Evidence map›Paper›PMID 36421736›Full record

ReviewBiomolecules2022

New Insights into Microglial Mechanisms of Memory Impairment in Alzheimer's Disease.

Na Li, Mingru Deng, Gonghui Hu, Nan Li, Haicheng Yuan, Yu Zhou

Open access · goldAbstract readReview
In one paragraph

Review in Biomolecules, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

22 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Designing Neural Dynamics: From Digital Twin Modeling to Regeneration.International journal of molecular sciences · 2025
    Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Evaluation of the Anti-Alzheimer Activity ofCurrent issues in molecular biology · 2025
    Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. [Lead exposure aggravates AβNan fang yi ke da xue xue bao = Journal of Southern Medical University · 2023
    Article
  15. Review
  16. Article
  17. Article
  18. Review
  19. Review
  20. 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

6 authors at 1 institution in 1 country.

Na LiDepartment of Rehabilitation Medicine, Affiliated Hospital of Qingdao University, Qingdao 266000, China.
Mingru DengDepartment of Neurology, Affiliated Qingdao Central Hospital of Qingdao University, Qingdao 266042, China.ORCID 0000-0002-5084-4813
Gonghui HuDepartment of Physiology and Pathophysiology, School of Basic Medical Sciences, Qingdao University, Qingdao 266071, China.ORCID 0000-0001-6825-9375
Nan LiDepartment of Health and Life Sciences, University of Health and Rehabilitation Sciences, Qingdao 266000, China.
Haicheng YuanDepartment of Neurology, Affiliated Qingdao Central Hospital of Qingdao University, Qingdao 266042, China.
Yu ZhouDepartment of Rehabilitation Medicine, Affiliated Hospital of Qingdao University, Qingdao 266000, China.
Qingdao University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alzheimer's disease (AD) is the most common progressive and irreversible neurodegeneration characterized by the impairment of memory and cognition. Despite years of studies, no effective treatment and prevention strategies are available yet. Identifying new AD therapeutic targets is crucial for better elucidating the pathogenesis and establishing a valid treatment of AD. Growing evidence suggests that microglia play a critical role in AD. Microglia are resident macrophages in the central nervous system (CNS), and their core properties supporting main biological functions include surveillance, phagocytosis, and the release of soluble factors. Activated microglia not only directly mediate the central immune response, but also participate in the pathological changes of AD, including amyloid-beta (Aβ) aggregation, tau protein phosphorylation, synaptic dissection, neuron loss, memory function decline, etc. Based on these recent findings, we provide a new framework to summarize the role of microglia in AD memory impairment. This evidence suggests that microglia have the potential to become new targets for AD therapy.

Indexed as

Alzheimer DiseaseMicrogliaAmyloid beta-PeptidesHumansMemory DisordersPhagocytosisAmyloid beta-PeptidesAlzheimer’s diseaseinflammationmemory impairmentmicrogliareviews

Identifiers

PMID36421736
PMCPMC9687453
OpenAlexW4309705161

What OpenQuestion 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 OpenQuestion graph.