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1.
J Epidemiol Community Health ; 63(6): 500-4, 2009 Jun.
Article in English | MEDLINE | ID: mdl-19228684

ABSTRACT

BACKGROUND: Relationships between ambient air pollution levels during pregnancy and adverse pregnancy outcomes have been investigated using one of three analytic approaches: ambient pollution levels have been contrasted over space, time or both space and time. Although the three approaches share a common goal, to estimate the causal effects of pollution on pregnancy outcomes, they face different challenges with respect to confounding. METHODS: A framework based on counterfactual effect definitions to examine issues related to confounding in spatial, temporal, and spatial-temporal analyses of air pollution and pregnancy outcomes is presented, and their implications for inference are discussed. RESULTS: In spatial analyses, risk factors that are spatially correlated with pollution levels are confounders; the primary challenges relate to the availability and validity of risk factor measurements. In temporal analyses, where smooth functions of time are commonly used to control for confounding, concerns relate to the adequacy of control and the possibility that abrupt changes in risk might be systematically related to pollution levels. Spatial-temporal approaches are subject to challenges faced in both spatial and temporal analyses. CONCLUSION: Each approach faces different challenges with respect to the likely sources of confounding and the ability to control for that confounding because of differences in the type, availability, and quality of information required. Thoughtful consideration of these differences should help investigators select the analytic approach that best promotes the validity of their research.


Subject(s)
Air Pollution/adverse effects , Pregnancy Outcome/epidemiology , Air Pollution/analysis , Confounding Factors, Epidemiologic , Environmental Monitoring/methods , Epidemiological Monitoring , Female , Humans , Maternal Exposure/adverse effects , Pregnancy
2.
Cancer Causes Control ; 13(2): 159-68, 2002 Mar.
Article in English | MEDLINE | ID: mdl-11936822

ABSTRACT

OBJECTIVE: Non-Hodgkin's lymphoma (NHL) encompasses diverse subtypes, and analyzing NHL as a single outcome may mask associations. In a new approach we evaluated associations with subtypes defined by the t(14;18) translocation, reasoning that cases within these subtypes would have more common risk factors than all NHL combined. METHODS: Archival biopsies from cases in a population-based NHL study were assayed for t(14;18) using polymerase chain reaction amplification. Exposures in 68 t(14;18)-positive and 114-negative cases were compared with 1245 controls. The expectation-maximization algorithm was used to fit polytomous regression models based on all available information, including data from 440 unclassified cases. RESULTS: Family history of hemolymphatic cancer was associated with t(14;18)-negative NHL (odds ratio (OR) 2.4, 95% confidence interval (CI) 1.4 3.9). but not t(14;18)-positive NHL. Cigarette smoking was weakly associated with t(14;18)-positive NHL (OR 1.7, CI 0.9-3.3), but ORs decreased as smoking increased. Chewing tobacco was associated with t(14;18)-positive NHL, particularly when used before age 18 (OR 2.5. CI 1.0-6.0, 13 exposed cases). Odds ratios for both case-subtypes were doubled among hair-dye users. CONCLUSIONS: Cigarette smoking was not clearly associated with t(14;18)-positive NHL. Family history may be a marker for factors that act specifically through t(14;18)-negative pathogenic mechanisms.


Subject(s)
Chromosomes, Human, Pair 14/genetics , Chromosomes, Human, Pair 18/genetics , Lymphoma, Non-Hodgkin/etiology , Lymphoma, Non-Hodgkin/genetics , Occupational Exposure , Smoking/adverse effects , Translocation, Genetic , Adolescent , Adult , Aged , Case-Control Studies , Family Health , Humans , Incidence , Lymphoma, Non-Hodgkin/epidemiology , Male , Middle Aged , Odds Ratio , Risk Factors
3.
Environ Health Perspect ; 109(11): 1133-7, 2001 Nov.
Article in English | MEDLINE | ID: mdl-11712998

ABSTRACT

In the early 1970s, the largest industrial accident in the United States resulted in widespread contamination of the food supply in Michigan with polybrominated biphenyls (PBBs). The chemical similarity of PBBs to compounds implicated as endocrine disruptors has raised the question of whether PBBs could affect the reproductive system. In the present analysis we examine the relation between serum measurements of PBBs and the frequency and duration of lactation. Persons who lived on or received food from farms exposed to PBBs were enrolled in a registry by the Michigan Department of Public Health. Female members of the cohort were invited to participate in a telephone survey of reproductive outcomes. The three outcomes of interest in the present analysis were a) the decision to breast-feed (yes/no); b) the duration, in months, of breast-feeding as the main source of nutrition; and c) the total duration, in months, of breast-feeding. None of the three outcomes was significantly associated with serum PBB levels, even after controlling for maternal age, previous history of breast-feeding, body mass index, maternal education, household income, history of smoking in the year before pregnancy, consumption of alcohol during the first trimester of pregnancy, history of thyroid disorder, gestational age of the infant in weeks, time to pregnancy, and year of birth.


