value
Not Working N = 1369Low skilled N = 2791Skilled N = 3129White Collar N = 471Not Working N = 7283Low skilled N = 666Skilled N = 508White Collar N = 70
Low F&V Intake59.962.453.347.6<0.00162.669.157.057.00.062
(54.6, 65.2)(59.7, 65.2)(50.7, 55.9)(43.3,51.8)(60.4, 64.8)(64.3, 74.0)(52.4, 61.6)(47.2, 66.8)
Smoked Tobacco Use21.229.321.012.6<0.0010.81.42.7
(17.2, 25.3)(27.1, 31.5)(19.1, 22.8)(8.5, 16.7)(0.5, 1.1)(0.6, 2.2)(0.0, 6.2)
Smokeless Tobacco19.028.016.613.50.0096.69.53.2
(14.5, 23.4)(25.2, 30.8)(14.6, 18.7)(8.5, 18.5)(5.7, 7.4)(5.6, 13.4)(1.6, 4.7)
BMI 23–24.9 kg/m214.917.017.515.40.84012.514.916.714.60.613
(11.3, 18.6)(14.9, 19.0)(15.5,19.5)(11.2, 19.5)(11.4, 13.6)(11.2, 18.5)(11.6, 21.7)(4.7, 24.4)
BMI 25–29.9 kg/m226.823.331.839.8<0.00132.726.432.125.70.433
(21.7, 31.9)(21.2, 25.3)(29.3, 34.3)(32.6, 47.0)(31.3, 34.1)(21.7, 31.1)(25.9, 38.4)(13.1, 38.3)
BMI ≥30 kg/m28.75.510.913.10.01922.713.621.833.10.028
(5.3, 12.1)(4.5, 6.6)(9.4, 12.4)(9.4, 16.9)(21.2, 24.1)(10.8, 16.4)(17.2, 26.5)(22.1, 44.1)
WHtR ≥0.558.654.464.871.7<0.00170.557.870.865.40.820
(54.6, 62.7)(51.7, 57.0)(62.5, 67.1)(65.9, 77.5)(69.0, 72.1)(52.5, 63.1)(66.0, 75.6)(58.5, 72.2)
Diabetes22.917.322.822.60.65023.318.720.620.70.580
(18.9, 26.9)(15.6, 18.9)(20.9, 24.6)(17.3, 28.0)(22.1, 24.5)(14.7, 22.7)(17.4, 23.7)(13.3, 28.1)
Hypertension35.527.731.531.50.50028.825.522.124.50.200
(29.8, 41.2)(25.6, 29.8)(29.3, 33.7)(26.4, 36.6)(27.7, 30.0)(20.4, 30.8)(19.2, 25.0)(16.5, 32.6)
Hypercholesterolemia38.940.244.353.4<0.00141.338.139.242.00.830
(35.7, 42.1)(37.6, 42.8)(41.8, 46.8)(48.4, 58.4)(39.6, 42.9)(32.9, 43.4)(34.9, 43.6)(32.4, 51.6)
Low HDL48.448.151.753.50.23069.268.071.473.10.470
(42.7, 54.1)(44.9, 51.3)(48.7, 54.6)(45.1, 61.8)(67.5, 70.9)(61.8, 74.2)(66.8, 76.1)(59.1, 87.2)
Hypertriglyceridemia32.234.440.445.10.00626.223.931.323.10.900
(26.4, 38.1)(31.9, 36.9)(38.2, 42.7)(36.6, 53.7)(24.9, 27.6)(19.0, 28.7)(26.9, 35.7)(12.6, 33.5)

Abbreviations: CVD, cardiovascular disease; F&V, fruit and vegetable; BMI, body mass index; WHtR, waist-to-height ratio; HDL, high-density lipoprotein cholesterol.

Definitions:

  • Diabetes (self-report or fasting blood glucose≥126 mg/dl or glycated hemoglobin≥6.5%);

  • Hypertension (self-report or measured blood pressure≥140/90 mmHg);

  • Hypercholesterolemia (self-report or total cholesterol≥200 mg/dl or low-density lipoprotein cholesterol≥130 mg/dl);

  • Low HDL (<40 mg/dl [males] and <50 mg/dl [females]);

  • Hypertriglyceridemia (≥150 mg/dl).

a

With 95% confidence intervals in parentheses.

