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A method to estimate the chronic health impact of air pollutants in U.S. residences.

BACKGROUND: Indoor air pollutants (IAPs) cause multiple health impacts. Prioritizing mitigation options that differentially affect individual pollutants and comparing IAPs with other environmental health hazards require a common metric of harm.

OBJECTIVES: Our objective was to demonstrate a methodology to quantify and compare health impacts from IAPs. The methodology is needed to assess population health impacts of large-scale initiatives-including energy efficiency upgrades and ventilation standards-that affect indoor air quality (IAQ).

METHODS: Available disease incidence and disease impact models for specific pollutant-disease combinations were synthesized with data on measured concentrations to estimate the chronic heath impact, in disabiliry-adjusted life-years (DALYs) lost, due to inhalation of a subset of IAPs in U.S. residences. Model results were compared with independent estimates of DALYs lost due to disease.

RESULTS: Particulate matter [less than or equal to] 2.5 pm in aerodynamic diameter ([PM.sub2.5]), acrolein, and formaldehyde accounted for the vast majority of DALY losses caused by IAPs considered in this analysis, with impacts on par or greater than estimates for secondhand tobacco smoke and radon. Confidence intervals of DALYs lost derived from epidemiology-based response functions are tighter than those derived from toxicology-based, interspecies extrapolations. Statistics on disease incidence in the United States indicate that the upper-bound confidence interval for aggregate IAP harm is implausibly high.

CONCLUSIONS: The approach demonstrated in this study may be used to assess regional and national initiatives that affect IAQ at the population level. Cumulative health impacts from inhalation in U.S. residences of the IAPs assessed in this study are estimated at 400-1,100 DALYs lost annually per 100,000 persons.

KEY WORDS: air toxics, criteria pollutants, DALYs, exposure, impact assessment, indoor air pollutants, indoor air quality. Environ Health Perspect 120:216-222 (2012). ehp.1 104035 [Online 17 November 2011]

Air pollutant concentrations in many homes exceed health-based standards for chronic and acute exposures (Logue et al. 2011). On average, Americans spend > 65% of their time in residences (Klepeis et al. 2001), and numerous studies have noted the importance of the indoor environment to cumulative air pollutant intake (Samet 1993; Weisel et al. 2005). Impact assessment methods have been applied to estimate aggregate chronic health impacts for outdoor air pollution [Muller and Mcndelsohn 2007; U.S. Environmental Protection Agency (EPA) 1999] and from pollutant inhalation in office buildings (Fisk Ct al. 2011). Yet, to our knowledge, no study has yet considered both disease incidence and severity to assess aggregate health impacts of air pollutant inhalation in residences.

Air pollutants known to be hazardous based on epidemiological and toxicological information include the "criteria pollutants" specified in the 1970 Clean Air Act Amendments (CAAA 1970) and hazardous air pollutants (HAPs) specified in the 1990 CAAA (1990). In addition, concern is growing that some bioaccumulating scmivolatile organic compounds and ultrafine particles--both ubiquItously present in residences--may cause substantial adverse health effects at typical environ mental levels. However, the current toxicological data is insufficient to quantify that impact. 'The U.S. EPA and the California EPA (CaIEPA) each publish health standards or guidelines for long-term exposure concentrations to protect against cancer and noncancer chronic effects. The hazard associated with residential air pollutant exposure can be quantified as the percentage of homes that exceed specified noncancer standards or as the incremental risk of cancer incidence across the population. These methods consider only disease potential for noncancer end points and disease incidence for cancer; they do not incorporate disease severity. Quantitatively comparing the effects of individual residential indoor air pollutants (TAPs) and comparing their estimated cumulative health impact with that of other environmental hazards requires a single metric that includes both disease incidence and severity. A comprehensive metric will fici1itate the evaluation of residential Indoor air quality (IAQ) interventions, inc1uding source control measures and ventilation.

Epiderniological and toxicological research has contributed to the development of tools to bridge the gap from measured pollutant exposure levels to disease incidence, and from disease incidence to health costs in disability-adjusted life-years (DALYs) lost. Concentration-response (C-R) relationships have been quantified for criteria pollutants. The U.S. EPA aggregated several of these disease incidence models for use in the cost-benefit analysis of the Clean Air Act (U.S. EPA 1999). Several studies have estimated the health impact per incidence of specitic diseascs (Hong et ai. 2010; Lvovsky et al. 2000; Melse et al. 2010). Huijbregts et al. (2005) published cumulative impact and effect fictors for cposure to air pollutants, including air toxics and ozone. These models provide the basis for performing a human health impact assessment for inhalation of IAPs.

