Evidence map›Paper›PMID 39061976›Full record

ArticleBiomedicines2024

Transcriptome Study in Sicilian Patients with Autism Spectrum Disorder.

Michele Salemi, Francesca A Schillaci, Giuseppe Lanza, Giovanna Marchese, Maria Grazia Salluzzo, Angela Cordella, Salvatore Caniglia, Maria Grazia Bruccheri, Anna Truda, Donatella Greco and 2 more

Abstract read
In one paragraph

Article in Biomedicines, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. 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

12 authors.

Michele SalemiOasi Research Institute-IRCCS, 94018 Troina, Italy.
Francesca A SchillaciOasi Research Institute-IRCCS, 94018 Troina, Italy.ORCID 0009-0004-7185-1176
Giuseppe LanzaOasi Research Institute-IRCCS, 94018 Troina, Italy.ORCID 0000-0002-5659-662X
Giovanna MarcheseGenomix4Life S.r.l., 84081 Baronissi, Italy.
Maria Grazia SalluzzoOasi Research Institute-IRCCS, 94018 Troina, Italy.
Angela CordellaGenomix4Life S.r.l., 84081 Baronissi, Italy.ORCID 0000-0001-9784-7010
Salvatore CanigliaOasi Research Institute-IRCCS, 94018 Troina, Italy.
Maria Grazia BruccheriOasi Research Institute-IRCCS, 94018 Troina, Italy.
Anna TrudaGenomix4Life S.r.l., 84081 Baronissi, Italy.
Donatella GrecoOasi Research Institute-IRCCS, 94018 Troina, Italy.
Raffaele FerriOasi Research Institute-IRCCS, 94018 Troina, Italy.ORCID 0000-0001-6937-3065
Corrado RomanoOasi Research Institute-IRCCS, 94018 Troina, Italy.ORCID 0000-0003-1049-0683

Funding

Italian Ministry of Health, Ricerca Corrente, grant number RC-2787064. RC-2787064
6 · The paper itself

Abstract

ASD is a complex condition primarily rooted in genetics, although influenced by environmental, prenatal, and perinatal risk factors, ultimately leading to genetic and epigenetic alterations. These mechanisms may manifest as inflammatory, oxidative stress, hypoxic, or ischemic damage. To elucidate potential variances in gene expression in ASD, a transcriptome analysis of peripheral blood mononuclear cells was conducted via RNA-seq on 12 ASD patients and 13 healthy controls, all of Sicilian ancestry to minimize environmental confounds. A total of 733 different statistically significant genes were identified between the two cohorts. Gene Set Enrichment Analysis (GSEA) and Gene Ontology (GO) terms were employed to explore the pathways influenced by differentially expressed mRNAs. GSEA revealed GO pathways strongly associated with ASD, namely the GO Biological Process term "Response to Oxygen-Containing Compound". Additionally, the GO Cellular Component pathway "Mitochondrion" stood out among other pathways, with differentially expressed genes predominantly affiliated with this specific pathway, implicating the involvement of different mitochondrial functions in ASD. Among the differentially expressed genes,

Indexed as

autism spectrum disordermRNAsRNA sequencingtranscriptome analysis

Identifiers

PMID39061976
PMCPMC11274004

What Socratic 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 Socratic graph.