Evidence map›Paper›PMID 42062633›Full record

ArticleMolecular neurobiology2026

MicroRNA-mRNA Regulatory Network Associated with Cognitive Impairment in Multiple Sclerosis.

Bruna De Felice, Federica Farinella, Giuseppe Romano, Concetta Montanino, Simona Bonavita, Deborah Archetto, Elisabetta Maida, Simona Raimo, Giacomo Lus, Maria Cropano and 2 more

Abstract read
In one paragraph

Article in Molecular neurobiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Bruna De FeliceDepartment of Environmental, Biological and Pharmaceutical Sciences and Technologies, University of Campania Luigi Vanvitelli, Caserta, Italy. bruna.defelice@unicampania.it.ORCID http://orcid.org/0000-0002-9132-5569
Federica FarinellaDepartment of Environmental, Biological and Pharmaceutical Sciences and Technologies, University of Campania Luigi Vanvitelli, Caserta, Italy.
Giuseppe RomanoDepartment of Advanced Medical and Surgical Sciences, University of Campania "Luigi Vanvitelli", Via Vivaldi 43, 81100, Caserta, Italy.
Concetta MontaninoDepartment of Environmental, Biological and Pharmaceutical Sciences and Technologies, University of Campania Luigi Vanvitelli, Caserta, Italy.
Simona BonavitaDepartment of Advanced Medical and Surgical Sciences, University of Campania "Luigi Vanvitelli", Via Vivaldi 43, 81100, Caserta, Italy.
Deborah ArchettoDepartment of Advanced Medical and Surgical Sciences, University of Campania "Luigi Vanvitelli", Via Vivaldi 43, 81100, Caserta, Italy.
Elisabetta MaidaDepartment of Advanced Medical and Surgical Sciences, University of Campania "Luigi Vanvitelli", Via Vivaldi 43, 81100, Caserta, Italy.
Simona RaimoDepartment of Medical and Surgical Sciences, "Magna Graecia" University of Catanzaro, Catanzaro, Italy.
Giacomo LusDepartment of Advanced Medical and Surgical Sciences, University of Campania "Luigi Vanvitelli", Via Vivaldi 43, 81100, Caserta, Italy.
Maria CropanoDepartment of Advanced Medical and Surgical Sciences, University of Campania "Luigi Vanvitelli", Via Vivaldi 43, 81100, Caserta, Italy.
Cinzia CoppolaDepartment of Advanced Medical and Surgical Sciences, University of Campania "Luigi Vanvitelli", Via Vivaldi 43, 81100, Caserta, Italy.
Elisabetta SignorielloDepartment of Advanced Medical and Surgical Sciences, University of Campania "Luigi Vanvitelli", Via Vivaldi 43, 81100, Caserta, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cognitive impairment (CI) is a frequent and disabling manifestation of multiple sclerosis (MS), yet its molecular underpinnings remain poorly understood. This study aimed to identify microRNA (miRNA) signatures and related gene expression changes associated with CI in MS. Forty-six people with MS underwent clinical, radiological, and cognitive assessment. Peripheral blood mononuclear cells were collected for miRNA profiling using the miRCURY LNA miRNA Focus PCR Panel and validated through RT-qPCR. Experimentally validated miRNA target genes were retrieved using miRWalk with miRTarBase filtering. Target networks were constructed in Cytoscape, followed by protein-protein interaction analysis using STRING and functional enrichment analysis with database for annotation, visualization, and integrated discovery (DAVID) ( https://davidbioinformatics.nih.gov/ ). Selected target genes were further evaluated by gene expression analysis. The results showed that three miRNAs (i.e., miR-146a-5p, miR-let-7a-5p, and miR-21-5p) were significantly dysregulated in patients with MS with CI compared to those with preserved cognition. Gene expression analysis identified differential regulations of IL-1B, IL-6, SLC16A10, and NEFL, supporting the involvement of inflammatory and neurodegenerative pathways. Correlation analyses indicated specific miRNA-mRNA relationships underlying these alterations. These findings suggest that the combined dysregulation of miR-146a-5p and miR-21-5p, together with their target genes, constitutes a molecular signature associated with CI in MS. This profile could contribute to the development of miRNA-based biomarkers for early detection and monitoring of cognitive dysfunction in MS.

Indexed as

Cognitive DysfunctionGene Regulatory NetworksMicroRNAsMultiple SclerosisRNA, MessengerAdultFemaleGene Expression ProfilingGene Expression RegulationHumansMaleMiddle AgedMicroRNAsRNA, MessengerCognitive impairmentMicroRNAsMRNAsMultiple sclerosis

Identifiers

PMID42062633
PMCPMC13132931

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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.