Gene-level association analysis of bivariate ordinal traits with functional regressions

IF 1.7 4区 医学 Q3 GENETICS & HEREDITY
Shuqi Wang, Chi-Yang Chiu, Alexander F. Wilson, Joan E. Bailey-Wilson, Elvira Agron, Emily Y. Chew, Jaeil Ahn, Momiao Xiong, Ruzong Fan
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引用次数: 1

Abstract

In genetic studies, many phenotypes have multiple naturally ordered discrete values. The phenotypes can be correlated with each other. If multiple correlated ordinal traits are analyzed simultaneously, the power of analysis may increase significantly while the false positives can be controlled well. In this study, we propose bivariate functional ordinal linear regression (BFOLR) models using latent regressions with cumulative logit link or probit link to perform a gene-based analysis for bivariate ordinal traits and sequencing data. In the proposed BFOLR models, genetic variant data are viewed as stochastic functions of physical positions, and the genetic effects are treated as a function of physical positions. The BFOLR models take the correlation of the two ordinal traits into account via latent variables. The BFOLR models are built upon functional data analysis which can be revised to analyze the bivariate ordinal traits and high-dimension genetic data. The methods are flexible and can analyze three types of genetic data: (1) rare variants only, (2) common variants only, and (3) a combination of rare and common variants. Extensive simulation studies show that the likelihood ratio tests of the BFOLR models control type I errors well and have good power performance. The BFOLR models are applied to analyze Age-Related Eye Disease Study data, in which two genes, CFH and ARMS2, are found to strongly associate with eye drusen size, drusen area, age-related macular degeneration (AMD) categories, and AMD severity scale.

双变量有序性状的基因水平关联分析及功能回归
在遗传学研究中,许多表型具有多个自然有序的离散值。表型可以相互关联。如果同时分析多个相关的有序特征,可以显著提高分析能力,同时可以很好地控制假阳性。在这项研究中,我们提出了二元功能有序线性回归(BFOLR)模型,使用具有累积logit链接或probit链接的潜在回归对二元有序性状和测序数据进行基于基因的分析。在提出的BFOLR模型中,遗传变异数据被视为物理位置的随机函数,遗传效应被视为物理位置的函数。BFOLR模型通过潜在变量考虑了两个有序性状之间的相关性。BFOLR模型建立在功能数据分析的基础上,可用于分析二元有序性状和高维遗传数据。该方法灵活,可以分析三种类型的遗传数据:(1)仅罕见变异,(2)仅常见变异,(3)罕见和常见变异的组合。大量的仿真研究表明,BFOLR模型的似然比检验能很好地控制I类误差,具有良好的功率性能。BFOLR模型用于分析年龄相关性眼病研究数据,其中发现两个基因CFH和ARMS2与眼膜大小、眼膜面积、年龄相关性黄斑变性(AMD)类别和AMD严重程度密切相关。
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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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