利用未知遗传相互作用的稳健关联测试:在囊性纤维化肺疾病中的应用

IF 1.7 4区 医学 Q3 GENETICS & HEREDITY
Sangook Kim, Yu-Chung Lin, Lisa J. Strug
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引用次数: 0

摘要

对于复杂的特征,如囊性纤维化(CF)中的肺部疾病,基因x基因或基因x环境的相互作用可以影响疾病的严重程度,但这些在很大程度上仍然未知。未解释的遗传相互作用在基因型群体中引入了数量性状的分布转移。联合定位和规模测试,或基因型组之间的完全分布差异可以解释未知的遗传相互作用,与传统的关联测试相比,可以增加基因鉴定的能力。在这里,我们提出了一种新的联合位置和规模检验(JLS),一种基于分位数回归的JLS (qJLS),它解决了以前的局限性。具体来说,qJLS没有分布假设,因此适用于非高斯特征;与现有的高斯特征下的JLS测试一样强大;并且在全基因组关联研究(GWAS)中具有计算效率。我们对未知遗传相互作用建模的模拟研究表明,qJLS对偏态和重尾误差分布具有鲁棒性,并且在正态性下与文献中其他JLS检验一样强大。在没有任何未知的遗传相互作用的情况下,qJLS在非高斯性状的关联检验中显示出比常规关联检验更大的功效,而在正态性下的功效略低。我们将qJLS方法应用于加拿大CF基因修饰研究(n = 1997),并在13号染色体上发现了一个全基因组显著变异rs9513900,该变异以前未被报道与CF肺部疾病有关。qJLS提供了一个强大的替代传统的遗传关联测试,其中相互作用可能有助于数量性状。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A Robust Association Test Leveraging Unknown Genetic Interactions: Application to Cystic Fibrosis Lung Disease

A Robust Association Test Leveraging Unknown Genetic Interactions: Application to Cystic Fibrosis Lung Disease

For complex traits such as lung disease in Cystic Fibrosis (CF), Gene x Gene or Gene x Environment interactions can impact disease severity but these remain largely unknown. Unaccounted-for genetic interactions introduce a distributional shift in the quantitative trait across the genotypic groups. Joint location and scale tests, or full distributional differences across genotype groups can account for unknown genetic interactions and increase power for gene identification compared with the conventional association test. Here we propose a new joint location and scale test (JLS), a quantile regression-basd JLS (qJLS), that addresses previous limitations. Specifically, qJLS is free of distributional assumptions, thus applies to non-Gaussian traits; is as powerful as the existing JLS tests under Gaussian traits; and is computationally efficient for genome-wide association studies (GWAS). Our simulation studies, which model unknown genetic interactions, demonstrate that qJLS is robust to skewed and heavy-tailed error distributions and is as powerful as other JLS tests in the literature under normality. Without any unknown genetic interaction, qJLS shows a large increase in power with non-Gaussian traits over conventional association tests and is slightly less powerful under normality. We apply the qJLS method to the Canadian CF Gene Modifier Study (n = 1,997) and identified a genome-wide significant variant, rs9513900 on chromosome 13, that had not previously been reported to contribute to CF lung disease. qJLS provides a powerful alternative to conventional genetic association tests, where interactions may contribute to a quantitative trait.

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来源期刊
Genetic Epidemiology
Genetic Epidemiology 医学-公共卫生、环境卫生与职业卫生
CiteScore
4.40
自引率
9.50%
发文量
49
审稿时长
6-12 weeks
期刊介绍: Genetic Epidemiology is a peer-reviewed journal for discussion of research on the genetic causes of the distribution of human traits in families and populations. Emphasis is placed on the relative contribution of genetic and environmental factors to human disease as revealed by genetic, epidemiological, and biologic investigations. Genetic Epidemiology primarily publishes papers in statistical genetics, a research field that is primarily concerned with development of statistical, bioinformatical, and computational models for analyzing genetic data. Incorporation of underlying biology and population genetics into conceptual models is favored. The Journal seeks original articles comprising either applied research or innovative statistical, mathematical, computational, or genomic methodologies that advance studies in genetic epidemiology. Other types of reports are encouraged, such as letters to the editor, topic reviews, and perspectives from other fields of research that will likely enrich the field of genetic epidemiology.
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