Evidence map›Paper›PMID 37880571›Full record

ArticleBMC bioinformatics2023

TreeKernel: interpretable kernel machine tests for interactions between -omics and clinical predictors with applications to metabolomics and COPD phenotypes.

Charlie M Carpenter, Lucas Gillenwater, Russell Bowler, Katerina Kechris, Debashis Ghosh

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

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Charlie M CarpenterDepartment of Biostatistics and Informatics, University of Colorado Denver, Anschutz Medical Campus, Denver, CO, USA. charles.carpenter@cuanschutz.edu.
Lucas GillenwaterComputational Bioscience Program, University of Colorado Denver, Anschutz Medical Campus, Denver, CO, USA.
Russell BowlerDepartment of Medicine, National Jewish Health, Denver, USA.
Katerina KechrisDepartment of Biostatistics and Informatics, University of Colorado Denver, Anschutz Medical Campus, Denver, CO, USA.
Debashis GhoshDepartment of Biostatistics and Informatics, University of Colorado Denver, Anschutz Medical Campus, Denver, CO, USA.

Funding

Genetic Epidemiology of COPDU01HL089897 · NHLBI · NATIONAL JEWISH HEALTH · PI CRAPO, JAMES D · 2007 to 2021
$56.9M
Addressing Sparsity in Metabolomics Data AnalysisU01CA235488 · NCI · UNIVERSITY OF COLORADO DENVER · PI GHOSH, DEBASHIS, KECHRIS-MAYS, KATHERINA · 2018 to 2021
$1.8M
NCI NIH HHS U01 CA235488NHLBI NIH HHS U01 HL089897
6 · The paper itself

Abstract

backgroundIn this paper, we are interested in interactions between a high-dimensional -omics dataset and clinical covariates. The goal is to evaluate the relationship between a phenotype of interest and a high-dimensional omics pathway, where the effect of the omics data depends on subjects' clinical covariates (age, sex, smoking status, etc.). For instance, metabolic pathways can vary greatly between sexes which may also change the relationship between certain metabolic pathways and a clinical phenotype of interest. We propose partitioning the clinical covariate space and performing a kernel association test within those partitions. To illustrate this idea, we focus on hierarchical partitions of the clinical covariate space and kernel tests on metabolic pathways.

resultsWe see that our proposed method outperforms competing methods in most simulation scenarios. It can identify different relationships among clinical groups with higher power in most scenarios while maintaining a proper Type I error rate. The simulation studies also show a robustness to the grouping structure within the clinical space. We also apply the method to the COPDGene study and find several clinically meaningful interactions between metabolic pathways, the clinical space, and lung function.

conclusionTreeKernel provides a simple and interpretable process for testing for relationships between high-dimensional omics data and clinical outcomes in the presence of interactions within clinical cohorts. The method is broadly applicable to many studies.

Indexed as

Pulmonary Disease, Chronic ObstructiveComputer SimulationHumansPhenotypeKernel functionsKernel interactionsKernel methodsMetabolic pathwaysMetabolomics

Identifiers

PMID37880571
PMCPMC10601228

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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 OpenQuestion graph.