Estimates likely unreliable due to small number of women in this occupation category.

Table 3.

Age and sex-standardized CVD risk factor prevalencea among male and female Chennai, Delhi and Karachi residents aged ≥20 years by occupation, CARRS (n = 16,287).

Male (N = 7760)
p-valueFemale (N = 8527)
p-value
Not Working N = 1369Low skilled N = 2791Skilled N = 3129White Collar N = 471Not Working N = 7283Low skilled N = 666Skilled N = 508White Collar N = 70
Low F&V Intake59.962.453.347.6<0.00162.669.157.057.00.062
(54.6, 65.2)(59.7, 65.2)(50.7, 55.9)(43.3,51.8)(60.4, 64.8)(64.3, 74.0)(52.4, 61.6)(47.2, 66.8)
Smoked Tobacco Use21.229.321.012.6<0.0010.81.42.7
(17.2, 25.3)(27.1, 31.5)(19.1, 22.8)(8.5, 16.7)(0.5, 1.1)(0.6, 2.2)(0.0, 6.2)
Smokeless Tobacco19.028.016.613.50.0096.69.53.2
(14.5, 23.4)(25.2, 30.8)(14.6, 18.7)(8.5, 18.5)(5.7, 7.4)(5.6, 13.4)(1.6, 4.7)
BMI 23–24.9 kg/m214.917.017.515.40.84012.514.916.714.60.613
(11.3, 18.6)(14.9, 19.0)(15.5,19.5)(11.2, 19.5)(11.4, 13.6)(11.2, 18.5)(11.6, 21.7)(4.7, 24.4)
BMI 25–29.9 kg/m226.823.331.839.8<0.00132.726.432.125.70.433
(21.7, 31.9)(21.2, 25.3)(29.3, 34.3)(32.6, 47.0)(31.3, 34.1)(21.7, 31.1)(25.9, 38.4)(13.1, 38.3)
BMI ≥30 kg/m28.75.510.913.10.01922.713.621.833.10.028
(5.3, 12.1)(4.5, 6.6)(9.4, 12.4)(9.4, 16.9)(21.2, 24.1)(10.8, 16.4)(17.2, 26.5)(22.1, 44.1)
WHtR ≥0.558.654.464.871.7<0.00170.557.870.865.40.820
(54.6, 62.7)(51.7, 57.0)(62.5, 67.1)(65.9, 77.5)(69.0, 72.1)(52.5, 63.1)(66.0, 75.6)(58.5, 72.2)
Diabetes22.917.322.822.60.65023.318.720.620.70.580
(18.9, 26.9)(15.6, 18.9)(20.9, 24.6)(17.3, 28.0)(22.1, 24.5)(14.7, 22.7)(17.4, 23.7)(13.3, 28.1)
Hypertension35.527.731.531.50.50028.825.522.124.50.200
(29.8, 41.2)(25.6, 29.8)(29.3, 33.7)(26.4, 36.6)(27.7, 30.0)(20.4, 30.8)(19.2, 25.0)(16.5, 32.6)
Hypercholesterolemia38.940.244.353.4<0.00141.338.139.242.00.830
(35.7, 42.1)(37.6, 42.8)(41.8, 46.8)(48.4, 58.4)(39.6, 42.9)(32.9, 43.4)(34.9, 43.6)(32.4, 51.6)
Low HDL48.448.151.753.50.23069.268.071.473.10.470
(42.7, 54.1)(44.9, 51.3)(48.7, 54.6)(45.1, 61.8)(67.5, 70.9)(61.8, 74.2)(66.8, 76.1)(59.1, 87.2)
