Evidence map›Paper›PMID 33800495›Full record

ArticleInternational journal of molecular sciences2021

Different miRNA Profiles in Plasma Derived Small and Large Extracellular Vesicles from Patients with Neurodegenerative Diseases.

Daisy Sproviero, Stella Gagliardi, Susanna Zucca, Maddalena Arigoni, Marta Giannini, Maria Garofalo, Martina Olivero, Michela Dell'Orco, Orietta Pansarasa, Stefano Bernuzzi and 11 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed, 5 pooled it
4.5field-weighted citation impact, top 4% 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

49 citing papers in PubMed, 5 syntheses or guidelines pooled it, 74 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

21 authors at 6 institutions in 2 countries.

Daisy SprovieroGenomic and post-Genomic Unit, IRCCS Mondino Foundation, 27100 Pavia, Italy.ORCID 0000-0001-5061-683X
Stella GagliardiGenomic and post-Genomic Unit, IRCCS Mondino Foundation, 27100 Pavia, Italy.ORCID 0000-0002-6589-6907
Susanna ZuccaGenomic and post-Genomic Unit, IRCCS Mondino Foundation, 27100 Pavia, Italy.
Maddalena ArigoniDepartment of Molecular Biotechnology and Health Sciences, Bioinformatics and Genomics Unit, University of Turin, 10126 Turin, Italy.
Marta GianniniGenomic and post-Genomic Unit, IRCCS Mondino Foundation, 27100 Pavia, Italy.
Maria GarofaloGenomic and post-Genomic Unit, IRCCS Mondino Foundation, 27100 Pavia, Italy.
Martina OliveroDepartment of Oncology, University of Turin, 10060 Turin, Italy.
Michela Dell'OrcoDepartments of Neurosciences, University of New Mexico School of Medicine, Albuquerque, NM 87131, USA.ORCID 0000-0002-0742-7037
Orietta PansarasaGenomic and post-Genomic Unit, IRCCS Mondino Foundation, 27100 Pavia, Italy.ORCID 0000-0002-3041-0612
Stefano BernuzziImmunohematological and Transfusional Service and Centre of Transplantation Immunology, IRCCS "San Matteo Foundation", 27100 Pavia, Italy.
Micol AvenaliNeurorehabilitation Unit, IRCCS Mondino Foundation, 27100 Pavia, Italy.
Matteo Cotta RamusinoUnit of Behavioral Neurology, IRCCS Mondino Foundation, 27100 Pavia, Italy.ORCID 0000-0003-3090-9648
Luca DiamantiNeuro-Oncology Unit, IRCCS Mondino Foundation, 27100 Pavia, Italy.
Brigida MinafraParkinson Unit and Movement Disorders Mondino Foundation IRCCS, 27100 Pavia, Italy.
Giulia PeriniUnit of Behavioral Neurology, IRCCS Mondino Foundation, 27100 Pavia, Italy.
Roberta ZangagliaParkinson Unit and Movement Disorders Mondino Foundation IRCCS, 27100 Pavia, Italy.
Alfredo CostaDepartment of Brain and Behavioral Sciences, University of Pavia, 27100 Pavia, Italy.ORCID 0000-0001-7312-8011
Mauro CeroniDepartment of Brain and Behavioral Sciences, University of Pavia, 27100 Pavia, Italy.
Nora I Perrone-BizzozeroDepartments of Neurosciences and Psychiatry and Behavioral Health, University of New Mexico School of Medicine, Albuquerque, NM 87131, USA.
Raffaele A CalogeroDepartment of Molecular Biotechnology and Health Sciences, Bioinformatics and Genomics Unit, University of Turin, 10126 Turin, Italy.ORCID 0000-0002-2848-628X
Cristina CeredaGenomic and post-Genomic Unit, IRCCS Mondino Foundation, 27100 Pavia, Italy.
Italian institute for Genomic Medicine · ITUniversity of Pavia · ITFondazione Istituto Neurologico Nazionale Casimiro Mondino · ITUniversity of Turin · ITUniversity of New Mexico · USIstituti di Ricovero e Cura a Carattere Scientifico · IT

Funding

Fondazione Cariplo Association between frailty trajectories and biological markers of aging 2017-0557Fondazione Cariplo Extracellular vesicles in the pathogenesis of Frontotemporal Dementia 2017-0747Fondazione Regionale per la Ricerca Biomedica FRRB 2015-0023Ministero della Salute 5*1000Ministero della Salute Ricerca Corrente 2018-2020Ministero della Salute Young research project GR-2016-02361552
6 · The paper itself

Abstract

Identifying biomarkers is essential for early diagnosis of neurodegenerative diseases (NDs). Large (LEVs) and small extracellular vesicles (SEVs) are extracellular vesicles (EVs) of different sizes and biological functions transported in blood and they may be valid biomarkers for NDs. The aim of our study was to investigate common and different miRNA signatures in plasma derived LEVs and SEVs of Alzheimer's disease (AD), Parkinson's disease (PD), Amyotrophic Lateral Sclerosis (ALS) and Fronto-Temporal Dementia (FTD) patients. LEVs and SEVs were isolated from plasma of patients and healthy volunteers (CTR) by filtration and differential centrifugation and RNA was extracted. Small RNAs libraries were carried out by Next Generation Sequencing (NGS). MiRNAs discriminate all NDs diseases from CTRs and they can provide a signature for each NDs. Common enriched pathways for SEVs were instead linked to ubiquitin mediated proteolysis and Toll-like receptor signaling pathways and for LEVs to neurotrophin signaling and Glycosphingolipid biosynthesis pathway. LEVs and SEVs are involved in different pathways and this might give a specificity to their role in the spreading of the disease. The study of common and different miRNAs transported by LEVs and SEVs can be of great interest for biomarker discovery and for pathogenesis studies in neurodegeneration.

Indexed as

Gene Expression ProfilingSignal TransductionAgedAged, 80 and overCirculating MicroRNAExtracellular VesiclesFemaleHumansMaleMiddle AgedNeurodegenerative DiseasesCirculating MicroRNAAlzheimer’s diseaseamyotrophic lateral sclerosisfrontotemporal dementialarge extracellular vesiclesmiRNAsParkinson’s diseaseRNA-seqsmall extracellular vesicles

Identifiers

PMID33800495
PMCPMC7962970
OpenAlexW3133875348

What OpenQuestion holds

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LicenceCC BY
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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.