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

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....

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Veröffentlicht in:Genetic epidemiology 2023-09, Vol.47 (6), p.409-431
Hauptverfasser: Wang, Shuqi, Chiu, Chi‐Yang, Wilson, Alexander F., Bailey‐Wilson, Joan E., Agron, Elvira, Chew, Emily Y., Ahn, Jaeil, Xiong, Momiao, Fan, Ruzong
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Sprache:eng
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Zusammenfassung: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.
ISSN:0741-0395
1098-2272
DOI:10.1002/gepi.22524