Hypertriglyceridemia32.234.440.445.10.00626.223.931.323.10.900
(26.4, 38.1)(31.9, 36.9)(38.2, 42.7)(36.6, 53.7)(24.9, 27.6)(19.0, 28.7)(26.9, 35.7)(12.6, 33.5)
Male (N = 7760)
p-valueFemale (N = 8527)
p-value
Not Working N = 1369Low skilled N = 2791Skilled N = 3129White Collar N = 471Not Working N = 7283Low skilled N = 666Skilled N = 508White Collar N = 70
Low F&V Intake59.962.453.347.6<0.00162.669.157.057.00.062
(54.6, 65.2)(59.7, 65.2)(50.7, 55.9)(43.3,51.8)(60.4, 64.8)(64.3, 74.0)(52.4, 61.6)(47.2, 66.8)
Smoked Tobacco Use21.229.321.012.6<0.0010.81.42.7
(17.2, 25.3)(27.1, 31.5)(19.1, 22.8)(8.5, 16.7)(0.5, 1.1)(0.6, 2.2)(0.0, 6.2)
Smokeless Tobacco19.028.016.613.50.0096.69.53.2
(14.5, 23.4)(25.2, 30.8)(14.6, 18.7)(8.5, 18.5)(5.7, 7.4)(5.6, 13.4)(1.6, 4.7)
BMI 23–24.9 kg/m214.917.017.515.40.84012.514.916.714.60.613
(11.3, 18.6)(14.9, 19.0)(15.5,19.5)(11.2, 19.5)(11.4, 13.6)(11.2, 18.5)(11.6, 21.7)(4.7, 24.4)
BMI 25–29.9 kg/m226.823.331.839.8<0.00132.726.432.125.70.433
(21.7, 31.9)(21.2, 25.3)(29.3, 34.3)(32.6, 47.0)(31.3, 34.1)(21.7, 31.1)(25.9, 38.4)(13.1, 38.3)
BMI ≥30 kg/m28.75.510.913.10.01922.713.621.833.10.028
(5.3, 12.1)(4.5, 6.6)(9.4, 12.4)(9.4, 16.9)(21.2, 24.1)(10.8, 16.4)(17.2, 26.5)(22.1, 44.1)
WHtR ≥0.558.654.464.871.7<0.00170.557.870.865.40.820
(54.6, 62.7)(51.7, 57.0)(62.5, 67.1)(65.9, 77.5)(69.0, 72.1)(52.5, 63.1)(66.0, 75.6)(58.5, 72.2)
Diabetes22.917.322.822.60.65023.318.720.620.70.580
(18.9, 26.9)(15.6, 18.9)(20.9, 24.6)(17.3, 28.0)(22.1, 24.5)(14.7, 22.7)(17.4, 23.7)(13.3, 28.1)
Hypertension35.527.731.531.50.50028.825.522.124.50.200
(29.8, 41.2)(25.6, 29.8)(29.3, 33.7)(26.4, 36.6)(27.7, 30.0)(20.4, 30.8)(19.2, 25.0)(16.5, 32.6)
Hypercholesterolemia38.940.244.353.4<0.00141.338.139.242.00.830
(35.7, 42.1)(37.6, 42.8)(41.8, 46.8)(48.4, 58.4)(39.6, 42.9)(32.9, 43.4)(34.9, 43.6)(32.4, 51.6)
Low HDL48.448.151.753.50.23069.268.071.473.10.470
(42.7, 54.1)(44.9, 51.3)(48.7, 54.6)(45.1, 61.8)(67.5, 70.9)(61.8, 74.2)(66.8, 76.1)(59.1, 87.2)
Hypertriglyceridemia32.234.440.445.10.00626.223.931.323.10.900
(26.4, 38.1)(31.9, 36.9)(38.2, 42.7)(36.6, 53.7)(24.9, 27.6)(19.0, 28.7)(26.9, 35.7)(12.6, 33.5)