In this study we combined disease incidence and DALY-based health impact models to develop a methodology for estimating the population-average health costs due to chronic inhalation of a broad suite of air pollutants in U.S. residences. We first analyzed published data to calculate mean exposure concentrations and estimated age-dependent inhalation intakes. We used disease incidence and disease impact models to predict pollutant-specific impacts and total DALY-based health costs to identify the residential IAPs that have the greatest impact on health in the United States. As a check on the method, and the estimated aggregate impact of IAP, we compared our findings with independent estimates of DALY losses related to secondhand smoke (SHS) to diseases that cou'd potentially result from air pollutant exposure and to all noncommunicable, non-psychiatric diseases in the United States.


IAP intake. To calculate pollutant inhalation in U.S. residences, we used a data compilation described by Logue et al. (2011) that includes summary statistics from 77 studies reporting residential air pollutant concentration measurements in the United States and other countries with similar lifestyles. The aggregate data were used to calculate concentrations relevant to assessing chronic residential exposures to 267 chemical air pollutants. Seventy of the pollutants had sufficient toxicological and epidemiological data to calculate chronic health impact using the methodology described below and were included in this study (Table 1). Our analysis did not extend to contaminants from biological sources such as molds and allergens. We thus refer to the suite of pollutants considered as "nonbiological."
Table 1. Pollutants included in analysis and assumed
population-average concentrations ([mu]g/[m.sub.3]).

Pollutant Concentration

1,1,2,2-Tetrachloroethane 0.42
1,1,2-Trichloroethane 0.46
1,1-Dichloroethene 1.2
1,2-Dibromoethane 0.14
1.2-Dichloroethane 0.34
1,3-Butadiene 0.46
1,4-Dichlorobenzene 50
2-Butoxyethanol 2.6
2-Ethylhexanol 3.7
2-Ethoxyethanol 0.43
2-Methoxyethanol 0.12
Acetaldehyde 22
Acrolein 2.3
Acrylonitrile 0.27
Ammonia 28
Arsenic 9.8 x [10.sup.-4]
Atrazine 5.9 x [10.sup.-4]
Benzaldehyde 2.5
Benzene 2.5
Benzo[a]pyrene 9.1 x [10.sup.-5]
Benzyl chloride 0.5
Beryllium 1.6 x [10.sup.-6]
Bis(2-ethylhexyl) phthalate 0.14
Bromodichloromethane 0.49
Bromoform 0.39
Cadmium 2.6 x [10.sup.-3]
Carbon disulfide 0.34
Carbon tetrachloride 0.68
Chloroethane 0.26
Chloroform 1.5
Chloromethane 1.8
Chromium 2.2 x [10.sup.-3]
Crotonaldehyde 4.7
Cyclohexane 5.2
Di(2-ethylhexyl) adipate 1.6 x [10.sup.-2]
Dibenzo[a,c+a,c]anthracene 1.4 x [10.sup.-5]
Dibromochloromethane 0.44
d-Limonine 23
Ethanol 860
Ethyl benzene 3.9
Formaldehyde 69
Hexachlorobutadiene 7.7
Hexane 7.3
Isopropylbenzene 0.4
Manganese 3.3 x [10.sup.-3]
Methyl ethyl ketone 7.4
Mercury 1.6 x [10.sup.-4]
Methyl methacrylate 0.27
Methylene chloride 8.2
Methyl isobutyl ketone 1.2
Methyl fert-butyl ether 12
Naphthalene 1.2
[NO.sub2] 13.1
o-Phenylphenol 0.13
Ozone 17.2
Pentachlorophenol 2.9 x [10.sup.-3]
[PM.sub.2.5] 15.9
Styrene 5.9
S02 2.9
Tetrachloroethene 1.7
Tetrahydrofuran 15
Toluene 2.3
Trichloroethene 0.16
Vinyl chloride 1.7
Xylene, o 8.2
Xylene, m/p 9.7
Xylenes 7.4

Abbreviations: CO. carbon monoxide; [NO.sub.2], nitrogen
dioxide; [PM.sub.2.5], particulate matter [less than or
equal to]15 [micro]m in aerodynamic diameter; [SO.sub.2],
sulfur dioxide. The data are for poltutats identified by
Logue et al, (2011) that had sufficient toxicologicaL and
epidemiological data to calcuate their health impact.

Determining annual population health impact. The annual health impact of residential TAPs was calculated by considering the total intake in residences as an increment adding to intake in other environments. The increment was calculated by considering in-home inhalation of aircontaining the population-mean exposure concentrations relative to the theoretical case of the population inhaling residential air containing no pollutants.