Subject(s)
Accidents, Occupational , Environmental Pollutants/adverse effects , Food Contamination , Lactation , Milk, Human/chemistry , Polychlorinated Biphenyls/adverse effects , Adolescent , Adult , Age Factors , Body Mass Index , Child , Child, Preschool , Cohort Studies , Decision Making , Environmental Pollutants/analysis , Female , Health Surveys , Humans , Income , Infant , Infant, Newborn , Michigan , Parity , Polychlorinated Biphenyls/analysis , Pregnancy , Risk Factors
4.
Epidemiology ; 12(6): 701-9, 2001 Nov.
Article in English | MEDLINE | ID: mdl-11679800

ABSTRACT

The t(14;18) translocation is a common somatic mutation in non-Hodgkin's lymphoma (NHL) that is associated with bcl-2 activation and inhibition of apoptosis. We hypothesized that some risk factors might act specifically along t(14;18)-dependent pathways, leading to stronger associations with t(14;18)-positive than t(14;18)-negative non-Hodgkin's lymphoma. Archival biopsies from 182 non-Hodgkin's lymphoma cases included in a case-control study of men in Iowa and Minnesota (the Factors Affecting Rural Men, or FARM study) were assayed for t(14;18) using polymerase chain reaction amplification; 68 (37%) were t(14;18)-positive. We estimated adjusted odds ratios (OR) and 95% confidence intervals (CI) for various agricultural risk factors and t(14;18)-positive and -negative cases of non-Hodgkin's lymphoma, based on polytomous logistic regression models fit using the expectation-maximization (EM) algorithm. T(14;18)-positive non-Hodgkin's lymphoma was associated with farming (OR 1.4, 95% CI = 0.9-2.3), dieldrin (OR 3.7, 95% CI = 1.9-7.0), toxaphene (OR 3.0, 95% CI = 1.5-6.1), lindane (OR 2.3, 95% CI = 1.3-3.9), atrazine (OR 1.7, 95% CI = 1.0-2.8), and fungicides (OR 1.8, 95% CI = 0.9-3.6), in marked contrast to null or negative associations for the same self-reported exposures and t(14;18)-negative non-Hodgkin's lymphoma. Causal relations between agricultural exposures and t(14;18)-positive non-Hodgkin's lymphoma are plausible, but associations should be confirmed in a larger study. Results suggest that non-Hodgkin's lymphoma classification based on the t(14;18) translocation is of value in etiologic research.


Subject(s)
Agricultural Workers' Diseases/genetics , Chromosomes, Human, Pair 14/drug effects , Chromosomes, Human, Pair 18/drug effects , Lymphoma, Non-Hodgkin/genetics , Translocation, Genetic/genetics , Adult , Aged , Agricultural Workers' Diseases/chemically induced , Agricultural Workers' Diseases/epidemiology , Agrochemicals/adverse effects , Algorithms , Apoptosis/genetics , Case-Control Studies , Chromosomes, Human, Pair 14/genetics , Chromosomes, Human, Pair 18/genetics , Confidence Intervals , Genes, bcl-2/genetics , Humans , Hydrocarbons, Chlorinated/adverse effects , Iowa/epidemiology , Lymphoma, Non-Hodgkin/chemically induced , Lymphoma, Non-Hodgkin/epidemiology , Male , Middle Aged , Minnesota/epidemiology , Odds Ratio , Polymerase Chain Reaction/methods , Risk Factors
5.
J Toxicol Environ Health A ; 63(4): 237-41, 2001 Jun 22.
Article in English | MEDLINE | ID: mdl-11437057

ABSTRACT

Agricultural exposures differ across the United States by region, calendar time period, and agricultural practice, but most of the published literature focuses on white men in the Midwest. A pilot study was conducted to explore the breadth and diversity of farming practices over time among African-American farmers in Georgia whose exposures may differ in important ways. Using a comprehensive life events calendar questionnaire, 17 male African-American farmers aged 36 to 86 yr residing in southeastern Georgia were interviewed regarding their agricultural history in July 1997. Most men (15/17) reported working on multiple farms in their lifetime; 3 men worked on 5 different farms during their lifetime. These farmers reported using more chemicals during their lifetime than farmers in the Midwest. Used motor oil was the most frequently reported insecticide applied to animals; this apparently common practice has not been described in the literature and should be better understood since its use may result in dermal exposure to polyaromatic hydrocarbons. Better characterization of regionally specific farming history and individual farming practices will facilitate studies of the health effects of farming.


