Evidence map›Paper›PMID 36299516›Full record

ReviewHeliyon2022

Deciphering the role of aberrant DNA methylation in NAFLD and NASH.

Meenakshi Vachher, Savita Bansal, Bhupender Kumar, Sandeep Yadav, Archana Burman

Abstract readReview
In one paragraph

Review in Heliyon, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Liver, ageing and disease.Nature reviews. Gastroenterology & hepatology · 2025
    Review
  5. Article
  6. Review
  7. Review
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  15. Review
  16. Review
  17. Article
  18. Epigenetic Regulation in Lean Nonalcoholic Fatty Liver Disease.International journal of molecular sciences · 2023
    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

5 authors.

Meenakshi VachherDepartment of Biochemistry, Institute of Home Economics, University of Delhi, F-4 Hauz Khas Enclave, New Delhi, India.
Savita BansalDepartment of Biochemistry, Institute of Home Economics, University of Delhi, F-4 Hauz Khas Enclave, New Delhi, India.
Bhupender KumarDepartment of Biochemistry, Institute of Home Economics, University of Delhi, F-4 Hauz Khas Enclave, New Delhi, India.
Sandeep YadavDepartment of Biochemistry, Institute of Home Economics, University of Delhi, F-4 Hauz Khas Enclave, New Delhi, India.
Archana BurmanDepartment of Biochemistry, Institute of Home Economics, University of Delhi, F-4 Hauz Khas Enclave, New Delhi, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The global incidence of nonalcoholic fatty liver disease (NAFLD) is mounting incessantly, and it is emerging as the most frequent cause of chronic and end stage liver disorders. It is the starting point for a range of conditions from simple steatosis to more progressive nonalcoholic steatohepatitis (NASH) and associated hepatocellular carcinoma (HCC). Dysregulation of insulin secretion and dyslipidemia due to obesity and other lifestyle variables are the primary contributors to establishment of NAFLD. Onset and progression of NAFLD is orchestrated by an interplay of metabolic environment with genetic and epigenetic factors. An incompletely understood mechanism of NAFLD progression has greatly hampered the progress in identification of novel prognostic and therapeutic strategies. Emerging evidence suggests altered DNA methylation pattern as a key determinant of NAFLD pathogenesis. Environmental and lifestyle factors can manipulate DNA methylation patterns in a reversible manner, which manifests as changes in gene expression. In this review we attempt to highlight the importance of DNA methylation in establishment and progression of NAFLD. Development of novel diagnostic, prognostic and therapeutic strategies centered around DNA methylation signatures and modifiers has also been explored.

Indexed as

5-methyl cytosineCpG islandsDietDNA methylationDNA methyl Transferase (DNMT)EpigeneticsFibrosisNonalcoholic fatty liver disease (NAFLD)Nonalcoholic steatohepatitis (NASH)Ten-eleven translocation (TET) enzymes

Identifiers

PMID36299516
PMCPMC9589178

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.