Evidence map›Paper›PMID 33969382›Full record

ArticleBiostatistics (Oxford, England)2022

Bayesian integrative analysis and prediction with application to atherosclerosis cardiovascular disease.

Thierry Chekouo, Sandra E Safo

Open access · greenAbstract read
In one paragraph

Article in Biostatistics (Oxford, England), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.5field-weighted citation impact, top 31% of its field
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

13 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Integrative Analysis of Multimodal Omics Data.Annual review of statistics and its application · 2026
    Article
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  12. sJIVE: Supervised Joint and Individual Variation Explained.Computational statistics & data analysis · 2022
    Article
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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

2 authors at 2 institutions in 2 countries.

Thierry ChekouoDepartment of Mathematics and Statistics, University of Calgary, 2500 University Dr NW, Calgary, AB, T2N1N4, Canada.ORCID 0000-0002-3594-9182
Sandra E SafoDivision of Biostatistics, University of Minnesota, 20 Delaware St SE, Minneapolis, MN 55455, USA.ORCID 0000-0001-9593-4778
University of Calgary · CAUniversity of Minnesota · US

Funding

University of Minnesota Clinical and Translational Science Institute (UMN CTSI)UL1TR002494 · NCATS · UNIVERSITY OF MINNESOTA · PI BLAZAR, BRUCE R, WEISDORF, DANIEL J · 2018 to 2022
$34.9M
Institutional Career Development CoreKL2TR002492 · NCATS · UNIVERSITY OF MINNESOTA · PI INGBAR, DAVID H · 2018 to 2022
$6.3M
National Institutes of Health (NIH) 5KL2TR002492-04Natural Sciences and Engineering Research Council of Canada (NSERC) Discovery RGPIN-2019-04810NCATS NIH HHS KL2 TR002492NCATS NIH HHS UL1 TR002494
6 · The paper itself

Abstract

The problem of associating data from multiple sources and predicting an outcome simultaneously is an important one in modern biomedical research. It has potential to identify multidimensional array of variables predictive of a clinical outcome and to enhance our understanding of the pathobiology of complex diseases. Incorporating functional knowledge in association and prediction models can reveal pathways contributing to disease risk. We propose Bayesian hierarchical integrative analysis models that associate multiple omics data, predict a clinical outcome, allow for prior functional information, and can accommodate clinical covariates. The models, motivated by available data and the need for exploring other risk factors of atherosclerotic cardiovascular disease (ASCVD), are used for integrative analysis of clinical, demographic, and genomics data to identify genetic variants, genes, and gene pathways likely contributing to 10-year ASCVD risk in healthy adults. Our findings revealed several genetic variants, genes, and gene pathways that are highly associated with ASCVD risk, with some already implicated in cardiovascular disease (CVD) risk. Extensive simulations demonstrate the merit of joint association and prediction models over two-stage methods: association followed by prediction.

Indexed as

AtherosclerosisCardiovascular DiseasesAdultBayes TheoremGenomicsHumansRisk AssessmentRisk FactorsBayesian variable selectionBiological informationCardiovascular diseaseFactor analysisIntegrative analysisJoint association and prediction

Identifiers

PMID33969382
PMCPMC9960952
OpenAlexW3027831021

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.