Subject(s)
Agricultural Workers' Diseases/epidemiology , Occupational Exposure/statistics & numerical data , Adult , Black or African American , Aged , Aged, 80 and over , Data Collection , Georgia/epidemiology , Humans , Male , Middle Aged , Pesticides , Surveys and Questionnaires
6.
Cancer Epidemiol Biomarkers Prev ; 9(11): 1223-32, 2000 Nov.
Article in English | MEDLINE | ID: mdl-11097231

ABSTRACT

Pancreatic cancer is a highly fatal cancer with few identified risk factors. Increased risk of pancreatic cancer in tobacco smokers and among diabetic patients is well established, and some reports have suggested associations with coffee consumption and occupational exposure to organochlorines. At present, there is little information regarding the possible association of these risk factors with the known genetic alterations found in pancreatic cancers, such as activation of the K-ras oncogene and inactivation of the p53 tumor suppressor gene. Knowledge of such relationships may help to understand the molecular pathways of pancreatic tumorigenesis. We investigated the association between these molecular defects and risk factors for pancreatic cancer in 61 newly diagnosed patients identified through an ongoing study of pancreatic cancer in the San Francisco Bay Area. Interview information was obtained regarding environmental exposures, medical history, and demographic factors. Serum levels of dichlorodiphenyltrichloroethylene (DDE) and polychlorinated biphenyls were available on a subset of 24 patients. Tumor blocks were located from local hospitals and used for K-ras mutational analysis at codon 12 and for p53 protein immunohistochemistry. The molecular analyses were facilitated through the use of laser capture microdissection, which provides a reliable method to obtain almost pure populations of tumor cells. Mutations in K-ras codon 12 were found in 46 (75%) of 61 pancreatic cancers. A prior diagnosis of diabetes was significantly associated with K-ras negative tumors (P = 0.002, Fisher's exact test). The absence of this mutation was also associated with increased serum levels of DDE, although this association was not statistically significant (P = 0.16, Wilcoxon's test). There was no difference in polychlorinated biphenyl levels between the K-ras wild-type and mutant groups. Immunohistochemical staining for p53 protein did not differ by patient characteristics or clinical history, but significant associations were found with poor glandular differentiation (P = 0.002, chi2 trend test), severe nuclear atypia (P = 0.0007, chi2 trend test), and high tumor grade (P = 0.004, chi2 trend test). Our results are suggestive of the presence of K-ras codon 12 mutation-independent tumorigenesis pathways in patients with prior diabetes and possibly in patients with higher serum levels of DDE. Our results also support a role for the p53 tumor suppressor protein in the maintenance of genomic integrity.


Subject(s)
Carcinogens/adverse effects , Environmental Exposure , Genes, p53/genetics , Genes, ras/genetics , Pancreatic Neoplasms/genetics , Aged , Case-Control Studies , DNA Mutational Analysis , Diabetes Complications , Dichlorodiphenyl Dichloroethylene/adverse effects , Female , Humans , Immunohistochemistry , Insecticides/adverse effects , Male , Medical History Taking , Middle Aged , Pancreatic Neoplasms/etiology , Risk Factors
7.
J Expo Anal Environ Epidemiol ; 10(5): 446-60, 2000.
Article in English | MEDLINE | ID: mdl-11051535

ABSTRACT

Substantial evidence supports an association of particulate matter (PM) with cardiorespiratory illnesses, but little is known regarding characteristics of PM that might contribute to this association and the mechanisms of action. The Atlanta superstation sponsored by the Electric Power Research Institute as part of the Aerosol Research and Inhalation Epidemiology Study (ARIES) study is monitoring chemical composition of ambient particles by size fraction, as well as a comprehensive suite of other pollutants, at a site in downtown Atlanta during the 25-month period, August 1, 1998-August 31, 2000. Our investigative team is making use of this unique resource in several morbidity studies, called the "Study of Particulates and Health in Atlanta (SOPHIA)". The study includes the following components: (1) a time series investigation of emergency department (ED) visits for the period during which the superstation is operating; (2) a time series investigation of ED visits during the 5 years prior to implementation of the superstation; and (3) a study of arrhythmic events in patients equipped with automatic implantable cardioverter defibrillators (AICDs) for the period January 1, 1993-August 31, 2000. Thirty-three of 39 Atlanta area EDs are participating in the ED studies, comprising over a million annual ED visits. In this paper, we present initial analyses of data from 18 of the 33 participating EDs. The preliminary data set includes 1,662,713 ED visits during the pre-superstation time period and 559,480 visits during the superstation time period. Visits for four case groupings--asthma, chronic obstructive pulmonary disease (COPD), dysrhythmia, and all cardiovascular diseases (CVDs) combined--have been assessed relative to daily air quality indices, controlling for long-term temporal trends and meteorologic variables, using general linear models, generalized estimating equations and generalized additive models. Single-pollutant models predicting case visitation rates using moving averages of 0-, 1-, and 2-day lagged air quality variables were run. For the pre-superstation period, PM10 (24-h), ozone (8-h), SO2 (1-h), NO2 (1-h) and CO (1-h) were studied. For the first 12 months of superstation operation, the following air quality variables of a priori interest were available: ozone (8-h), NO2 (1-h), SO2 (1-h), CO (1-h), and 24-h measurements of PM10, coarse PM (PM 2.5-10 microm), PM2.5, polar VOCs, 10-100 nm particulate count and surface area, and in the PM2.5 fraction: sulfates, acidity, water-soluble metals, organic matter (OM), and elemental carbon (EC). During the pre-superstation time period, statistically significant, positive associations were observed for adult asthma with ozone, and for COPD with ozone, NO2 and PM10. During the superstation time period, the following statistically significant, positive associations were observed: dysrhythmia with CO, coarse PM, and PM2.5 EC; and all CVDs with CO, PM2.5 EC and PM2.5 OM. While covariation of many of the air quality indices limits the informativeness of this analysis, the study provides one of the first assessments of PM components in relation to ED visits.


