Multifactor dimensionality reduction reveals gene-gene interactions associated with multiple sclerosis susceptibility in African Americans

被引:41
作者
Brassat, D.
Motsinger, A. A.
Caillier, S. J.
Erlich, H. A.
Walker, K.
Steiner, L. L.
Cree, B. A. C.
Barcellos, L. F.
Pericak-Vance, M. A.
Schmidt, S.
Gregory, S.
Hauser, S. L.
Haines, J. L.
Oksenberg, J. R.
Ritchie, M. D.
机构
[1] Vanderbilt Univ, Dept Mol Physiol & Biophys, Ctr Human Genet Res, Nashville, TN 37232 USA
[2] Univ Calif San Francisco, Sch Med, Dept Neurol, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Sch Med, Ctr Human Genet, San Francisco, CA 94143 USA
[4] Roche Mol Syst, Dept Human Genet, Alameda, CA USA
[5] Univ Calif Berkeley, Div Epidemiol, Sch Publ Hlth, Berkeley, CA 94720 USA
[6] Duke Univ, Med Ctr, Ctr Human Genet, Durham, NC USA
关键词
D O I
10.1038/sj.gene.6364299
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Multiple sclerosis (MS) is a common disease of the central nervous system characterized by inflammation, myelin loss, gliosis, varying degrees of axonal pathology, and progressive neurological dysfunction. Multiple sclerosis exhibits many of the characteristics that distinguish complex genetic disorders including polygenic inheritance and environmental exposure risks. Here, we used a highly efficient multilocus genotyping assay representing variation in 34 genes associated with inflammatory pathways to explore gene-gene interactions and disease susceptibility in a well-characterized African-American case-control MS data set. We applied the multifactor dimensionality reduction (MDR) test to detect epistasis, and identified single-IL4R(Q576R)- and three-IL4R(Q576R), IL5RA(-80), CD14(-260)- locus association models that predict MS risk with 75-76% accuracy (P < 0.01). These results demonstrate the importance of exploring both main effects and gene-gene interactions in the study of complex diseases.
引用
收藏
页码:310 / 315
页数:6
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