Evidence map›Paper›PMID 34510387›Full record

ArticleHuman cell2021

Role of long non-coding RNAs in Down syndrome patients: a transcriptome analysis study.

Michele Salemi, Rossella Cannarella, Giovanna Marchese, Maria Grazia Salluzzo, Maria Ravo, Concetta Barone, Mariangela Lo Giudice, Aldo E Calogero, Corrado Romano

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Article in Human cell, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.6field-weighted citation impact, top 39% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

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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

9 authors at 2 institutions in 1 country.

Michele Salemi *Oasi Research Institute-IRCCS, Troina, EN, Italy. micezia@tiscali.it.ORCID http://orcid.org/0000-0003-1075-8993
Rossella Cannarella *Department of Clinical and Experimental Medicine, University of Catania, Catania, Italy.
Giovanna MarcheseGenomix4Life Srl, Baronissi, SA, Italy.
Maria Grazia SalluzzoOasi Research Institute-IRCCS, Troina, EN, Italy.
Maria RavoGenomix4Life Srl, Baronissi, SA, Italy.
Concetta BaroneOasi Research Institute-IRCCS, Troina, EN, Italy.
Mariangela Lo GiudiceOasi Research Institute-IRCCS, Troina, EN, Italy.
Aldo E CalogeroDepartment of Clinical and Experimental Medicine, University of Catania, Catania, Italy.
Corrado RomanoOasi Research Institute-IRCCS, Troina, EN, Italy.
Oasi Maria SS · ITUniversity of Catania · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Down syndrome (DS) is defined by the presence of a third copy of chromosome 21. Several comorbidities can be found in these patients, such as intellectual disability (ID), muscle weakness, hypotonia, congenital heart disease, and autoimmune diseases. The molecular mechanisms playing a role in the development of such comorbidities are still unclear. The regulation and expression of genes that map to chromosome 21 are dynamic and complex, so it is important to perform global gene expression studies with high statistical power to fully characterize the transcriptome in DS patients. This study was undertaken to evaluate mRNAs and lncRNA expression in patients with DS versus a matched cohort of healthy subjects. RNA sequencing was used to perform this transcriptome study. Differential expression analysis revealed 967 transcripts with padj ≤ 0.05. Among them, 447 transcripts were differentially expressed in patients with DS compared to controls. Particularly, 203 transcripts were down expressed (151 protein-coding mRNAs, 45 lncRNAs, 1 microRNA, 1 mitochondrial tRNA, 1 ribozyme, and 1 small nuclear RNA) and 244 were over expressed (210 protein-coding mRNAs and 34 lncRNAs). Interestingly, deregulated lncRNAs are involved in pathways that play a role in developmental disorders, neurological diseases, DNA replication and repair mechanisms, and cancer development in DS patients. In conclusion, these results suggest a role of lncRNAs in the phenotype of DS patients.

Indexed as

AdultChromosomes, Human, Pair 21Cohort StudiesComorbidityDevelopmental DisabilitiesDNA RepairDNA ReplicationDown SyndromeFemaleGene Expression ProfilingHumansMaleMiddle AgedNeoplasmsNervous System DiseasesOligonucleotide Array Sequence AnalysisRNA, Long NoncodingRNA, MessengerDown syndromelncRNAsmRNAsRNA sequencingTranscriptome

Identifiers

PMID34510387
OpenAlexW3199866785

What OpenQuestion holds

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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.