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. 2019 May 8;127(5):057003. doi: 10.1289/EHP3915

Health Effects of Household Solid Fuel Use: Findings from 11 Countries within the Prospective Urban and Rural Epidemiology Study

Perry Hystad 1,, MyLinh Duong 2, Michael Brauer 3, Andrew Larkin 1, Raphael Arku 4, Om P Kurmi 5, Wen Qi Fan 6, Alvaro Avezum 7, Igbal Azam 8, Jephat Chifamba 9, Antonio Dans 10, Johan L du Plessis 11, Rajeev Gupta 12, Rajesh Kumar 13, Fernando Lanas 14, Zhiguang Liu 15, Yin Lu 16, Patricio Lopez-Jaramillo 17, Prem Mony 18, Viswanathan Mohan 19, Deepa Mohan 19, Sanjeev Nair 20, Thandi Puoane 21, Omar Rahman 22, Ah Tse Lap 15, Yanga Wang 16, Li Wei 16, Karen Yeates 23, Sumathy Rangarajan 5, Koon Teo 5, Salim Yusuf 5; [on behalf of Prospective Urban and Rural Epidemiological (PURE) Study investigators]
PMCID: PMC6791569  PMID: 31067132

Abstract

Background:

Household air pollution (HAP) from solid fuel use for cooking affects 2.5 billion individuals globally and may contribute substantially to disease burden. However, few prospective studies have assessed the impact of HAP on mortality and cardiorespiratory disease.

Objectives:

Our goal was to evaluate associations between HAP and mortality, cardiovascular disease (CVD), and respiratory disease in the prospective urban and rural epidemiology (PURE) study.

Methods:

We studied 91,350 adults 35–70 y of age from 467 urban and rural communities in 11 countries (Bangladesh, Brazil, Chile, China, Colombia, India, Pakistan, Philippines, South Africa, Tanzania, and Zimbabwe). After a median follow-up period of 9.1 y, we recorded 6,595 deaths, 5,472 incident cases of CVD (CVD death or nonfatal myocardial infarction, stroke, or heart failure), and 2,436 incident cases of respiratory disease (respiratory death or nonfatal chronic obstructive pulmonary disease, pulmonary tuberculosis, pneumonia, or lung cancer). We used Cox proportional hazards models adjusted for individual, household, and community-level characteristics to compare events for individuals living in households that used solid fuels for cooking to those using electricity or gas.

Results:

We found that 41.8% of participants lived in households using solid fuels as their primary cooking fuel. Compared with electricity or gas, solid fuel use was associated with fully adjusted hazard ratios of 1.12 (95% CI: 1.04, 1.21) for all-cause mortality, 1.08 (95% CI: 0.99, 1.17) for fatal or nonfatal CVD, 1.14 (95% CI: 1.00, 1.30) for fatal or nonfatal respiratory disease, and 1.12 (95% CI: 1.06, 1.19) for mortality from any cause or the first incidence of a nonfatal cardiorespiratory outcome. Associations persisted in extensive sensitivity analyses, but small differences were observed across study regions and across individual and household characteristics.

Discussion:

Use of solid fuels for cooking is a risk factor for mortality and cardiorespiratory disease. Continued efforts to replace solid fuels with cleaner alternatives are needed to reduce premature mortality and morbidity in developing countries. https://doi.org/10.1289/EHP3915

Introduction

Approximately 2.5 billion individuals globally are exposed to household air pollution (HAP) from cooking with solid fuels such as coal, wood, dung, or crop residues (Smith et al. 2014). Concentrations of air pollutants, especially fine particulate matter [PM2.5μm  in aerodynamic diameter  (PM2.5)], can be several orders of magnitude higher in homes cooking with solid fuels compared with those using clean fuels such as electricity or liquefied petroleum gas (LPG) (Clark et al. 2013; Shupler et al. 2018). PM2.5 in outdoor air has been linked to mortality, ischemic heart disease (IHD), stroke, and respiratory diseases (Kim et al. 2015).

Despite the large population exposed and the potential for adverse health effects, few prospective cohort studies have examined the health effects of HAP. Only four studies have examined HAP and mortality and reached contradictory conclusions (Alam et al. 2012; Kim et al. 2016; Mitter et al. 2016; Yu et al. 2018). Further, studies have not examined HAP and fatal as well as nonfatal cardiovascular disease (CVD) events. There is growing evidence of the adverse effects of HAP on respiratory diseases and lung cancer; however, most studies are cross sectional or case–control in design, with relatively small sample sizes and limited geographic coverage (Gordon et al. 2014). To date, few prospective studies have examined HAP exposures and respiratory events in adults, and the existing studies have reported contradictory findings (Chan et al. 2019; Ezzati and Kammen 2001; Mitter et al. 2016).

Given the absence of direct epidemiological data, the Global Burden of Disease (GBD) study estimated the potential impact of HAP on health using exposure–response relationships that pooled data from studies on outdoor air pollution, secondhand smoke, and active smoking (Burnett et al. 2014). These predictions indicated that 1.6 million deaths were attributable to HAP exposure in 2017, of which 39% were from IHD and stroke and 55% from respiratory outcomes [>90% from chronic obstructive pulmonary disease (COPD) and acute lower respiratory infections (ALRI)] (GBD 2017 Risk Factor Collaborators 2018). Given the lack of direct epidemiological evidence and this large predicted burden, there is an urgent need to directly characterize the health effects associated with HAP.

Within the Prospective Urban and Rural Epidemiology (PURE) study, we conducted an analysis of 91,350 adults from 467 urban and rural communities in 11 low- to middle-income countries (LMICs) where solid fuels are commonly used for cooking. We examined associations between cooking with solid fuels—as a proxy indicator of HAP exposure—and cause-specific mortality, incident cases of CVD [CVD death and incidence of nonfatal myocardial infarction (MI), stroke, and heart failure (HF)] and incident cases of respiratory disease [respiratory death, nonfatal COPD, pulmonary tuberculosis (TB), pneumonia, or lung cancer]. We estimated associations between solid fuel use for cooking and these outcomes, controlling for extensive individual, household, and community covariates.

