Evidence map›Paper›PMID 39796173›Full record

ArticleInternational journal of molecular sciences2025

Research on Prediction of Multiple Degenerative Diseases and Biomarker Screening Based on DNA Methylation.

Ruoting Tian, Hao Zhang, Chencai Wang, Shengyang Zhou, Li Zhang, Han Wang

Abstract read
In one paragraph

Article in International journal of molecular sciences, 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. Review
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

6 authors.

Ruoting TianCollege of Computer Science and Engineering, Changchun University of Technology, Changchun 130051, China.
Hao ZhangSchool of Information Science and Engineering (School of Software), Yanshan University, Qinhuangdao 066000, China.
Chencai WangCollege of Computer Science and Engineering, Changchun University of Technology, Changchun 130051, China.
Shengyang ZhouCollege of Computer Science and Engineering, Changchun University of Technology, Changchun 130051, China.
Li ZhangCollege of Computer Science and Engineering, Changchun University of Technology, Changchun 130051, China.
Han WangSchool of Information Science and Technology, Institute of Computational Biology, Northeast Normal University, Changchun 130117, China.ORCID 0000-0002-4302-1886

Funding

Fundamental Research Funds for the Central Universities 2412023YQ002Jilin Scientific and Technological Development Program 20230201090GXNational Natural Science Foundation of China 62372099
6 · The paper itself

Abstract

The aging process will lead to a gradual functional decline in the human body, and even accelerate a significantly increased risk of degenerative diseases. DNA methylation patterns change markedly with one's age, serving as a biomarker of biological age and closely linked to the occurrence and progression of age-related diseases. Currently, diagnostic methods for individual degenerative diseases are relatively mature. However, aging often accompanies the onset of multiple degenerative diseases, presenting certain limitations in existing diagnostic models. Additionally, some identified DNA methylation biomarkers are typically applicable to only one or a few types of cancer or diseases, further restricting their utility. We endeavor to screen for biomarkers associated with multiple degenerative diseases from the perspective of aging-related co-morbid mechanisms and to perform multiple degenerative disease diagnoses. In this study, we explored research based on methylation correlations and patterns to investigate shared mechanisms across multiple degenerative diseases, identifying a set of biomarkers associated with them. We validated these biomarkers with biological omics analysis and the prediction of multiple classes of degenerative diseases, screened the biomarkers from 600 to 110 by biological omics analysis, and demonstrated the validity and predictive ability of the screened 110 biomarkers. We propose a disease diagnostic model based on a multi-scale one-dimensional convolutional neural network (MSDCNN) and a multi-class degenerative disease prediction model (ResDegNet). The two models are well trained and tested to accurately diagnose diseases and categorize four types of degenerative diseases. The research identified 110 biomarkers associated with degenerative diseases, providing a foundation for further exploration of age-related degenerative conditions. This work aims to facilitate early diagnosis, the identification of biomarkers, and the development of therapeutic targets for drug interventions.

Indexed as

BiomarkersDNA MethylationNeurodegenerative DiseasesAgingHumansNeural Networks, ComputerBiomarkersbiomarkerdegenerative diseaseDNA methylation

Identifiers

PMID39796173
PMCPMC11719970

What Socratic holds

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LicenceCC BY
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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.