The DALY metric allows quantification and comparison of the health costs from varied disease end points that can result from various pollutants. As a measure of equivalent years of life lost (YLL) due to illness or disease, DALY loss quantifies overall disease costs (impacts) due to both mortality and morbidity. DALY losses include YLL due to premature mortality and equivalent YLL due to reduced health or disability (YLD). For each disease, the DALYs lost per incidence are calculated as follows:

[DALY.sub.disease] = [YLL.sub.disease] + [YID.sub.disease] [1]

The equivalent life-years lost to reduced health are weighted from 0 to 1. based on the severity of the disease. For example, a 5-year illness that reduces quality of life to 4/5 that of a healthy year is valued at 1 DALY lost.

Several authors have determined the DALYs 1ost per incidence of specific diseases using the preeminent work of Murray and Lopez (1996a, 1996b) [Huijbregts et al. 2005; Lvovsky et al. 2000; World Health Organization (WHO) 2009]. Multiplying disease incidence by a "DALY factor" yields total DALYs lost per disease incidence:

DALYs = ([??]DALYs/[??]adisease incidence) x disease incidence. [2]

Equation 2 uses a partial derivative in recognition that DALY losses are incrementally affected by causes other than disease. The total burden of disease in a community can be calculated as the aggregate, across all diseases, of DALY factors multiplied by disease incidence rates.

Our analysis used two approaches to calculate DALY losses from estimated exposure concentrations. For criteria pollutants [ozone, nitrogen dioxide ([NO.sub.2]), particulate matter [less than or equal to]2.5 [micro]m in aerodynamic diameter ([PM.sub.2.5]), sulfur dioxide ([SO.sub.2]), and carbon monoxide (CO)] we used an intake-incidence-DALY (IND) method that uses epidemiology-based C-R functions to quantify disease incidence rates; these are combined with estimates of DALY losses per disease incidence reported in the literature. For noncriteria pollutants we used an intake-DALY (ID) approach using the work of Huijbregts et al. (2005) to calculate the health impact associated with intake of noncriteria pollutants based on animal toxicity literature. The IND approach is preferred because it does not require interspecies extrapolations, which generally involve larger uncertainties than the epidemiologically based C-R functions. However, the IND approach can he used only for pollutants with information on C-R functions in humans. Ozone was the only pollutant for which both the IND and ID approaches could be applied.

Although the disease incidence relationships in the IND and ID approaches are accepted health impact models, they are nevertheless simplifications of populationwide responses to chronic inhalation exposure. Our approaches use linear (i.e., IND) and nearly linear (i.e., ID) disease incidence models without effect thresholds. For these types of disease incidence models, only the mean of the concentration distribution is needed to estimate population impact. Existence of a threshold concentration for disease incidence, or a strongly nonlinear disease-to-intake response, would necessitate accurate determination of the shape of the population intake distribution. A discussion of the impact of threshold effects on our DALY loss estimates is included in the "Discussion." The potential impacts of nonlinear response functions are beyond the scope of the present study.

The IND approach. The first step of the IND method comprises the application of C-R functions to determine disease incidence. For almost all of the disease outcomes, the CR function follows the formula:

[increment of Incidence] = - {[y.sub.o] x [exp(-[beta] [increment of [C.sub.exposure]) - 1]} population, [3]

where [y.sub.o] is the baseline prevalence of illness per year, [beta] is the coefficient of the concentration change, [C.sub.exposure] is the exposure-related conccntration, and population is the number of persons exposed. For each pollutant and outcome, [y.sub.0] and [beta] vary. Respiratory illness due to long-term [NO.sub.2] intake requires a slightly different C-R functional form but still relies on a [beta] with specifed uncertainty.

When aggregating C-R functions and DALY factors, we tried to include all of the diseases with available established relationships between concentrations and disease incidence. We did nor include diseases/outcomes that were negligible compared wjth the other diseases included. The health end points selected and DALY loss per incidence of disease are summarized in Table 2.
Table 2. Criteria pollutant C-R function outcomes and DALYs lost
pr incidence.

Pollutant Outcome [beta]-Coefficient [y.sub.0]
 (95% CI)

[PM.sub.2.5] Total 0.058(0.002, 0.010) 7.4x[10.sup.-3]
 (Pope et al.
 Chronic 0.091(0.078, 0.105) 0.4x[10.sup.-3]
 (Abbey et al.
 Nonfatal 0.025 (0.002, 0.2x[10.sup.-3]
 stroke (Brook 0.048)
 et al. 2010)

CO Hospital
 (Burnett et
 al. 1999)
 Asthma 0.033(0.016, 0.050) 1.8x[10.sup.-3]
 Lung disease 0.025(0.000, 0.057) 2.1x[10.sup.-3]
 Dysrhythmias 0.058(0.012, 0.102) 2.4x[10.sup.-3]
 Heart failure 0.034 (0.002, 3.4x[10.sup.-3]

