What Cure Models Can Teach us About Genome-Wide Survival Analysis

被引:0
作者
Sven Stringer
Damiaan Denys
René S. Kahn
Eske M. Derks
机构
[1] VU Amsterdam,Department of Complex Trait Genetics, Center for Neurogenomics and Cognitive Research (CNCR), Neuroscience Campus Amsterdam (NCA)
[2] Academic Medical Center,Department of Psychiatry
[3] University Medical Center,Department of Psychiatry, Rudolf Magnus Institute of Neuroscience
来源
Behavior Genetics | 2016年 / 46卷
关键词
Proportional hazards model; Logistic regression; Cox regression; Accelerated failure time model; Simulation study;
D O I
暂无
中图分类号
学科分类号
摘要
The aim of logistic regression is to estimate genetic effects on disease risk, while survival analysis aims to determine effects on age of onset. In practice, genetic variants may affect both types of outcomes. A cure survival model analyzes logistic and survival effects simultaneously. The aim of this simulation study is to assess the performance of logistic regression and traditional survival analysis under a cure model and to investigate the benefits of cure survival analysis. We simulated data under a cure model and varied the percentage of subjects at risk for disease (cure fraction), the logistic and survival effect sizes, and the contribution of genetic background risk factors. We then computed the error rates and estimation bias of logistic, Cox proportional hazards (PH), and cure PH analysis, respectively. The power of logistic and Cox PH analysis is sensitive to the cure fraction and background heritability. Our results show that traditional Cox PH analysis may erroneously detect age of onset effects if no such effects are present in the data. In the presence of genetic background risk even the cure model results in biased estimates of both the odds ratio and the hazard ratio. Cure survival analysis takes cure fractions into account and can be used to simultaneously estimate the effect of genetic variants on disease risk and age of onset. Since genome-wide cure survival analysis is not computationally feasible, we recommend this analysis for genetic variants that are significant in a traditional survival analysis.
引用
收藏
页码:269 / 280
页数:11
相关论文
共 78 条
[1]  
Bergen SE(2014)Genetic modifiers and subtypes in schizophrenia: investigations of age at onset, severity, sex and family history Schizophr Res 154 48-53
[2]  
O’Dushlaine CT(2008)Genetic and genomic discovery using family studies Circulation 118 1057-1063
[3]  
Lee PH(2012)smcure: an R-Package for estimating semiparametric mixture cure models Comput Methods Programs Biomed 108 1255-1260
[4]  
Fanous AH(1977)Maximum likelihood from incomplete data via the EM algorithm. Journal of the Royal Statistical Society Series B (Methodological) 39 1-38
[5]  
Ruderfer DM(1984)Biased estimates of treatment effect in randomized experiments with nonlinear regressions and omitted covariates Biometrika 71 431-444
[6]  
Ripke S(2014)Large-scale genomics unveils the genetic architecture of psychiatric disorders Nat Neurosci 17 782-790
[7]  
Sullivan PF(2010)Meta-analysis of genome-wide association studies of attention-deficit/hyperactivity disorder J Am Acad Child Adolesc Psychiatry 49 884-897
[8]  
Smoller JW(2012)Cure models as a useful statistical tool for analyzing survival Clin Cancer Res 18 3731-3736
[9]  
Purcell SM(2014)Use of the word “cure” in the oncology literature Am J Hosp Palliat Med 32 477-483
[10]  
Corvin A(2003)Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits Bioinformatics 19 149-150