A robust and adaptive framework for interaction testing in quantitative traits between multiple genetic loci and exposure variables

被引:2
|
作者
Hecker, Julian [1 ,2 ]
Prokopenko, Dmitry [2 ,3 ,4 ]
Moll, Matthew [1 ,2 ,5 ]
Lee, Sanghun [6 ,7 ]
Kim, Wonji [1 ,2 ]
Qiao, Dandi [1 ,2 ]
Voorhies, Kirsten [2 ,8 ]
Kim, Woori [2 ,9 ,10 ]
Vansteelandt, Stijn [11 ,12 ]
Hobbs, Brian D. [1 ,2 ,5 ]
Cho, Michael H. [1 ,2 ,5 ]
Silverman, Edwin K. [1 ,2 ,5 ]
Lutz, Sharon M. [2 ,7 ,8 ]
DeMeo, Dawn L. [1 ,2 ]
Weiss, Scott T. [1 ,2 ]
Lange, Christoph [1 ,2 ,7 ]
机构
[1] Brigham & Womens Hosp, Dept Med, Channing Div Network Med, 75 Francis St, Boston, MA 02115 USA
[2] Harvard Med Sch, Boston, MA 02115 USA
[3] Massachusetts Gen Hosp, Genet & Aging Unit, Boston, MA 02114 USA
[4] Massachusetts Gen Hosp, McCance Ctr Brain Hlth, Dept Neurol, Boston, MA 02114 USA
[5] Brigham & Womens Hosp, Div Pulm & Crit Care Med, 75 Francis St, Boston, MA 02115 USA
[6] Dankook Univ, Grad Sch, Dept Med Consilience, Div Med, Yongin, South Korea
[7] Harvard TH Chan Sch Publ Hlth, Dept Biostat, Boston, MA USA
[8] Harvard Pilgrim Hlth Care, Dept Populat Med, PRecis Med Translat Res PROMoTeR Ctr, Boston, MA USA
[9] Brigham & Womens Hosp, Dept Neurol, Ann Romney Ctr Neurol Dis, Syst Biol & Comp Sci Program, 75 Francis St, Boston, MA 02115 USA
[10] Broad Inst MIT & Harvard, Cambridge, MA 02142 USA
[11] Univ Ghent, Dept Appl Math Comp Sci & Stat, Ghent, Belgium
[12] London Sch Hyg & Trop Med, Dept Med Stat, London, England
来源
PLOS GENETICS | 2022年 / 18卷 / 11期
关键词
GENOME-WIDE ASSOCIATION; SET-BASED TEST; ENVIRONMENT INTERACTION; COMMON VARIANTS; RARE VARIANTS; MARKER-SET; REGRESSION; SELECTION;
D O I
10.1371/journal.pgen.1010464
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The identification and understanding of gene-environment interactions can provide insights into the pathways and mechanisms underlying complex diseases. However, testing for gene-environment interaction remains a challenge since a.) statistical power is often limited and b.) modeling of environmental effects is nontrivial and such model misspecifications can lead to false positive interaction findings. To address the lack of statistical power, recent methods aim to identify interactions on an aggregated level using, for example, polygenic risk scores. While this strategy can increase the power to detect interactions, identifying contributing genes and pathways is difficult based on these relatively global results. Here, we propose RITSS (Robust Interaction Testing using Sample Splitting), a gene-environment interaction testing framework for quantitative traits that is based on sample splitting and robust test statistics. RITSS can incorporate sets of genetic variants and/or multiple environmental factors. Based on the user's choice of statistical/machine learning approaches, a screening step selects and combines potential interactions into scores with improved interpretability. In the testing step, the application of robust statistics minimizes the susceptibility to main effect misspecifications. Using extensive simulation studies, we demonstrate that RITSS controls the type 1 error rate in a wide range of scenarios, and we show how the screening strategy influences statistical power. In an application to lung function phenotypes and human height in the UK Biobank, RITSS identified highly significant interactions based on subcomponents of genetic risk scores. While the contributing single variant interaction signals are weak, our results indicate interaction patterns that result in strong aggregated effects, providing potential insights into underlying gene-environment interaction mechanisms. Author summary The understanding of gene-environment interactions provides potential insights into the pathways and mechanisms underlying complex diseases, but they are hard to detect since effect sizes are expected to be small. To facilitate the detection of such interactions in quantitative traits, we propose a robust and flexible approach called RITSS that can incorporate sets of genetic variants and multiple environmental factors. RITSS can utilize any suitable machine/statistical learning approach to screen for interactions and rigorously tests these aggregated signals using sample splitting and robust test statistics. We demonstrate the validity and power of our approach in extensive simulation studies. Furthermore, in an application to lung function and height data in the UK Biobank, RITSS discovers highly significant interactions based on subcomponents of genetic risk scores.
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页数:19
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