Evidence map›Paper›PMID 34950142›Full record

SynthesisFrontiers in immunology2021

Long Non-Coding RNAs, Novel Offenders or Guardians in Multiple Sclerosis: A Scoping Review.

Abbas Jalaiei, Mohammad Reza Asadi, Hani Sabaie, Hossein Dehghani, Jalal Gharesouran, Bashdar Mahmud Hussen, Mohammad Taheri, Soudeh Ghafouri-Fard, Maryam Rezazadeh

Open access · goldAbstract readMeta-AnalysisScoping Review
In one paragraph

Synthesis in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 25% 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, 1 synthesis or guideline pooled it, 18 citations in OpenAlex.

  1. Pooled it
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  3. Review
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  5. Review
  6. Article
  7. Review
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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 3 countries.

Abbas JalaieiMolecular Medicine Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Mohammad Reza AsadiMolecular Medicine Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Hani SabaieMolecular Medicine Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Hossein DehghaniDepartment of Molecular Medicine, School of Medicine, Birjand University of Medical Sciences, Birjand, Iran.
Jalal GharesouranDepartment of Medical Genetics, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran.
Bashdar Mahmud HussenDepartment Pharmacognosy, College of Pharmacy, Hawler Medical University, Erbil, Iraq.
Mohammad TaheriSkull Base Research Center, Loghman Hakim Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Soudeh Ghafouri-FardDepartment of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Maryam RezazadehMolecular Medicine Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Tabriz University of Medical Sciences · IRShahid Beheshti University of Medical Sciences · IRBirjand University of Medical Sciences · IRHawler Medical University · IQ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple sclerosis (MS), a chronic inflammatory demyelinating disease of the central nervous system, is one of the most common neurodegenerative diseases worldwide. MS results in serious neurological dysfunctions and disability. Disturbances in coding and non-coding genes are key components leading to neurodegeneration along with environmental factors. Long non-coding RNAs (lncRNAs) are long molecules in cells that take part in the regulation of gene expression. Several studies have confirmed the role of lncRNAs in neurodegenerative diseases such as MS. In the current study, we performed a systematic analysis of the role of lncRNAs in this disorder. In total, 53 studies were recognized as eligible for this systematic review. Of the listed lncRNAs, 52 lncRNAs were upregulated, 37 lncRNAs were downregulated, and 11 lncRNAs had no significant expression difference in MS patients compared with controls. We also summarized some of the mechanisms of lncRNA functions in MS. The emerging role of lncRNAs in neurodegenerative diseases suggests that their dysregulation could trigger neuronal death

Indexed as

BiomarkersGene Expression RegulationAdaptive ImmunityAnimalsDisease Models, AnimalDisease SusceptibilityGene Regulatory NetworksGenetic Predisposition to DiseaseHumansMultiple SclerosisRNA InterferenceRNA, Long NoncodingBiomarkersRNA, Long NoncodingexpressionlncRNAsmultiple sclerosisneurodegenerative diseasepolymorphism

Identifiers

PMID34950142
PMCPMC8688805
OpenAlexW4200516080

What Socratic 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 Socratic graph.