Thomas Duncan C
From the Department of Preventive Medicine, University of Southern California, Los Angeles, CA.
Epidemiology. 2017 Jul;28(4):470-478. doi: 10.1097/EDE.0000000000000668.
Screening behavior depends on previous screening history and family members' behaviors, which can act as both confounders and intermediate variables on a causal pathway from screening to disease risk. Conventional analyses that adjust for these variables can lead to incorrect inferences about the causal effect of screening if high-risk individuals are more likely to be screened. Analyzing the data in a manner that treats screening as randomized conditional on covariates allows causal parameters to be estimated; inverse probability weighting based on propensity of exposure scores is one such method considered here. I simulated family data under plausible models for the underlying disease process and for screening behavior to assess the performance of alternative methods of analysis and whether a targeted screening approach based on individuals' risk factors would lead to a greater reduction in cancer incidence in the population than a uniform screening policy. Simulation results indicate that there can be a substantial underestimation of the effect of screening on subsequent cancer risk when using conventional analysis approaches, which is avoided by using inverse probability weighting. A large case-control study of colonoscopy and colorectal cancer from Germany shows a strong protective effect of screening, but inverse probability weighting makes this effect even stronger. Targeted screening approaches based on either fixed risk factors or family history yield somewhat greater reductions in cancer incidence with fewer screens needed to prevent one cancer than population-wide approaches, but the differences may not be large enough to justify the additional effort required. See video abstract at, http://links.lww.com/EDE/B207.
筛查行为取决于既往筛查史和家庭成员的行为,这些因素在从筛查到疾病风险的因果路径中既可能是混杂因素,也可能是中间变量。如果高危个体更有可能接受筛查,那么对这些变量进行调整的传统分析可能会导致对筛查因果效应的错误推断。以将筛查视为基于协变量随机化的方式分析数据,可以估计因果参数;基于暴露分数倾向的逆概率加权就是这里考虑的一种方法。我在关于潜在疾病过程和筛查行为的合理模型下模拟了家庭数据,以评估替代分析方法的性能,以及基于个体风险因素的靶向筛查方法是否会比统一筛查政策在人群中导致更大幅度的癌症发病率降低。模拟结果表明,使用传统分析方法时,可能会大幅低估筛查对后续癌症风险的影响,而使用逆概率加权可以避免这种情况。德国一项关于结肠镜检查和结直肠癌的大型病例对照研究显示了筛查的强大保护作用,但逆概率加权使这种作用更强。基于固定风险因素或家族史的靶向筛查方法在预防一例癌症所需筛查次数较少的情况下,癌症发病率降低幅度略大于全人群筛查方法,但差异可能不够大,不足以证明所需的额外努力是合理的。见视频摘要:http://links.lww.com/EDE/B207 。