Evidence map›Paper›PMID 37101379›Full record

ArticleGenetic epidemiology2023

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

Shuqi Wang, Chi-Yang Chiu, Alexander F Wilson, Joan E Bailey-Wilson, Elvira Agron, Emily Y Chew, Jaeil Ahn, Momiao Xiong, Ruzong Fan

Abstract read
In one paragraph

Article in Genetic epidemiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Shuqi WangDepartment of Biostatistics, Bioinformatics, and Biomathematics, Georgetown University Medical Center, Washington, DC, USA.
Chi-Yang ChiuDivision of Biostatistics, Department of Preventive Medicine, University of Tennessee Health Science Center, Memphis, TN, USA.ORCID 0000-0002-4837-3194
Alexander F WilsonComputational and Statistical Genomics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA.ORCID 0000-0002-6682-8156
Joan E Bailey-WilsonComputational and Statistical Genomics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA.ORCID 0000-0002-9153-2920
Elvira AgronNational Eye Institute, National Institute of Health, Bethesda, MD, USA.
Emily Y ChewNational Eye Institute, National Institute of Health, Bethesda, MD, USA.
Jaeil AhnDepartment of Biostatistics, Bioinformatics, and Biomathematics, Georgetown University Medical Center, Washington, DC, USA.
Momiao XiongHuman Genetics Center, University of Texas-Houston, Houston, TX, USA.
Ruzong FanDepartment of Biostatistics, Bioinformatics, and Biomathematics, Georgetown University Medical Center, Washington, DC, USA.ORCID 0000-0002-7603-2135

Funding

The Age-Related Eye Disease Study 2 (AREDS2)ZIAEY000485 · NEI · NATIONAL EYE INSTITUTE · PI CHEW, EMILY Y · 2009 to 2015
$990k
Age-Related Eye Disease Follow-up Study (AREDS) Follow-up StudyZIAEY000489 · NEI · NATIONAL EYE INSTITUTE · PI CHEW, EMILY Y · 2009 to 2025
$639k
AREDS II Ancillary Genetics StudyZIAAT000018 · NCCIH · NATIONAL CENTER FOR COMPLEMENTARY & INTEGRATIVE HEALTH · PI CHEW, EMILY · 2011 to 2013
$237k
Age-related Eye Disease Study (AREDS)Z01EY000394 · NEI · NATIONAL EYE INSTITUTE · PI CHEW, EMILY Y · 2002 to 2005
–
Intramural NIH HHS Z01 EY000394Intramural NIH HHS ZIA AT000018Intramural NIH HHS ZIA EY000485Intramural NIH HHS ZIA EY000489
6 · The paper itself

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.

Indexed as

Macular DegenerationModels, GeneticComputer SimulationHumansLinear ModelsPhenotypeassociation mappingbivariate ordinal traitscomplex diseasefunctional data analysislatent regression modelsrare variantssequence data

Identifiers

PMID37101379
PMCPMC13452082

What Socratic holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.