Evidence map›Paper›PMID 33143364›Full record

ReviewInternational journal of molecular sciences2020

DNA Methylation in Nonalcoholic Fatty Liver Disease.

Jeongeun Hyun, Youngmi Jung

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed
9.2field-weighted citation impact, top 1% 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

66 citing papers in PubMed, 102 citations in OpenAlex.

  1. Review
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  15. NORE1A loss promotes MASLD/MASH.Transgenic research · 2024
    Article
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6 more citing papers are in PubMed but not listed here.

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 1 country.

Jeongeun HyunInstitute of Tissue Regeneration Engineering (ITREN), Dankook University, Cheonan 31116, Korea.ORCID 0000-0003-1144-2552
Youngmi JungDepartment of Integrated Biological Science, Pusan National University, Pusan 46241, Korea.
Dankook University · KRPusan National University · KR

Funding

National Research Foundation of Korea 2018R1A2A3075038National Research Foundation of Korea 2020R1F1A1073695
6 · The paper itself

Abstract

Nonalcoholic fatty liver disease (NAFLD) is a widespread hepatic disorder in the United States and other Westernized countries. Nonalcoholic steatohepatitis (NASH), an advanced stage of NAFLD, can progress to end-stage liver disease, including cirrhosis and liver cancer. Poor understanding of mechanisms underlying NAFLD progression from simple steatosis to NASH has limited the development of effective therapies and biomarkers. An accumulating body of studies has suggested the importance of DNA methylation, which plays pivotal roles in NAFLD pathogenesis. DNA methylation signatures that can affect gene expression are influenced by environmental and lifestyle experiences such as diet, obesity, and physical activity and are reversible. Hence, DNA methylation signatures and modifiers in NAFLD may provide the basis for developing biomarkers indicating the onset and progression of NAFLD and therapeutics for NAFLD. Herein, we review an update on the recent findings in DNA methylation signatures and their roles in the pathogenesis of NAFLD and broaden people's perspectives on potential DNA methylation-related treatments and biomarkers for NAFLD.

Indexed as

DNA MethylationEpigenesis, GeneticGene Expression RegulationAnimalsDisease ProgressionHumansNon-alcoholic Fatty Liver Disease5-hydroxymethylcytosine (5-hmC)5-methylcytosine (5-mC)biomarkercytosine-phospho-guanine dinucleotide (CpG)DNA methylationDNA methyltransferase (DNMT)epigeneticsnonalcoholic fatty liver disease (NAFLD)nonalcoholic steatohepatitis (NASH)ten eleven translocation (TET)

Identifiers

PMID33143364
PMCPMC7662478
OpenAlexW3096106003

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.