NPO Drug Safety Research Unit Japan|, 6-2-9-2F, Soto-Kanda, Chiyoda-ku, Tokyo, 101-0021, Japan.
Department of Pharmacy, Tokyo University of Science, Chiba, Japan.
BMC Med Res Methodol. 2021 Oct 17;21(1):214. doi: 10.1186/s12874-021-01408-5.
Case-crossover studies have been widely used in various fields including pharmacoepidemiology. Vines and Farrington indicated in 2001 that when within-subject exposure dependency exists, conditional logistic regression can be biased. However, this bias has not been well studied.
We have extended findings by Vines and Farrington to develop a weighting method for the case-crossover study which removes bias from within-subject exposure dependency. Our method calculates the exposure probability at the case period in the case-crossover study which is used to weight the likelihood formulae presented by Greenland in 1999. We simulated data for the population with a disease where most patients receive a cyclic treatment pattern with within-subject exposure dependency but no time trends while some patients stop and start treatment. Finally, the method was applied to real-world data from Japan to study the association between celecoxib and peripheral edema and to study the association between selective serotonin reuptake inhibitor (SSRI) and hip fracture in Australia.
When the simulated rate ratio of the outcome was 4.0 in a case-crossover study with no time-varying confounder, the proposed weighting method and the Mantel-Haenszel odds ratio reproduced the true rate ratio. When a time-varying confounder existed, the Mantel-Haenszel method was biased but the weighting method was not. When more than one control period was used, standard conditional logistic regression was biased either with or without time-varying confounding and the bias increased (up to 8.7) when the study period was extended. In real-world analysis with a binary exposure variable in Japan and Australia, the point estimate of the odds ratio (around 2.5 for the association between celecoxib and peripheral edema and around 1.6 between SSRI and hip fracture) by our weighting method was equal to the Mantel-Haenszel odds ratio and stable compared with standard conditional logistic regression.
Case-crossover studies may be biased from within-subject exposure dependency, even without exposure time trends. This bias can be identified by comparing the odds ratio by the Mantel-Haenszel method and that by standard conditional logistic regression. We recommend using our proposed method which removes bias from within-subject exposure dependency and can account for time-varying confounders.
病例交叉研究已广泛应用于包括药物流行病学在内的多个领域。Vines 和 Farrington 于 2001 年指出,当个体内暴露依赖性存在时,条件逻辑回归可能会产生偏差。然而,这种偏差尚未得到很好的研究。
我们扩展了 Vines 和 Farrington 的发现,为病例交叉研究开发了一种加权方法,以消除个体内暴露依赖性引起的偏差。我们的方法计算了病例交叉研究中病例期的暴露概率,该概率用于加权 Greenland 于 1999 年提出的似然公式。我们模拟了具有疾病人群的数据,其中大多数患者接受周期性治疗模式,具有个体内暴露依赖性,但没有时间趋势,而一些患者停止和开始治疗。最后,该方法应用于来自日本的真实世界数据,以研究塞来昔布与外周水肿之间的关联,以及研究澳大利亚选择性 5-羟色胺再摄取抑制剂(SSRIs)与髋部骨折之间的关联。
当病例交叉研究中无时间变化混杂因素时,结果的模拟率比值为 4.0,提出的加权方法和 Mantel-Haenszel 比值比重现了真实的率比值。当存在时间变化的混杂因素时,Mantel-Haenszel 方法存在偏差,但加权方法没有。当使用多个对照期时,标准条件逻辑回归存在偏差,无论是否存在时间变化的混杂因素,且当研究期延长时,偏差增加(高达 8.7)。在日本和澳大利亚具有二元暴露变量的真实世界分析中,我们加权方法的比值比(塞来昔布与外周水肿之间的关联约为 2.5,SSRIs 与髋部骨折之间的关联约为 1.6)的点估计值与 Mantel-Haenszel 比值比相等,且与标准条件逻辑回归相比是稳定的。
即使没有暴露时间趋势,病例交叉研究也可能受到个体内暴露依赖性的偏差影响。这种偏差可以通过比较 Mantel-Haenszel 方法和标准条件逻辑回归的比值比来识别。我们建议使用我们提出的方法,该方法可以消除个体内暴露依赖性的偏差,并可以考虑时间变化的混杂因素。