Methods

The PURE Cohort and Household Air Pollution Substudy

The PURE study is a large multinational cohort study of individuals 35–70 y of age enrolled from 21 countries in five continents. The methodology of the PURE study has been described in detail elsewhere (Dehghan et al. 2017; Teo et al. 2009; Yusuf et al. 2014). Briefly, PURE countries were selected to cover a wide range of socioeconomic and environmental settings, especially in LMICs, where health-related data are sparse. The primary sampling unit was the “community” in urban areas, selected based on known information of the geographical area such as a set of contiguous postal codes or groups of streets corresponding roughly to a neighborhood. Rural communities were small villages at least 50km from cities. Many of these communities were remote with few health facilities. Communities were clustered into centers (representing regions) within countries. Households with at least one member 35–70 y of age with no plans to move in the next 5 y were approached for recruitment. This HAP analysis was restricted to the subset of individuals living in centers where at least 10% of the participants primarily used solid fuels for cooking. This resulted in a study population of 91,350 adults from 467 urban and rural communities in 11 countries (Bangladesh, Brazil, Chile, China, Colombia, India, Pakistan, Philippines, South Africa, Tanzania, and Zimbabwe).

Data Collection

Baseline data included in this analysis were collected from 2002 to 2015. Standardized interview-based questionnaires were used to collect individual and household information on demographics, socioeconomic status (SES), risk factors, and medical histories (Corsi et al. 2013; Teo et al. 2009; Yusuf et al. 2014).

Face-to-face or telephone interviews were conducted with participants at least every 3 y during follow-up to document events. Up to three attempts were made to interview all households. The PURE study includes LMICs where there is unreliable or no death or clinical event registries. To determine a probable cause of death, hospitalization, or event, we obtained information from interviews of participants or their relatives, additional details from hospital records, medically certified cause of death, and verbal autopsies where medical information was not available (Gajalakshmi et al. 2002). Additional information on CVD (MI, stroke, and HF) were collected and used for event adjudication, conducted centrally in each county by trained physicians using standardized definitions. To ensure a consistent approach and high accuracy for event classification across all countries and over time, the first 100 CVD events per year for China and India, and 50 events per year for other countries, were adjudicated both locally and centrally by an adjudication chair (Dehghan et al. 2017; Teo et al. 2009; Yusuf et al. 2014).

We examined a range of outcomes hypothesized to be related to HAP. Mortality outcomes included all-cause mortality, cause-specific mortality due to any CVD, any respiratory condition, any cancer, all other causes combined (excluding CVD, respiratory, and cancer mortality), and accidental mortality (deaths due to accident or trauma in the absence of other causes) as well as deaths due to unspecified causes (not classified). We estimated associations with fatal and nonfatal CVD (MI, stroke, HF), and hospitalization (defined as any medical procedure occurring in a hospital environment or a length of stay for at least 12 h in a hospital, clinic, or emergency room or other similar location) for CVD (MI, stroke, HF), as well as fatal and nonfatal major respiratory diseases (COPD, TB, pneumonia, lung cancer), and hospitalization for major respiratory diseases (COPD, TB, pneumonia, lung cancer). In addition, we examined a composite outcome that included deaths from any cause and the first incidence of any major nonfatal CVD (MI, stroke, HF) or major respiratory outcome (COPD, TB, pneumonia, lung cancer), hereafter referred to as “incident cardiorespiratory disease and all-cause mortality.” We estimated associations with asthma diagnoses as a separate outcome because there is little evidence of an association between HAP and asthma in adults (Po et al. 2011) and asthma may be underdiagnosed in LMICs. We also estimated associations with fatal and nonfatal injuries and injury hospitalizations, which we assumed would not be associated with household use of solid fuels for cooking. Detailed criteria for each outcome are provided in the section, “PURE Event Definitions,” in the Supplemental Material.

HAP exposure was derived from the baseline household questionnaire, which asked, “What is the primary fuel used for cooking?” We compared primary use of solid fuels for cooking (charcoal, coal, wood, agriculture/crop, animal dung, shrub/grass) with primary use of clean fuels (electricity/gas). We excluded kerosene from our analysis (n=2,170) because this fuel was used by only a small number of communities and its use results in different air pollution emissions compared with solid fuels (Smith et al. 2014). We have a separate paper examining cooking with kerosene currently under review. We also explored the influence of a chimney inside the cooking area, other ventilation in the cooking area (windows, exhaust, or partially open to the outside), and solid fuel use for heating.

Statistical Analysis

We assessed the associations between solid fuels for cooking at baseline, compared with clean fuels, for each outcome separately using Cox proportional hazards models with SAS (version 9.4; SAS Institute Inc.). For each outcome examined, participants were censored at the time of the event (death or incident CVD and respiratory disease), at the time of loss to follow-up (if a participant could not be contacted or requested to be removed from the study), or the date of last follow-up (given that PURE event surveillance is ongoing, the date of last follow-up can vary between centers). Interaction terms between solid fuel use and time (p-interaction = 0.88, 0.72, 0.87, and 0.56 for all-cause mortality, CVD, respiratory disease, and the composite outcome, respectively) did not improve model fit; therefore, we concluded that the proportion hazards assumption was met.

The base model (Model 1) included age (continuous), sex, baseline year, and strata variables for center and urban/rural status. Strata variables can be viewed as a robust form of control where individuals are only compared with other individuals in the same strata. Center refers to a unique geographical region of PURE participants, for which 28 regions are included in this analysis (Figure 1). All centers had urban and rural communities, which were also included as strata.

Figure 1.

Figure 1 is a world map marking PURE community locations. The locations are scattered around parts of China, parts of India, in the east and south of Africa, and parts of South America.

Map of PURE communities included in the analysis of HAP. Communities were included if they were located in centers with 10% of PURE participants reporting primary use of solid fuels for cooking at baseline.

Model 2 adjusted for additional individual risk factors, including smoking (current, former, never); alcohol use (current, former, never); physical activity (low, moderate, high) assessed using the International Physical Activity Questionnaire (IPAQ) (Craig et al. 2003); body mass index (BMI) (<20/2030/30kg/m3); an alternative healthy eating index (quintiles) developed from dietary intake information collected with a validated food frequency questionnaire (Iqbal et al. 2009); baseline chronic conditions (yes/no; including baseline CVD, diabetes, respiratory disease, and HIV/AIDS); current CVD medication use (yes/no); hypertension (yes/no); the INTERHEART risk score (continuous), a composite index of individual risk measures (Yusuf et al. 2004); and the outdoor average PM2.5 concentrations (continuous) at baseline [based on geographically weighted regression of satellite-based estimates and ground-based PM2.5 measurements at a 1×1km resolution (van Donkelaar et al. 2016)]. Missing data indicator terms were modeled for all categorical variables with missing data. Details regarding the derivation of the physical activity, INTERHEART risk score, and alternative healthy eating index variables are provided in the section, “Calculation Details for Covariate Measures,” in the Supplemental Material.

