ﻻ يوجد ملخص باللغة العربية
Typically, case-control studies to estimate odds-ratios associating risk factors with disease incidence from logistic regression only include cases with newly diagnosed disease. Recently proposed methods allow incorporating information on prevalent cases, individuals who survived from disease diagnosis to sampling, into cross-sectionally sampled case-control studies under parametric assumptions for the survival time after diagnosis. Here we propose and study methods to additionally use prospectively observed survival times from prevalent and incident cases to adjust logistic models for the time between disease diagnosis and sampling, the backward time, for prevalent cases. This adjustment yields unbiased odds-ratio estimates from case-control studies that include prevalent cases. We propose a computationally simple two-step generalized method-of-moments estimation procedure. First, we estimate the survival distribution based on a semi-parametric Cox model using an expectation-maximization algorithm that yields fully efficient estimates and accommodates left truncation for the prevalent cases and right censoring. Then, we use the estimated survival distribution in an extension of the logistic model to three groups (controls, incident and prevalent cases), to accommodate the survival bias in prevalent cases. In simulations, when the amount of censoring was modest, odds-ratios from the two-step procedure were equally efficient as those estimated by jointly optimizing the logistic and survival data likelihoods under parametric assumptions. Even with 90% censoring they were as efficient as estimates obtained using only cross-sectionally available information under parametric assumptions. This indicates that utilizing prospective survival data from the cases lessens model dependency and improves precision of association estimates for case-control studies with prevalent cases.
The use of case-crossover designs has become widespread in epidemiological and medical investigations of transient associations. However, the most popular reference-select strategy, the time-stratified schema, is not a suitable solution for controlli
Can two separate case-control studies, one about Hepatitis disease and the other about Fibrosis, for example, be combined together? It would be hugely beneficial if two or more separately conducted case-control studies, even for entirely irrelevant p
We propose a method to test for the presence of differential ascertainment in case-control studies, when data are collected by multiple sources. We show that, when differential ascertainment is present, the use of only the observed cases leads to sev
Most clinical trials involve the comparison of a new treatment to a control arm (e.g., the standard of care) and the estimation of a treatment effect. External data, including historical clinical trial data and real-world observational data, are comm
We propose the variable selection procedure incorporating prior constraint information into lasso. The proposed procedure combines the sample and prior information, and selects significant variables for responses in a narrower region where the true p