Evidence map›Paper›PMID 40972407›Full record

ArticleArtificial intelligence in medicine2025

Pathway information on methylation analysis using deep neural network (PROMINENT): An interpretable deep learning method with pathway prior for phenotype prediction using gene-level DNA methylation.

Soyeon Kim, Laizhi Zhang, Yidi Qin, Rebecca I Caldino Bohn, Hyun Jung Park

Abstract read
In one paragraph

Article in Artificial intelligence in medicine, 2025. 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.

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

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.

Soyeon KimDivision of Pulmonary Medicine, Department of Pediatrics, School of Medicine, University of Pittsburgh, Pittsburgh, PA, United States.
Laizhi ZhangDepartment of Human Genetics, School of Public Health, University of Pittsburgh, Pittsburgh, PA, United States.
Yidi QinDepartment of Human Genetics, School of Public Health, University of Pittsburgh, Pittsburgh, PA, United States.
Rebecca I Caldino BohnDepartment of Human Genetics, School of Public Health, University of Pittsburgh, Pittsburgh, PA, United States.
Hyun Jung ParkDepartment of Human Genetics, School of Public Health, University of Pittsburgh, Pittsburgh, PA, United States. Electronic address: hyp15@pitt.edu.

Funding

VECTOR CORE FACILITYP30CA047904 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI CHRISTOPHER J. BAKKENIST · 1988 to 2026
$158.0M
Project 5: Microenvironment manipulation using anti-angiogenics to improve immunotherapy in melanomaP50CA254865 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI WANG, HONG · 2021 to 2025
$10.4M
Inflammation Phenotypes in Pediatric Sepsis Induced Multiple Organ Failure RenewalR01GM108618 · NIGMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI JOSEPH A CARCILLO · 2014 to 2026
$5.4M
Identifying Genetic and Epigenetic Risk Factors Regulating Gene Expression for Childhood AsthmaK01HL153792 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI KIM, SOYEON · 2020 to 2025
$699k
High-Throughput Computing for Genomics and Bioinformatics ResearchS10OD028483 · OD · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI LEE, ADRIAN V · 2021 to 2021
$574k
NCI NIH HHS P30 CA047904NCI NIH HHS P50 CA254865NHLBI NIH HHS K01 HL153792NIGMS NIH HHS R01 GM108618NIH HHS S10 OD028483
6 · The paper itself

Abstract

backgroundDNA methylation is a key epigenetic marker that influences gene expression and phenotype regulation, and is affected by both genetic and environmental factors. Traditional linear regression methods such as elastic nets have been employed to assess the cumulative effects of multiple DNA methylation markers on phenotypes. However, these methods often fail to capture the complex nonlinear nature of the data. Recent deep learning approaches, such as MethylNet, have improved the prediction accuracy but lack interpretability and efficiency.

findingsTo address these limitations, we introduced Pathway Information on Methylation Analysis using a Deep Neural Network (PROMINENT), a novel interpretable deep learning method that integrates gene-level DNA methylation data with biological pathway information for phenotype prediction. PROMINENT enhances interpretability and prediction accuracy by incorporating gene- and pathway-level priors from databases such as Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG). It employs SHapley Additive exPlanations (SHAP) to prioritize significant genes and pathways. Evaluated across various datasets, childhood asthma, idiopathic pulmonary fibrosis (IPF), and first-episode psychosis (FEP)-PROMINENT consistently outperformed existing methods in terms of prediction accuracy and computational efficiency. PROMINENT also identified crucial genes and pathways involved in disease mechanisms.

conclusionsPROMINENT represents a significant advancement in leveraging DNA methylation data for phenotype prediction, offering both high accuracy and interpretability within reasonable computational time. This method holds promise for elucidating the epigenetic underpinnings of complex diseases and enhancing the utility of DNA methylation data in biomedical research.

Indexed as

Deep LearningDNA MethylationNeural Networks, ComputerAsthmaChildEpigenesis, GeneticHumansPhenotypePsychotic DisordersDeep learningDNA methylationGenePathwayPhenotype prediction

Identifiers

PMID40972407
PMCPMC13273382

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.