Model 3 included all Model 2 covariates plus education (primary, secondary, trade or college/university); percent of household income spent on food (quintiles); and a strata variable for household wealth index (categorized into country-specific tertiles), which was created from a combination of household assets (Gupta et al. 2017), as described in Supplemental Material.

Exploratory stratified analyses were conducted to examine associations by key characteristics identified as potential modifiers of HAP exposure or health effects. These were identified a priori from the literature and included the following: region (China, South Asia, other countries), urban versus rural communities, sex (male/female), age (60, <60 y), education (primary education/>primary education), household wealth index (tertiles), occupation (professional or skilled/unskilled/homemaker), smoking status (ever/never smoker), CVD medication use (yes/no), hypertension (yes/no), chronic condition (yes/no) at baseline, BMI (<20/2030/30kg/m3), INTERHEART risk score (<5, 5–11, 11), presence of a chimney in the kitchen (yes/no), any kitchen ventilation (yes/no), solid fuel use for heating (yes/no), and outdoor PM2.5 concentration (<50/50μg/m3 annual average).

We evaluated the robustness of our findings using several sensitivity analyses. First, to examine consistency in associations across different regions and solid fuel types, we explored models for biomass and coal use separately for China, South Asia (India, Pakistan, Bangladesh) and other countries (Brazil, Chile, Colombia, Philippines, South Africa, Tanzania, Zimbabwe) combined into a single group due to smaller sample size. Second, we conducted all analyses for urban and rural communities separately because most households with solid fuel use were in rural communities and there could be important unmeasured context-specific differences between urban and rural areas. Third, we evaluated the sensitivity of our fully adjusted model results to removing or adding specific variables. These included removing covariates that may lie on the causal pathway between HAP and CVD/respiratory events and mortality (baseline chronic conditions, hypertension, CVD medication); removing the household wealth index (which is highly related to solid fuel use); removing outdoor PM2.5 concentrations because emissions from cooking with solid fuels contributes about one-third of ambient air pollution levels in South and South East Asia (Chafe et al. 2014); adding secondhand smoke exposure, occupational class, additional diet variables and lipids (these were not included in the main model due to large amounts of missing data); and adding a community random effect variable (n=467 communities) in order to evaluate clustering of individuals and unmeasured community characteristics. Finally, to examine potential residual confounding and heterogeneity in the effect of HAP by regions and countries, we estimated the effect by center and pooled the estimates using a random effects meta-regression model.

Results

Figure 1 illustrates the location of study communities included in this analysis, and Table 1 presents descriptive statistics. Participants from China and India contributed to 47.4% and 26.4% of the total study population, respectively. In urban areas, 8.2% of participants used solid fuel for cooking compared with 71.7% in rural communities. Solid fuel users had lower INTERHEART risk scores (urban=9.3, rural=8.2) compared with individuals using clean fuels (urban=9.8, rural=9.8), indicating a higher overall risk for CVD in individuals using clean fuels for cooking. Conversely, indicators of SES (education, percentage of household income spent on food, and household wealth index) were lower for solid fuel users. This complex relationship between solid fuel use and traditional CVD risk factors (e.g., diet, smoking, physical activity) and SES is illustrated in Figure S1.

Table 1.

Characteristics of 91,350 individuals living in centers with >10% solid fuel use for cooking, stratified by urban/rural status and solid fuel use for cooking versus electricity or gas.

