A Nonparametric Test to Detect Quantitative Trait Loci Where the Phenotypic Distribution Differs by Genotypes

被引:21
作者
Aschard, Hugues [1 ]
Zaitlen, Noah [2 ]
Tamimi, Rulla M. [1 ,3 ]
Lindstroem, Sara [1 ]
Kraft, Peter [1 ,4 ]
机构
[1] Harvard Univ, Sch Publ Hlth, Dept Epidemiol, Boston, MA 02115 USA
[2] Univ Calif San Francisco, Dept Med, San Francisco, CA USA
[3] Brigham & Womens Hosp, Channing Div Network Med, Boston, MA 02115 USA
[4] Harvard Univ, Sch Publ Hlth, Dept Biostat, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
nonparametric test; gene-gene and gene-environment interactions; quantitative traits; genome-wide association studies; quantitative trait; GENE-ENVIRONMENT INTERACTIONS; GENOME-WIDE ASSOCIATION; MAMMOGRAPHIC DENSITY; MISSING HERITABILITY; STRATEGIES; ORDER; RISK;
D O I
10.1002/gepi.21716
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Searching for genetic variants involved in gene-gene and gene-environment interactions in large-scale data raises multiple methodological issues. Many existing methods have focused on the problem of dimensionality, trying to explore the largest number of combinations between risk factors while considering simple interaction models. Despite evidence demonstrating the efficacy of these methods in simulated data, their application in real data has been unsuccessful so far. The classical test of a linear marginal genetic effect has been widely used for agnostic genome-wide association studies, with the underlying idea that most variants involved in interactions might display marginal effect on the phenotypic mean. Although this approach may allow for the identification of genetic variants involved in interactions in many scenarios, the linear marginal effects of some causal alleles on the phenotypic mean might not be always detectable at genome-wide significance level. We introduce in this study a general association test for quantitative trait loci that compare the distributions of phenotypic values by genotypic classes as opposed to most standard tests that compare phenotypic means by genotypic classes. Using simulations we show that in presence of interactions, this approach can be more powerful than the standard test of the linear marginal effect, with a gain of power increasing with increasing interaction effect and decreasing frequencies of the interacting exposures. We demonstrate the potential utility of our method on real data by analyzing mammographic density genome-wide data from the Nurses' Health Study.
引用
收藏
页码:323 / 333
页数:11
相关论文
共 40 条
[1]   Inclusion of Gene-Gene and Gene-Environment Interactions Unlikely to Dramatically Improve Risk Prediction for Complex Diseases [J].
Aschard, Hugues ;
Chen, Jinbo ;
Cornelis, Marilyn C. ;
Chibnik, Lori B. ;
Karlson, Elizabeth W. ;
Kraft, Peter .
AMERICAN JOURNAL OF HUMAN GENETICS, 2012, 90 (06) :962-972
[3]   Symmetry of projection in the quantitative analysis of mammographic images [J].
Byng, JW ;
Boyd, NF ;
Little, L ;
Lockwood, G ;
Fishell, E ;
Jong, RA ;
Yaffe, MJ .
EUROPEAN JOURNAL OF CANCER PREVENTION, 1996, 5 (05) :319-327
[4]   Naive application of permutation testing leads to inflated type I error rates [J].
Churchill, G. A. ;
Doerge, R. W. .
GENETICS, 2008, 178 (01) :609-610
[5]   Epidemiological methods for studying genes and environmental factors in complex diseases [J].
Clayton, D ;
McKeigue, PM .
LANCET, 2001, 358 (9290) :1356-1360
[6]   The Nurses' Health Study: Lifestyle and health among women [J].
Colditz, GA ;
Hankinson, SE .
NATURE REVIEWS CANCER, 2005, 5 (05) :388-396
[7]   Detecting gene-gene interactions that underlie human diseases [J].
Cordell, Heather J. .
NATURE REVIEWS GENETICS, 2009, 10 (06) :392-404
[8]   Gene-Environment Interactions in Genome-Wide Association Studies: A Comparative Study of Tests Applied to Empirical Studies of Type 2 Diabetes [J].
Cornelis, Marilyn C. ;
Tchetgen, Eric J. Tchetgen ;
Liang, Liming ;
Qi, Lu ;
Chatterjee, Nilanjan ;
Hu, Frank B. ;
Kraft, Peter .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 2012, 175 (03) :191-202
[9]   Detecting Interacting Genetic Loci with Effects on Quantitative Traits Where the Nature and Order of the Interaction Are Unknown [J].
Davies, Joanna L. ;
Hein, Jotun ;
Holmes, Chris C. .
GENETIC EPIDEMIOLOGY, 2010, 34 (04) :299-308
[10]   Bias Due to Two-Stage Residual-Outcome Regression Analysis in Genetic Association Studies [J].
Demissie, Serkalem ;
Cupples, L. Adrienne .
GENETIC EPIDEMIOLOGY, 2011, 35 (07) :592-596