[NO.sub.2] Hospital
 (Burnett et
 al. 1999)
 Respiratory 0.004 (0.000, 9.5x[10.sup.-3]
 issues 0.008)
 Congestive 0.003 (0.001, 3.4x[10.sup.-3]
 heart failure 0.004)
 Ischemic heart 0.003 (0.002, 8.0x[10.sup.-3]
 disease 0.004)
 Respiratory 0.028 (0.002, N/A
 illness, 0.053)
 indicated by
 et al. 1992)

Ozone Mortality 0.001 (0.000, 7.7x[10.sup.-3]
 (Jerrett et 0.002)
 al. 2010;
 Samet et al.
 (Burnett et
 al. 1999)
 Asthma 0.003(0.001, 0.004) 1.8x[10.sup.-3]
 Lung disease 0.003(0.001, 0.005) 2.1x[10.sup.-3]
 Respiratory 0.002(0.001, 0.003) 5.8x[10.sup.-3]
 Dysrhythmias 0.002 (0.000, 2.4x[10.sup.-3]

[SO.sub.2] Hospital 0.002 (0.000, 8.0x[10.sup.-3]
 admissions 0.003)
 (Burnett et
 al. 1999)

Pollutant DALYs lost per
 incidence (95%

[PM.sub.2.5] 1.4 (0.14,14)
 (Pope 2007; Pope
 et al. 2002,
 1.2 (0.12,12)
 (Lvovsky et al.
 2000; Melse et
 al. 2010)
 0 complications:
 9.5 (9.25, 9.75)
 1 complication:
 > 1
 13.1 (12.2,14.0)
 (Hong et

CO 4x[10.sup.-4]
 (Lvovsky et al.

[NO.sub.2] 4x[10.sup.-4]
 (Lvovsky et al.
 (Lvovsky etal.

Ozone 1.0(0.1,10) (Levy
 et al. 2001;
 Lvovsky et al.
 (Lvovsky et al.

[SO.sub.2] 4x[10.sup.-4]
 (Lvovsky et al.

N/A, not applicable. [y.sub.0] is the baseline prevalence
of illness per year, and [beta] is the coefficient of the
concentration change used for inputs into Equation 3.

Chronic [PM.sub.2.5], exposure affects both the respiratory and cardiovascular systems. The three outcomes that we included were all-cause mortality, chronic bronchitis, and stroke. Pope et al. (2002) predicted incidence rates of all-cause mortality and the average YLL per unit increase in [PM.sub.2.5] (Pope er al. 2009); we divided the former by the latter to get DALYs lost per incidence. The 95th percentile range of the DALYs lost per death was set to represent the span of values seen in the literature (Lvovsky et al. 2000; Pope et al. 2009). Recent studies have shown that chronic [PM.sub.2.5] exposure can lead to heart disease and thickening of arterial walls (Kunzli et al. 2004). The total impact of [PM.sub.2.5] on cardiovascular health is nor known. However, recent work by Miller et al. (2007) has shown associations between chronic [PM.sub.2.5] and stroke, an outcome of heart disease, in women. The end point of nonftal stroke was included in the analysis using the hazard ratios derived by Miller et al. (2007) for both men and women. This is likely an underestimation of the total impact of [PM.sub.2.5] on heart disease. The DALYS lost per nonfatal stroke incidence were taken from Brook et al. (2010). The incidence of stroke predicted was split among 0, 1, and > 1 complications and the percentage of stroke that resulted in death was determined based on the findings of Brook et al. (2010). Burnett et al. (1999) developed a C-R function for hospital admissions associated with long-term [PM.sub.2.5] exposure. However, because the impact was negligible compared with the impact of mortality, chronic bronchitis, and stroke, we did not include this outcome. There is evidence that [PM.sub.2.5] exposure is associated with other health outcomes, including diabetes and reduced lung function; however, these findings are relatively new and have not been included in this work.

For CO and [SO.sub.2], the only outcomes relevant to chronic exposure appear to be hospital admissions. Chronic ozone and [NO.sub.2] exposure have been associated with early death and respiratory illness, respectively. The input pacameters into the C-R functions for these outcomes are the same as those used in the U.S. EPA cost-benefit analysis of the Clean Air Act (U.S. EPA 1999). For hospital admission and respiratory illness, we used the DALY loss/incidence values available in the literature. For ozone mortality, as with PM25, it is unclear how much life is lost because of early death. Values in the literature range from a few weeks to 10 years; we chose a large range of values to represent this uncertainty (Levy et al. 2001; Lvovsky et al. 2000).