Characteristic All participants Urban (n=43,001) Rural (n=48,349)
Solid fuel Clean fuel Solid fuel Clean fuel
Individuals (n) 91,350 3,513 39,488 34,674 13,675
Households (n) 62,056 2,618 27,009 23,377 9,052
Communities (n) 467 137 210 254 199
Age (mean±SD) 50.2±10.0 50.5±10.4 51.2±10.0 49.3±10.0 49.4±9.7
Sex
 Female 53,758 (58.9) 2,266 (64.5) 23,493 (59.5) 20,038 (57.8) 7,961 (58.2)
 Male 37,592 (41.2) 1,247 (35.3) 15,995 (40.5) 14,636 (42.2) 5,714 (41.8)
INTERHEART risk score (mean±SD) 9.2±5.3 9.3±5.3 9.8±5.4 8.2±5.0 9.8±5.5
Education
Primary school 40,865 (44.70) 1,809 (51.5) 9,782 (24.8) 22,313 (64.4) 6,961 (50.9)
 Secondary school 37,785 (41.4) 1,390 (39.6) 19,120 (48.4) 11,364 (32.8) 5,911 (43.2)
 Trade, college/university 12,378 (13.6) 307 (8.7) 10,475 (26.5) 834 (2.4) 762 (5.6)
 Missing 322 (0.4) 7 (0.2) 111 (0.3) 163 (2.4) 41 (0.3)
Income spent on food (%)
<30 19,960 (21.9) 540 (15.4) 9,499 (24.1) 6,241 (18) 3,680 (26.9)
 30–50 22,854 (25.0) 845 (24.1) 11,997 (30.4) 6,944 (20.0) 3,068 (22.4)
 50–66 20,475 (22.4) 823 (23.4) 9,573 (24.2) 7,445 (21.5) 2,634 (19.3)
>66 24,334 (26.6) 1,222 (34.8) 7,067 (17.9) 12,784 (36.9) 3,261 (19.3)
 Missing 3,727 (4.1) 83 (2.4) 1,352 (3.4) 1,260 (3.6) 1,032 (7.6)
Household wealth index (tertile)
 T1 (lowest) 31,211 (34.2) 767 (21.8) 3,327 (8.4) 22,177 (64.0) 4,940 (36.1)
 T2 29,518 (32.3) 1,663 (47.3) 12,672 (32.1) 9,793 (28.2) 5,390 (39.4)
 T3 (highest) 30,550 (33.4) 1,081 (30.8) 23,452 (59.4) 2,673 (7.7) 3,344 (24.5)
 Missing 71 (0.1) 2 (0.1) 37 (0.1) 31 (0.1) 1 (0.0)
Smoking status
 Former 6,077 (6.7) 245 (7.0) 2,958 (7.5) 1,836 (5.3) 1,038 (7.6)
 Current 20,248 (22.2) 640 (18.2) 7,227 (18.3) 9,325 (26.9) 3,056 (22.4)
 Never 63,822 (69.9) 2,599 (74.0) 28,902 (73.2) 22,927 (66.1) 9,394 (68.7)
 Missing 1,203 (1.3) 29 (0.8) 401 (1.0) 586 (1.7) 187 (1.4)
Alcohol use
 Former 4,088 (4.5) 152 (4.3) 1,819 (4.6) 1,371 (4.0) 746 (5.5)
 Current 17,899 (19.6) 691 (19.7) 7,349 (18.6) 6,578 (19.0) 3,281 (24.0)
 Never 68,531 (75.0) 2,660 (75.7) 30,065 (76.1) 26,301 (75.9) 9,505 (69.5)
 Missing 832 (0.9) 10 (0.3) 255 (0.7) 424 (1.2) 143 (1.1)
BMI (kg/m3)
<20 13,326 (14.6) 524 (14.9) 2,830 (7.2) 8,569 (24.7) 1,403 (10.3)
 20–30 63,920 (70.0) 2,227 (63.4) 29,690 (75.2) 22,073 (63.7) 9,930 (72.6)
>30 9,592 (10.5) 582 (16.6) 5,361 (13.6) 1,980 (5.7) 1,669 (12.2)
 Missing 4,512 (4.9) 180 (5.1) 1,607 (4.1) 2,052 (5.9) 673 (4.9)
Physical activity
 Low 14,896 (16.3) 568 (16.2) 7,234 (18.3) 4,978 (14.4) 2,116 (15.5)
 Moderate 32,316 (35.4) 1,111 (31.6) 15,949 (40.4) 10,894 (31.4) 4,362 (31.9)
 High 38,178 (41.8) 1,636 (46.6) 14,847 (37.6) 15,955 (46.0) 5,740 (42.0)
 Missing 5,960 (6.5) 198 (5.6) 1,458 (3.7) 2,847 (8.2) 1,457 (10.7)
Alternative Healthy Eating Index (quartile)
 Q1 21,752 (23.8) 1,040 (29.6) 7,668 (19.4) 9,516 (27.4) 3,528 (25.8)
 Q2 21,241 (23.3) 905 (25.8) 8,794 (22.3) 8,304 (24.0) 3,238 (23.7)
 Q3 21,848 (23.9) 768 (21.9) 9,904 (25.1) 8,083 (23.3) 3,093 (22.6)
 Q4 22,288 (24.4) 299 (17.1) 11,115 (28.2) 7,361 (21.2) 3,213 (23.5)
 Missing 4,221 (4.6) 201 (5.7) 2,007 (5.1) 1,410 (4.1) 603 (4.4)
Chronic conditiona
 Yes 14,597 (16.0) 633 (18.0) 7,617 (19.3) 4,359 (12.6) 1,988 (14.5)
 No 76,753 (84.0) 2,880 (82.0) 31,871 (80.7) 30,315 (87.4) 11,687 (85.5)
Hypertension
 Yes 34,414 (37.7) 1,338 (38.1) 16,191 (41.0) 11,345 (32.7) 5,540 (40.5)
 No 52,464 (57.4) 1,989 (56.6) 21,722 (55.0) 21,218 (61.2) 7,535 (55.1)
 Missing 4,472 (4.9) 186 (5.3) 1,575 (4.0) 2,111 (6.1) 600 (4.4)
CVD medication use
 Yes 11,526 (12.6) 392 (11.2) 6,594 (16.7) 2,592 (7.5) 1,948 (14.2)
 No 79,824 (87.4) 3,121 (88.8) 32,894 (83.3) 32,082 (92.5) 11,727 (85.8)
Outdoor PM2.5 (μg/m3; mean±SD) 42.9±24.9 37.9±24.8 50.7±25.9 37.3±21.3 35.7±23.6
Region/country (%)
 China 43,278 (47.4%) 762 (21.7%) 19,331 (49.0%) 16,884 (48.7%) 6,301 (46.1%)
 South Asiab 28,406 (31.1%) 1,599 (45.5%) 11,396 (28.9%) 12,473 (36.0%) 2,938 (21.5%)
 Otherc 19,666 (21.5%) 1,152 (32.8%) 8,761 (22.2%) 5,317 (15.3%) 4,436 (32.4%)
a

Chronic conditions include baseline CVD, diabetes, respiratory disease, and HIV/AIDS.

b

Pakistan, India, Bangladesh.

c

Brazil, Chile, Colombia, Philippines, South Africa, Tanzania, Zimbabwe.

After a median follow-up period of 9.1 y, we recorded 6,595 deaths, 5,472 incident cases of CVD, and 2,436 incident cases of major respiratory disease. Table 2 summarizes the associations between solid fuels use, relative to clean fuels, for each outcome. Model 1 showed large associations for mortality and respiratory disease and relatively weaker associations with CVD. Model 2 included risk factor adjustments, which resulted in the overall association with mortality and respiratory disease being largely unchanged from Model 1 but also increased the estimates of effect for CVD mortality [hazard ratio (HR) 1.18; 95% confidence interval (CI): 1.04, 1.34] and incident cases of fatal and nonfatal CVD (1.14; 95% CI: 1.05, 1.23). Model 3 included further adjustment for SES measures, which resulted in attenuation of all associations. Here, solid fuel use was associated with an HR of 1.12 (95% CI: 1.04, 1.21) for all-cause mortality, 1.08 (95% CI: 0.99, 1.17) for CVD, and 1.14 (95% CI: 1.00, 1.30) for respiratory disease. The fully adjusted HRs were slightly larger for CVD (95% CI: 1.10, 1.00, 1.22) and respiratory (95% CI: 1.17, 0.98, 1.38) disease that had documented hospitalization. The HR for the composite outcome of incident cardiorespiratory disease and all-cause mortality was 1.12 (95% CI: 1.06, 1.91) in the fully adjusted model. No associations were observed in fully adjusted models between injury events or hospitalizations, although a positive association was observed for injury deaths.

Table 2.

