Evidence map›Paper›PMID 37510393›Full record

ArticleGenes2023

The Effect of DNA Methylation in the Development and Progression of Chronic Kidney Disease in the General Population: An Epigenome-Wide Association Study Using the Korean Genome and Epidemiology Study Database.

Ji-Eun Kim, Min-Jee Jo, Eunjung Cho, Shin-Young Ahn, Young-Joo Kwon, Jeong-An Gim, Gang-Jee Ko

Open access · goldAbstract read
In one paragraph

Article in Genes, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. 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

7 authors at 1 institution in 1 country.

Ji-Eun KimDepartment of Internal Medicine, Korea University Guro Hospital, Seoul 08308, Republic of Korea.ORCID 0000-0003-3094-2229
Min-Jee JoDepartment of Internal Medicine, Korea University Guro Hospital, Seoul 08308, Republic of Korea.
Eunjung ChoDepartment of Internal Medicine, Korea University Guro Hospital, Seoul 08308, Republic of Korea.
Shin-Young AhnDepartment of Internal Medicine, Korea University Guro Hospital, Seoul 08308, Republic of Korea.ORCID 0000-0002-6844-0614
Young-Joo KwonDepartment of Internal Medicine, Korea University Guro Hospital, Seoul 08308, Republic of Korea.
Jeong-An GimMedical Science Research Center, Korea University College of Medicine, Korea University Guro Hospital, Seoul 08308, Republic of Korea.
Gang-Jee KoDepartment of Internal Medicine, Korea University Guro Hospital, Seoul 08308, Republic of Korea.ORCID 0000-0001-7927-8651
Korea University Medical Center · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAlthough knowledge of the genetic factors influencing kidney disease is increasing, epigenetic profiles, which are associated with chronic kidney disease (CKD), have not been fully elucidated. We sought to identify the DNA methylation status of CpG sites associated with reduced kidney function and examine whether the identified CpG sites are associated with CKD development.

methodWe analyzed DNA methylation patterns of 440 participants in the Korean Genome and Epidemiology Study (KoGES) with estimated glomerular filtration rates (eGFRs) ≥ 60 mL/min/1.73 m

resultsIn the CKD prediction analysis, methylation profiles of a total of 403,129 CpG sites were evaluated at baseline in 440 participants, and increased and decreased methylation of 268 and 189 CpG sites, respectively, were significantly correlated with the development of CKD in multivariable logistic regression. During kidney function slope analysis using follow-up methylation profiles of 49 participants, the percent methylation changes in 913 CpG sites showed a linear relationship with the percent change in eGFR during 8 years. During functional enrichment analyses for significant CpG sites found in the CKD prediction and kidney function slope analyses, we found that those CpG sites represented MAPK, PI3K/Akt, and Rap1 pathways. In addition, three CpG sites from three genes,

conclusionIt is suggested that DNA methylation on specific genes is associated with the development of CKD and the deterioration of kidney function.

Indexed as

DNA MethylationRenal Insufficiency, ChronicEpigenomeHumansPhosphatidylinositol 3-KinasesRepublic of KoreaPhosphatidylinositol 3-KinasesCHCHD4chronic kidney diseaseDNA methylationNPHS2

Identifiers

PMID37510393
PMCPMC10379047
OpenAlexW4385225615

What OpenQuestion 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 OpenQuestion graph.