Evidence map›Paper›PMID 26073484›Full record

ArticleJournal of the neurological sciences2015

Blood circulating microparticle species in relapsing-remitting and secondary progressive multiple sclerosis. A case-control, cross sectional study with conventional MRI and advanced iron content imaging outcomes.

J S Alexander, R Chervenak, B Weinstock-Guttman, I Tsunoda, M Ramanathan, N Martinez, S Omura, F Sato, G V Chaitanya, A Minagar and 7 more

Open access · greenAbstract read
In one paragraph

Article in Journal of the neurological sciences, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

14 citing papers in PubMed, 28 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Dysregulated Sulfide Metabolism in Multiple Sclerosis: Serum and Vascular Endothelial Inflammatory Responses.Pathophysiology : the official journal of the International Society for Pathophysiology · 2022
    Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Short-Term High-Intensity Treadmill Exercise Promotes Ceramide-Dependent Extracellular Vesicle Secretion in the Central Nervous System of Mice.Medical science monitor : international medical journal of experimental and clinical research · 2021
    Article
  11. Review
  12. Extracellular Vesicles in Neuroinflammation.Frontiers in cell and developmental biology · 2020
    Review
  13. Article
  14. Article
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

17 authors at 6 institutions in 1 country.

J S AlexanderDepartment of Molecular and Cellular Physiology, Louisiana State University Health-Shreveport, LA, USA.
R ChervenakDepartment Microbiology & Immunology, Center for Molecular and Tumor Virology, Louisiana State University Health-Shreveport, LA, USA.
B Weinstock-GuttmanThe Jacobs Neurological Institute, Department of Neurology, University of Buffalo, Buffalo, NY, USA.
I TsunodaDepartment Microbiology & Immunology, Center for Molecular and Tumor Virology, Louisiana State University Health-Shreveport, LA, USA.
M RamanathanDepartment of Pharmaceutical Sciences, State University of New York, Buffalo, NY, USA.
N MartinezDepartment Microbiology & Immunology, Center for Molecular and Tumor Virology, Louisiana State University Health-Shreveport, LA, USA.
S OmuraDepartment Microbiology & Immunology, Center for Molecular and Tumor Virology, Louisiana State University Health-Shreveport, LA, USA.
F SatoDepartment Microbiology & Immunology, Center for Molecular and Tumor Virology, Louisiana State University Health-Shreveport, LA, USA.
G V ChaitanyaDepartment of Molecular and Cellular Physiology, Louisiana State University Health-Shreveport, LA, USA.
A MinagarDepartment of Neurology, Louisiana State University Health-Shreveport, LA, USA. Electronic address: aminag@lsuhsc.edu.
J McGeeDepartment of Neurology, Louisiana State University Health-Shreveport, LA, USA.
M H JenningsDepartment of Molecular and Cellular Physiology, Louisiana State University Health-Shreveport, LA, USA.
C MonceauxDepartment of Molecular and Cellular Physiology, Louisiana State University Health-Shreveport, LA, USA.
F BeckerDepartment of Molecular and Cellular Physiology, Louisiana State University Health-Shreveport, LA, USA; Department for General and Visceral Surgery, Muenster, Germany.
U CvekComputer Sciences Department, Louisiana State University-Shreveport, LA, USA.
M TrutschlComputer Sciences Department, Louisiana State University-Shreveport, LA, USA.
R ZivadinovThe Jacobs Neurological Institute, Department of Neurology, University of Buffalo, Buffalo, NY, USA; Buffalo Neuroimaging Analysis Center, Department of Neurology, University of Buffalo, Buffalo, NY, USA.
Louisiana State University Health Sciences Center Shreveport · USLouisiana State University · USLouisiana State University in Shreveport · USBuffalo Psychiatric Center · USJacobs Institute · USUniversity at Buffalo, State University of New York · US

Funding

COBRE Center for Molecular and Tumor VirologyP30GM110703 · NIGMS · LOUISIANA STATE UNIV HSC SHREVEPORT · PI SAPP, MARTIN · 2014 to 2018
$4.8M
Axonal degeneration can trigger demyelinating diseaseR21NS059724 · NINDS · UNIVERSITY OF UTAH · PI TSUNODA, IKUO · 2008 to 2009
$357k
NIGMS NIH HHS P30 GM110703NIGMS NIH HHS P30GM110703NINDS NIH HHS R21 NS059724
6 · The paper itself

Abstract

backgroundAlthough multiple sclerosis (MS) is thought to represent an excessive and inappropriate immune response to several central nervous system (CNS) autoantigens, increasing evidence also suggests that MS may also be a neurovascular inflammatory disease, characterized by endothelial activation and shedding of cell membrane microdomains known as 'microparticles' into the circulation.

objectiveTo investigate the relationships between these endothelial biomarkers and MS.

methodsWe examined the relative abundance of CD31(+)/PECAM-1, CD51(+)CD61(+) (αV-β3) and CD54(+) (ICAM-1) bearing microparticles in sera of healthy individuals, patients with relapsing-remitting MS, and secondary-progressive MS. We also investigated the correlation among circulating levels of different microparticle species in MS with conventional MRI (T2- and T1-lesion volumes and brain atrophy), as well as novel MR modalities [assessment of iron content on susceptibility-weighted imaging (SWI)-filtered phase].

resultsDifferences in circulating microparticle levels were found among MS groups, and several microparticle species (CD31(+)/CD51(+)/CD61(+)/CD54(+)) were found to correlate with conventional MRI and SWI features of MS.

conclusionThese results indicate that circulating microparticles' profiles in MS may support mechanistic roles for microvascular stress and injury which is an underlying contributor not only to MS initiation and progression, but also to pro-inflammatory responses.

Indexed as

AdultAntigens, CDBrainCase-Control StudiesCross-Sectional StudiesFemaleFlow CytometryHumansMagnetic Resonance ImagingMaleMiddle AgedMultiple Sclerosis, Chronic ProgressiveMultiple Sclerosis, Relapsing-RemittingSeverity of Illness IndexAntigens, CDAtrophyEndothelial microparticlesIron depositionMRIMultiple sclerosisSerum

Identifiers

PMID26073484
PMCPMC4550483
OpenAlexW1778415602

What OpenQuestion holds

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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.