Abbreviations: CVD, cardiovascular disease; F&V, fruit and vegetable; BMI, body mass index; WHtR, waist-to-height ratio; HDL, high-density lipoprotein cholesterol.

Definitions:

  • Diabetes (self-report or fasting blood glucose≥126 mg/dl or glycated hemoglobin≥6.5%);

  • Hypertension (self-report or measured blood pressure≥140/90 mmHg);

  • Hypercholesterolemia (self-report or total cholesterol≥200 mg/dl or low-density lipoprotein cholesterol≥130 mg/dl);

  • Low HDL (<40 mg/dl [males] and <50 mg/dl [females]);

  • Hypertriglyceridemia (≥150 mg/dl).

a

With 95% confidence intervals in parentheses.

Estimates likely unreliable due to small number of women in this occupation category.

The vast majority of women reported not working outside the home. Also, the small numbers of women white-collar professionals meant those estimates were unstable. As such, the only significant difference observed was gradation of higher prevalence of obesity across non-working, low skilled, skilled, and white-collar women (p=0.028) (Table 3).

We noted 26–30% of participants across cities had two risk factors while 25–31% had three or more risk factors (Figure 1); although there were statistical differences noted, there were no patterned differences in the prevalence of one, two or three or more risk factors across education, wealth or occupation groups.

Age and sex-standardized prevalence (%)†* of multiple risk factors among Chennai, Delhi and Karachi residents aged 20 years or over by education (a), assets accumulated (b) and occupation (c), CARRS (n = 16,287).
Figure 1.

Age and sex-standardized prevalence (%)†* of multiple risk factors among Chennai, Delhi and Karachi residents aged 20 years or over by education (a), assets accumulated (b) and occupation (c), CARRS (n = 16,287).

*With 95% confidence intervals (error bars).

†Proportion of adults with one, two and three or more cardiovascular disease (CVD) risk factors (out of: current tobacco use (smoked or smokeless), central adiposity (waist-to-height ratio ≥0.5), diabetes, hypertension and hypercholesterolaemia).

Wald tests comparing prevalence of one, two and three or more CVD risk factors across education, asset and occupation groups were statistically significant.

Comparing our imputed analysis to complete case data (Table 4), there were some differences in estimates and almost all estimates using imputed data were lower than for the complete case analysis, except for low F&V intake (4 percentage points [ppt] higher) and hypercholesterolemia (8 ppt higher). When standardized to the world’s age and sex distribution, prevalence of central adiposity, diabetes, hypertension, and ≥3 risk factors were all significantly higher –between 1 and 3ppt– than our non-standardized estimates.

Table 4.