The C-R functions are formulated to cal-culate the increment of disease incidence per increment of exposure concentration, not total disease incidence for a given exposure concentration. According to population-weighted demographics (Kiepeis et al. 2001; U.S. Census Bureau 2010), summarized in Table 3, the "average" American spends 70% of the time in residences. The chronic exposure-relevant concentration contributed from indoor exposure was therefore set to 70% of the indoor concentration:
Table 3. Residential occupancy characteristics.

 Percent of Cancer Percent Air intake
 of day ([m.sup.3]/day)
Age (years) population ADAF spent

[less than or equal 3 10 75 7

2-16 19 3 75 13

[greater than or 78 1 59 15
to] 16

Population average - 1.6 70 14.4

The percentage of the population in each of these age groups was
determined from the U.S. Census Bureau (2010). The percentage of
time each age groups spends at home was determined from the National
Human Activity Pattern Study (Klepeis et al. 2001). The age-dependent
inhalation rate was taken from U.S. EPA (2009).

[increment of [C.sub.exposure]] = 0.7 [C.sub.indoors] [4]

Incidence rates were combined with DALY factors to calculate total health impacts by pollutant (Equation 2). A Monte Carlo approach was used to calculate impacts by pollutant by sampling with replacement from the available distributions of DALY factors and [beta]. We assumed that all DALY factor distributions are log-normal.

The ID approach. The ID approach extrapolated directly from indoor concentrations to total DALYs lost due to intake of specific pollutants. From this standpoint, it is convenient to rewrite Equation 2 as follows:

DALYs = ([??] DALY/[??] disease incidence) x ([??] adiscase incidence/[??] intake) intake, [5]

where intake is the mass of pollutant that an individual inhales over a given time frame. Huijbregts et al. (2005) computed expected ranges of human impact for cancer and non-cancer chronic effects of 1,192 substances, applying equal weightings for a year lost, independent of age (i.e., zero discounting). Using the values determined by Huijbregts et al. (2005), the DALYs lost for 1 year of breathing pollutant i is calculated using the following equations:

[DALYs.sub.i] = ([??] DALY/[??] intake) x intake, [6]

[DALYs.sub.i] = [C.sub.i] x V x [([[??] DALY.sub.cancer]/[[??] intake).sub.i] x ADAF + ([[[??] DALY.sub.noncancer]/[??] intake).sub.i]], [7]

where [??] DALY/[[??] intake.sub.i] are the cancer and noncancer mass intake-based DALY factors, [C.sub.i] is the indoor concentration, V is volume of air breathed in the residence each year, and ADAF is the age-dependent adjustment factor for cancer exposure as described below.

The age at which carcinogens are inhaled has an appreciable effect on total toxicity, and the U.S. EPA has developed ADAFs to calculate cancer health impact as a function of exposure age (U.S. EPA 2005). To align with U.S. EPA-recommended ADAFs, we considered three age groups: <- 2, 2-16, and > 16 years of age (U.S. EPA 2005). A population-weighted average annual air intake volume and ADAF were calculated by combining age distribution of the U.S. population, age-specific inhalation rates, and time spent at home (Table 3).

Huijbregts et al. (2005) presented, for each chemical, both a central estimate (50th percentile value) and the estimated uncertainty of the DALY losses per mass intake of pollutant; uncertainty was assumed to be log-normal, characterized by a factor, [k.sub.i], calculated as follows:

[k.sub.i]= [(97.5th percentile/2.5th pcrcentile).sup.0.5], [8]

which includes the aggregated uncertainty of the rate of disease incidence as well as the uncertainty in the DALY losses per incidence of disease. We used a Monte Carlo approach to sample with replacement from uncertainty distributions of DALY factors derived from the central estimate of the DALY factor and the k1 value, to determine the central estimate and 95% confidence interval (CI) for combined cancer and noncancer DALY losses for each pollutant. A Monte Carlo approach was also used to determine the total DALYs lost from all of the pollutants analyzed using the IND and ID methods.

Despite the availability of a DALY factor for bromomethane, DALY-based impacts are not presented for this compound because the limited available concentration data (New York State Department of Health 2006) appear more indicative of a local outdoor source than of general conditions in U.S. homes (Logue et al. 2011).

Radon, SHS, and acute CO poisoning deaths. The population-average DALYs lost to radon, SHS, and acute CO poisoning deaths were determined based on estimates of disease incidence from the literature. We included DALY loss estimates for these pollutants fbr two reasons: a) to compare health impacts calculated for a subset of SHS pollutants using the IND and ID methodologies to independent estimates of overall DALY losses associated with SHS exposure (as described below), and b) to compare estimated TAP-associated DALY losses calculated in the present study with estimates for these three established indoor health hazards.

