Evidence map›Paper›PMID 37298088›Full record

SynthesisInternational journal of molecular sciences2023

DNA Methylation Biomarkers for Young Children with Idiopathic Autism Spectrum Disorder: A Systematic Review.

Andrea Stoccoro, Eugenia Conti, Elena Scaffei, Sara Calderoni, Fabio Coppedè, Lucia Migliore, Roberta Battini

Open access · goldAbstract readSystematic Review
In one paragraph

Synthesis in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
4.6field-weighted citation impact, top 5% 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

16 citing papers in PubMed, 26 citations in OpenAlex.

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  13. Decoding the genetic landscape of autism: A comprehensive review.World journal of clinical pediatrics · 2024
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  15. 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 2 institutions in 1 country.

Andrea StoccoroDepartment of Translational Research and of New Surgical and Medical Technologies, University of Pisa, 56100 Pisa, Italy.ORCID 0000-0002-6768-8466
Eugenia ContiDepartment of Developmental Neuroscience, IRCCS Stella Maris Foundation, 56128 Pisa, Italy.
Elena ScaffeiDepartment of Developmental Neuroscience, IRCCS Stella Maris Foundation, 56128 Pisa, Italy.ORCID 0000-0002-7941-362X
Sara CalderoniDepartment of Developmental Neuroscience, IRCCS Stella Maris Foundation, 56128 Pisa, Italy.ORCID 0000-0002-6250-5739
Fabio CoppedèDepartment of Translational Research and of New Surgical and Medical Technologies, University of Pisa, 56100 Pisa, Italy.ORCID 0000-0002-3081-6647
Lucia MiglioreDepartment of Translational Research and of New Surgical and Medical Technologies, University of Pisa, 56100 Pisa, Italy.
Roberta BattiniDepartment of Developmental Neuroscience, IRCCS Stella Maris Foundation, 56128 Pisa, Italy.
University of Pisa · ITFondazione Stella Maris · IT

Funding

Ministero della Salute Ricerca Corrente 2020 to IRCCS Fondazione Stella MarisUniversity of Pisa Bando PRA-Progetti di Ricerca di Ateneo" (Institutional Research Grants) 2020-2021 "Multimod-al non-invasive approach in young females with autism and their parents: a feasibility study
6 · The paper itself

Abstract

Autism spectrum disorder (ASD) is a complex neurodevelopmental condition, the underlying pathological mechanisms of which are not yet completely understood. Although several genetic and genomic alterations have been linked to ASD, for the majority of ASD patients, the cause remains unknown, and the condition likely arises due to complex interactions between low-risk genes and environmental factors. There is increasing evidence that epigenetic mechanisms that are highly sensitive to environmental factors and influence gene function without altering the DNA sequence, particularly aberrant DNA methylation, are involved in ASD pathogenesis. This systematic review aimed to update the clinical application of DNA methylation investigations in children with idiopathic ASD, investigating its potential application in clinical settings. To this end, a literature search was performed on different scientific databases using a combination of terms related to the association between peripheral DNA methylation and young children with idiopathic ASD; this search led to the identification of 18 articles. In the selected studies, DNA methylation is investigated in peripheral blood or saliva samples, at both gene-specific and genome-wide levels. The results obtained suggest that peripheral DNA methylation could represent a promising methodology in ASD biomarker research, although further studies are needed to develop DNA-methylation-based clinical applications.

Indexed as

Autism Spectrum DisorderDNA MethylationBiomarkersChildChild, PreschoolEpigenesis, GeneticHumansPhenotypeBiomarkersautism spectrum disorderDNA methylationepigeneticsidiopathic ASDperipheral biomarkers

Identifiers

PMID37298088
PMCPMC10252672
OpenAlexW4377820723

What OpenQuestion holds

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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.