Gene‐level association analysis of ordinal traits with functional ordinal logistic regressions. Issue 5 (19th April 2022)

• Record Type: Journal Article
• Authors: Chiu, Chi‐Yang; Wang, Shuqi; Zhang, Bingsong; Luo, Yutong; Simpson, Claire; Zhang, Wei; Wilson, Alexander F.; Bailey‐Wilson, Joan E.; Agron, Elvira; Chew, Emily Y.; Zhang, Jun; Xiong, Momiao; Fan, Ruzong
• Is Part Of: Genetic epidemiology. Volume 46:Issue 5/6(2022)
• Page Start: 234
• Page End: 255
• Publication Date: 2022-04-19
• Subjects: association mapping -- complex disease -- functional data analysis -- ordinal traits -- rare variants -- sequence data; Genetic epidemiology -- Periodicals; Heredity -- Periodicals; Medical geography -- Periodicals; 614
• DOI: 10.1002/gepi.22451
• Languages: English
• ISSNs: 0741-0395

Abstract

Abstract: In this paper, we develop functional ordinal logistic regression (FOLR) models to perform gene‐based analysis of ordinal traits. In the proposed FOLR 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 FOLR models are built upon functional data analysis which can be revised to analyze the ordinal traits and high dimension genetic data. The proposed methods are capable of dealing with dense genotype data which is usually encountered in analyzing the next‐generation sequencing 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. Simulation studies show that the likelihood ratio test statistics of the FOLR models control type I errors well and have good power performance. The proposed methods achieve the goals of analyzing ordinal traits directly, reducing high dimensionality of dense genetic variants, being computationally manageable, facilitating model convergence, properly controlling type I errors, and maintaining high power levels. The FOLR models are applied to analyze Age‐Related Eye Disease Study data, in which two genes are found to strongly associate with four ordinal traits.