Crude and standardized prevalencea of CVD risk factors using complete and imputed data for Chennai, Delhi and Karachi residents aged ≥20 years, CARRS Study.

Complete case analysis (n = 10,976)
Multiple Imputation analysis (n = 16,287)
Crude Prevalence (%)95% CIsRegional Standardized Prevalence (%)95% CIsGlobal Standardized Prevalence (%)95% CIs
Mean age (SD): 42.2 (13.3)Mean age (SD): 42.2 (13.3)Mean age (SD): 42.6 (15.9)
Behavioural Risk Factors
 Low F&V intake55.9(53.5, 58.3)59.7(58.3, 61.2)57.2(55.0, 59.4)
 Tobacco Smoking12.9(11.4, 14.6)12.1(11.4, 12.7)12.5(11.8, 13.2)
 Smokeless Tobacco Use12.1(10.7, 13.7)13.7(12.7, 14.6)12.7(11.7, 13.7)
Weight-related Risk Factors
 BMI 23–24.9 kg/m215.3(14.5, 16.2)15.0(14.3, 15.8)15.3(14.5, 16.0)
 BMI 25–29.9 kg/m233.7(32.6, 35.0)30.5(29.5, 31.6)31.6(30.4, 32.8)
 BMI ≥30 kg/m218.0(16.7, 19.3)15.3(14.5, 16.1)16.0(15.1, 16.9)
 Waist height ratio≥0.572.2(70.6, 73.7)65.2(64.2, 66.3)67.8(66.7, 68.9)
Metabolic Risk Factors
 Diabetes25.1(23.4, 26.9)21.7(21.0, 22.4)25.0(24.1, 25.8)
 Hypertension32.3(28.9, 34.1)29.4(28.5, 30.3)32.6(31.6, 33.6)
 Hypercholesterolemia33.7(32.0, 35.4)41.9(40.9, 43.0)43.5(42.3, 44.6)
 HDL < 40(M) < 50(F)62.6(60.8, 64.4)59.5(58.3, 60.8)59.9(58.4, 61.3)
 Hypertriglyceridemia33.2(31.7, 34.8)31.5(30.4, 32.6)33.1(31.9, 34.3)
Number of Risk Factors
 1 Risk Factor29.6(28.3, 31.1)29.2(28.2, 30.2)27.3(26.3, 28.3)
 2 Risk Factors28.0(26.9, 29.0)27.8(27.0, 28.7)28.0(27.2, 28.9)
 ≥3 Risk Factors29.3(27.4, 31.3)28.7(27.9, 29.4)32.0(31.2, 32.9)
Complete case analysis (n = 10,976)
Multiple Imputation analysis (n = 16,287)
Crude Prevalence (%)95% CIsRegional Standardized Prevalence (%)95% CIsGlobal Standardized Prevalence (%)95% CIs
Mean age (SD): 42.2 (13.3)Mean age (SD): 42.2 (13.3)Mean age (SD): 42.6 (15.9)
Behavioural Risk Factors
 Low F&V intake55.9(53.5, 58.3)59.7(58.3, 61.2)57.2(55.0, 59.4)
 Tobacco Smoking12.9(11.4, 14.6)12.1(11.4, 12.7)12.5(11.8, 13.2)
 Smokeless Tobacco Use12.1(10.7, 13.7)13.7(12.7, 14.6)12.7(11.7, 13.7)
Weight-related Risk Factors
 BMI 23–24.9 kg/m215.3(14.5, 16.2)15.0(14.3, 15.8)15.3(14.5, 16.0)
 BMI 25–29.9 kg/m233.7(32.6, 35.0)30.5(29.5, 31.6)31.6(30.4, 32.8)
 BMI ≥30 kg/m218.0(16.7, 19.3)15.3(14.5, 16.1)16.0(15.1, 16.9)
 Waist height ratio≥0.572.2(70.6, 73.7)65.2(64.2, 66.3)67.8(66.7, 68.9)
Metabolic Risk Factors
 Diabetes25.1(23.4, 26.9)21.7(21.0, 22.4)25.0(24.1, 25.8)
 Hypertension32.3(28.9, 34.1)29.4(28.5, 30.3)32.6(31.6, 33.6)
 Hypercholesterolemia33.7(32.0, 35.4)41.9(40.9, 43.0)43.5(42.3, 44.6)
 HDL < 40(M) < 50(F)62.6(60.8, 64.4)59.5(58.3, 60.8)59.9(58.4, 61.3)
 Hypertriglyceridemia33.2(31.7, 34.8)31.5(30.4, 32.6)33.1(31.9, 34.3)
Number of Risk Factors
 1 Risk Factor29.6(28.3, 31.1)29.2(28.2, 30.2)27.3(26.3, 28.3)
 2 Risk Factors28.0(26.9, 29.0)27.8(27.0, 28.7)28.0(27.2, 28.9)
 ≥3 Risk Factors29.3(27.4, 31.3)28.7(27.9, 29.4)32.0(31.2, 32.9)
a