Associations (hazard ratios [95% confidence intervals]) between individuals living in households using solid fuels for cooking, compared with clean fuels, and cause-specific mortality, CVD, and respiratory disease during a median of 9.1-y follow-up.

Health outcome Events Model 1 (base model) Model 2 (+risk factors) Model 3 (+SES)
All-cause mortality 6,595 1.24 (1.15, 1.33) 1.24 (1.16, 1.34) 1.12 (1.04, 1.21)
Cause-specific mortalitya
 CVD 2,104 1.08 (0.95, 1.22) 1.18 (1.04, 1.34) 1.04 (0.91, 1.19)
 Respiratory 356 1.82 (1.32, 2.51) 1.54 (1.11, 2.12) 1.34 (0.95, 1.89)
 Cancer 1,126 1.26 (1.06, 1.49) 1.22 (1.03, 1.45) 1.15 (0.96, 1.38)
 Other causes 1,034 1.50 (1.22, 1.84) 1.49 (1.21, 1.84) 1.25 (1.00, 1.55)
 Injury 393 1.39 (1.03, 1.87) 1.31 (0.97, 1.77) 1.24 (0.89, 1.72)
 Not classified 1,544 1.21 (1.05, 1.40) 1.17 (1.01, 1.35) 1.07 (0.91, 1.25)
CVD (fatal+nonfatal)b 5,472 1.06 (0.98, 1.14) 1.14 (1.05, 1.23) 1.08 (0.99, 1.17)
 MI 2,363 1.01 (0.90, 1.13) 1.12 (1.00, 1.26) 1.07 (0.94, 1.22)
 Stroke 2,685 1.12 (1.00, 1.26) 1.16 (1.03, 1.30) 1.12 (0.99, 1.27)
 Heart failure 476 1.10 (0.84, 1.43) 1.20 (0.92, 1.56) 1.13 (0.85, 1.50)
CVD hospitalizationc 4,407 1.05 (0.96, 1.15) 1.14 (1.04, 1.25) 1.10 (1.00, 1.22)
Respiratory disease (fatal+nonfatal)d 2,436 1.29 (1.14, 1.46) 1.24 (1.10, 1.41) 1.14 (1.00, 1.30)
 TB 530 1.68 (1.26, 2.23) 1.48 (1.11, 1.96) 1.29 (0.95, 1.74)
 COPD 708 1.31 (1.05, 1.63) 1.28 (1.02, 1.59) 1.15 (0.91, 1.44)
 Pneumonia 893 1.17 (0.95, 1.44) 1.20 (0.98, 1.48) 1.17 (0.94, 1.46)
 Lung cancer 239 0.84 (0.58, 1.24) 0.83 (0.57, 1.22) 0.79 (0.53, 1.18)
Respiratory hospitalizatione 1,517 1.30 (1.11, 1.52) 1.29 (1.10, 1.51) 1.17 (0.98, 1.38)
Incident cardiorespiratory disease+all -cause mortalityf 11,111 1.18 (1.12, 1.25) 1.20 (1.14, 1.27) 1.12 (1.06, 1.19)
Asthmag 693 1.15 (0.93, 1.43) 1.05 (0.84, 1.31) 0.88 (0.69, 1.11)
Injuryh 3,461 1.05 (0.94, 1.16) 1.05 (0.94, 1.17) 1.01 (0.90, 1.14)
Injury hospitalization 1,213 1.16 (0.98, 1.37) 1.15 (0.97, 1.36) 1.02 (0.85, 1.22)

Model 1: Age, sex, baseline year, strata for center and urban/rural status.

Model 2: Model  1+INTERHEART risk score, smoking, physical activity, alcohol use, alternative healthy eating index, BMI, baseline chronic condition, baseline CVD medication use, baseline hypertensive status, outdoor PM2.5.

Model 3: Model  2+education, percentage income spent on food, and strata for household wealth index tertile.

a

Cause-specific death.

b

Fatal and nonfatal myocardial infarction, stroke, and heart failure.

c

Documented hospitalization for myocardial infarction, stroke, or heart failure.

d

Fatal and nonfatal COPD, pneumonia, tuberculosis, and lung cancer.

e

Documented hospitalization for COPD, pneumonia, tuberculosis, and lung cancer.

f

Composite outcome: mortality from any cause or the first incidence of any major nonfatal CVD (MI, stroke, HF) or respiratory outcome (tuberculosis, COPD, pneumonia, or lung cancer, but not asthma) as an indicator of all health outcomes likely related to HAP.

g

Physician diagnosis of asthma. Not included as a major respiratory disease outcome due to lack of evidence for association with HAP.

h

Fatal or nonfatal injury. Hospitalizations refer to injuries with a documented hospital admission.

Stratified analyses are illustrated in Figure 2, and model estimates provided in Table S1. There was general consistency in the associations observed across individual, household, and geographic variables. Greater variation was seen for CVD and respiratory events, but this is partially due to smaller sample sizes. For all-cause mortality, we observed larger associations in China (HR=1.20; 95% CI: 1.04, 1.38) compared with South Asia (HR=1.06; 95% CI: 0.95, 1.20) and other countries (HR=1.15; 95% CI: 0.98, 1.34); for men (HR=1.15; 95% CI: 1.03, 1.28) compared with women (HR=1.08; 95% CI: 1.00, 1.22); for ever-smokers (HR=1.19; 95% CI: 1.06, 1.34) compared with never smokers (HR=1.07; 95% CI: 0.96, 1.19); and for individuals with no chimney in their kitchen (HR=1.16; 95% CI: 1.05, 1.29) compared with homes with chimneys (HR=1.04; 95% CI: 0.80, 1.34).

Figure 2.

Figure 2 is a forest plot showing fully adjusted hazard ratios for all-cause mortality, cardiovascular disease, respiratory disease, and cardiorespiratory disease and mortality. The stratification under the main model is as follows: regions; urban or rural; sex; age; primary education; home wealth index; employment status; smoking status; CVD medication use; hypertension status; baseline chronic condition status; BMI; inter heart risk score; presence of chimney in the kitchen; kitchen ventilation; solid fuel use; and outdoor PM 2.5.

Fully adjusted hazard ratios and 95% confidence intervals for all-cause mortality, CVD events (fatal and nonfatal MI, stroke, and HF), respiratory disease (fatal and nonfatal COPD, pneumonia, tuberculosis, and lung cancer), and incident cardiorespiratory disease and all-cause mortality, stratified by individual, household and community characteristics, comparing solid fuel use for cooking to electricity/gas. The shaded regions represent 95% CI of the overall fully adjusted model. Full model estimates are provided in Table S1.

