{"title":"A comparison of cause-specific and competing risk models to assess risk factors for dementia","authors":"M. Waller, G. Mishra, A. Dobson","doi":"10.1515/em-2019-0036","DOIUrl":null,"url":null,"abstract":"Abstract The study of dementia risk factors is complicated by the competing risk of dying. The standard approaches are the cause-specific Cox proportional hazard model with deaths treated as censoring events (and removed from the risk set) and the Fine and Gray sub-distribution hazard model in which those who die remain in the risk set. An alternative approach is to modify the risk set between these extremes. We propose a novel method of doing this based on estimating the time at which the person might have been diagnosed if they had not died using a parametric survival model, and then applying the cause-specific and Fine and Gray models to the modified dataset. We compare these methods using data on dementia from the Australian Longitudinal Study on Women’s Health and discuss the assumptions and limitations of each model. The results from survival models to assess risk factors for dementia varied considerably between the cause-specific model and the models designed to account for competing risks. Therefore, when assessing risk factors in the presence of competing risks it is important to examine results from: the cause-specific model, different models which account for competing risks, and the model which assesses risk factors associated with the competing risk.","PeriodicalId":37999,"journal":{"name":"Epidemiologic Methods","volume":"36 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Epidemiologic Methods","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1515/em-2019-0036","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Mathematics","Score":null,"Total":0}
引用次数: 2
Abstract
Abstract The study of dementia risk factors is complicated by the competing risk of dying. The standard approaches are the cause-specific Cox proportional hazard model with deaths treated as censoring events (and removed from the risk set) and the Fine and Gray sub-distribution hazard model in which those who die remain in the risk set. An alternative approach is to modify the risk set between these extremes. We propose a novel method of doing this based on estimating the time at which the person might have been diagnosed if they had not died using a parametric survival model, and then applying the cause-specific and Fine and Gray models to the modified dataset. We compare these methods using data on dementia from the Australian Longitudinal Study on Women’s Health and discuss the assumptions and limitations of each model. The results from survival models to assess risk factors for dementia varied considerably between the cause-specific model and the models designed to account for competing risks. Therefore, when assessing risk factors in the presence of competing risks it is important to examine results from: the cause-specific model, different models which account for competing risks, and the model which assesses risk factors associated with the competing risk.
死亡的竞争风险使痴呆危险因素的研究变得复杂。标准方法是病因特异性Cox比例风险模型,其中死亡被视为审查事件(并从风险集中删除),以及Fine和Gray子分布风险模型,其中死亡的人仍在风险集中。另一种方法是修改这两个极端之间的风险设置。我们提出了一种新的方法,该方法基于使用参数生存模型估计如果患者没有死亡,则患者可能被诊断的时间,然后将原因特定模型和Fine and Gray模型应用于修改后的数据集。我们使用澳大利亚妇女健康纵向研究的痴呆数据对这些方法进行比较,并讨论每个模型的假设和局限性。用于评估痴呆风险因素的生存模型的结果在病因特异性模型和用于考虑竞争风险的模型之间差异很大。因此,在评估存在竞争风险的风险因素时,重要的是要检查以下结果:特定原因模型,考虑竞争风险的不同模型,以及评估与竞争风险相关的风险因素的模型。
期刊介绍:
Epidemiologic Methods (EM) seeks contributions comparable to those of the leading epidemiologic journals, but also invites papers that may be more technical or of greater length than what has traditionally been allowed by journals in epidemiology. Applications and examples with real data to illustrate methodology are strongly encouraged but not required. Topics. genetic epidemiology, infectious disease, pharmaco-epidemiology, ecologic studies, environmental exposures, screening, surveillance, social networks, comparative effectiveness, statistical modeling, causal inference, measurement error, study design, meta-analysis