Prevalence data and 95% confidence intervals are age- and sex-standardized to the world’s population.

Abbreviations: CVD, cardiovascular disease; F&V, fruit and vegetable; BMI, body mass index; WHtR, waist-to-height ratio; HDL, high-density lipoprotein cholesterol.

Definitions:

  • Diabetes (self-report or fasting blood glucose≥126 mg/dl or glycated hemoglobin≥6.5%);

  • Hypertension (self-report or measured blood pressure≥140/90 mmHg);

  • Hypercholesterolemia (self-report or total cholesterol≥200 mg/dl or low-density lipoprotein cholesterol ≥130 mg/dl);

  • Low HDL (<40 mg/dl [males] and <50 mg/dl [females]);

  • Hypertriglyceridemia (≥150 mg/dl).

Table 4.

Crude and standardized prevalencea of CVD risk factors using complete and imputed data for Chennai, Delhi and Karachi residents aged ≥20 years, CARRS Study.

Complete case analysis (n = 10,976)
Multiple Imputation analysis (n = 16,287)
Crude Prevalence (%)95% CIsRegional Standardized Prevalence (%)95% CIsGlobal Standardized Prevalence (%)95% CIs
Mean age (SD): 42.2 (13.3)Mean age (SD): 42.2 (13.3)Mean age (SD): 42.6 (15.9)
Behavioural Risk Factors
 Low F&V intake55.9(53.5, 58.3)59.7(58.3, 61.2)57.2(55.0, 59.4)
 Tobacco Smoking12.9(11.4, 14.6)12.1(11.4, 12.7)12.5(11.8, 13.2)
 Smokeless Tobacco Use12.1(10.7, 13.7)13.7(12.7, 14.6)12.7(11.7, 13.7)
Weight-related Risk Factors
 BMI 23–24.9 kg/m215.3(14.5, 16.2)15.0(14.3, 15.8)15.3(14.5, 16.0)
 BMI 25–29.9 kg/m233.7(32.6, 35.0)30.5(29.5, 31.6)31.6(30.4, 32.8)
 BMI ≥30 kg/m218.0(16.7, 19.3)15.3(14.5, 16.1)16.0(15.1, 16.9)
 Waist height ratio≥0.572.2(70.6, 73.7)65.2(64.2, 66.3)67.8(66.7, 68.9)
Metabolic Risk Factors
 Diabetes25.1(23.4, 26.9)21.7(21.0, 22.4)25.0(24.1, 25.8)
 Hypertension32.3(28.9, 34.1)29.4(28.5, 30.3)32.6(31.6, 33.6)
 Hypercholesterolemia33.7(32.0, 35.4)41.9(40.9, 43.0)43.5(42.3, 44.6)
 HDL < 40(M) < 50(F)62.6(60.8, 64.4)59.5(58.3, 60.8)59.9(58.4, 61.3)
 Hypertriglyceridemia33.2(31.7, 34.8)31.5(30.4, 32.6)33.1(31.9, 34.3)
Number of Risk Factors
 1 Risk Factor29.6(28.3, 31.1)29.2(28.2, 30.2)27.3(26.3, 28.3)
 2 Risk Factors28.0(26.9, 29.0)27.8(27.0, 28.7)28.0(27.2, 28.9)
 ≥3 Risk Factors29.3(27.4, 31.3)28.7(27.9, 29.4)32.0(31.2, 32.9)
Complete case analysis (n = 10,976)
Multiple Imputation analysis (n = 16,287)
Crude Prevalence (%)95% CIsRegional Standardized Prevalence (%)95% CIsGlobal Standardized Prevalence (%)95% CIs
Mean age (SD): 42.2 (13.3)Mean age (SD): 42.2 (13.3)Mean age (SD): 42.6 (15.9)
Behavioural Risk Factors
 Low F&V intake55.9(53.5, 58.3)59.7(58.3, 61.2)57.2(55.0, 59.4)
 Tobacco Smoking12.9(11.4, 14.6)12.1(11.4, 12.7)12.5(11.8, 13.2)
 Smokeless Tobacco Use12.1(10.7, 13.7)13.7(12.7, 14.6)12.7(11.7, 13.7)
Weight-related Risk Factors
 BMI 23–24.9 kg/m215.3(14.5, 16.2)15.0(14.3, 15.8)15.3(14.5, 16.0)
 BMI 25–29.9 kg/m233.7(32.6, 35.0)30.5(29.5, 31.6)31.6(30.4, 32.8)
 BMI ≥30 kg/m218.0(16.7, 19.3)15.3(14.5, 16.1)16.0(15.1, 16.9)
 Waist height ratio≥0.572.2(70.6, 73.7)65.2(64.2, 66.3)67.8(66.7, 68.9)
Metabolic Risk Factors
 Diabetes25.1(23.4, 26.9)21.7(21.0, 22.4)25.0(24.1, 25.8)
 Hypertension32.3(28.9, 34.1)29.4(28.5, 30.3)32.6(31.6, 33.6)
 Hypercholesterolemia33.7(32.0, 35.4)41.9(40.9, 43.0)43.5(42.3, 44.6)
 HDL < 40(M) < 50(F)62.6(60.8, 64.4)59.5(58.3, 60.8)59.9(58.4, 61.3)
 Hypertriglyceridemia33.2(31.7, 34.8)31.5(30.4, 32.6)33.1(31.9, 34.3)
Number of Risk Factors
 1 Risk Factor29.6(28.3, 31.1)29.2(28.2, 30.2)27.3(26.3, 28.3)
 2 Risk Factors28.0(26.9, 29.0)27.8(27.0, 28.7)28.0(27.2, 28.9)
 ≥3 Risk Factors29.3(27.4, 31.3)28.7(27.9, 29.4)32.0(31.2, 32.9)
a

Prevalence data and 95% confidence intervals are age- and sex-standardized to the world’s population.

Abbreviations: CVD, cardiovascular disease; F&V, fruit and vegetable; BMI, body mass index; WHtR, waist-to-height ratio; HDL, high-density lipoprotein cholesterol.

Definitions:

  • Diabetes (self-report or fasting blood glucose≥126 mg/dl or glycated hemoglobin≥6.5%);

  • Hypertension (self-report or measured blood pressure≥140/90 mmHg);

  • Hypercholesterolemia (self-report or total cholesterol≥200 mg/dl or low-density lipoprotein cholesterol ≥130 mg/dl);

  • Low HDL (<40 mg/dl [males] and <50 mg/dl [females]);

  • Hypertriglyceridemia (≥150 mg/dl).