Sensitivity Analyses

Findings for biomass and coal use for cooking are presented in Table S2. Coal use for cooking was almost exclusively used in China (n=8,850 individuals), whereas only 133 homes in South Asia and 378 homes in other countries reported primary use of coal for cooking. Overall, we observed larger fully adjusted associations with mortality for biomass use (HR=1.14; 95% CI: 1.05, 1.24) than for coal use (HR=1.05; 95% CI: 0.88, 1.24) compared with electricity or gas. When restricted to China, we observed elevated associations for mortality only for biomass use (HR=1.35; 95% CI: 1.13, 1.61) and not for coal use (HR=0.99; 95% CI: 0.81, 1.20), as well as larger associations for the combined incident cardiorespiratory disease and all-cause mortality outcome for biomass (HR=1.15; 95% CI: 1.02, 1.30) compared with coal use (HR=1.07; 95% CI: 0.94, 1.21).

Effect estimates from models restricted to urban or rural communities are provided in Table S3. In rural communities, solid fuel use for cooking, compared with clean fuel use, was associated with a fully adjusted HR of 1.13 (95% CI: 1.03, 1.23) for all-cause mortality, 1.03 (95% CI: 0.94, 1.14) for CVD, 1.18 (95% CI: 1.00, 1.38) for respiratory disease, and 1.11 (95% CI: 1.04, 1.19) for the combined incident cardiorespiratory disease and all-cause mortality outcome. Stroke (HR=1.12; 95% CI: 0.97, 1.28) and CVD hospitalizations (HR=1.10; 95% CI: 0.98, 1.24) were the only CVD outcomes increased with solid fuel use in rural communities. In urban communities, solid fuel use was associated with a fully adjusted HR of 1.12 (95% CI: 0.95, 1.31) for all-cause mortality, 1.23 (95% CI: 1.04, 1.44) for CVD, 1.07 (95% CI: 0.85, 1.34) for respiratory disease, and 1.17 (95% CI: 1.04, 1.32) for the combined incident cardiorespiratory disease and all-cause mortality.

Effect estimates from sensitivity analyses are provided in Table S4. Results from our fully adjusted model did not change appreciably when we removed baseline chronic conditions, hypertension, and CVD medication use; removed outdoor PM2.5; added secondhand smoke exposure, occupational class, additional diet and lipid variables; and added a community random effect variable. The largest change occurred when we removed the household wealth index from the model (highly correlated with solid fuel use), which increased all associations. Here, solid fuel use compared with clean fuel use was associated with a fully adjusted HR of 1.17 (95% CI: 1.09, 1.26) for all-cause mortality, 1.09 (95% CI: 1.01, 1.18) for CVD, 1.19 (95% CI: 1.05, 1.35) for respiratory disease, and 1.15 (95% CI: 1.09, 1.22) for the combined incident cardiorespiratory disease and all-cause mortality.

Finally, to examine potential residual confounding and heterogeneity in the effect of HAP by centers, regions, and countries, we estimated fully adjusted models by center and pooled the estimates using random effects meta-regression. Figure 3 illustrates the center-specific results for all-cause mortality and the combined incident cardiorespiratory disease and all-cause mortality. For all-cause mortality, the overall pooled HR was 1.10 (95% CI: 0.99, 1.23) with an I2=18.8, p=0.19. For the combined outcomes, the overall pooled HR was 1.11 (1.02, 1.20) with an I2=23.9, p=0.13. Region-specific HR estimates and I2 statistics are provided in Table S5. Due to sample size limitations, we did not run center-specific models for CVD or respiratory events.

Figure 3.

Figure 3 is a forest plot showing fully adjusted hazard ratios for all-cause mortality and cardiorespiratory disease and mortality. The stratification is as follows: South Asia pooled HR; China pooled HR; other countries pooled HR; and all countries pooled HR.

Center-specific fully adjusted hazard ratios and 95% confidence intervals comparing solid fuel use for cooking with electricity/gas. The pooled HR for all-cause mortality is 1.10 (95% CI: 0.99, 1.23) with an I2  statistic=18.9%, p=0.19 and for the incident cardiorespiratory disease and all-cause mortality composite the HR is 1.11 (95% CI: 1.02, 1.20) with an I2  statistic=23.9%, p=0.13.

Discussion

Findings from our diverse cohort of 91,350 adults living in 467 urban and rural communities in 11 countries suggest that the residents of households that used solid fuels for cooking had higher all-cause mortality, fatal and nonfatal CVD, and fatal and nonfatal major respiratory conditions compared with residents of households that used clean fuels for cooking.

Our findings contribute to the existing evidence suggesting an association between HAP and all-cause and CVD mortality. Within the China Kadoorie Biobank study (271,217 participants, 15,468 deaths over a 7.5-y follow-up period), solid fuels use for cooking, compared with clean fuel use, was associated with an HR of 1.11 (95% CI: 1.03, 1.20) for all-cause mortality and 1.20 (95% CI: 1.02, 1.41) for CVD mortality (Yu et al. 2018). When we restricted our models to China, we estimated an HR of 1.12 (95% CI: 1.04, 1.38) for all-cause mortality when comparing solid to clean fuel users but found no association for CVD mortality. Although our study included 12 diverse regions in China, this sample is not representative of the entire Chinese population. In another study of 74,941 women in Shanghai, the estimated HRs for women reporting ever using coal for cooking, compared with never, were 1.12 (95% CI: 1.05, 1.21) for all-cause mortality and 1.18 (95% CI: 1.02, 1.37) for CVD mortality (Kim et al. 2016). In rural Bangladesh, a cohort study of 22,337 individuals (1,154 deaths over 10 y) observed incident rate ratios of 1.10 (95% CI: 0.89, 1.37) for noncommunicable disease mortality and 1.07 (95% CI: 0.82, 1.41) for CVD mortality, again comparing solid fuel use for cooking to gas (Alam et al. 2012). Finally, the Iran Golestan Cohort Study examined 50,045 individuals and estimated HRs per 10-y use of wood for cooking of 1.01 (95% CI: 0.97, 1.05) for all-cause mortality and 1.03 (95% CI: 0.97, 1.08) for CVD mortality (Mitter et al. 2016). These four cohorts demonstrate the variability in results linking HAP to mortality. In comparison, we observed HRs for all-cause and CVD mortality for individuals using solid fuels for cooking, compared with clean fuels, of 1.12 (95% CI: 1.04, 1.21) and 1.08 (95% CI: 0.99, 1.17), respectively. Our all-cause mortality finding was robust across study regions, urban/rural status, and individuals’ sociodemographic characteristics, whereas CVD mortality was more variable.

