Evidence map›Paper›PMID 40804668›Full record

ReviewBMC nephrology2025

DNA methylation in chronic kidney disease.

Ye Cheng, Pei Liu, Guiling Xie, Wenjun Li, Huan Jing, Yanna Chen, Hongtao Chen, Youlin Fan, Jun Zhou

Abstract readReview
In one paragraph

Review in BMC nephrology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. 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

9 authors.

Ye Cheng *Department of Anesthesiology, The Third Affiliated Hospital of Southern Medical University, Guangzhou, Guangdong Province, China.
Pei Liu *Department of Anesthesiology, The Third Affiliated Hospital of Southern Medical University, Guangzhou, Guangdong Province, China.
Guiling XieDepartment of Anesthesiology, The Third Affiliated Hospital of Southern Medical University, Guangzhou, Guangdong Province, China.
Wenjun LiDepartment of Anesthesiology, The Third Affiliated Hospital of Southern Medical University, Guangzhou, Guangdong Province, China.
Huan JingDepartment of Anesthesiology, The First People's Hospital of Foshan, Foshan, Guangdong Province, China.
Yanna ChenDepartment of Anesthesiology, The Third Affiliated Hospital of Southern Medical University, Guangzhou, Guangdong Province, China.
Hongtao ChenDepartment of Anesthesiology, The Eighth People's Hospital of Guangzhou, Guangzhou, Guangdong Province, China.
Youlin FanDepartment of Anesthesiology, Guangzhou Panyu Central Hospital of Panyu District, Guangzhou, Guangdong Province, China.
Jun ZhouDepartment of Anesthesiology, The Third Affiliated Hospital of Southern Medical University, Guangzhou, Guangdong Province, China. zhounjun7843@126.com.

Funding

Natural Science Foundation of Guangdong Province 2019A1515011087Natural Science Foundation of Guangdong Province 2021A1515012453Natural Science Foundation of Xinjiang Uygur Autonomous Region (2018D01C016
6 · The paper itself

Abstract

Chronic kidney disease (CKD) is a condition that affects people on a global scale. After various stages of progression, CKD is finally characterized by renal fibrosis. As the most pervasive and well-studied epigenetic modification, DNA methylation has recently been associated with the development of renal fibrosis. Gaining a better understanding of the link between DNA methylation and CKD would provide new targets or enable the development of epigenetic therapies for CKD. This review discusses the mechanisms by which DNA methylation regulates gene expression during the pathological process of CKD, including the role of DNA methyltransferases (DNMTs). This review summarizes DNA methylation in CKD, particularly its crucial role in CKD-related conditions, such as diabetic kidney disease (DKD) and chronic allograft injury. Conventional demethylating agents have been discussed as well as the need for less toxic demethylating agents for clinical applications. Finally, some of the problems and obstacles specified in previous DNA methylation studies have been considered. This information aims to promote further investigations into the role of DNA methylation in CKD by providing novel insights into the mechanism by which methylation affects the progression and regression of CKD, which would result in the development of alternate treatments.

Indexed as

DNA MethylationRenal Insufficiency, ChronicEpigenesis, GeneticHumansChronic allograft injuryChronic kidney diseaseDemethylating agentsDiabetic kidney diseaseDNA methyltransferasesRenal fibrosis

Identifiers

PMID40804668
PMCPMC12345035

What OpenQuestion holds

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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 OpenQuestion graph.