Abstract
SETTING
The National Longitudinal Mortality Study (NLMS) offers the advantage of assessing mortality in a representative population of the United States.
OBJECTIVE
To evaluate health disparities associated with lung cancer and chronic obstructive pulmonary disease (COPD) mortality in the United States and whether these associations are similar between these outcomes.
DESIGN
The NLMS is a prospective study. Data are from NLMS cohort years 1985, 1992, 1993, 1995, and 1996 were included representing nearly 1.5 million person years. Lung cancer and COPD mortality relative risks from Cox regression analysis including residential characteristics, marital status, education, health insurance, and family income were evaluated.
RESULTS
By 1998, 1,273 lung cancer deaths and 772 COPD deaths occurred. Lung cancer mortality rates were approximately two times higher than COPD mortality rates among race and ethnic groups. Cox regression analysis revealed that low education (Relative Risk (RR) = 1.77, significant, p=0.01) and low family income (RR = 1.50, significant, p=0.01) are associated with lung cancer and COPD mortality controlling for age, race/ethnicity, gender and smoking status.
CONCLUSIONS
COPD and lung cancer mortality have similar associations with health disparities indicators in the NLMS data with some differences in the magnitude of the effect.
Keywords: cancer, mortality, lung diseases, health disparities, income, education
Introduction
Death rates from chronic lung diseases including chronic bronchitis, emphysema, and chronic obstructive pulmonary disease (COPD) by smoking status are not readily available. Mortality rates from world estimates1 vary, and may reflect differences in diagnosis, cause of death attribution,2 or mortality files3. Cancer mortality rates may be found through nationally representative registries4 or those representing smaller, well-described populations. Despite the decreases in smoking5,6 and decreased lung cancer deaths7, lung cancer remains among the top five cancer causes of death4. Smoking remains a top contributor to COPD disease8, 9.
This analysis examines health disparities, including socioeconomic factors, adjusted for smoking, associated with death from lung cancer and chronic obstructive pulmonary disease (COPD) using the National Longitudinal Mortality Study (NLMS), a population-based mortality study in the United States. The Surveillance, Epidemiology, and End Results (SEER)-NLMS data were introduced as a unique, population-based research resource that is valuable for health disparity research on cancer burden (10). Although cancer rates have been decreasing (11), a data gap exists in the research of health disparities for cancer and other outcomes. Prompted by Congressional action in 1997 and 2000, the Institute of Medicine (IOM) issued a review of the NIH Strategic Plan, and recommended inclusion of information on racial and ethnic subpopulations and detailed socioeconomic data in population-based studies that evaluate health disparities. Risk estimates from NLMS cohorts, which are followed, offer person-year contributions to the mortality risk estimates, rather than cross-sectional mortality estimates. Results are presented of health disparities factors on the burden of lung cancer and COPD using the NLMS tobacco use cohorts, a subset of the NLMS data. The NLMS tobacco use cohorts include self-declared smoking status that will allow adjustment for smoking as part of the evaluation of health disparities.
Study Population and Methods
The study population includes a subset of the NLMS12–14, a mortality follow-up of selected cohorts of respondents to the Current Population Survey (CPS) and the 1980 U.S. Census. The CPS is conducted monthly by personal and telephone interview on a national probability sample of about 60,000 households from the civilian non-institutionalized U.S. population by the U.S. Census Bureau for the Bureau of Labor Statistics15. Responses are obtained for household members concerning employment status and labor, demographic, economic, and social characteristics. Records were selected from five NLMS cohorts with information on tobacco use: the CPS survey for September 1985, and the March CPS surveys of 1992, 1993, 1995, and 1996. Smoking status (never smoked, current smoker, and former smoker) and other variables are collected only at the time of the survey.
NLMS cohort vital status is followed through the National Death Index (NDI), a national file of death certificate information collected and maintained by the National Center for Health Statistics (NCHS). For this paper, cause of death is defined as the underlying cause of death determined by professional nosologists according to the International Classification of Diseases, 9th Revision (ICD-9)16. Mortality follow-up is measured from the last day of interview for the source survey until date of death or censoring at the end of follow-up of the study, December 31, 1998. Confidentiality of NLMS data is governed by the U.S. Federal Policy for the Protection of Human Subjects, and is identical to Subpart A or 45 CFR Part 46 of the Health and Human Services regulation.
