Modifications to the Patient Rule-Induction Method That Utilize Non-Additive Combinations of Genetic and Environmental Effects to Define Partitions That Predict Ischemic Heart Disease

被引:8
作者
Dyson, Greg [1 ]
Frikke-Schmidt, Ruth [2 ]
Nordestgaard, Borge G. [3 ,4 ]
Tybjaerg-Hansen, Anne [2 ,4 ]
Sing, Charles F. [1 ]
机构
[1] Univ Michigan, Dept Human Genet, Ann Arbor, MI 48109 USA
[2] Univ Copenhagen Hosp, Rigshosp, Mol Genet Sect, Dept Clin Biochem, DK-2100 Copenhagen, Denmark
[3] Herlev Univ Hosp, Dept Clin Biochem, DK-2730 Herlev, Denmark
[4] Bispebjerg Hosp, Copenhagen City Heart Study, Copenhagen, Denmark
基金
英国医学研究理事会;
关键词
CPM; PRIM; interaction; non-additivity; IHD; APOLIPOPROTEIN-E; GENOTYPE; TRIGLYCERIDES; LIPOPROTEIN; GENOMICS; SNPS;
D O I
10.1002/gepi.20383
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
This article extends the Patient Rule-Induction Method (PRIM) for modeling Cumulative incidence of disease developed by Dyson et al. (Genet Epidemiol 31:515-527) to include the simultaneous consideration of non-additive combinations of predictor variables, a significance test of each combination, an adjustment for multiple testing and a confidence interval for the estimate of the cumulative incidence of disease in each partition. We employ the partitioning algorithm component of the Combinatorial Partitioning Method to construct combinations of predictors, permutation testing to assess the significance of each combination, theoretical arguments for incorporating a multiple testing adjustment and bootstrap resampling to produce the confidence intervals. An illustration of this revised PRIM utilizing a sample of 2,258 European male participants from the Copenhagen City Heart Study is presented that assesses the utility of genetic variants in predicting the presence of ischemic heart disease beyond the established risk factors. Genet. Epidemiol. 33: 317-324, 2009. (C) 2008 Wiley-Liss, Inc.
引用
收藏
页码:317 / 324
页数:8
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