Evidence mapPaperPMID 39404430Full record

ArticleCells2024

Identification of

Valeria Lodde, Ignazio Roberto Zarbo, Gabriele Farina, Aurora Masia, Paolo Solla, Ilaria Campesi, Giuseppe Delogu, Maria Rosaria Muroni, Dimitrios Tsitsipatis, Myriam Gorospe and 2 more

Abstract read
In one paragraph

Article in Cells, 2024. 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
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

6 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. 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

12 authors.

Valeria LoddeDepartment of Biomedical Sciences, University of Sassari, Sassari 07100, Italy.ORCID 0000-0001-6904-1431
Ignazio Roberto ZarboDepartment of Medicine, Surgery and Pharmacy, University of Sassari, Sassari 07100, Italy.
Gabriele FarinaUnit of Clinical Neurology, AOU, Sassari 07100, Italy.
Aurora MasiaDepartment of Medicine, Surgery and Pharmacy, University of Sassari, Sassari 07100, Italy.
Paolo SollaDepartment of Medicine, Surgery and Pharmacy, University of Sassari, Sassari 07100, Italy.ORCID 0000-0002-2982-0665
Ilaria CampesiDepartment of Biomedical Sciences, University of Sassari, Sassari 07100, Italy.ORCID 0000-0002-1681-6448
Giuseppe DeloguDepartment of Biomedical Sciences, University of Sassari, Sassari 07100, Italy.
Maria Rosaria MuroniDepartment of Medicine, Surgery and Pharmacy, University of Sassari, Sassari 07100, Italy.
Dimitrios TsitsipatisLaboratory of Genetics and Genomics, National Institute on Aging Intramural Research Program, National Institutes of Health, Baltimore, MD 21224, USA.
Myriam GorospeLaboratory of Genetics and Genomics, National Institute on Aging Intramural Research Program, National Institutes of Health, Baltimore, MD 21224, USA.
Matteo FlorisDepartment of Biomedical Sciences, University of Sassari, Sassari 07100, Italy.ORCID 0000-0003-4385-9336
Maria Laura IddaDepartment of Biomedical Sciences, University of Sassari, Sassari 07100, Italy.

Funding

Fondazione Italiana Sclerosi Multipla Grant N. 2021/S/2
6 · The paper itself

Abstract

Multiple sclerosis (MS) is a demyelinating autoimmune disease characterized by early onset, for which the interaction of genetic and environmental factors is crucial. Dysregulation of the immune system as well as myelinization-de-myelinization has been shown to correlate with changes in RNA, including non-coding RNAs. Recently, circular RNAs (circRNAs) have emerged as a key player in the complex network of gene dysregulation associated with MS. Despite several efforts, the mechanisms driving circRNA regulation and dysregulation in MS still need to be properly elucidated. Here, we explore the panorama of circRNA expression in PBMCs purified from five newly diagnosed MS patients and five healthy controls (HCs) using the Arraystar Human circRNAs microarray. Experimental validation was then carried out in a validation cohort, and a possible correlation with disease severity was tested. We identified 64 differentially expressed circRNAs, 53 of which were downregulated in PBMCs purified from MS compared to the HCs. The discovery dataset was subsequently validated using qRT-PCR with an independent cohort of 20 RRMS patients and 20 HCs. We validated seven circRNAs differentially expressed in the RRMS group versus the HC group.

Indexed as

BiomarkersLeukocytes, MononuclearMultiple SclerosisRNA, CircularAdultCase-Control StudiesFemaleGene Expression ProfilingGene Expression RegulationHumansMaleMiddle AgedBiomarkersRNA, Circularbiomarkerscircular RNAsimmune regulationmultiple sclerosisnew diagnosis

Identifiers

PMID39404430
PMCPMC11475351

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.