Evidence map›Paper›PMID 40607503›Full record

SynthesisEpigenomics2025

DNA methylation studies in mouse models of depression: a systematic review.

Mohammad Mustakim Billah, Chu Guo, Kazunari Mizuno, Yutaka Nakachi, Miki Bundo, Kazuya Iwamoto

Abstract readSystematic Review
In one paragraph

Synthesis in Epigenomics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

6 authors.

Mohammad Mustakim BillahDepartment of Molecular Brain Sciences, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.
Chu GuoDepartment of Molecular Brain Sciences, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.
Kazunari MizunoDepartment of Molecular Brain Sciences, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.
Yutaka NakachiDepartment of Molecular Brain Sciences, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.ORCID 0000-0003-1964-2495
Miki BundoDepartment of Molecular Brain Sciences, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.ORCID 0000-0002-5786-0509
Kazuya IwamotoDepartment of Molecular Brain Sciences, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.ORCID 0000-0002-1780-692X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMajor depression (MD) is caused by both genetic and environmental factors. Epigenetic mechanisms, particularly DNA methylation (5mC) and hydroxymethylation (5hmC), are thought to mediate gene - environment interactions. However, findings in mouse models remain dispersed.

objectiveThis review evaluates the studies on 5mC and 5hmC in mouse models of depression.

methodsWe systematically searched PubMed, Scopus, and Web of Science using terms related to 5mC/5hmC, depression, and mouse, until December 2024. We grouped the articles as candidate, global, cellular, and comprehensive studies and summarized the findings accordingly.

resultsSixty-eight studies met inclusion criteria. The main findings were environmental models, especially chronic stress paradigms, which were most frequently used to induce depression models. Candidate gene studies focused on Bdnf and Nr3c1, while global and cellular assays revealed both regional and widespread 5mC/5hmC changes. Genome-wide approaches revealed that epigenetic changes are not limited to isolated loci rather affect broad genomic regions involved in neural development and plasticity.

conclusionThis review provides a comprehensive summary of existing research on epigenetic changes in terms of DNA methylation in mouse models of depression. Broader application of standardized, integrative, and cell-type-specific approaches is needed to fully elucidate the role of epigenetic regulation in the pathology of MD.

Indexed as

DepressionDNA MethylationEpigenesis, GeneticMajor Depressive Disorder5-MethylcytosineAnimalsDisease Models, AnimalHumansMice5-MethylcytosinedepressionDNA methylationhydroxymethylationmicestress

Identifiers

PMID40607503
PMCPMC12330240

What Socratic holds

Textmetadata
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.