To our knowledge, our study is the first prospective cohort to examine household solid fuel use for cooking—a proxy indicator of exposure to HAP—as a risk factor for both fatal and nonfatal CVD. This is highly relevant given that a large portion of CVD events in our study were not fatal (2,104 CVD deaths resulted from 5,472 incident cases of CVD) and health care access plays a key role in CVD survival rates. The inclusion of individual education and a household asset index, which may capture a component of health care access, attenuated model results for CVD death from an HR of 1.18 (95% CI: 1.04, 1.34) in Model 2 (controlling for all CVD risk factors) to 1.04 (95% CI: 0.91, 1.19) in the fully adjusted model. For all CVD events (including fatal and nonfatal CVD), this attenuation was less severe, attenuating associations from an HR of 1.14 (95% CI: 1.05, 1.23) in Model 2 to 1.08 (95% CI: 0.99, 1.17) in the fully adjusted model. Overall, we also observed a larger association with stroke events (HR: 1.12; 95% CI: 0.99, 1.27) compared with MI (HR: 1.07; 95% CI: 0.94, 1.22), which corresponds to the larger association observed in the China Kadoorie Biobank study for stroke death compared with IHD (Yu et al. 2018). In addition, CVD events with a documented hospitalization remained elevated (HR: 1.10; 95% CI: 1.00, 1.22) in fully adjusted models, comparing individuals using solid fuels for cooking versus those using clean fuels. Although some studies have examined HAP and surrogate markers (e.g., inflammation processes, atherosclerosis, blood pressure) that correlate with CVD outcomes (Fatmi and Coggon 2016), these are not necessarily a reliable basis for public health interventions. By contrast, our study is based on a large number of CVD deaths and nonfatal events that were accrued during systematic and prospective follow-up, and our results add to the body of evidence suggesting that HAP is a risk factor for CVD.

We also observed associations between HAP and major respiratory disease, which aligns with and strengthens the existing literature. A longitudinal analysis of 280,000 Chinese nonsmokers comparing solid fuels users with clean fuels users estimated an HR of 1.36 (95% CI: 1.32, 1.40) for major respiratory diseases, including chronic lower respiratory disease, COPD, and ALRI (Chan et al. 2019). Here we estimated an overall HR of 1.14 (95% CI: 1.00, 1.30) for respiratory disease, including TB, COPD, pneumonia, and lung cancer, for individuals cooking with solid fuels compared with clean fuels. We did not observe an association between HAP and asthma, which is consistent with prior studies (Po et al. 2011). A systematic review of 24 HAP and COPD studies estimated increased odds ratios (ORs) of 2.30 (95% CI: 1.73, 2.06) for women and 1.90 (95% CI: 1.15, 3.13) for men exposed to HAP (Smith et al. 2014). A recent study not included in this meta-analysis of 12,396 adults in 13 LMICs estimated an OR of 1.41 (95% CI: 1.18, 1.68) for COPD in homes using biomass compared with clean fuels (Siddharthan et al. 2018). In our study, we estimated an HR of 1.15 (95% CI: 0.91, 1.44) for COPD for individuals using solid fuels for cooking, compared with clean fuels. A systematic review of 12 studies of HAP and TB estimated that individuals exposed to HAP had a pooled OR of 1.30 (95% CI: 1.04, 1.62) compared with individuals who were not exposed (Sumpter and Chandramohan 2013). We estimated an HR of 1.29 (95% CI: 0.95, 1.74) for TB in those exposed to HAP compared with those using clean fuels. Finally, for pneumonia we observed an HR of 1.17 (95% CI: 0.94, 1.46) for individuals using solid fuels for cooking. Although there is a strong body of evidence for the increased risk of pneumonia in children (Smith et al. 2011, 2014), this has not been documented for adults (Shen et al. 2009). We did not observe any association with lung cancer; however, there were only 239 lung cancer cases documented during follow-up.

We observed mixed findings for individual and household characteristics that could modify HAP exposures or susceptibility to HAP health effects. We observed reductions in associations between solid fuels used for cooking and health events if kitchens had a chimney, especially for all-cause mortality and CVD. The magnitude of these differences align with other large cohort findings of the impact of ventilation (Yu et al. 2018, 2018). Surprisingly, we did not see larger associations for women, who would be expected to have higher air pollution exposure levels if they are responsible for cooking in the household, although we did not have information on whether individuals were responsible for cooking. We also did not observe larger associations if homes reported using solid fuels for cooking, although most households reporting heating were in China and used coal. Similarly, associations with solid fuels for cooking were not stronger in areas with higher outdoor PM2.5 concentrations (dichotomized as <50  or50μg/m3). Although we observed some differences in the effects of HAP by smoking status, these were small and varied by outcome, which aligns with the mixed findings in the literature (Brook et al. 2010).

We relied on reported history of primary cooking fuels at baseline as our indicator for long-term HAP exposure, comparing individuals who lived in households using solid fuel to households using gas or electricity. To our knowledge, the use of fuel types as a surrogate for HAP is the only approach that has been used to date to examine mortality and CVD (e.g., Alam et al. 2012; Kim et al. 2016; Mitter et al. 2016; Yu et al. 2018) due to the difficultly of measuring household PM2.5 for large populations over long time periods. Recent global estimates suggest a 110880μg/m3 difference between electricity/gas and biomass kitchens (Shupler et al. 2018), which supports the use of fuel types as an indicator of HAP in our study. Importantly, these measurement studies also highlight the exposure misclassification present and potential attenuation of our HAP effect estimates when fuel surrogates are used to represent air pollution exposures. Ongoing research in the PURE cohort will address this limitation by measuring PM2.5 concentrations in a subset of 4,500 study homes (along with 1,800 personal samples) (Arku et al. 2018). Future analyses will implement regression calibration approaches (Weller et al. 2007) to integrate this monitoring data to adjust our estimates of solid fuel use versus electricity or gas for measurement error. We will also develop a predictive household PM2.5 model to apply to the entire cohort to examine associations between predicted household PM2.5 concentrations and disease events (Arku et al. 2018).

