Evidence map›Paper›PMID 34201498›Full record

ArticleInternational journal of molecular sciences2021

CD163 as a Potential Biomarker of Monocyte Activation in Ischemic Stroke Patients.

Rosaria Greco, Chiara Demartini, Anna Maria Zanaboni, Elena Tumelero, Alessandra Persico, Elisa Candeloro, Andrea Morotti, Diana Amantea, Cristina Tassorelli

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 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

19 citing papers in PubMed, 26 citations in OpenAlex.

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  19. Ischemic Brain Neurodegeneration.International journal of molecular sciences · 2022
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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

9 authors at 4 institutions in 1 country.

Rosaria GrecoIRCCS Mondino Foundation, Via Mondino 2, 27100 Pavia, Italy.
Chiara DemartiniIRCCS Mondino Foundation, Via Mondino 2, 27100 Pavia, Italy.
Anna Maria ZanaboniIRCCS Mondino Foundation, Via Mondino 2, 27100 Pavia, Italy.
Elena TumeleroIRCCS Mondino Foundation, Via Mondino 2, 27100 Pavia, Italy.
Alessandra PersicoIRCCS Mondino Foundation, Via Mondino 2, 27100 Pavia, Italy.
Elisa CandeloroDepartment of Neurology and Stroke Unit, Neurology and Stroke Units, ASST-Settelaghi, Ospedale di Circolo Varese, Viale Borri 57, 21100 Varese, Italy.
Andrea MorottiNeurology Unit, Department of Neurological Sciences and Vision, ASST-Ospedali Civili, 25121 Brescia, Italy.
Diana AmanteaSection of Preclinical and Translational Pharmacology, Department of Pharmacy, Health and Nutritional Sciences, University of Calabria, 87036 Rende, Italy.ORCID 0000-0002-7513-3495
Cristina TassorelliIRCCS Mondino Foundation, Via Mondino 2, 27100 Pavia, Italy.
University of Pavia · ITFondazione Audiologica Varese · ITUniversity of Brescia · ITUniversity of Calabria · IT

Funding

Italian Ministry of Health RC2017-2019
6 · The paper itself

Abstract

In ischemic stroke patients, a higher monocyte count is associated with disease severity and worse prognosis. The complex correlation between subset phenotypes and functions underscores the importance of clarifying the role of monocyte subpopulations. We examined the subtype-specific distribution of the CD163+ and CD80+ circulating monocytes and evaluated their association with the inflammatory status in 26 ischemic stroke patients and 16 healthy controls. An increased percentage of CD163+/CD16+ and CD163+/CD14++ events occurred 24 and 48 h after a stroke compared to the controls. CD163+ expression was more pronounced in CD16+ non-classical and intermediate monocytes, as compared to CD14+ classical subtype, 24 h after stroke. Conversely, the percentage of CD80+/CD16+ events was unaffected in patients; meanwhile, the percentage of CD80+/CD14+ events significantly increased only 24 h after stroke. Interleukin (IL)-1beta, TNF-alpha, and IL-4 mRNA levels were higher, while IL-10 mRNA levels were reduced in total monocytes from patients versus controls, at either 24 h or 48 h after stroke. The percentage of CD163+/CD16+ events 24 h after stroke was positively associated with NIHSS score and mRS at admission, suggesting that stroke severity and disability are relevant triggers for CD163+ expression in circulating CD16+ monocytes.

Indexed as

AgedAged, 80 and overAntigens, CDAntigens, Differentiation, MyelomonocyticB7-1 AntigenBiomarkersCase-Control StudiesCD163 AntigenCross-Sectional StudiesCytokinesFemaleGPI-Linked ProteinsHumansIschemic StrokeMaleMiddle AgedAntigens, CDAntigens, Differentiation, MyelomonocyticB7-1 AntigenBiomarkersCD163 AntigenCD80 protein, humanCytokinesFCGR3B protein, humanGPI-Linked ProteinsReceptors, Cell SurfaceReceptors, IgGacute ischemic strokeCD163+CD80+cytokinesperipheral blood monocytes

Identifiers

PMID34201498
PMCPMC8268853
OpenAlexW3175959703

What OpenQuestion 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 OpenQuestion graph.