RESUMO
Among the scientific interests of cancer epidemiology is the identification of both environmental and genetic factors associated with cancer development. Observational designs requiring sophisticated methodology are applied to control for potential confounding factors. The enormous biotechnological potential developed in the last two decades has allowed the integration of a plethora of new biomarkers in epidemiological studies to better define the exposure and "neoclassic" outcomes, as well as incorporating genetic susceptibility factors in both classical and new epidemiological designs. The integration of scopes, objectives, data and tools coming from different disciplines also benefits epidemiology, thus evolving into "systems epidemiology". In this manuscript, we review the basic concepts of study designs and data analysis and introduce readers to the more innovative aspects that are now being applied in epidemiological studies.
Assuntos
Neoplasias/epidemiologia , Interpretação Estatística de Dados , Humanos , Neoplasias/genética , Projetos de PesquisaRESUMO
Glutathione S-transferase (GST) polymorphism may contribute to the individual variability in detoxifying lung carcinogens. This effect might be particularly relevant at low-level exposure to environmental carcinogens, such as in nonsmokers exposed to environmental tobacco smoke (ETS). We conducted a case-control study among 122 nonsmoking lung cancer cases and 121 nonsmoking controls from eight countries. Information on environmental exposures was obtained through a personal interview. The presence of GSTM1 and GSTT1 genes was determined using multiplex PCR. GSTM1-positive samples were then analyzed for *1A and *1B polymorphism using an allele-specific amplification-PCR method. GSTM1*2 (null) individuals had an odds ratio (OR) of lung cancer of 1.5 [95% confidence interval (CI), 0.9-2.7]; the risk associated with this genotype was higher for cases with squamous and small cell carcinomas (OR, 2.3; 95% CI, 0.9-6.1) than for cases with adenocarcinomas. It was also elevated in individuals with long-term exposure to indoor wood combustion (OR, 3.1; 95% CI, 0.9-9.9), in subjects who mainly lived in a rural setting (OR, 3.6; 95% CI, 1.0-13), and in cases exposed to occupational carcinogens (OR, 10.7; 96% CI, 0.4-260) but not in subjects exposed to ETS. GSTT1*2 subjects did not show a risk of lung cancer. Our study suggests that the effect of GSTM1 polymorphism in nonsmokers is similar to that found in smokers. It does not seem to interact with ETS exposure, although we cannot exclude that it does in association with exposure to other specific environmental carcinogens.