Software for Generating Liability Distributions for Pedigrees Conditional on Their Observed Disease States and Covariates

被引:8
作者
Campbell, Desmond D. [3 ]
Sham, Pak C. [1 ,2 ]
Knight, Jo [4 ,5 ]
Wickham, Harvey
Landau, Sabine [3 ]
机构
[1] Univ Hong Kong, Genome Res Ctr, Pokfulam, Hong Kong, Peoples R China
[2] Univ Hong Kong, State Key Lab Brain & Cognit Sci, Dept Psychiat, Pokfulam, Hong Kong, Peoples R China
[3] Kings Coll London, Dept Biostat, Inst Psychiat, London WC2R 2LS, England
[4] Kings Coll London, Guys Hosp, Sch Med, Dept Med & Mol Genet, London WC2R 2LS, England
[5] Guys & St Thomas NHS Fdn Trust, NIHR, Biomed Res Ctr, London, England
关键词
multifactorial; complex; disease; prediction; Gibbs sampler; risk; family history; family history score; risk factor; age of onset; right censoring; WIDE LINKAGE ANALYSIS; VARIANCE-COMPONENTS ANALYSIS; NATIONAL COMORBIDITY SURVEY; MIXED MODELS GLMMS; DSM-IV DISORDERS; LIFETIME PREVALENCE; MULTIPLE IMPUTATION; HIGH-RISK; HISTORY; DEPRESSION;
D O I
10.1002/gepi.20446
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
For many multifactorial diseases, aetiology is poorly understood. A major research aim is the identification of disease predictors (environmental, biological, and genetic markers). In order to achieve this, a two-stage approach is proposed. The initial or synthesis stage combines observed pedigree data with previous genetic epidemiological research findings, to produce estimates of pedigree members' disease risk and predictions of their disease liability. A further analysis stage uses the latter as inputs to look for associations with potential disease markers. The incorporation of previous research findings into an analysis should lead to power gains. It also allows separate predictions for environmental and genetic liabilities to be generated. This should increase power for detecting disease predictors that are environmental or genetic in nature. Finally, the approach brings pragmatic benefits in terms of data reduction and synthesis, improving comprehensibility, and facilitating the use of existing statistical genetics tools. In this article we present a statistical model and Gibbs sampling approach to generate liability predictions for multifactorial disease for the synthesis stage. We have implemented the approach in a software program. We apply this program to a specimen disease pedigree, and discuss the results produced, comparing its results with those generated under a more naive model. We also detail simulation studies that validate the software's operation. Genet. Epidemiol. 34:159-170, 2010. (C) 2009 Wiley-Liss, Inc.
引用
收藏
页码:159 / 170
页数:12
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