Subject(s)
Air Pollutants/adverse effects , Cardiovascular Diseases/epidemiology , Emergency Service, Hospital/statistics & numerical data , Environmental Monitoring/methods , Respiratory Tract Diseases/epidemiology , Adult , Air Pollutants/analysis , Cardiovascular Diseases/etiology , Data Collection , Epidemiological Monitoring , Female , Georgia/epidemiology , Humans , Male , Middle Aged , Pacemaker, Artificial , Respiratory Tract Diseases/etiology , Statistics, Nonparametric , Urban Population
8.
Epidemiology ; 11(6): 641-7, 2000 Nov.
Article in English | MEDLINE | ID: mdl-11055623

ABSTRACT

Accidental contamination of the Michigan food chain with polybrominated biphenyls (PBBs) led to the exposure of more than 4,000 individuals in 1973. Because PBB exposure is suspected to disrupt endocrine function, we assessed pubertal development in females 5-24 years of age (N = 327) who were exposed to PBB in utero and, in many cases, through breastfeeding. We estimated in utero PBB exposure using maternal serum PBB measurements taken after exposure (1976-1979) and extrapolated to time of pregnancy using a model of PBB decay. We found that breastfed girls exposed to high levels of PBB in utero (> or =7 parts per billion) had an earlier age at menarche (mean age = 11.6 years) than breastfed girls exposed to lower levels of PBB in utero (mean age = 12.2-12.6 years) or girls who were not breastfed (mean age = 12.7 years). This association persisted after adjustment for potential confounders (menarche ratio = 3.4, 95% confidence interval = 1.3-9.0). Perinatal PBB exposure was associated with earlier pubic hair stage in breastfed girls, but little association was found with breast development. The associations observed here lend support to the hypothesis that pubertal events may be affected by pre- and postnatal exposure to organohalogens.


Subject(s)
Food Contamination , Menarche/drug effects , Polybrominated Biphenyls/pharmacology , Prenatal Exposure Delayed Effects , Adolescent , Adult , Breast Feeding , Child , Child, Preschool , Educational Status , Female , Humans , Logistic Models , Maternal Age , Michigan , Polybrominated Biphenyls/blood , Polychlorinated Biphenyls/blood , Polychlorinated Biphenyls/pharmacology , Pregnancy
9.
Am J Epidemiol ; 151(8): 798-810, 2000 Apr 15.
Article in English | MEDLINE | ID: mdl-10965977

ABSTRACT

Pediatric emergency room visits for asthma were studied in relation to air quality indices in a spatio-temporal investigation of approximately 130,000 visits (approximately 6,000 for asthma) to the major emergency care centers in Atlanta, Georgia, during the summers of 1993-1995. Generalized estimating equations, logistic regression, and Bayesian models were fitted to the data. In logistic regression models comparing estimated exposures of asthma cases with those of the nonasthma patients, controlling for temporal and demographic covariates and using residential zip code to link patients to spatially resolved ozone levels, the estimated relative risk per 20 parts per billion (ppb) increase in the maximum 8-hour ozone level was 1.04 (p < 0.05). The estimated relative risk for particulate matter less than or equal to 10 microm in aerodynamic diameter (PM10) was 1.04 per 15 microg/m3 (p < 0.05). Exposure-response trends (p < 0.01) were observed for ozone (>100 ppb vs. <50 ppb: odds ratio = 1.23, p = 0.003) and PM10 (>60 microg/m3 vs. <20 microg/m3: odds ratio = 1.26, p = 0.004). In models with ozone and PM10, both terms became nonsignificant because of collinearity of the variables (r= 0.75). The other analytical approaches yielded consistent findings. This study supports accumulating evidence regarding the relation of air pollution to childhood asthma exacerbation.