To estimate the health impact from radon, SHS, and acute Go, we used Equation 2 with disease incidence estimates from the literature, summarized in Table 4. For radon and acute CO poisoning, only the end point of premature death was used to estimate DALY losses. The DALYs lost per incidence of various SHS outcomes and per early mortality due to acute CO poisoning and radon were taken from the literature and are also summarized in 1 able 4.
Table 4. Health outcomes attributable to SHS, radon, and acute
CO poisoning in the United States and the DALYs lost per
incidence of each health outcome.

Outcome Annual U.S. DALYs lost per incidence
Asthma 202,300 40/1,000 cases (Lvovsky et al. 2000)
episodes (CalEPA
Otitis media 790,000 22/1,000 cases (de Hollander et al. 1999)
visits (CalEPA

Sudden 430 (CalEPA 78 (current U.S. life expectancy)/case
infant death 2005) (Xuetal.2010)
Cardiac 46,000 (95% 1/case (de Hollander et al. 1999)
death CI: 22,700,

Lung cancer 3,400 14/case (de Hollander et al.
death (CalEPA 1999;
Melseetal.2010) 2005)
Radon lung

Smokers 18,000 (95% 14/case (de Hollander et al. 1999;
 CI: 5,600, Melseetal.2010)
 (U.S. EPA

Nonsmokers 3,000 (95% 14/case (de Hollander et al. 1999;
 CI: 950, Melseetal.2010)
 (U.S. EPA

CO acute 1.53 deaths 32 (Xuetal.2010)
poisoning per million
deaths persons
 (95% CI:
 for Disease
 Control and

Comparison with DALY losses estimated by other methods. Results from this study were compared with three other estimates of populationwide DALY losses for the United States. Although our study used an impact assessment approach, the studies used for comparison are cumulative risk assessment (CRA and burden of disease studies (Ezzati and Lopez 2004; McKenna et al. 2005; WHO 2009). The burden of disease studies used available statistics to determine the disease incidence rate as a function of age, sex, and geographical location. A DALY value was then assigned based on YLL and disability incurred. The CRA studies determined the fraction of disease or death attributable to a specific risk factor based on epidemiological studies of specific populations. This is similar to, but far more complex than, our method of estimating health impacts due to SHS and radon. If the disease rate and DALY factors were accurate, and if we used the same discount ratings and time weightings for the age at which years of life are lost, both methods should estimate the same number of DALYs lost associated with a specific risk factor. Indoor air, independent of the impact of household use of solid fuels, had not been studied in a CRA analysis thus far. We compared results from our methodology with CPA results with the caveat that the methods are far from equivalent and the comparison should he seen only as a point of reference. The comparison also provides a useful tool for bounding uncertainties for our impact assessment method.

The WHO compiled disease incidence data for all communicable and noncommunicable diseases and injuries to determine the total number of DALYs lost per year for 192 countries (WHO 2009). McKenna et al. (2005) aggregated US. mortality and morbidity data to determine the top 20 causes of DALY losses for men and women in 1996. Ezzati and Lopez (2004) estimated the total DALYs lost due to smoking and tobacco use in industrialized nations by determining the impact of disease beyond what would be expected in non-smoking homes. The total DALY losses that we estimated for all TAPs analyzed with the IND and ID methods were compared with estimates from these studies to discern whether the full CI of the aggregate TAP impact of indoor residential air is plausible. Additionally, we used our IND and ID methodology to calculate health impact for a suite of measured SHS components, and we compared the aggregate CI of the DALYs lost for these components with CRA-derived DALY estimates.

SHS is a complex mixture of chemicals. Nazaroff and Singer (2004) estimated increases in specific volatile organic compound concentrations (1,3-butadiene, 2-butanone, acetaldehyde, acetonitrile, acrolein, acrylo-nitrile, benzene, ethyl benzene, formaldehyde, naphthalene, phenol, strene, toluene, and xylenes) expected for average smoking activity. Sirnons et al. (2007) found that homes with smokers had [PM.sub.2.5] concentrations that averaged 16 [micro]g/[m.sub.3] higher than those in the homes of nonsmokers. We applied the IND and ID modeling frameworks established here to determine the additional DALYs lost due to living in a household that had indoor Concentrations elevated by the specified levels. We used the Monte Carlo sampling to determine an aggregate CI for the DALYs lost due to exposure to this chemical mixture.


Figure 1 shows the estimated number of DALYs lost due to indoor inhalation intake of HAPs and ozone based on the ID approach. Formaldehyde and acrolein had the largest estimated number of DALYS lost, 46 (95% CI: 0.2, 14,000) and 47 (95% CI: 2.4, 1,050), respectively, higher than the upper hound of the CI for all hut two other pollutants, ozone and acetaldehyde. of the 65 pollutants compared using the ID method, only 15 had 95% CIs that overlapped with the 95% CI for formaldehyde.