Data analysis
The ICD-9 underlying lung disease death codes included in the analyses are bronchitis (ICD-9 490), chronic bronchitis (ICD-9 491), emphysema (ICD-9 492), asthma (ICD-9 493), bronchiectasis (ICD-9 494), chronic airway obstruction (ICD-9 496), and lung cancer (ICD-9 162.2–162.9). COPD utilizes the codes for bronchitis, chronic bronchitis, and emphysema (490-492) and CAO (496). While 494 and 495 are included in the NCHS definition of COPD, these conditions are not included. Direct, age adjusted mortality rates per 100,000 person years17 based on the NCHS year 2000 standard million population are presented with frequency distributions for demographic and smoking characteristics for persons aged 25 years and older. White race was split into Hispanic and non-Hispanic, owing to very low Hispanic ethnicity found among blacks or other race.
Geographic and residential variables in the analysis include urban or rural residence, residence in a standard metropolitan statistical area (SMSA) in a central city, SMSA residence not in a central city, or residence in a non SMSA area, and U.S. Census division. Referent groups for geographic and residential variables are urban residence, residence in an SMSA central city, and Pacific division.
Socio-economic status (SES) included marital status (widowed or divorced, separated, married, and never married), education (less than high school diploma, high school diploma, and education beyond a high school diploma), health insurance (insured/not insured), family income in 1990 U.S. dollars, and percent of poverty level using 1990 standings. Major occupation was analyzed by the 1990 categorization of U.S. occupations18. Referent groups for these variables are married, greater than high school education for education, having health insurance, more than $60,000 in family income in U.S. 1990 dollars, and living at greater than or equal to 400 percent of the 1990 U.S. poverty level.
Cox proportional hazards regression models19 were used to estimate relative risks (RR) and 99 percent confidence intervals for the risk of dying from the underlying cause of death for geographic, residence, and SES variables. Stratified analysis by calendar year was used in consideration of the baseline hazard of each of the CPS cohorts20. Cox regression models were adjusted for age in years, gender, race/ethnicity (non-Hispanic white, Hispanic white, black, other). A global test of whether all levels of a categorical variable are equal to zero was conducted using the test statement for the Cox regression models in SAS to address the possibility of a type-1 error20. The proportional hazards assumption was verified graphically (results not shown). 189,924 individuals had sufficient data for mortality analysis representing 1,653,653 person years.
Results
Mortality
Of 189,924 individuals at risk of death, 94,027 or 49.51% were never smokers, 49,532 or 26.08% were current smokers, and 46,368 or 24.51% were former smokers. Death rates for lung cancer and COPD by demographic factors and smoking are shown in Table 1. Lung cancer mortality rates were highest among those aged 65 to 74 years, males, and among black individuals (Table 1). COPD mortality rates were highest among 65 to 74 year olds, males, and non-Hispanic whites. Mortality rates by smoking were highest among current smokers followed by former smokers for both lung cancer and COPD.
Table 1.
Lung cancer (n = 1,273) | Chronic obstructive pulmonary disease (n = 772) | |||||
---|---|---|---|---|---|---|
# Deaths | Person-years | Rateb | # Deaths | Person-years | Rateb | |
Baseline Age | ||||||
25 to 44 | 64 | 941,144.25 | 12.20 | 10 | 941,144.25 | 2.02 |
45 to 54 | 129 | 243,211.56 | 19.50 | 45 | 243,211.56 | 10.00 |
55 to 64 | 391 | 217,166.26 | 49.88 | 170 | 217,166.26 | 26.86 |
65 to 74 | 447 | 162,254.60 | 52.71 | 303 | 162,254.60 | 36.93 |
75 to 84 | 217 | 75,209.34 | 26.92 | 211 | 75,209.34 | 25.69 |
85+ | 25 | 14,667.11 | 4.09 | 33 | 14,667.11 | 5.40 |
Gender | ||||||
Male | 795 | 764,304.43 | 103.60 | 433 | 764,304.43 | 46.18 |
Female | 478 | 889,348.67 | 46.72 | 339 | 889,348.67 | 25.17 |
Race/Ethnicitya | ||||||
Hispanic white | 14 | 79,031.09 | 27.33 | 7 | 79,031.09 | 11.26 |
Non-Hispanic | 1115 | 1,343,013.61 | 72.89 | 705 | 1,343,013.61 | 35.16 |
White | ||||||
Black | 104 | 147,045.28 | 75.41 | 36 | 147,045.28 | 22.17 |
Others | 19 | 53,221.51 | 46.96 | 8 | 53,221.51 | 19.76 |
Unknown | 21 | 31,341.61 | 55.16 | 16 | 31,341.61 | 31.92 |
Smoking Status | ||||||
Never | 143 | 837,868.96 | 15.56 | 98 | 837,868.96 | 9.62 |
Current | 679 | 466,200.34 | 184.29 | 342 | 466,200.34 | 106.72 |
Former | 451 | 349,583.80 | 84.78 | 332 | 349,583.80 | 63.12 |
Hispanic ethnicity includes white Hispanic. White, black and other are non-Hispanic.