Subject(s)
Air Pollutants/adverse effects , Asthma/therapy , Emergency Service, Hospital/statistics & numerical data , Adolescent , Asthma/epidemiology , Child , Child, Preschool , Environmental Exposure , Female , Georgia/epidemiology , Humans , Incidence , Infant , Infant, Newborn , Male , Oxidants, Photochemical/adverse effects , Ozone/adverse effects , Retrospective Studies
10.
Am J Epidemiol ; 152(1): 41-9, 2000 Jul 01.
Article in English | MEDLINE | ID: mdl-10901328

ABSTRACT

Electric and magnetic fields (EMFs) have been hypothesized to increase the risk of breast cancer, and electric blankets represent an important source of exposure to EMFs. The authors examined the relation between electric blanket use and invasive breast cancer in the Nurses' Health Study. On the biennial questionnaire in 1992, 87,497 women provided information on this exposure during three consecutive time periods. In a prospective analysis with 301,775 person-years of follow-up through 1996 (954 cases), the relative risk for any electric blanket use was not elevated (relative risk (RR) = 1.08, 95% confidence interval (CI): 0.95, 1.24) after controlling for breast cancer risk factors. There was a weak association between breast cancer and electric blanket use at least 16 years before diagnosis and long-term use in age-adjusted analyses but not in multivariate models. In a retrospective analysis of 1,318,683 person-years of follow-up (2,426 cases), the multivariate relative risk associated with use before disease follow-up began was null (RR = 1.05, 95% CI: 0.95, 1.16). Similar results were obtained in analyses stratified by menopause and restricted to estrogen receptor-positive breast cancers. While 95% confidence intervals for these estimates did not exclude small risks, overall, results did not support an association between breast cancer risk and exposure to EMFs from electric blankets.


Subject(s)
Bedding and Linens , Breast Neoplasms/epidemiology , Breast Neoplasms/etiology , Electricity/adverse effects , Adult , Female , Humans , Incidence , Middle Aged , Nurses , Prospective Studies , Retrospective Studies , Risk Factors , Surveys and Questionnaires
11.
Am J Ind Med ; 38(1): 19-27, 2000 Jul.
Article in English | MEDLINE | ID: mdl-10861763

ABSTRACT

BACKGROUND: Epidemiologic data for an association between radiation exposure and non-Hodgkin's lymphoma (NHL) have been inconclusive though the strongest evidence has been provided by studies of patients treated with radiotherapy. METHODS: We evaluated the association between occupational radiation exposure and non-Hodgkin's lymphoma in men using a population-based case-control study with 1,056 case and 1,860 control subjects sampled from eight geographic areas in the United States. Because dosimetry data were not available, doses were estimated for individuals who reported occupational radiation exposure using a radiation job exposure matrix developed for this purpose. Conditional logistic regression was used to model the association between reported occupational radiation exposure and NHL incidence. RESULTS: We found that most men (> 90%) did not report exposure to occupational sources of radiation. Among those who reported exposure, estimated cumulative doses were low, with an estimated mean of less than 0.02 Gray and a maximum of 0.12 Gray. The risk for NHL was not associated with ever having reported an occupational radiation exposure (OR = 0.90, 95% CI = 0.74-1.10) nor was there evidence of a dose-response relationship between risk and either the estimated cumulative doses or duration of exposure. CONCLUSIONS: The findings in this study are consistent with results from most current research on occupational radiation and NHL risk that have found no increased risk of NHL at low levels of occupational radiation exposure. While it should be noted that exposure misclassification likely biased our results toward the null, this large population-based case-control study adds to existing evidence which suggests that there is little to no increased risk for NHL associated with exposure to low levels of radiation such as that commonly found in many occupational settings.


Subject(s)
Lymphoma, Non-Hodgkin/epidemiology , Occupational Exposure/adverse effects , Radiation Injuries/epidemiology , Adult , Case-Control Studies , Comorbidity , Data Collection , Dose-Response Relationship, Radiation , Female , Humans , Incidence , Logistic Models , Lymphoma, Non-Hodgkin/etiology , Male , Middle Aged , Odds Ratio , Radiation Dosage , Risk Assessment , Survival Rate
12.
Cancer Epidemiol Biomarkers Prev ; 9(2): 199-205, 2000 Feb.
Article in English | MEDLINE | ID: mdl-10698482

ABSTRACT

Occupational exposure to p,p'-dichlorodiphenyltrichloroethane (DDT) has been associated with increased pancreatic cancer risk. We measured organochlorine levels in serum obtained at the study enrollment from 108 pancreatic cancer cases and 82 control subjects aged 32-85 years in the San Francisco Bay Area between 1996 and 1998. Cases were identified using rapid case-ascertainment methods; controls were frequency-matched to cases on age and sex via random digit dial and random sampling of Health Care Financing Administration lists. Serum organochlorine levels were adjusted for lipid content to account for variation in the lipid concentration in serum between subjects. Median concentrations of p,p'-dichlorodiphenyldichloroethylene (DDE, 1290 versus 1030 ng/g lipid; P = 0.05), polychlorinated biphenyls (PCBs; 330 versus 220 ng/g lipid; P<0.001), and transnonachlor (54 versus 28 ng/g lipid; P = 0.03) were significantly greater among cases than controls. A significant dose-response relationship was observed for total PCBs (P for trend <0.001). Subjects in the highest tertile of PCBs (> or =360 ng/g lipid) had an odds ratio (OR) of 4.2 [95% confidence interval (CI) = 1.8-9.4] compared to the lowest tertile. The OR of 2.1 for the highest level of p,p'-DDE (95% CI = 0.9-4.7) diminished (OR = 1.1; 95% CI = 0.4-2.8) when PCBs were included in the model. Because pancreatic cancer is characterized by cachexia, the impact of this on the serum organochlorine levels in cases is difficult to predict. One plausible effect of cachexia is bioconcentration of organochlorines in the diminished lipid pool, which would lead to a bias away from the null. To explore this, a sensitivity analysis was performed assuming a 10-40% bioconcentration of organochlorines in case samples. The OR associated with PCBs remained elevated under conditions of up to 25% bioconcentration.


