Evidence map›Paper›PMID 39766772›Full record

ReviewGenes2024

Can Global DNA Methylation Be Influenced by Polymorphisms in Genes Involved in Epigenetic Mechanisms? A Review.

Naila Francis Paulo de Oliveira, Darlene Camati Persuhn, Maria Cristina Leme Godoy Dos Santos

Abstract readReview
In one paragraph

Review in Genes, 2024. 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. Article
  2. International journal of molecular medicine · 2026
    Review
  3. Article
  4. Review
  5. DNA Methylation ofBiology · 2025
    Article
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

3 authors.

Naila Francis Paulo de OliveiraDepartment of Molecular Biology, Center for Exact and Natural Sciences, Federal University of Paraíba-UFPB, João Pessoa 58051-900, PB, Brazil.ORCID 0000-0002-0855-2518
Darlene Camati PersuhnDepartment of Molecular Biology, Center for Exact and Natural Sciences, Federal University of Paraíba-UFPB, João Pessoa 58051-900, PB, Brazil.ORCID 0000-0001-5291-5454
Maria Cristina Leme Godoy Dos SantosDepartment of Celular Biology, Federal University of Paraná-UFPR, Curitiba 80060-000, PR, Brazil.ORCID 0000-0002-0507-1604

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGlobal methylation refers to the total methylation in the DNA and can also be inferred from the Line 1 and Alu regions, as these repeats are very abundant in the genome. The main function of DNA methylation is to control gene expression and is associated with both normal and pathological mechanisms. DNA methylation depends on enzymes that generate the methyl radical (e.g., methylenetetrahydrofolate reductase-MTHFR) and attach this radical to the DNA (DNA methyltransferases-DNMT). Genetic variants such as single nucleotide polymorphisms (SNP) in these genes can lead to changes in the activity or expression of MTHFR and DNMT proteins and consequently influence the DNA methylation profile. This review focuses on studies investigating inter-individual variations in the global DNA methylation profile associated with genetic polymorphisms in the

methodsA narrative review was conducted, taking into account articles published in the last 15 years.

resultsIt was found that the SNPs rs1801131, rs1801133 and rs1537514 in the

conclusionsIt is concluded that polymorphisms in the

Indexed as

DNA MethylationEpigenesis, GeneticMethylenetetrahydrofolate Reductase (NADPH2)Polymorphism, Single NucleotideDNA (Cytosine-5-)-MethyltransferasesHumansDNA (Cytosine-5-)-MethyltransferasesMethylenetetrahydrofolate Reductase (NADPH2)MTHFR protein, humanDNA methylationDNMTepigeneticgeneticglobal methylationMTHFRpolymorphism

Identifiers

PMID39766772
PMCPMC11675890

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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.