Mortality rate is direct adjusted per 100,000 person years.
Smoking and Lung Disease Mortality
The adjusted relative risk for smoking and lung cancer death was 13.24 (99% confidence interval 10.36 to 16.91) and 5.27 (99% confidence interval 4.09 to 6.80) for current and former smokers respectively as compared with non-smokers in a model adjusted for age, gender and race/ethnicity. In a similar model for COPD mortality, the adjusted relative risks were 12.40 (99% confidence interval 8.79 to 17.50) and 6.72 (99% confidence interval 4.77 to 9.47) for current and former smokers respectively as compared with non-smokers (results not shown).
Table 2 presents frequencies and the results of the Cox regression analyses for geographic, residential, and SES factors for time until lung cancer or COPD mortality adjusted for age, race/ethnicity, gender, and smoking. Rural residence and type of SMSA residence did not show increased mortality risk from either lung cancer or COPD relative to those with urban residence or residence in a Central City SMSA. Risk of death from COPD was increased for the Mountain US Census division (RR=1.40, p=0.03, Table 2).
Table 2.
Lung Cancer | Chronic Obstructive Pulmonary Disease | |||||
---|---|---|---|---|---|---|
# Deaths | RRa | 99% CIa | # Deaths | RRa | 99%CIa | |
Urban/Rural Residence | ||||||
Rural | 365 | 0.91 | 0.78, 1.07 | 225 | 0.94 | 0.77, 1.16 |
Urban | 908 | 1.00 | 547 | 1.00 | ||
SMSAb | ||||||
SMSA not Central City | 464 | 0.94 | 0.78,1.14 | 266 | 0.87 | 0.68, 1.12 |
Not an SMSA | 476 | 0.90 | 0.75,1.09 | 308 | 0.93 | 0.74, 1.19 |
SMSA, Central City | 333 | 1.00 | 198 | 1.00 | ||
US Census Division | ||||||
New England | 110 | 0.92 | 0.65,1.29 | 74 | 1.00 | 0.65, 1.54 |
MidAtlantic | 215 | 1.12 | 0.83,1.50 | 102 | 0.90 | 0.61, 1.34 |
East North Central | 206 | 1.09 | 0.81,1.47 | 131 | 1.22 | 0.83, 1.78 |
West North Central | 112 | 0.88 | 0.63,1.23 | 70 | 0.91 | 0.59, 1.40 |
South Atlantic | 249 | 1.07 | 0.80,1.43 | 136 | 1.04 | 0.71, 1.51 |
East South Central | 70 | 1.10 | 0.74,1.63 | 39 | 1.13 | 0.67, 1.89 |
West South Central | 112 | 1.19 | 0.85,1.67 | 63 | 1.22 | 0.78, 1.90 |
Mountain | 74 | 0.74 | 0.51,1.08 | 73 | 1.40 | 0.92, 2.12 |
Pacific | 125 | 1.00 | 74 | 1.00 | ||
Marital Status | ||||||
Widowed/Divorced | 341 | 0.97 | 0.81,1.17 | 284 | 1.33c | 1.07, 1.66 |
Separated | 26 | 1.11 | 0.66,1.86 | 15 | 1.66 | 0.84, 3.30 |
Never Married | 49 | 0.69 | 0.47,1.01 | 22 | 0.95 | 0.59, 1.52 |
Married | 857 | 1.00 | 441 | 1.00 | ||
Education | ||||||
<HS Diploma | 578 | 1.77c | 1.45,2.17 | 388 | 1.87c | 1.44, 2.42 |
HS Diploma | 451 | 1.50c | 1.22,1.84 | 245 | 1.40c | 1.07, 1.85 |
>HS Diploma | 244 | 1.00 | 139 | 1.00 | ||
Health Insurance Status | ||||||
No Health Insurance | 24 | 1.35 | 0.79,2.32 | 6 | 0.86 | 0.30, 2.50 |
Health Insurance | 401 | 1.00 | 258 | 1.00 | ||
Family Income 1990 US$ | ||||||
<$10,000 | 251 | 1.50c | 1.12,2.00 | 205 | 2.46c | 1.65, 3.66 |
$10,000–$20,000 | 338 | 1.45c | 1.10,1.90 | 251 | 2.13c | 1.45, 3.13 |
$20,000–$40,000 | 422 | 1.43c | 1.10,1.87 | 213 | 1.61c | 1.09, 2.37 |
$40,000–$60,000 | 138 | 1.33 | 0.97,1.83 | 47 | 1.08 | 0.65, 1.80 |
>=$60,000 | 80 | 1.00 | 30 | 1.00 |
RR, relative risk; CI, confidence interval
SMSA, Standard metropolitan statistical area
p<0.01
Risk by marital status did not differ from the referent category, married, for lung cancer mortality in the smoking-adjusted models (Table 2). Mortality risk from COPD, however, was increased significantly for those who were widowed or divorced (RR=1.33, p<0.01) and increased, but not significantly, for those who were separated relative to those who were married.