Subject(s)
Hydrocarbons, Chlorinated , Insecticides/adverse effects , Pancreatic Neoplasms/etiology , Adult , Aged , Aged, 80 and over , Cachexia , Case-Control Studies , Dose-Response Relationship, Drug , Female , Humans , Insecticides/blood , Male , Middle Aged , Occupational Exposure , Pancreatic Neoplasms/epidemiology , Pancreatic Neoplasms/physiopathology , Risk Factors
13.
Am J Ind Med ; 37(5): 532-41, 2000 May.
Article in English | MEDLINE | ID: mdl-10723047

ABSTRACT

BACKGROUND: Elevated rates of nasal and nasopharyngeal cancers have been associated with wood-related occupational exposures, including chlorophenols, formaldehyde, and wood dust. METHODS: Occupational information was obtained from 43 nasal carcinoma cases, 92 nasopharyngeal carcinoma cases, and 1909 controls, by interview. Exact conditional logistic regression was used to evaluate the association of these cancers with chlorophenol exposure, estimated from a review of verbatim responses. RESULTS: Both nasal and nasopharyngeal cancers were significantly associated with estimated duration of chlorophenol exposure. For nasopharyngeal cancer, elevated risk was observed among those who held jobs assigned medium or high intensity chlorophenol exposure (n(exposed)=18, OR=1.94, 95% CI=1.03-3.50) and among those with 10+ years in jobs assigned high intensity with high certainty (n(exposed)=3, OR=9.07, 95% CI=1.41-42. 9). Controlling for estimated formaldehyde and wood dust exposure did not alter these findings, as much of the estimated chlorophenol exposure was among machinists. CONCLUSIONS: These findings support the hypothesis that occupational exposure to chlorophenol is a risk factor for nasal and nasopharyngeal cancer, although the role of machining-related exposures warrants further assessment.


Subject(s)
Chlorophenols/adverse effects , Nasopharyngeal Neoplasms/epidemiology , Nose Neoplasms/epidemiology , Occupational Diseases/epidemiology , Occupational Exposure/statistics & numerical data , Adult , Case-Control Studies , Confidence Intervals , Confounding Factors, Epidemiologic , Dust/adverse effects , Fixatives/adverse effects , Formaldehyde/adverse effects , Humans , Logistic Models , Male , Middle Aged , Odds Ratio , Population Surveillance , Risk Factors , Smoking/epidemiology , Time Factors , United States/epidemiology , Wood
14.
Environ Health Perspect ; 108(2): 147-52, 2000 Feb.
Article in English | MEDLINE | ID: mdl-10656855

ABSTRACT

Accidental contamination of the food chain in Michigan in 1973 with polybrominated biphenyls (PBBs) led to the establishment of a registry of exposed individuals in 1976. Serum was collected and analyzed for PBB at the time of enrollment and for targeted studies in the following years. We used the archived PBB data to study the elimination of PBB and to identify factors associated with elimination. A total of 380 women >= 16 years of age who had an initial PBB level of 2 ppb and at least two serum samples drawn when they were not pregnant were included in the analysis. The mean initial PBB level was 20.9 ppb (median 4) and mean time between the first and last measurement was 4.2 years (range 0.5-11.1). PBB was assumed to reach equilibrium in the body before substantial amounts were eliminated and before the first serum measurements were taken; therefore, the entire body was modeled as a single compartment for PBB with exponential decay. Subject-specific decay rate estimates were regressed on predictor variables including initial age, body mass index (BMI), smoking history, breast-feeding duration, and parity. In women with an initial PBB level < 10 ppb, the median half-life was 12.9 years; in those with > 10 ppb, the median half-life was 28.7 years. Decay was significantly slower among women with an initial BMI at or above the median (BMI >= 23). The calculated half-life values are estimates of decay and can be used to estimate body burden of PBB at various points in time other than at the time of serum collection.


