Evidence map›Paper›PMID 26277791›Full record

ArticleJournal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology2016

Targeted Stage-Specific Inflammatory microRNA Profiling in Urine During Disease Progression in Experimental Autoimmune Encephalomyelitis: Markers of Disease Progression and Drug Response.

Jaspreet Singh, Mandar Deshpande, Hamid Suhail, Ramandeep Rattan, Shailendra Giri

Abstract read
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In one paragraph

Article in Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 23% 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

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 48 citations in OpenAlex.

  1. Role of miR-155 in inflammatory autoimmune diseases: a comprehensive review.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2022
    Pooled it
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  14. MiR-155: An Important Regulator of Neuroinflammation.International journal of molecular sciences · 2021
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  18. microRNA and exosome profiling in multiple sclerosis.Multiple sclerosis (Houndmills, Basingstoke, England) · 2020
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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

5 authors at 1 institution in 1 country.

Jaspreet SinghDepartment of Neurology, E&R Building, Room 4051 Henry Ford Health System, Detroit, MI, 48202, USA.
Mandar DeshpandeDepartment of Neurology, E&R Building, Room 4051 Henry Ford Health System, Detroit, MI, 48202, USA.
Hamid SuhailDepartment of Neurology, E&R Building, Room 4051 Henry Ford Health System, Detroit, MI, 48202, USA.
Ramandeep RattanDepartment of Neurology, E&R Building, Room 4051 Henry Ford Health System, Detroit, MI, 48202, USA.
Shailendra GiriDepartment of Neurology, E&R Building, Room 4051 Henry Ford Health System, Detroit, MI, 48202, USA. SGIRI1@hfhs.org.
Henry Ford Health System · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recently, microRNAs (miRNAs) have been implicated in regulating neuroinflammatory and demyelinative responses in multiple sclerosis (MS) and its mouse model of experimental autoimmune encephalomyelitis (EAE). miRNAs have also been studied as biomarkers of disease pathology and drug-response in MS. However, no complete miRNA profiling at various stages of EAE disease has been examined, especially in the urine. We carried out a systematic analysis of miRNAs in the urine exosomes as well as in the plasma and spinal cord at pre-onset, onset and peak stages of EAE established in the chronic B6 mice model. For the first time, we provide evidence that urine exosomes can be a specific and sensitive source of miRNA biomarkers for all 3 stages of EAE disease. In a significant observation, we observed that miR-155-5p expression increased in urine exosomes, plasma and spinal cord 6 days before the onset of disease, suggesting its early involvement in the pathology of EAE disease. We also analyzed the effect of Glatiramer acetate (GA; copaxone) treatment, an approved treatment for MS patients, in modulating miRNA expression at the peak of EAE disease. We identified miR-155-5p, miR-27a-3p, miR-9-5p and miR-350-5p as putative GA-treatment responsive miRNA biomarkers. Since, EAE is a mainly CD4 cells mediated disease, we also examined the above set of miRNAs and found to be significantly altered in T cells polarized to Th1 and Th17 phenotype, similar to urine exosomes. Thus, urine exosome miRNAs hold the potential to be defined as novel accessible stage-specific biomarkers of EAE (MS) disease as well as treatment response.

Indexed as

AnimalsBiomarkersDisease ProgressionEncephalomyelitis, Autoimmune, ExperimentalExosomesFemaleGene Expression ProfilingGlatiramer AcetateImmunosuppressive AgentsMiceMice, Inbred C57BLMicroRNAsReal-Time Polymerase Chain ReactionBiomarkersGlatiramer AcetateImmunosuppressive AgentsMicroRNAsBiomarkerCopaxoneExperimental autoimmune encephalomyelitismicroRNAMultiple sclerosisUrinary exosomes

Identifiers

PMID26277791
OpenAlexW1466499198

What OpenQuestion holds

Textmetadata
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.