Adjusted mortality risks for lung cancer and COPD were significantly increased for those with less than a high school diploma (RR=1.77, p<0.01 for lung cancer; RR=1.87, p<0.01 for COPD) relative to those with education beyond a high school diploma. Mortality risk was significantly elevated for those with a high school diploma (RR=1.50, p<0.01 for lung cancer and RR=1.40, p<0.01 for COPD) relative to those with an education beyond a high school diploma.
Lung cancer mortality risk was non-significantly increased for those who were not insured relative to those insured (RR=1.35). Access to health insurance did not impact mortality risk for COPD, RR=0.86.
Mortality risk for lung cancer and COPD was significantly increased for lower family income. There is a significant trend for increasing risk of mortality for both lung cancer and COPD with decreasing income (results not shown). Lung cancer mortality risk significantly increased for those with less than a high school education relative to greater than a high school education (results not shown). COPD mortality risk by education and smoking was similar. Significant trend relationships for increased lung cancer and COPD mortality risk and decreasing income were detected among current and former smokers (results not shown).
Discussion
The NLMS data provide mortality rates for outcomes that may not be obtainable otherwise. Mortality rates for lung cancer and COPD are presented by demographic background and by smoking. The Cox regression analysis focuses on potential health disparities factors in a representative sample of the U.S. population, controlling for self-reported smoking.
A primary risk factor for chronic obstructive pulmonary disease (COPD) is smoking21–23. In a study of male British doctors, COPD mortality rates were less than half for former smokers compared with current smokers22. Our results agree with previous studies that former smokers have a decreased risk of lung cancer mortality compared with current smokers24. COPD rates among former smokers in our analysis were slightly more than half the rate among current smokers.
No significant differences for lung cancer mortality risk for urban and rural residence and SMSA residence were found. Non-SMSA dwellers had decreased COPD mortality risk relative to SMSA dwellers may indicate a role for air quality in the risk of COPD death. Fine particulate air pollution has been previously associated with daily mortality25. An extension of the Harvard Six Cities Study found total, cardiovascular, and lung cancer mortality positively associated with ambient PM2.5 concentrations; reduced PM2.5 concentrations were associated with reduced mortality risk25. SMSA central city residents may be exposed to higher concentrations of particulate matter, reflecting higher risks of mortality. Residents who do not live in these areas have reduced mortality. An airborne particulate matter source apportionment workgroup reported that soil sources and residual oil sources were more consistent in explaining PM2.5 sources and traffic sources were not consistently correlated with PM2.526.
The magnitude of COPD mortality risk was slightly higher than that of lung cancer for U.S. Census divisions with an increased risk. Underlying reasons for these differences are unknown; lung cancer mortality is not subject to the reversibility that can be observed with lung diseases where particulate air pollution is a major risk factor27. Lung cancer and COPD mortality risk decreased in the West North Central division relative to the Pacific region, perhaps due to better air quality.