Subject(s)
Environmental Pollutants/pharmacokinetics , Food Contamination , Polybrominated Biphenyls/pharmacokinetics , Adolescent , Adult , Aged , Body Mass Index , Cohort Studies , Environmental Pollutants/blood , Female , Half-Life , Humans , Longitudinal Studies , Michigan , Middle Aged , Polybrominated Biphenyls/blood , Registries
16.
J Expo Anal Environ Epidemiol ; 10(6 Pt 2): 743-54, 2000.
Article in English | MEDLINE | ID: mdl-11138666

ABSTRACT

There are limited data on the concentrations of common contaminants--polychlorinated biphenyls (PCBs), dichlorodiphenyl dichloroethene (pp'-DDE) and hexachlorobenzene (HCB)--in umbilical cord blood. Cord blood provides the primary direct measure of prenatal exposure to these contaminants, the key determinant of PCBs' neurodevelopmental toxicities. The objective of this study was to characterize cord blood levels of PCBs, pp'-DDE, and HCB among 751 infants who were born between 1993 and 1998 to mothers residing adjacent to a PCB-contaminated harbor in New Bedford, Massachusetts, and for whom the neurodevelopmental toxicities of these compounds are being studied. We refined standard analytic methods to optimize the sensitivity and precision of trace-level PCB, p,p'-DDE, and HCB measurements in blood. Using these methods, we measured the concentrations of 51 individual PCBs, their sum (sum(PCB)), p,p'-DDE, and HCB in cord serum. With correction for background contamination, the respective mean+/-SD cord serum concentrations of sum(PCB), p,p'-DDE, and HCB were 0.54+/-0.83, 0.48+/-0.94, and 0.03+/-0.04 ng/g serum. These concentrations were generally lower than those in most of the few published studies with congener-specific measures of PCBs in cord blood. However, for less-chlorinated PCB congeners (e.g., congeners 99 and 118), study samples had concentrations comparable to those in other populations, including groups at risk for high dietary PCB exposure. Of note, the contaminated harbor sediment has a relatively high proportion of less-chlorinated PCB congeners. Thus, although the sum(PCB) in study infants was not higher than concentrations in infants studied elsewhere, the relative predominance of less-chlorinated congeners was generally consistent with the characteristics of the contaminated site.


Subject(s)
Dichlorodiphenyl Dichloroethylene/blood , Environmental Exposure , Environmental Pollutants/blood , Fetal Blood/chemistry , Fungicides, Industrial/blood , Hexachlorobenzene/blood , Polychlorinated Biphenyls/blood , Female , Hazardous Waste , Humans , Infant Welfare , Infant, Newborn , Male , Risk Factors
17.
Am J Ind Med ; 36(3): 348-59, 1999 Sep.
Article in English | MEDLINE | ID: mdl-10469999

ABSTRACT

BACKGROUND: A job exposure matrix (JEM) was developed for a population based case control study to assess the possible association between occupational radiation and non-Hodgkin's lymphoma. METHODS: Using published radiation monitoring data, we developed a radiation JEM composed of estimated annual dose distributions, categorized by time period, for a broad range of occupational and industrial groups. RESULTS: When information is available to correctly assess an individual's exposure status, the annual dose distributions in the JEM can be used in conjunction with job histories to estimate the distribution of possible cumulative doses for individuals. The median of the cumulative dose distribution can then be used in standard epidemiologic analysis. In addition, methods can be applied that incorporate the uncertainty about each individual's true dose into risk estimates and associated confidence intervals. CONCLUSIONS: The JEM can be useful in estimating occupational radiation exposures in other studies, particularly population based case control studies which include detailed occupational histories.


Subject(s)
Lymphoma, Non-Hodgkin/etiology , Models, Biological , Neoplasms, Radiation-Induced/etiology , Occupational Diseases/etiology , Occupational Exposure , Radiation Dosage , Adult , Aged , Case-Control Studies , Confidence Intervals , Humans , Lymphoma, Non-Hodgkin/epidemiology , Male , Middle Aged , Neoplasms, Radiation-Induced/epidemiology , Occupational Diseases/epidemiology , Population Surveillance , Radiation Monitoring , Radiometry , Risk Assessment , Risk Factors , Time Factors , United States/epidemiology
18.
J Occup Environ Med ; 41(4): 267-72, 1999 Apr.
Article in English | MEDLINE | ID: mdl-10224592

ABSTRACT

Occupational exposure to chlorophenols is suspected to increase non-Hodgkin's lymphoma (NHL) risk. This association was examined using data on 995 NHL cases and 1783 controls from the Selected Cancers Study, a population-based case-control study of men aged 32 to 60 years from eight population-based cancer registries conducted from 1984 to 1988. Potential chlorophenol exposure was characterized by an industrial hygienist using intensity estimates and confidence ratings, based upon review of verbatim job histories. Cases with substantial chlorophenol exposure had a significantly greater number of years of chlorophenol exposure (median years: cases, 4.0; controls, 2.0; P = 0.046); however, in conditional logistic regression models, the odds ratio for more than 8 years of substantial exposure was 1.51 (95% CI, 0.88 to 2.59). Overall, the findings do not provide strong support for an association with NHL risk. Chlorophenol exposure in this study is not based upon measured values and, therefore, may fail to characterize actual chlorophenol exposures accurately. Because of the large presence of machinists in the potentially chlorophenol-exposed group, these results may be underestimated by exposure misclassification if these subjects were not exposed to chlorophenolic biocides. However, these results are consistent with other findings, which suggest that chlorophenol exposure is not likely to be a strong risk factor for NHL.


