Evidence mapPaperPMID 38017342Full record

ReviewMolecular neurobiology2024

Clusterin is a Potential Therapeutic Target in Alzheimer's Disease.

Nazhakaiti Palihati, Yuanhong Tang, Yajuan Yin, Ding Yu, Gang Liu, Zhenzhen Quan, Junjun Ni, Yan Yan, Hong Qing

Abstract readReview
PubMed Publisher
In one paragraph

Review in Molecular neurobiology, 2024. 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
3.9field-weighted citation impact, top 6% 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, 17 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Clusterin: structure, function and roles in disease.International journal of medical sciences · 2025
    Review
  10. Article
  11. Review
  12. Article
  13. Review
  14. 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

9 authors at 2 institutions in 1 country.

Nazhakaiti PalihatiKey Laboratory of Molecular Medicine and Biotherapy, School of Life Science, Beijing Institute of Technology, Beijing, 100081, China.
Yuanhong TangKey Laboratory of Molecular Medicine and Biotherapy, School of Life Science, Beijing Institute of Technology, Beijing, 100081, China.
Yajuan YinDepartment of Cardiology, The First Hospital of Hebei Medical University, Shijiazhuang, 050000, Hebei, China.
Ding YuDepartment of Cardiology, The First Hospital of Hebei Medical University, Shijiazhuang, 050000, Hebei, China.
Gang LiuDepartment of Cardiology, The First Hospital of Hebei Medical University, Shijiazhuang, 050000, Hebei, China.
Zhenzhen QuanKey Laboratory of Molecular Medicine and Biotherapy, School of Life Science, Beijing Institute of Technology, Beijing, 100081, China.
Junjun NiKey Laboratory of Molecular Medicine and Biotherapy, School of Life Science, Beijing Institute of Technology, Beijing, 100081, China.
Yan YanDepartment of Cardiology, The First Hospital of Hebei Medical University, Shijiazhuang, 050000, Hebei, China. 15128470659@163.com.ORCID http://orcid.org/0000-0003-3416-4460
Hong QingKey Laboratory of Molecular Medicine and Biotherapy, School of Life Science, Beijing Institute of Technology, Beijing, 100081, China. hqing@bit.edu.cn.
Beijing Institute of Technology · CNHebei Medical University · CN

Funding

Innovative Research Group Project of the National Natural Science Foundation of China 92049102Natural Science Foundation of Beijing Municipality 7222113
6 · The paper itself

Abstract

In recent years, Clusterin, a glycosylated protein with multiple biological functions, has attracted extensive research attention. It is closely associated with the physiological and pathological states within the organism. Particularly in Alzheimer's disease (AD) research, Clusterin plays a significant role in the disease's occurrence and progression. Numerous studies have demonstrated a close association between Clusterin and AD. Firstly, the expression level of Clusterin in the brain tissue of AD patients is closely related to pathological progression. Secondly, Clusterin is involved in the deposition and formation of β-amyloid, which is a crucial process in AD development. Furthermore, Clusterin may affect the pathogenesis of AD through mechanisms such as regulating inflammation, controlling cell apoptosis, and clearing pathological proteins. Therefore, further research on the relationship between Clusterin and AD will contribute to a deeper understanding of the etiology of this neurodegenerative disease and provide a theoretical basis for developing early diagnostic and therapeutic strategies for AD. This also makes Clusterin one of the research focuses as a potential biomarker for AD diagnosis and treatment monitoring.

Indexed as

Alzheimer DiseaseClusterinAmyloid beta-PeptidesAnimalsBiomarkersBrainHumansMolecular Targeted TherapyAmyloid beta-PeptidesBiomarkersClusterinAlzheimer’s disease (AD)Amyloid beta (Aβ)ClusterinNeurodegenerative disordersNeurotoxicityTau

Identifiers

PMID38017342
OpenAlexW4389151516

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.