Our results concur with increased risk of death from COPD in the Mountain division described previously28, 29. Particulate matter is associated with non-malignant respiratory diseases and mortality based on changes in PM 2.527. Many areas of the Mountain region are exposed to dusty industries, including farming and mining. Reduced oxygen concentration in the Mountain division may make lung function more difficult among those with pulmonary challenges. Lifestyle factors, including diet and physical fitness, and environmental factors, including air pollution, particulate matter, and other air toxics specific to the U.S. Census divisions, in consideration of population density would be recommended for further analysis. COPD and lung cancer mortality risk among those widowed, divorced, or separated compared with married individuals, is similar to a finding that unmarried individuals have a higher risk compared with married persons30. Lower socio-economic status (lower education and low income) and a higher percentage of households at the poverty level resulted in higher mortality risks for lung cancer and COPD among current and former smokers. Higher incidence and mortality of lung cancer has been associated with socioeconomic disadvantage including working class jobs, lower education, and lower income31–33.
Lack of health insurance had a greater impact on lung cancer mortality than COPD mortality, as there was a non-significant increased mortality risk for lung cancer for those lacking health insurance. COPD, lung cancer, and heart disease, share inflammation as part of their pathology34. Death from COPD may be underreported on death certificates when the ante-mortem symptoms are less severe as opposed to COPD cases that have moderate to severe symptoms35. Access to care determines which lung cancer patients receive surgery, which increases their chances for long term survival. Conversely, it is possible for COPD patients to survive with or without care until they become eligible for Medicare. Future studies of health insurance should explore lung cancer and non-cancer lung diseases, interventions and effects on morbidity and mortality to increase our understanding of the role of health insurance.
The strengths and limitations of these data and the analysis should be carefully considered. These data are prospective and mortality rates are based on person years of observation; strengths include self-reported lifestyle factors and self-reported tobacco exposure. Vital status was determined using the NDI after the CPS interviews were conducted. Smoking (never, current and former smoker) was collected only at the time of interview. Cigarettes smoked per day, number of years of smoking and pack years, and time since cessation are not available in the CPS.
A potential limiting factor of the analysis is multiple comparisons. Our concern was whether variables that have more than three or four levels, such as U.S. Census division are associated with mortality risk. Results of the global test of association to address the possibility of type-1 errors indicated that U.S. Census division, income, and education for lung cancer, and income, education, and poverty level for COPD were significant indicating a global association for each level of these variables. The significance of the global test for U.S. Census division for lung cancer (p=0.03) and marginal significance for COPD agrees with our relative risk findings. Level of significance is also considered when there is concern of type-1 error; many associations are highly significant (p<0.01).
In summary, our analysis agrees with previous associations of self-declared smoking status and mortality from lung diseases. While the same health disparity indicators were often associated with both lung cancer and COPD mortality, the magnitude of the risk differs between the two outcomes. Etiologies of lung cancer and other lung diseases differ, however these results may guide surveillance efforts for cancer and non-cancer lung causes of death, provide information to the public, shape research questions, and focus prevention efforts for respiratory health in various subpopulations. Future research using NLMS and SEER data will ascertain the importance of histologic and staging factors for lung cancer mortality with health disparity indicators.
Acknowledgments
Dr. Lewis constructed the analysis with statistical advice from Dr. Clegg and Dr. Johnson. Dr. Johnson supervised the analysis at the Bureau of the Census. Dr. Lewis wrote the manuscript with review by Dr. Clegg and Dr. Johnson. This paper has been reviewed and cleared by the National Cancer Institute and the U.S. Bureau of the Census for publication.
Footnotes
This paper is released to inform interested parties of research and to encourage discussion. Any views expressed on statistical, methodological, technical, or operational issues are those of the authors and not necessarily those of the U.S. Census Bureau.
Contributor Information
Denise Riedel Lewis, Surveillance Research Program, National Cancer Institute, National Institutes of Health, Department of Health and Human Services, Bethesda, MD USA.
