Evidence map›Paper›PMID 30040732›Full record

ReviewJournal of Alzheimer's disease : JAD2018

Neuro-Immuno-Gene- and Genome-Editing-Therapy for Alzheimer's Disease: Are We There Yet?

Sudhanshu P Raikwar, Ramasamy Thangavel, Iuliia Dubova, Mohammad Ejaz Ahmed, Pushpavathi Govindhasamy Selvakumar, Duraisamy Kempuraj, Smita Zaheer, Shankar Iyer, Asgar Zaheer

Abstract readReview
In one paragraph

Review in Journal of Alzheimer's disease : JAD, 2018. 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
–field-weighted citation impact
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. Review
  2. Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Current Clinical Applications of In Vivo Gene Therapy with AAVs.Molecular therapy : the journal of the American Society of Gene Therapy · 2021
    Review
  10. Review
  11. Review
  12. Tuning up Transcription Factors for Therapy.Molecules (Basel, Switzerland) · 2020
    Review
  13. CRISPR/Cas9 Editing of Glia Maturation Factor Regulates Mitochondrial Dynamics by Attenuation of the NRF2/HO-1 Dependent Ferritin Activation in Glial Cells.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2019
    Article
  14. Glia Maturation Factor in the Pathogenesis of Alzheimer's disease.Open access journal of neurology & neurosurgery · 2019
    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

9 authors.

Sudhanshu P RaikwarDepartment of Neurology, Center for Translational Neuroscience, School of Medicine, University of Missouri, Columbia, MO, USA.
Ramasamy ThangavelDepartment of Neurology, Center for Translational Neuroscience, School of Medicine, University of Missouri, Columbia, MO, USA.
Iuliia DubovaDepartment of Neurology, Center for Translational Neuroscience, School of Medicine, University of Missouri, Columbia, MO, USA.
Mohammad Ejaz AhmedDepartment of Neurology, Center for Translational Neuroscience, School of Medicine, University of Missouri, Columbia, MO, USA.
Pushpavathi Govindhasamy SelvakumarDepartment of Neurology, Center for Translational Neuroscience, School of Medicine, University of Missouri, Columbia, MO, USA.
Duraisamy KempurajDepartment of Neurology, Center for Translational Neuroscience, School of Medicine, University of Missouri, Columbia, MO, USA.
Smita ZaheerDepartment of Neurology, Center for Translational Neuroscience, School of Medicine, University of Missouri, Columbia, MO, USA.
Shankar IyerDepartment of Neurology, Center for Translational Neuroscience, School of Medicine, University of Missouri, Columbia, MO, USA.
Asgar ZaheerDepartment of Neurology, Center for Translational Neuroscience, School of Medicine, University of Missouri, Columbia, MO, USA.

Funding

Therapeutic potential of GMF suppresssion in inflammation and neurodegenerationR01AG048205 · NIA · UNIVERSITY OF MISSOURI-COLUMBIA · PI ZAHEER, ASGAR · 2015 to 2019
$1.6M
BLRD VA I01 BX002477NIA NIH HHS R01 AG048205
6 · The paper itself

Abstract

Alzheimer's disease (AD) is a highly complex neurodegenerative disorder and the current treatment strategies are largely ineffective thereby leading to irreversible and progressive cognitive decline in AD patients. AD continues to defy successful treatment despite significant advancements in the field of molecular medicine. Repeatedly, early promising preclinical and clinical results have catapulted into devastating setbacks leading to multi-billion dollar losses not only to the top pharmaceutical companies but also to the AD patients and their families. Thus, it is very timely to review the progress in the emerging fields of gene therapy and stem cell-based precision medicine. Here, we have made sincere efforts to feature the ongoing progress especially in the field of AD gene therapy and stem cell-based regenerative medicine. Further, we also provide highlights in elucidating the molecular mechanisms underlying AD pathogenesis and describe novel AD therapeutic targets and strategies for the new drug discovery. We hope that the quantum leap in the scientific advancements and improved funding will bolster novel concepts that will propel the momentum toward a trajectory leading to a robust AD patient-specific next generation precision medicine with improved cognitive function and excellent life quality.

Indexed as

Genetic TherapyPrecision MedicineStem Cell TransplantationAlzheimer DiseaseAnimalsGene EditingHumansAAVAlzheimer’s diseaseCRISPRgene editinggene therapyregenerative medicinestem cells

Identifiers

PMID30040732
PMCPMC6130335

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.