Evidence map›Paper›PMID 35867206›Full record

ReviewMolecular neurobiology2022

Dysregulated miRNAs in Progression and Pathogenesis of Alzheimer's Disease.

Tania Arora, Vikash Prashar, Randeep Singh, Tushar Singh Barwal, Harish Changotra, Arti Sharma, Jyoti Parkash

Abstract readReview
PubMed Publisher
In one paragraph

Review in Molecular neurobiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
4.4field-weighted citation impact, top 4% 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

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 34 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. Review
  20. Review
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

7 authors at 2 institutions in 1 country.

Tania AroraDepartment of Zoology, School of Biological Sciences, Central University of Punjab, Ghudda 151 401, Bathinda, Punjab, India.
Vikash PrasharDepartment of Zoology, School of Biological Sciences, Central University of Punjab, Ghudda 151 401, Bathinda, Punjab, India.
Randeep SinghDepartment of Zoology, School of Biological Sciences, Central University of Punjab, Ghudda 151 401, Bathinda, Punjab, India.
Tushar Singh BarwalDepartment of Zoology, School of Biological Sciences, Central University of Punjab, Ghudda 151 401, Bathinda, Punjab, India.
Harish ChangotraDepartment of Biochemistry and Molecular Biology, Guru Nanak Dev University, Amritsar, 143101, Punjab, India.
Arti SharmaDepartment of Computational Biology, School of Biological Sciences, Central University of Punjab, Ghudda 151 401, Bathinda, Punjab, India.
Jyoti ParkashDepartment of Zoology, School of Biological Sciences, Central University of Punjab, Ghudda 151 401, Bathinda, Punjab, India. jyoti.parkash@cup.edu.in.ORCID http://orcid.org/0000-0002-6399-700X
Central University of Punjab · INGuru Nanak Dev University · IN

Funding

Science and Engineering Research Board CRG/2015/000240Science and Engineering Research Board CRG/2020/003257University Grants Commission F.30-312/2016 (BSR)
6 · The paper itself

Abstract

Alzheimer's disease (AD) is a progressive degeneration of neurons due to the accumulation of amyloid-β peptide (Aβ) and hyper-phosphorylation of tau protein in the neuronal milieu leading to increased oxidative stress and apoptosis. Numerous factors contribute towards the progression of AD, including miRNA, which are 22-24 nucleotides long sequence which acts as critical regulators of cellular processes by binding to 3' UTR of mRNA, regulating its expression post-transcriptionally. This review aims to determine the miRNA with the most significant dysregulation in the brain and cerebrospinal fluid (CSF) of human patients. A systemized inclusion/exclusion criterion has been utilized based on selected keywords followed by screening of those articles to conclude a list of 8 highly dysregulated miRNAs based on the fold change of AD vs control patients, which could be used in clinical testing as these miRNAs play central role in the pathophysiology of AD. Furthermore, a network study of highly dysregulated miRNA estimated the association of these miRNA in the mediation of Aβ generation and aggregation, inhibition of autophagy, reduction of Aβ clearance, microglial and astrocytic activation, neuro-inflammation, tau hyper-phosphorylation, and synaptic loss.

Indexed as

Alzheimer DiseaseMicroRNAsAmyloid beta-PeptidesBrainHumansNeuronstau ProteinsAmyloid beta-PeptidesMicroRNAstau ProteinsAlzheimer’s diseaseBrainCerebrospinal fluidDysregulationmiRNANetwork study

Identifiers

PMID35867206
OpenAlexW4286717546

What Socratic 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 Socratic graph.