Evidence map›Paper›PMID 29453930›Full record

ArticleStatistical applications in genetics and molecular biology2018

Ensemble survival tree models to reveal pairwise interactions of variables with time-to-events outcomes in low-dimensional setting.

Jean-Eudes Dazard, Hemant Ishwaran, Rajeev Mehlotra, Aaron Weinberg, Peter Zimmerman

Abstract read
In one paragraph

Article in Statistical applications in genetics and molecular biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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.

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
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

5 authors.

Jean-Eudes DazardCase Western Reserve University, School of Medicine, Center for Proteomics and Bioinformatics, Cleveland, OH 44106, USA.ORCID http://orcid.org/0000-0003-4720-3684
Hemant IshwaranThe University of Miami, Department of Epidemiology and Public Health, Division of Biostatistics, Miami, FL 33136, USA.
Rajeev MehlotraCase Western Reserve University, School of Medicine, Center for Global Health and Diseases, Cleveland, OH 44106, USA.
Aaron WeinbergCase Western Reserve University, School of Dental Medicine, Department of Biological Sciences, Cleveland, OH 44106, USA.
Peter ZimmermanCase Western Reserve University, School of Medicine, Center for Global Health and Diseases, Cleveland, OH 44106, USA.

Funding

WG3: HIV, Co-infections and Co-morbiditiesP30AI036219 · NIAID · CASE WESTERN RESERVE UNIVERSITY · PI Alan David Levine · 1994 to 2026
$50.0M
Miami Clinical and Translational Science InstituteUL1TR000460 · NCATS · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI SACCO, RALPH L. · 2012 to 2016
$16.9M
Proj. 4-The Genetic Variation of Innate Immune Genes w/Oral Manifestations of HIVP01DE019759 · NIDCR · CASE WESTERN RESERVE UNIVERSITY · PI CHANCE, MARK R · 2009 to 2013
$9.0M
NextGen Random ForestsR01GM125072 · NIGMS · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI ISHWARAN, HEMANT · 2017 to 2020
$1.4M
RF-SRC: A Unified Data ToolR01CA163739 · NCI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI ISHWARAN, HEMANT · 2012 to 2015
$966k
NCATS NIH HHS UL1 TR000460NCI NIH HHS R01 CA163739NIAID NIH HHS P30 AI036219NIDCR NIH HHS P01 DE019759NIGMS NIH HHS R01 GM125072
6 · The paper itself

Abstract

Unraveling interactions among variables such as genetic, clinical, demographic and environmental factors is essential to understand the development of common and complex diseases. To increase the power to detect such variables interactions associated with clinical time-to-events outcomes, we borrowed established concepts from random survival forest (RSF) models. We introduce a novel RSF-based pairwise interaction estimator and derive a randomization method with bootstrap confidence intervals for inferring interaction significance. Using various linear and nonlinear time-to-events survival models in simulation studies, we first show the efficiency of our approach: true pairwise interaction-effects between variables are uncovered, while they may not be accompanied with their corresponding main-effects, and may not be detected by standard semi-parametric regression modeling and test statistics used in survival analysis. Moreover, using a RSF-based cross-validation scheme for generating prediction estimators, we show that informative predictors may be inferred. We applied our approach to an HIV cohort study recording key host gene polymorphisms and their association with HIV change of tropism or AIDS progression. Altogether, this shows how linear or nonlinear pairwise statistical interactions of variables may be efficiently detected with a predictive value in observational studies with time-to-event outcomes.

Indexed as

Models, StatisticalAcquired Immunodeficiency Syndromebeta-DefensinsCohort StudiesConfidence IntervalsDNA Copy Number VariationsEpistasis, GeneticHIV-1HIV InfectionsHumansKaplan-Meier EstimateModels, GeneticProportional Hazards ModelsViral Tropismbeta-DefensinsDEFB4A protein, humanepistasisgenetic variations interactionsinteraction detection and modelingrandom survival foresttime-to-event analysis

Identifiers

PMID29453930
PMCPMC5844232

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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.