Examining data from each city (Appendices 3–6), the same pattern of low fruit/vegetable intake among lower educated was evident in Delhi and Karachi, and higher tobacco use was noted among Delhi and Chennai’s lower educated groups. The pattern of higher overweight, obesity, central obesity and diabetes prevalence among the highest educated was only evident in Delhi. The pattern of less behavioural risk factors and higher overweight, obesity, central obesity, diabetes, hypercholesterolaemia, and hypertriglyceridemia among the wealthiest was evident in Delhi, but not other cities. There was no patterning of CVD risk across occupations in any city.

Discussion

Main findings

In this large representative urban South Asian population, smoked and smokeless tobacco use were two to four times more prevalent in low education and less wealthy strata than their respective higher SES counterparts. Low fruit/vegetable intake was also more common in low education and wealth strata. The opposite was true for weight-related risks – prevalence of overweight, obesity and central adiposity were 1.5 times as prevalent in higher than lower education or wealth groups. Prevalence estimates for diabetes and hypercholesterolaemia were statistically higher among the most educated and wealthiest compared to their less educated and less wealthy counterparts, but not patterned across occupation groups. Hypertension was more prevalent among more affluent as well. The prevalence of multiple risk factors was not different across SES groups.

Comment

This mixed pattern of higher behavioural risk factors among the socioeconomically disadvantaged and higher weight profiles among advantaged groups are consistent with other reports from developing countries like Mexico,24 Guatemala25 and previous reports from India.15,16 At the individual and household level, lower SES and corresponding behaviours might reflect a preoccupation with food quantity over quality and low awareness of tobacco’s harms. With higher wealth, there is greater access to calorie-dense foods without corresponding increases in activity levels leading to a positive energy balance, or higher weight may be a socially desirable status symbol.

Our data show different patterns of association between different SES indicators and metabolic risks. This correctly reflects lack of correlation between occupation and other SES indicators in South Asia, as was observed in our analyses (Appendix 2).There were some differences in metabolic risks by education, and higher metabolic risks concentrated among the wealthiest and technical or professional occupations for men. This implies some epidemiological transition may be on-going. Higher prevalence among the educated was also noted in a review of studies that collected data between 1975 and 2007.26 However, these differences in the prevalence of a few percentage points should be taken in context, as 80% of our populations, which are representative of their respective cities, belong to lower-middle SES groups (only 16% completed tertiary education, 3% were white-collar occupations and 11% earn≥US$400 per month). As such the absolute number of people in lower-middle SES that are affected by CVD risk is very high. These estimates become even more stark when one considers that India and Pakistan’s current combined urban population outnumbers 450 million; two-thirds of them have excess central adiposity and a quarter have one or more metabolic risk factor. Also, lower SES groups in our study had a higher prevalence of behavioural risks, which foretells of impending metabolic and cardiovascular abnormalities. It appears CVD has cross-population impacts, no matter which SES group one belongs to.

Several hypotheses have been proposed27,28 to explain these paradoxical social gradients in behavioural, weight-related and metabolic risks. SES-CVD risk factor relationships may evolve as societies transition. Our data show that these large city populations are not in early phases of the CVD epidemic in which risk-prone behaviours (e.g. tobacco use, poor diets) are confined to the affluent and educated; nor are these cities in advanced epidemiological phases in which the advantaged exhibit healthier behaviours and metabolic profiles. Our data suggest that different SES groups have different risk profiles.

We noted that CVD risk factors were very prevalent, despite a fairly young average age across cities, and these estimates would be between 1 and 5 ppt higher for weight and metabolic risks when standardized to an older global population. This may reflect a period effect in which South Asia’s young adults are exposed to economic and nutritional/lifestyle transitions. Also, this corroborates findings from the INTERHEART study showing a higher prevalence of CVD risks in South Asians partly explained the younger age of first MI between South Asian and other countries.2

Examining SES-CVD relationships may have implications for societal action and policies as identifying modifiable exposure–outcome associations may help guide the design of appropriate interventions. For example, our findings suggest that identifying and implementing suitable and effective tobacco awareness, prevention and cessation interventions for lower SES groups may have important benefits. Demand for tobacco has been shown to be especially price-elastic among lower SES groups.29 Meanwhile, addressing metabolic risks appears to be necessary across SES groups.