Limin X. Clegg, Office of Healthcare Inspections, Office of Inspector General, U.S. Department of Veterans Affairs, Washington, D.C., USA
Norman J. Johnson, U.S. Census Bureau, Suitland, MD, USA
References
- 1.Lopez AD, Mathers CD, Ezzati M, Jamison DT, Murray CJL. Global burden of disease and risk factors. Washington: The World Bank; 2006. [PubMed] [Google Scholar]
- 2.Mannino DM, Buist AS. Global burden of COPD: risk factors, prevalence, and future trends. The Lancet. 2007;370:765–773. doi: 10.1016/S0140-6736(07)61380-4. [DOI] [PubMed] [Google Scholar]
- 3.Mannino DM, Brown C, Giovino GA. Obstructive lung disease deaths in the United States from 1979 through 1993. An analysis using multiple-cause mortality data. Am J Respir Crit Care Med. 1997;156:814–818. doi: 10.1164/ajrccm.156.3.9702026. [DOI] [PubMed] [Google Scholar]
- 4.Ries LAG, Melbert D, Krapcho M, et al., editors. SEER Cancer Statistics Review, 1975–2005. National Cancer Institute; Bethesda, MD: [accessed 8/1/2008]. http://seer.cancer.gov/csr/1975_2005/, based on November 2007 SEER data submission. [Google Scholar]
- 5.Rock VJ, Malarcher A, Kahende JW, Asman K, Husten C, Caraballo R. Cigarette Smoking Among Adults United States, 2006. MMWR. 2007;56:1157–1161. [PubMed] [Google Scholar]
- 6.Maurice E, Trosclair A, Merritt R, Caraballo R, Malarcher A, Pechacek T. Cigarette Smoking Among Adults United States 2004. MMWR. 2005;54:1121–1124. [PubMed] [Google Scholar]
- 7.American Cancer Society. Cancer Facts and Figures 2006. Atlanta: American Cancer Society; 2006. [Google Scholar]
- 8.Chapman KR, Mannino DM, Soriano JB, et al. Epidemiology and costs of chronic obstructive pulmonary disease. Eur Respir J. 2006;27:188–207. doi: 10.1183/09031936.06.00024505. [DOI] [PubMed] [Google Scholar]
- 9.Sharma S, Graham L Chronic obstructive pulmonary disease (COPD) eMedicineHealth. [accessed 9/8/2008];Practical Guide to Health. http://www.emedicinehealth.com.
- 10.Clegg LX, Reichman ME, Miller BA, et al. Impact of socioeconomic status on cancer incidence and stage at diagnosis: selected findings from the surveillance, epidemiology, and end results: National Longitudinal Mortality Study. Cancer Causes Control. 2008 November 12; doi: 10.1007/s10552-008-9256-0. Epub ahead of print. www.springerlink.com/content/7t515j4283714t9k/fulltext.pdf. [DOI] [PMC free article] [PubMed]
- 11.Jemal A, Thun MJ, Ries LAG, et al. Annual report to the Nation on the status of cancer, 1975–2005, featuring trends in lung cancer, tobacco use, and tobacco control. J Natl Cancer Inst. 2008;100:1672–1694. doi: 10.1093/jnci/djn389. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.Rogot E, Sorlie PD, Johnson NJ, Glover CS, Treasure DW. 1st data book. Publication No. 88-2896. Bethesda, MD: National Institutes of Health; 1988. A mortality study of one million persons by demographic, social and economic factors: 1979–1981 follow-up. [Google Scholar]
- 13.Rogot E, Sorlie PD, Johnson NJ, Schmidt C. 2nd data book. Publication No. 92-3297. Bethesda, MD: National Institutes of Health; 1992. A mortality study of 1.3 million persons by demographic, social and economic factors: 1979–1985 follow-up. [Google Scholar]
- 14.Sorlie PD, Backlund E, Keller JB. U.S. mortality by economic, demographic, and social characteristics: The National Longitudinal Mortality Study. Am J Public Health. 1995;85:949–956. doi: 10.2105/ajph.85.7.949. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15.U.S. Bureau of the Census. The current population survey: design and methodology. (Technical paper #40) Washington, D.C: U.S. Department of Commerce; 1978. [Google Scholar]
- 16.World Health Organization. Manual of the International Statistical Classification of Diseases, Injuries, and Causes of Death. Ninth revision. Geneva, Switzerland: World Health Organization; 1977. International Classification of Diseases. [Google Scholar]
- 17.Breslow NE, Day NE. Volume II: The Design and Analysis of Cohort Studies. Lyon: International Agency for Research on Cancer; 1987. Statistical Methods in Cancer Research; pp. 51–57. [PubMed] [Google Scholar]
