The additive genetic gamma frailty model for linkage analysis of age-of-onset variation

被引:17
作者
Li, H [1 ]
机构
[1] Univ Calif Davis, Sch Med, Dept Med, Rowe Program Human Genet, Davis, CA 95616 USA
[2] Univ Calif Davis, Sch Med, Div Stat, Davis, CA 95616 USA
关键词
D O I
10.1046/j.1469-1809.1999.6350455.x
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Age of onset is a key factor in the linkage analysis of many complex diseases. Current methods in nonparametric linkage analysis are mainly concentrated on the affected relative pairs or affected family members with age of onset information either ignored or taken into account by specifying age-dependent penetrances for liability classes. On the other hand, gamma frailty models were developed in the biostatistics literature to model familial aggregation of age of onset. However, these frailty models cannot be used directly for linkage analysis. This: paper extends the gamma frailty model by incorporating inheritance vector information and provides a semiparametric approach for linkage testing. For a given inheritance vector at the putative disease locust we construct an additive genetic gamma frailty for each individual within a nuclear family and use the Cox proportional hazard model to model age of onset. We derive the conditional hazard ratio parameter for sib pairs and define a likelihood ratio based LOD score statistic under our model. The fill algorithm is used. for estimating the parameters and the maximum likelihood functions. Simulated data sets are used to illustrate these new statistical methods.
引用
收藏
页码:455 / 468
页数:14
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