Subject(s)
Chlorophenols/adverse effects , Lymphoma, Non-Hodgkin/chemically induced , Lymphoma, Non-Hodgkin/epidemiology , Occupational Exposure/adverse effects , Adult , Case-Control Studies , Humans , Logistic Models , Male , Middle Aged , Odds Ratio , Risk Factors , United States/epidemiology
19.
Epidemiology ; 10(3): 300-6, 1999 May.
Article in English | MEDLINE | ID: mdl-10230842

ABSTRACT

Herbicides, chlorophenols, and other occupational exposures are suspected risk factors for soft-tissue sarcoma, but the epidemiologic evidence is inconsistent. Given that soft-tissue sarcomas represent a heterogeneous mix of cancer subtypes and that these subtypes have different disease patterns by race, sex, and age at diagnosis, studying all soft-tissue sarcomas combined may mask subtype-specific associations. Using the Selected Cancers Study, a large population-based case-control study of sarcoma conducted among U.S. men aged 30 to 60 in 1984 to 1988, we explored the occupational risk factors for soft-tissue sarcoma subtypes and skeletal sarcoma. The analysis included 251 living sarcoma cases (48 dermatofibrosarcoma protuberans, 32 malignant fibrohistiocytic sarcoma, 67 leiomyosarcoma, 53 liposarcoma, and 51 skeletal sarcoma) and 1908 living controls. Exact conditional logistic regression models suggested patterns of subtype specificity for occupational exposures. Self-reported herbicide use was associated with malignant fibrohistiocytic sarcoma (OR = 2.9, 95% CI = 1.1-7.3). We found elevated risks for chlorophenol exposure and cutting oil exposure and malignant fibrohistiocytic sarcoma and leiomyosarcoma. We found no occupational risk factor for liposarcoma. Polytomous regression models identified different odds ratios across subtypes for plywood exposure and exposure to wood and saw dust. Although exploratory, this analysis suggests that occupational risk factors for sarcoma are not uniform across subtypes.


Subject(s)
Bone Neoplasms/etiology , Bone Neoplasms/pathology , Occupational Diseases/etiology , Occupational Diseases/pathology , Occupational Exposure/adverse effects , Sarcoma/etiology , Sarcoma/pathology , Soft Tissue Neoplasms/etiology , Soft Tissue Neoplasms/pathology , Adult , Age Distribution , Bone Neoplasms/epidemiology , Case-Control Studies , Dust/adverse effects , Herbicides/adverse effects , Humans , Logistic Models , Male , Middle Aged , Occupational Diseases/epidemiology , Occupational Exposure/analysis , Population Surveillance , Registries , Regression Analysis , Risk Factors , Sarcoma/epidemiology , Soft Tissue Neoplasms/epidemiology , United States/epidemiology , Wood
20.
Environ Mol Mutagen ; 33(2): 111-22, 1999.
Article in English | MEDLINE | ID: mdl-10217065

ABSTRACT

Both K-ras and p53 gene mutations are found commonly in pancreatic tumors. Analysis of the mutational patterns may provide insight into disease etiology. To further describe the mutational patterns of pancreatic cancer and to assess the evidence to date, we performed a pooled analysis of the published data on genetic mutations associated with pancreatic ductal adenocarcinoma. We included data from studies that evaluated point mutations in the two genes most studied in pancreatic cancer, K-ras and p53. A majority of the 204 tumors had mutations in at least one gene, with 29% having both K-ras and p53 mutations, 39% with K-ras mutation alone, and 16% having p53 mutation alone. Sixteen percent of tumors lacked mutation in either gene. K-ras mutations were present in high frequencies in all tumor grades (>69%). A statistically significant trend was observed for p53 mutation with higher tumor grade (P = 0.04). For K-ras, G2 and G3 grades, combined, had notably higher prevalences of mutation than G1 (P = 0.004). CGT mutations in K-ras codon 12 were marginally associated with lower tumor grade (P for trend = 0.09), and these tumors were somewhat less likely to have a p53 mutation than tumors with other K-ras mutations (P = 0.06). In the 59 K-ras+/p53+ tumors, 64% had the same type of mutation (transition or transversion) in both genes, suggesting a common mechanism. The mutational pattern of p53 in pancreatic cancer is similar to bladder cancer, another smoking-related cancer, but not to lung cancer. Analyses of molecular data, such as that performed here, present new avenues for epidemiologists in the study of the etiology of specific cancers.


Subject(s)
Adenocarcinoma/genetics , Genes, p53 , Genes, ras , Mutation , Pancreatic Neoplasms/genetics , Adenocarcinoma/pathology , Humans , Pancreatic Neoplasms/pathology
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