Our study has several strengths, including the prospective design, large sample size, inclusion of multiple countries and communities to increase the generalizability of results, collection of extensive individual and household information to control for confounding, and comprehensive and systematic information on outcomes using standardized definitions. However, there are also specific limitations. First, we have no information on the use of secondary fuels, the time spent cooking with solid fuels, or prior cooking fuel types used in childhood or young adulthood. HAP exposure may also vary by cultural, gender, age, and household characteristics (Balakrishnan et al. 2011). Our assumption of similar exposures for any given solid fuel type, although common in the HAP literature, likely leads to exposure misclassification that would bias our results towards the null. We partially address this issue in the center-specific meta-analysis approach, which demonstrated similar findings to our overall model. Second, there were 1,544 deaths for which we did not have an assigned cause of death (because they occurred at home without any medical care). The overall association between these deaths and solid fuel use was 1.07 (95% CI: 0.91, 1.25). A proportion of these may be CVD deaths, but it is unlikely that this would explain the weaker association observed in our study between solid fuel use and CVD compared with other causes of death. Currently, 32% of the deaths in our study population were from CVD, which concurs with existing estimates in LMICs (Roth et al. 2015). Third, differentiating asthma and COPD is a challenge in low resource settings. However, there were clear differences in the direction of association between HAP with asthma and COPD in our study, which agrees with the underlying pathophysiology of asthma as allergic or related to cellular permeability in contrast to COPD and the development of fibrosis. Fourth, we did not distinguish between ischemic and hemorrhagic stroke given the lack of available data in many low-income PURE countries. Fifth, we did not have sufficient power to examine the effects of specific fuel types (e.g., dung, wood, agricultural products) or more specific outcomes (e.g., cancer types), but these analyses will be possible once more events accrue during further follow-up. Sixth, we included a missing category for information not reported for several covariates, but overall missingness was limited for variables included in the main analyses. Finally, an important limitation inherent to any study of HAP is separating the HAP effect from other poverty-related effects. For all outcomes, education resulted in the greatest attenuation of the effects of solid fuel use for cooking but did not explain all SES-related attenuation. The household wealth index also resulted in attenuation of the HAP model estimates. In addition, we examined injury events as a possible negative control (although injury events includes burns, which may be associated with solid fuel use) and observed no associations between all documented events (n=3,461) or hospitalizations (n=1,213) but a positive association with deaths (n=393). Overall, we did not observe consistent patterns in our solid fuel health estimates across SES variables (education, home wealth index, occupation, percentage of income spent on food, and medication use) that would suggest our results are due to residual confounding by poverty-related effects.

Conclusions

We showed an increase in the risks of all-cause mortality, CVD, and respiratory disease among individuals living in households using solid fuels for cooking, compared with those using clean fuels. The results from this large, diverse population of 91,350 adults from 467 urban and rural communities in 11 LMICs adds to the strength of evidence supporting HAP as an important risk factor for chronic disease. Given that approximately 2.5 billion individuals live in households still using solid fuels for cooking, replacing these with cleaner energy sources may represent an important approach to reducing premature mortality and morbidity in LMICs.

Supplementary Material

Acknowledgments

The main PURE study and its components are funded by the Population Health Research Institute, the Canadian Institutes of Health Research, and the Heart and Stroke Foundation of Ontario and through unrestricted grants from several pharmaceutical companies [with major contributions from AstraZeneca (Canada), Sanofi-Aventis (France and Canada), Boehringer Ingelheim (Germany and Canada), Servier, and GlaxoSmithKline] and additional contributions from Novartis and King Pharma. The PURE-AIR study is funded by Canadian Institutes for Health Research (CIHR; grant 136893) and by the Office of the Director, National Institutes of Health (NIH; award DP5OD019850). The content is solely the responsibility of the authors and does not necessarily represent the official views of the CIHR or the NIH. Various national or local organizations in participating countries also contributed: Fundacion ECLA (Argentina); Independent University, Bangladesh and Mitra and Associates (Bangladesh); Unilever Health Institute (Brazil); Public Health Agency of Canada and Champlain Cardiovascular Disease Prevention Network, Canadian Institutes of Health Research, Heart and Stroke Foundation of Canada, and Population Health Research Institute (Canada); Universidad de la Frontera (Chile); National Center for Cardiovascular Diseases (China); Colciencias (grant 6566-04-18062; Colombia); Indian Council of Medical Research (India); Ministry of Science, Technology and Innovation of Malaysia [grant 100–IRDC/BIOTEK 16/6/21 (13/2007) and grant 07-05-IFN-BPH 010], Ministry of Higher Education of Malaysia [grant 600-RMI/LRGS/5/3 (2/2011)], Universiti Teknologi MARA, and Universiti Kebangsaan Malaysia (UKM-Hejim-Komuniti-15-2010) (Malaysia); Polish Ministry of Science and Higher Education (grant 290/W-PURE/2008/0), and Wroclaw Medical University (Poland); North-West University, South Africa and Netherlands Programme on Alternatives in Development (SANPAD), National Research Foundation, Medical Research Council of South Africa, South African Sugar Association (SASA), and Faculty of Community and Health Sciences (UWC; South Africa); AFA Insurance; Swedish Council for Working Life and Social Research, Swedish Research Council for Environment, Agricultural Sciences and Spatial Planning, Swedish Heart and Lung Foundation, Swedish Research Council, the Swedish State under LäkarUtbildningsAvtalet agreement, and the Västra Götaland Region (FOUU; Sweden); Metabolic Syndrome Society, AstraZeneca, and Sanofi-Aventis (Turkey); and Sheikh Hamdan Bin Rashid Al Maktoum award for Medical Sciences and Dubai Health Authority (United Arab Emirates). S.Y. holds the Heart and Stroke Foundation/Marion W. Burke Chair in Cardiovascular Disease. A complete list of PURE Project office staff, national coordinators, investigators, and key staff is provided in the section, “PURE Project Investigators and Staff,” in the Supplemental Material.

Footnotes

Supplemental Material is available online (https://doi.org/10.1289/EHP3915).

The authors declare they have no actual or potential competing financial interests.

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