- 18.U.S. Bureau of the Census. Census of Population and Housing. CPH-R-3. Washington, D.C: Government Printing Office; 1990. Alphabetical Index of Industries and Occupations. [Google Scholar]
- 19.Cox DR. Regression models and life tables (with discussion) J Royal Stat Soc. 1972;B34:187–220. [Google Scholar]
- 20.Allison PD. Survival Analysis Using the SAS System: A Practical Guide. Cary NC: SAS Institute, Inc; 1995. p. 182. [Google Scholar]
- 21.Mannino DM, Watt G, Hole D, et al. The natural history of chronic obstructive pulmonary disease. Eur Respir J. 2006;27:627–643. doi: 10.1183/09031936.06.00024605. [DOI] [PubMed] [Google Scholar]
- 22.Doll R, Peto R, Boreham J, Sutherland I. Mortality in relation to smoking: 50 years’ observations on male British doctors. Br J Cancer. 2005;92:426–429. doi: 10.1038/sj.bjc.6602359. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23.Lam TH, Ho SY, Hedley AJ, Mak KH, Peto R. Mortality and smoking in Hong Kong: case-control study of all adult deaths in 1998. BMJ. 2001;323:361. doi: 10.1136/bmj.323.7309.361. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24.Peto R, Darby S, Deo H, Silcocks P, Whitley E, Doll R. Smoking, smoking cessation, and lung cancer in the UK since 1950: combination of national statistics with two case-control studies. BMJ. 2000;321:323–329. doi: 10.1136/bmj.321.7257.323. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25.Schwartz J, Dockery DW, Neas LM. Is daily mortality associated specifically with fine particles? J Air Waste Manag Assoc. 1996;46:927–939. [PubMed] [Google Scholar]
- 26.Thurston GD, Ito K, Mar T, et al. Workgroup Report: Workshop on source apportionment of particulate matter health effects intercomparison of results and implications. Environ Health Perspect. 2005;113:1768–1774. doi: 10.1289/ehp.7989. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 27.Laden F, Schwartz J, Speizer FE, Dockery DW. Reduction in fine particulate air pollution and mortality. Extended follow-up of the Harvard Six Cities Study. Am J Respir Crit Care Med. 2006;173:667–672. doi: 10.1164/rccm.200503-443OC. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28.Nandram B, Sendransk J, Pickle LW. Bayesian analysis and mapping of mortality rates for chronic obstructive pulmonary disease. J Amer Stat Assoc. 2000;95(452):1110–1118. [Google Scholar]
- 29.Pickle LW, Mungiole M, Jones GK, White AA. Atlas of United States Mortality. (PHS) DHHS Publication No. 97-1015. Hyattsville, Maryland: National Center for Health Statistics; 1996. [Google Scholar]
- 30.Johnson NJ, Backlund E, Sorlie PD, Loveless CA. Marital status and mortality: The National Longitudinal Mortality Study. Ann Epidemiol. 2000;10:224–238. doi: 10.1016/s1047-2797(99)00052-6. [DOI] [PubMed] [Google Scholar]
- 31.Barbeau EM, Krieger N, Soobader M-J. Working Class Matters: Socioeconomic Disadvantage, Race/Ethnicity, Gender, and Smoking in NHIS 2000. Amer J Pub Health. 2004;94:269–278. doi: 10.2105/ajph.94.2.269. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 32.Krieger N, Quesenberry C, Jr, Peng T, et al. Social class, race/ethinicity, and incidence of breast, cervix, colon, lung, and prostate cancer among Asian, Black, Hispanic, and White residents of the San Francisco Bay Area, 1988–92 (United States) Cancer Causes Control. 1999;10:525–537. doi: 10.1023/a:1008950210967. [DOI] [PubMed] [Google Scholar]
- 33.Singh GK, Miller BA, Hankey BF. Changing area socioeconomic patterns in U.S. cancer mortality, 1950–1998: Part II lung and colorectal cancer. J Nat Cancer Inst. 2002;94:916–925. doi: 10.1093/jnci/94.12.916. [DOI] [PubMed] [Google Scholar]
- 34.Rennard SI. Lessons from multidisciplinary cross-fertilization. Chronic obstructive pulmonary disease, lung cancer, and heart disease. Proc Am Thorac Soc. 2008;5:865–868. doi: 10.1513/pats.200807-060TH. [DOI] [PubMed] [Google Scholar]
- 35.Camilli AE, Robbins DR, Lebowitz MD. Death certificate reporting of confirmed airways obstructive disease. Am J Epidemiol. 1991;133:795–800. doi: 10.1093/oxfordjournals.aje.a115958. [DOI] [PubMed] [Google Scholar]