A Dimension Reduction Approach for Modeling Multi-Locus Interaction in Case-Control Studies

被引:6
作者
Basu, Saonli [1 ]
Pan, Wei
Oetting, William S. [2 ,3 ]
机构
[1] Univ Minnesota, Div Biostat, Sch Publ Hlth, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Coll Pharm, Dept Expt & Clin Pharmacol, Minneapolis, MN 55455 USA
[3] Univ Minnesota, Inst Human Genet, Minneapolis, MN 55455 USA
关键词
Case-control study; Gene-gene interaction; Dimension reduction; GENETIC PATHWAY; ASSOCIATION; REGRESSION; IMMUNOSUPPRESSION; POLYMORPHISMS; TACROLIMUS; CYP3A5; TESTS; POWER; MDR1;
D O I
10.1159/000328842
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Studying one locus or one single nucleotide polymorphism (SNP) at a time may not be sufficient to understand complex diseases because they are unlikely to result from the effect of only one SNP. Each SNP alone may have little or no effect on the risk of the disease, but together they may increase the risk substantially. Analyses focusing on individual SNPs ignore the possibility of interaction among SNPs. In this paper, we propose a parsimonious model to assess the joint effect of a group of SNPs in a case-control study. The model implements a data reduction strategy within a likelihood framework and uses a test to assess the statistical significance of the effect of the group of SNPs on the binary trait. The primary advantage of the proposed approach is that the dimension reduction technique produces a test statistic with degrees of freedom significantly lower than a multiple logistic regression with only main effects of the SNPs, and our parsimonious model can incorporate the possibility of interaction among the SNPs. Moreover, the proposed approach estimates the direction of association of each SNP with the disease and provides an estimate of the average effect of the group of SNPs positively and negatively associated with the disease in the given SNP set. We illustrate the proposed model on simulated and real data, and compare its performance with a few other existing approaches. Our proposed approach appeared to outperform the other approaches for independent SNPs in our simulation studies. Copyright (C) 2011 S. Karger AG, Basel
引用
收藏
页码:234 / 245
页数:12
相关论文
共 31 条
[1]  
[Anonymous], 2005, R LANG ENV STAT COMP
[2]   A Likelihood-Based Trait-Model-Free Approach for Linkage Detection of Binary Trait [J].
Basu, S. ;
Stephens, M. ;
Pankow, J. S. ;
Thompson, E. A. .
BIOMETRICS, 2010, 66 (01) :205-213
[3]   Multiplexed genotyping with sequence-tagged molecular inversion probes [J].
Hardenbol, P ;
Banér, J ;
Jain, M ;
Nilsson, M ;
Namsaraev, EA ;
Karlin-Neumann, GA ;
Fakhrai-Rad, H ;
Ronaghi, M ;
Willis, TD ;
Landegren, U ;
Davis, RW .
NATURE BIOTECHNOLOGY, 2003, 21 (06) :673-678
[4]   Pair-Wise Multifactor Dimensionality Reduction Method to Detect Gene-Gene Interactions in A Case-Control Study [J].
He, H. ;
Oetting, W. S. ;
Brott, M. J. ;
Basu, S. .
HUMAN HEREDITY, 2010, 69 (01) :60-70
[5]   Pathway-based association analysis of genome-wide screening data suggest that genes associated with the γ-aminobutyric acid receptor signaling pathway are involved in neuroleptic-induced, treatment-resistant tardive dyskinesia [J].
Inada, Toshiya ;
Koga, Minori ;
Ishiguro, Hiroki ;
Horiuchi, Yasue ;
Syu, Aoi ;
Yoshio, Takashi ;
Takahashi, Nagahide ;
Ozaki, Norio ;
Arinami, Tadao .
PHARMACOGENETICS AND GENOMICS, 2008, 18 (04) :317-323
[6]   Immunosuppression: practice and trends [J].
Kaufman, DB ;
Shapiro, R ;
Lucey, MR ;
Cherikh, WS ;
Bustami, RT ;
Dyke, DB .
AMERICAN JOURNAL OF TRANSPLANTATION, 2004, 4 :38-53
[7]   Effects of CYP3A5 and MDR1 single nucleotide polymorphisms on drug interactions between tacrolimus and fluconazole in renal allograft recipients [J].
Kuypers, Dirk R. ;
de Jonge, Hylke ;
Naesens, Maarten ;
Vanrenterghem, Yves .
PHARMACOGENETICS AND GENOMICS, 2008, 18 (10) :861-868
[8]   A powerful and flexible multilocus association test for quantitative traits [J].
Kwee, Lydia Coulter ;
Liu, Dawei ;
Lin, Xihong ;
Ghosh, Debashis ;
Epstein, Michael P. .
AMERICAN JOURNAL OF HUMAN GENETICS, 2008, 82 (02) :386-397
[9]   A genomic pathway approach to a complex disease: Axon guidance and parkinson disease [J].
Lesnick, Timothy G. ;
Papapetropoulos, Spiridon ;
Mash, Deborah C. ;
Ffrench-Mullen, Jarlath ;
Shehadeh, Lina ;
de Andrade, Mariza ;
Henley, John R. ;
Rocca, Walter A. ;
Ahlskog, J. Eric ;
Maraganore, Demetrius M. .
PLOS GENETICS, 2007, 3 (06) :984-995
[10]   Semiparametric regression of multidimensional genetic pathway data: Least-squares kernel machines and linear mixed models [J].
Liu, Dawei ;
Lin, Xihong ;
Ghosh, Debashis .
BIOMETRICS, 2007, 63 (04) :1079-1088