Figure 2 plots disease incidence and DALYs lost using the TND method for chronic exposure to criteria pollutants. The estimated DALYs lost because of incidences of stroke, chronic bronchitis, and premature death due to [PM.sub.2.5] contributed substantially to annual health impacts. Mortality due to ozone is also a significant contributor to the total DALYs lost. The estimated number of DALY losses associated with hospitalization was relatively iow for each pollutant. NO2 is potentially a significant acute health hazard, but we did not consider acute effects in this analysis. Nonlethal chronic exposure to CO and [SO.sub.2] are not substantial contributors to DALYs lost from the outcomes we evaluated. There is concern that indoor concentrations of CO may have an adverse effect on certain susceptible populations (U.S. EPA 2010); however, the current empirical evidence is insufficient to reliably quantify the health impact from chronic CO exposure.

Figure 3 shows the estimated DALYs lost from exposure to the 12 analyzed lAPs with the highest DALY losses per year per 100,000 persons. Figure 3 also shows estimates of DALYs lost per 100,000 persons per year attributed to SHS [51 (95% CI: 42, 60)], acute CO deaths [4.9 (95% CI: 4.7, 5.1)], and radon exposure for smokers [79 (95% CI: 25, 255)] and nonsmokers [13 (95% CI: 4, 42)]. For smokers, we overestimated the DALY losses attributable to radon per se because a portion of the DALY losses for smokers exposed to radon would result solely from smoking. For ozone, the IND and ID approaches estimated annual DALY losses per 100,000 persons of 6.7 (95% CI: 0.3, 160) and 2.3 (95% Cl: (1.2, 26), respectively. There is substantial overlap in the Cis for both approaches, although the IND CI is smaller. These results suggest that [PM.sub.2.5], acrolein, fbrmaldehyde, radon, and SHS are the most harmful nonbiological air pollutants in residences on a population basis. In addition, we calculated that intake of the subset of compounds in SHS noted above would cause an annual loss of 1,000 DALYs (95% CI: 300, 14,000) per 100,000 residents in households with SHS, and a population-averaged annual loss of 110 DALYS (95% CI: 40, 1,600) per 100,000 residents in all U.S. households.

Our analysis yielded a central estimate for the DALYs lost due to all IAPs analyzed using the TND and ID methods of 1, 1 00 DALYs per 100,000 persons (95% CI: 400, 13,000) per year. For 80% of the Monte Carlo samples, indoor [PM.sub.2.5] was associated with the largest number of DALY losses, whereas acrolein and formaldehyde were the dominant contributors for 16% and 4% of the samples, respectively, and another IAP was the dominant contributor other than these three in <- 0.25% of the Monte Carlo samples. For 90% of the samples, acrolein, formaldehyde, and [PM.sub.2.5] contributed > 80% of the total DALYs lost. This reinforces the finding that these three pollutants account for most chronic health effects associated with indoor air in nonsmoking homes.


Although there is large uncertainty in the number of DALY losses estimated for each pollutant by the IND and ID models, several clear findings emerge. Our analysis demonstrates that in most U.S. residences [PM.sub.2.5], acrolein, and formaldehyde dominate health impacts due to chronic exposures to non-biological air pollutants. The DALY losses from these three pollutants appear to be much larger than the DALY losses due to CO deaths from acute poisoning in homes. SHS and radon are also significant contributors to populationwide DALY losses, but these exposures occur in a smaller fraction of homes.

Formaldehyde is primarily emitted from materials throughout the home. Similarly, acrolein is also emitted from such materials; however, cooking is also a potentially significant indoor source (Seaman et al. 2007). [PM.sub.2.5] concentrations indoors, unlike acrolein and formaldehyde, are due to both indoor and outdoor sources, and outdoor concentrations may exceed indoor levels in many locations (Weisel et al. 2005).

Our analysis yielded a central estimate of 1,100 DALY losses per 100,000 persons (95% CI: 400, 13,000) per year for IAPs, excluding radon and SHS. For the United States overall, WHO (2009) estimated a total burden of 7,700 DALY losses per year per 100,000 persons for all noncommunicable, nonpsychiatric diseases combined. McKenna et al. (2005) identified the top 20 diseases that drive the health burden in the United States. Of those top 20 diseases, those with an indoor-air connection account for the loss of 3,000 DALYs per 100,000 persons per year (McKenna et al. 2005). Ezzati and Lopez (2004) estimated that the population-average burden of both firsthand (smokers) and secondhand tobacco smoke in industrialized nations is 12% of the annual DALYs lost, which we assume would represent 1,700 DALY losses per 100,000 persons per year, that is, 12% of the total DALY losses estimated for the United States by WHO (2009). Estimated DALY losses due to indoor PM,5, acrolein, and Formaldehyde combined [1,100 (95% Cl: 700, 13,000)] were substantially greater than DALY losses due to the remaining 67 IAPs analyzed using the IND and ID methods combined [40 (95% CI: 10,70)].

