A family-based association test to detect gene–gene interactions in the presence of linkage

被引:0
作者
Lizzy De Lobel
Lutgarde Thijs
Tatiana Kouznetsova
Jan A Staessen
Kristel Van Steen
机构
[1] Ghent University,Department of Applied Mathematics and Computer Science
[2] KU Leuven,Division of Hypertension and Cardiovascular Rehabilitation, Department of Cardiovascular Diseases
[3] Maastricht University,Department of Epidemiology
[4] Systems and Modeling Unit,Department of Electrical Engineering and Computer Science
[5] Montefiore Institute,undefined
[6] University of Liège,undefined
[7] Bioinformatics and Modeling,undefined
[8] GIGA-R,undefined
[9] University of Liège,undefined
来源
European Journal of Human Genetics | 2012年 / 20卷
关键词
QTDT; epistasis; association; linkage;
D O I
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中图分类号
学科分类号
摘要
For many complex diseases, quantitative traits contain more information than dichotomous traits. One of the approaches used to analyse these traits in family-based association studies is the quantitative transmission disequilibrium test (QTDT). The QTDT is a regression-based approach that models simultaneously linkage and association. It splits up the association effect in a between- and a within-family genetic component to adjust and test for population stratification and includes a variance components method to model linkage. We extend this approach to detect gene–gene interactions between two unlinked QTLs by adjusting the definition of the between- and within-family component and the variance components included in the model. We simulate data to investigate the influence of the epistasis model, linkage disequilibrium patterns between the markers and the QTLs, and allele frequencies on the power and type I error rates of the approach. Results show that for some of the investigated settings, power gains are obtained in comparison with FAM-MDR. We conclude that our approach shows promising results for candidate-gene studies where too few markers are available to correct for population stratification using standard methods (for example EIGENSTRAT). The proposed method is applied to real-life data on hypertension from the FLEMENGHO study.
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页码:973 / 980
页数:7
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  • [1] Martin ER(2006)A novel method to identify gene-gene effects in nuclear families: the MDR-PDT Genet Epidemiol 30 111-123
  • [2] Ritchie MD(2005)Identifying susceptibility genes by using joint tests of association and linkage and accounting for epistasis BMC Genet 6 S147-177
  • [3] Hahn L(2010)FAM-MDR: a flexible family-based multifactor dimensionality reduction technique to detect epistasis using related individuals PLoS ONE 5 e10304-292
  • [4] Kang S(2007)Type I error rates in association versus joint linkage/association tests in related individuals Genet Epidemiol 31 173-1022
  • [5] Moore JH(2000)A general test of association for quantitative traits in nuclear families Am J Hum Genet 66 279-551
  • [6] Millstein J(1997)Power of variance component linkage analysis to detect epistasis Genet Epidemiol 14 1017-543
  • [7] Siegmund KD(2000)Pedigree tests of transmission disequilibrium Eur J Hum Genet 8 545-585
  • [8] Conti DV(1994)Robust variance-components approach for assessing genetic linkage in pedigrees Am J Hum Genet 54 535-6546
  • [9] Gauderman WJ(2007)Genomewide rapid association using mixed model and regression: a fast and simple method for genomewide pedigree-based quantitative trait loci association analysis Genetics 177 577-417
  • [10] Cattaert T(2008)Improving strategies for detecting genetic patterns of disease susceptibility in association studies Stat Med 27 6532-1358