Evidence map›Paper›PMID 31037054›Full record

ArticleFrontiers in neuroscience2019

Leukocyte Derived Microvesicles as Disease Progression Biomarkers in Slow Progressing Amyotrophic Lateral Sclerosis Patients.

Daisy Sproviero, Sabrina La Salvia, Federico Colombo, Susanna Zucca, Orietta Pansarasa, Luca Diamanti, Alfredo Costa, Luca Lova, Marta Giannini, Stella Gagliardi and 5 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in neuroscience, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

23 citing papers in PubMed, 32 citations in OpenAlex.

  1. TDP-43: [GU]-ardian of the transcriptome.Molecular neurodegeneration · 2026
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  7. Circulating GLASTFrontiers in molecular biosciences · 2024
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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

15 authors at 4 institutions in 2 countries.

Daisy SprovieroGenomic and Post-Genomic Center, IRCCS Mondino Foundation, Pavia, Italy.
Sabrina La SalviaGenomic and Post-Genomic Center, IRCCS Mondino Foundation, Pavia, Italy.
Federico ColomboFlow Cytometry and Cell Sorting Unit, Humanitas Clinical and Research Center - IRCCS, Rozzano, Italy.
Susanna ZuccaGenomic and Post-Genomic Center, IRCCS Mondino Foundation, Pavia, Italy.
Orietta PansarasaGenomic and Post-Genomic Center, IRCCS Mondino Foundation, Pavia, Italy.
Luca DiamantiDepartment of Brain and Behavioral Sciences, University of Pavia, Pavia, Italy.
Alfredo CostaDepartment of Brain and Behavioral Sciences, University of Pavia, Pavia, Italy.
Luca LovaDepartment of Brain and Behavioral Sciences, University of Pavia, Pavia, Italy.
Marta GianniniGenomic and Post-Genomic Center, IRCCS Mondino Foundation, Pavia, Italy.
Stella GagliardiGenomic and Post-Genomic Center, IRCCS Mondino Foundation, Pavia, Italy.
Eliana LauranzanoLaboratory of Pharmacology and Brain Pathology, Humanitas Clinical and Research Center - IRCCS, Rozzano, Italy.
Michela MatteoliLaboratory of Pharmacology and Brain Pathology, Humanitas Clinical and Research Center - IRCCS, Rozzano, Italy.
Mauro CeroniDepartment of Brain and Behavioral Sciences, University of Pavia, Pavia, Italy.
Andrea MalaspinaNeurodegeneration Group, Centre for Neuroscience and Trauma, Blizard Institute, Queen Mary University of London, London, United Kingdom.
Cristina CeredaGenomic and Post-Genomic Center, IRCCS Mondino Foundation, Pavia, Italy.
Center for Genomic Science · ITUniversity of Pavia · ITHumanitas University · ITQueen Mary University of London · GB

Funding

Motor Neurone Disease Association MALASPINA/APR13/817-791Motor Neurone Disease Association TURNER/OCT15/972-797
6 · The paper itself

Abstract

The lack of biomarkers in Amyotrophic Lateral Sclerosis (ALS) makes it difficult to determine the stage of the disease in patients and, therefore, it delays therapeutic trials. Microvesicles (MVs) are possible biomarkers implicated in physiological and pathological functions, however, their role in ALS remains unclear. We investigated whether plasma derived microvesicles could be overrepresented in a group of 40 patients affected by ALS compared to 28 Alzheimer's Disease (AD) patients and 36 healthy volunteers. Leukocyte derived MVs (LMVs) compared to endothelial, platelet, erythrocyte derived MVs, were mostly present in ALS patients compared to AD patients and healthy donors. Correlation analysis corrected for the presence of confounding variables (riluzole, age at onset, site of onset, gender) was tested between PRL (Progression Rate at the Last visit) and LMVs, and a statistically significant value was found (Pearson partial correlation

Indexed as

amyotrophic lateral sclerosisbiomarkersdisease progressionmicrovesiclesSOD1TDP-43

Identifiers

PMID31037054
PMCPMC6476347
OpenAlexW2937986807

What OpenQuestion holds

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LicenceCC BY
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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 OpenQuestion graph.