Our estimate of DALYs lost to SHS components in the 11% of homes estimated to have SHS is of similar magnitude to the mean estimate of DALY losses from LAP inhalation in nonsmoking homes. For the SHS analysis, pollutants that contribute the most to DALY losses are again [PM.sub.2.5] and acrolein. Having a smoker in a residence, on average, doubles the concentrations of these two components relative to homes without smokers (Nazaroff and Singer 2004; Sirnons et al. 2007), effectively doubling the DALY loss estimates. The complete chemical mixture of SHS should be more toxic than the limited subset of components examined here, but the DALY loss estimate derived from the literature-reported health end points due to SHS is in the lower bound ol the 95% CI. This result suggests that the component-based method used in this study may tend to overestimate DALY losses or that an insufficient number of health end points are attributed to SHS.

Both the IND and ID approaches rely on no-threshold disease incidence models that are linear or effectively linear over the concentration range of the analysis. The health impacts of [PM.sub.2.5] are broadly thought to be linear at low doses (Schwartz et al. 2002). Threshold effects may signifcantly reduce the actual health impacts due to formaldehyde (a cancer hazard) and acrolein exposure (a noncancer hazard). Although some studies have identified genotoxic efficts for formaldehyde (Viegas et al. 2010), others have identified strong threshold effects (Salthammer and Bahadir 2009). Various thresholds for exposure to avoid cancer have been suggested, ranging from 120 [micro]g/[m.sub.3] suggested by the German Federal Institute for Risk Assessment and WHO to 12[micro]g/[m.sub.3] suggested by Naya and Nakanishi (2005). Given the distribution of formaldehyde concentrations determined for residences, threshold effect Levels of 12 [micro]g/[m.sub.3] and 120 [micro]g/[m.sub.3] would result in 32% and 87% reductions in predicted DALY Losses, respectively. A high threshold would result in [PM.sub.2.5] and acrolein being the prime indoor pollutants of concern and Formaldehyde being of lesser importance.

Less information is available on threshold levels for acrolein exposure. We determined the impact on the DALY Loss estimate for a threshold equal to the CalEPA noncancer reference exposure Level (0.35 [micro]g/[m.sup.3]). Given the determined distribution of acrolein concentrations indoors, this would result in a 20% reduction in DALY losses.


Using the methodology established here, we estimated that the total annual health impact of IAP inhalation in U.S. residences, excluding radon and SHS, is 1,100 DALY losses per 100,000 persons (95% CI: 400, 13,000). The upper bound of the range was twice as high as the number of DALY losses due to all noncommunicable, nonpsychiatric diseases as estimated by WHO (2009) based on disease statistics. The upper bound of the CI estimated for the DALYs lost due to exposure to a subset of pollutants in SHS using the methodology was also implausibly high. The total annual DALYs lost due to IAPs is likely in the lower half of the calculated range, that is, between the central estimate (1,100) and lower bound of the 95% CI (400) in DALY losses per 100,000 persons.

Because the upper-bound Cl for all IAP-related DALY losses is too high, the upper-bound for CIs of at least some of the individual pollutants included must also be too high. Because the vast majority of the total DALY losses were due to acrolein, [PM.sub.2.5], and formaldehyde, further statistical analysis may be able to narrow the currently large CIs for impacts from these pollutants.


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Address correspondence to .J.M. Logue, I Cyclotron Rd.. MS 90R3083, Berkeley, CA 94720 USA. Telephone: (510) 486-5945. Fax: (510) 486-6658. E-mail:

Funding was provided by the U.S. Department of Energy Building Technologies Program, Office of Energy Efficiency and Renewable Energy under Department of Energy contract DE-ACO2-05CH11231; by the U.S. Department of Housing and Urban Development Office of Healthy Homes and Lead Hazard Control through interagency agreement I-PHI-01070; by the U.S. Environmental Protection Agency Office of Air and Radiaion through interagency agreement DW-89-92322201-0; and by the California Euergy Commission through con tract 500-08-061.

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

Received 3 June 2011; accepted 17 November 201 11.

Environmental Energy Technologies Division, Lawrence Berkeley National Lab, Berkeley, California, USA
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Title Annotation:Research
Author:Logue, Jennifer M.; Price, Phillip N.; Sherman, Max H.; Singer, Brett C.
Publication:Environmental Health Perspectives
Article Type:Report
Geographic Code:1USA
Date:Feb 1, 2012
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