Evidence map›Paper›PMID 30201881›Full record

ReviewBiomolecules2018

The Biology of Glial Cells and Their Complex Roles in Alzheimer's Disease: New Opportunities in Therapy.

Saif Shahriar Rahman Nirzhor, Rubayat Islam Khan, Sharmind Neelotpol

Abstract readReview
In one paragraph

Review in Biomolecules, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing 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

29 citing papers in PubMed.

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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

3 authors.

Saif Shahriar Rahman NirzhorDepartment of Pharmacy, BRAC University, Dhaka 1212, Bangladesh. saif.rahman@bracu.ac.bd.
Rubayat Islam KhanDepartment of Pharmacy, BRAC University, Dhaka 1212, Bangladesh. rubayat.khan@bracu.ac.bd.ORCID 0000-0003-3264-564X
Sharmind NeelotpolDepartment of Pharmacy, BRAC University, Dhaka 1212, Bangladesh. sharmind@bracu.ac.bd.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Even though Alzheimer's disease (AD) is of significant interest to the scientific community, its pathogenesis is very complicated and not well-understood. A great deal of progress has been made in AD research recently and with the advent of these new insights more therapeutic benefits may be identified that could help patients around the world. Much of the research in AD thus far has been very neuron-oriented; however, recent studies suggest that glial cells, i.e., microglia, astrocytes, oligodendrocytes, and oligodendrocyte progenitor cells (NG2 glia), are linked to the pathogenesis of AD and may offer several potential therapeutic targets against AD. In addition to a number of other functions, glial cells are responsible for maintaining homeostasis (i.e., concentration of ions, neurotransmitters, etc.) within the central nervous system (CNS) and are crucial to the structural integrity of neurons. This review explores the: (i) role of glial cells in AD pathogenesis; (ii) complex functionalities of the components involved; and (iii) potential therapeutic targets that could eventually lead to a better quality of life for AD patients.

Indexed as

Alzheimer DiseaseAnimalsHumansNeurogliaAlzheimer’s diseaseastrocytesAβ-peptidesglial cellsmicroglianeurodegenerative diseaseNG2 gliaoligodendrocytes

Identifiers

PMID30201881
PMCPMC6164719

What OpenQuestion holds

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Registered trials

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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.