Lubin J H, Boice J D, Samet J M
Epidemiology and Biostatistics Program, National Cancer Institute, Bethesda, Maryland 20892-7368, USA.
Radiat Res. 1995 Dec;144(3):329-41.
To date, epidemiological studies of risk from residential radon have not convincingly demonstrated an association with lung cancer. These case-control studies, however, have inherent limitations due to errors in estimates of exposure to indoor radon. These errors take on special significance because the level of residential risk predicted from studies of underground miners is relatively low and possibly at the limit detectable by current epidemiological methods. To illustrate the problem caused by errors in exposure assessment, a series of case-control studies were simulated and resulting dose-response relationships evaluated. For each of four assumed error distributions for exposure to radon progeny, 10 indoor radon studies of 700 cases and 700 controls were generated randomly from a population with a risk of radon-induced lung cancer based on extrapolations from studies of underground miners. When exposures were assumed as known without error, 6 of 10 studies failed to find a significant dose response, in accord with the theoretical power of the study of 0.47. For simulations in which exposures were measured with error, the situation was worse, as the power of the study was reduced further and it was even less likely that a single study would result in a significant finding. For each error scenario, combining data from the 10 simulated studies did result in a significant dose response. However, the pooled results are somewhat misleading, because the effects of mobility, missing radon measurements, residential occupancy and potential confounding variables such as cigarette smoking were not taken into account. Empirical estimates of power were computed using 1,000 simulated case-control studies. When mobility and missing radon measurements in prior homes were incorporated into the design, the power of the study decreased, reducing the chance of detecting a significant effect of exposure. Enlarging study size to 2,000 cases and 2,000 controls increased the power of the study to 0.90 when exposure error was absent and subjects lived in one home only, but power was below 0.40 under realistic conditions for exposure error and mobility. When studies were generated under an assumption that exposure does not increase risk, up to 15% of simulated studies with 700 cases and 700 controls resulted in an estimated dose-response parameter in excess of the dose response from studies of miners. With increasing mobility and exposure error, it became virtually impossible to distinguish between the distributions of risk estimates from simulated studies based on an underlying excess relative risk of 0.015/working level month from estimates based on no risk from exposure.(ABSTRACT TRUNCATED AT 400 WORDS)
迄今为止,关于室内氡气风险的流行病学研究尚未令人信服地证明其与肺癌存在关联。然而,这些病例对照研究存在固有局限性,因为在估计室内氡气暴露量时存在误差。这些误差具有特殊意义,因为根据地下矿工研究预测的室内风险水平相对较低,可能处于当前流行病学方法可检测的极限。为说明暴露评估误差所导致的问题,模拟了一系列病例对照研究,并对所得的剂量反应关系进行评估。对于四种假定的氡子体暴露误差分布中的每一种,从基于地下矿工研究推断出的有氡致肺癌风险的人群中,随机生成10项针对700例病例和700名对照的室内氡气研究。当假定暴露量无误差已知时,10项研究中有6项未能发现显著的剂量反应,这与该研究0.47的理论效能相符。对于测量暴露量存在误差的模拟情况,情况更糟,因为研究的效能进一步降低,单个研究得出显著结果的可能性更小。对于每种误差情况,将10项模拟研究的数据合并确实得出了显著的剂量反应。然而,汇总结果存在一定误导性,因为未考虑迁移、氡气测量缺失、居住情况以及吸烟等潜在混杂变量的影响。使用1000项模拟病例对照研究计算了效能的经验估计值。当在设计中纳入迁移和先前住所氡气测量缺失的情况时,研究的效能降低,检测暴露显著效应的机会减少。当暴露无误差且受试者仅居住在一个家中时,将研究规模扩大到2000例病例和2000名对照可使研究效能提高到0.90,但在存在暴露误差和迁移的实际情况下,效能低于0.40。当在暴露不会增加风险的假设下生成研究时,在700例病例和700名对照的模拟研究中,高达15%的研究得出的估计剂量反应参数超过了矿工研究中的剂量反应。随着迁移和暴露误差的增加,几乎不可能区分基于潜在超额相对风险为0.015/工作水平月的模拟研究的风险估计分布与基于暴露无风险的估计分布。(摘要截于400字)