Analysis of Bivariate Survival Data Based on Copulas with Log-Generalized Extreme Value Marginals

2016 ◽  
pp. 495-512
Twin Research ◽  
2000 ◽  
Vol 3 (1) ◽  
pp. 51-57 ◽  
Author(s):  
Alexander Z Begun ◽  
Ivan A Iachine ◽  
Anatoli I Yashin

AbstractThe traditional frailty models used in genetic analysis of bivariate survival data assume that individual frailty (and longevity) is influenced by thousands of genes, and that the contribution of each separate gene is small. This assumption, however, does not have a solid biological basis. It may just happen that one or a small number of genes makes a major contribution to determining the human life span. To answer the questions about the nature of the genetic influence on life span using survival data, models are needed that specify the influence of major genes on individual frailty and longevity. The goal of this paper is to test the nature of genetic influences on individual frailty and longevity using survival data on Danish twins. We use a new bivariate survival model with one major gene influencing life span to analyse survival data on MZ (monozygotic) and DZ (dizygotic) twins. The analysis shows that two radically different classes of model provide an equally good fit to the data. However, the asymptotic behaviour of some conditional statistics is different in models from different classes. Because of the limited sample size of bivariate survival data we cannot draw reliable conclusions about the nature of genetic effects on life span. Additional information about tails of bivariate distribution or risk factors may help to solve this problem. Twin Research (2000) 3, 51–57.


Author(s):  
Hong Zhu ◽  
Mei-Cheng Wang

AbstractIn disease registries, bivariate survival data are typically collected under interval sampling. It refers to a situation when entry into a registry is at the time of the first failure event (i.e., HIV infection) within a calendar time window. For all the cases in the registry, time of the initiating event (i.e., birth) is retrospectively identified, and subsequently the second failure event (i.e., death) is observed during follow-up. In this paper we discuss how interval sampling introduces bias into the data. Given the sampling design that the first event occurs within a specific time interval, the first failure time is doubly truncated, and the second failure time is possibly informatively right censored. Consider semi-stationary condition that the disease progression is independent of when the initiating event occurs. Under this condition, this paper adopts copula models to assess association between the bivariate survival times with interval sampling. We first obtain bias-corrected estimators of marginal survival functions, and estimate association parameter of copula model by a two-stage procedure. In the second part of the work, covariates are incorporated into the survival distributions via the proportional hazards models. Inference of the association measure in copula model is established, where the association is allowed to depend on covariates. Asymptotic properties of proposed estimators are established, and finite sample performance is evaluated by simulation studies. The method is applied to a community-based AIDS study in Rakai to investigate dependence between age at infection and residual lifetime without and with adjustment for HIV subtype.


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