Limitations and strengths

These cross-sectional urban data limit causal inferences and generalizations as South Asia is made up of diverse countries, states and cities. Furthermore, characterizing SES is challenging,18,30 as is the interpretation of SES indicators, especially when gender interacts (e.g. should wealthy homemakers get assigned to high or low SES groups?). We used categorical exposure variables and covariates, which may reduce power and obscure patterns, especially if some groups have small sample sizes. SES is dynamic and we cannot account for how rapidly participants’ wealth was accrued, or for the considerable heterogeneity within each SES group. Although caste, a hereditary class system in Hindu society, may be another important SES indicator in India, the concept does not exist in Pakistan and was therefore not examined. There may have been a slight misclassification of CVD risk factors as self-reported diabetes, hypertension and dyslipidaemia and measured indicators may not have captured all those actively using medications.

These concerns are counterbalanced by some important strengths. The cities surveyed are typical Indian and Pakistani metropolises. Compared to existing SES-CVD literature from South Asia, ours is one of a few studies14,16 that used multiple SES indicators and examined sample populations that are representative of 44 million people from across the SES spectrum. A study of employees at ten Indian industries included a specific, homogenous population representing specific educational and occupation phenotypes.13 The studies of 11 urban middle-class cities16 and 1800 rural villages15 both had response rates less than 50% and the latter relied on self-reported risk factors. Another study in 20 Andra Pradesh villages had 80% response, but data were self-reported.31 The use of self-report is particularly prone to underestimation of chronic diseases, as was persuasively shown from 2007 data across six Indian states where differences between the self-reported and measured prevalence of five chronic diseases were evident.14 Data in our study were collected using uniform methods and tools across sites. We performed multiple imputation (standardized to regional population structures to account for city-level differences) and sensitivity analyses to test for influences of missing data and city-specific variation.

Conclusions

SES-CVD relationships in South Asia are heterogeneous and still unravelling. The socioeconomically advantaged and disadvantaged in the region face some overlapping and some divergent risks. Addressing these will be challenging. Already, South Asians experience metabolic risks at younger ages and no SES group is spared. These recent data offer a helpful guide towards recognizing future risks as well as customizing interventions to address CVD in the region. Further surveillance is also needed to monitor these transitions and impacts of interventions.

Acknowledgements

The authors would like to thank and recognize Dr Bob Gerzoff and Dr Kai M Bullard (US Centers for Disease Control and Prevention) for their help with statistical analyses, data management and multiple imputation.

Funding

The CARRS Study and authors MKA, MMK, VM, NT, KMVN and DP were funded in whole or in part by the National Heart, Lung, and Blood Institute of the National Institutes of Health, Department of Health and Human Services (contract no. HHSN268200900026C) and the United Health Group (Minneapolis, MN, USA). Authors BB and RS were supported by grant number 1 D43 HD065249 from the Fogarty International Centre and the Eunice Kennedy Shriver National Institute of Child Health and Human Development at the National Institutes of Health.

Conflict of interest

The authors have no conflicts of interest to disclose.

Contributorship statement

The CARRS Study Group includes the following:

  • Steering Committee: Dorairaj Prabhakaran, KM Venkat Narayan, K Srinath Reddy, Nikhil Tandon, V Mohan, Muhammed M Kadir, Mohammed K Ali

  • Conduct and operations: Dorairaj Prabhakaran, Nikhil Tandon, KM Venkat Narayan, Mohammed K Ali, Roopa Shivashankar, Imran Naeem, R Pradeepa, M Deepa

  • Coordinating Centre (Delhi): Dorairaj Prabhakaran, Nikhil Tandon, Roopa Shivashankar, Vamadevan S Ajay, Deksha Kapoor

  • Data management and statistical team: Dimple Kondal, Shivam Pandey, Praggya, Naveen

  • Laboratory: Lakshmy Ramakrishnan, Ruby Gupta, Savita

  • Reporting: Mohammed K Ali, Nikhil Tandon, KM Venkat Narayan and Dorairaj Prabhakaran conceived of the analysis and study question, and wrote the manuscript. Authors Binukumar and Roopa conducted analyses. All other authors contributed to editing and revising of manuscript.

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