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

SOD1 TDP-43 amyotrophic lateral sclerosis biomarkers disease progression microvesicles

Journal

Frontiers in neuroscience
ISSN: 1662-4548
Titre abrégé: Front Neurosci
Pays: Switzerland
ID NLM: 101478481

Informations de publication

Date de publication:
2019
Historique:
received: 20 12 2018
accepted: 25 03 2019
entrez: 1 5 2019
pubmed: 1 5 2019
medline: 1 5 2019
Statut: epublish

Résumé

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

Identifiants

pubmed: 31037054
doi: 10.3389/fnins.2019.00344
pmc: PMC6476347
doi:

Types de publication

Journal Article

Langues

eng

Pagination

344

Subventions

Organisme : Motor Neurone Disease Association
ID : MALASPINA/APR13/817-791
Pays : United Kingdom
Organisme : Motor Neurone Disease Association
ID : TURNER/OCT15/972-797
Pays : United Kingdom

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Auteurs

Daisy Sproviero (D)

Genomic and Post-Genomic Center, IRCCS Mondino Foundation, Pavia, Italy.

Sabrina La Salvia (S)

Genomic and Post-Genomic Center, IRCCS Mondino Foundation, Pavia, Italy.

Federico Colombo (F)

Flow Cytometry and Cell Sorting Unit, Humanitas Clinical and Research Center - IRCCS, Rozzano, Italy.

Susanna Zucca (S)

Genomic and Post-Genomic Center, IRCCS Mondino Foundation, Pavia, Italy.

Orietta Pansarasa (O)

Genomic and Post-Genomic Center, IRCCS Mondino Foundation, Pavia, Italy.

Luca Diamanti (L)

Department of Brain and Behavioral Sciences, University of Pavia, Pavia, Italy.
Division of General Neurology, IRCCS Mondino Foundation, Pavia, Italy.

Alfredo Costa (A)

Department of Brain and Behavioral Sciences, University of Pavia, Pavia, Italy.
Division of General Neurology, IRCCS Mondino Foundation, Pavia, Italy.

Luca Lova (L)

Department of Brain and Behavioral Sciences, University of Pavia, Pavia, Italy.
Becton Dickinson Italia S.p.A., Milan, Italy.

Marta Giannini (M)

Genomic and Post-Genomic Center, IRCCS Mondino Foundation, Pavia, Italy.
Department of Brain and Behavioral Sciences, University of Pavia, Pavia, Italy.

Stella Gagliardi (S)

Genomic and Post-Genomic Center, IRCCS Mondino Foundation, Pavia, Italy.

Eliana Lauranzano (E)

Laboratory of Pharmacology and Brain Pathology, Humanitas Clinical and Research Center - IRCCS, Rozzano, Italy.

Michela Matteoli (M)

Laboratory of Pharmacology and Brain Pathology, Humanitas Clinical and Research Center - IRCCS, Rozzano, Italy.
IN-CNR, Milan, Italy.

Mauro Ceroni (M)

Department of Brain and Behavioral Sciences, University of Pavia, Pavia, Italy.
Division of General Neurology, IRCCS Mondino Foundation, Pavia, Italy.

Andrea Malaspina (A)

Neurodegeneration Group, Centre for Neuroscience and Trauma, Blizard Institute, Queen Mary University of London, London, United Kingdom.

Cristina Cereda (C)

Genomic and Post-Genomic Center, IRCCS Mondino Foundation, Pavia, Italy.

Classifications MeSH