Evidence map›Paper›PMID 32635934›Full record

ReviewJournal of neuroinflammation2020

TREM2 ectodomain and its soluble form in Alzheimer's disease.

Jiaolong Yang, Zhihui Fu, Xingyu Zhang, Min Xiong, Lanxia Meng, Zhentao Zhang

Open access · goldAbstract readReview
In one paragraph

Review in Journal of neuroinflammation, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed, 1 pooled it
5.7field-weighted citation impact, top 3% 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

59 citing papers in PubMed, 1 synthesis or guideline pooled it, 110 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Observational
  4. Review
  5. Article
  6. Review
  7. TREM2 promotes adipogenesis of PDGFR-αFrontiers in endocrinology · 2026
    Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Review
  13. Review
  14. Dehydroervatamine as a promising novel TREM2 agonist, attenuates neuroinflammation.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2025
    Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Article
  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

6 authors at 2 institutions in 1 country.

Jiaolong YangDepartment of Neurology, Renmin Hospital of Wuhan University, Wuhan, 430060, China.
Zhihui FuDepartment of Neurology, Renmin Hospital of Wuhan University, Wuhan, 430060, China.
Xingyu ZhangDepartment of Neurology, Renmin Hospital of Wuhan University, Wuhan, 430060, China.
Min XiongDepartment of Neurology, Renmin Hospital of Wuhan University, Wuhan, 430060, China.
Lanxia MengDepartment of Neurology, Renmin Hospital of Wuhan University, Wuhan, 430060, China.
Zhentao ZhangDepartment of Neurology, Renmin Hospital of Wuhan University, Wuhan, 430060, China. Zhentao104@gmail.com.
Wuhan University · CNRenmin Hospital of Wuhan University · CN

Funding

National Natural Science Foundation of China No.81822016,81771382, and 81571249
6 · The paper itself

Abstract

Triggering receptor expressed on myeloid cells 2 (TREM2) is a receptor mainly expressed on the surface of microglia. It mediates multiple pathophysiological processes in various diseases. Recently, TREM2 has been found to play a role in the development of Alzheimer's disease (AD). TREM2 is a transmembrane protein that is specifically expressed on microglia in the brain. It contains a long ectodomain that directly interacts with the extracellular environment to regulate microglial function. The ectodomain of TREM2 is processed by a disintegrin and metalloprotease, resulting in the release of a soluble form of TREM2 (sTREM2). Recent studies have demonstrated that sTREM2 is a bioactive molecule capable of binding ligands, activating microglia, and regulating immune responses during the AD continuum. Clinical studies revealed that sTREM2 level is elevated in cerebrospinal fluid (CSF) of AD patients, and the sTREM2 level is positively correlated with the levels of classical CSF biomarkers, namely t-tau and p-tau, indicating that it is a reliable predictor of the early stages of AD. Herein, we summarize the key results on the generation, structure, and function of sTREM2 to provide new insights into TREM2-related mechanisms underlying AD pathogenesis and to promote the development of TREM2-based therapeutic strategy.

Indexed as

Alzheimer DiseaseAnimalsBiomarkersHumansMembrane GlycoproteinsMicrogliaProtein IsoformsReceptors, ImmunologicSolubilitytau ProteinsBiomarkersMAPT protein, humanMembrane GlycoproteinsProtein IsoformsReceptors, Immunologictau ProteinsTREM2 protein, humanAlzheimer’s diseaseMicrogliaNeuroinflammationTriggering receptor expressed on myeloid cells 2

Identifiers

PMID32635934
PMCPMC7341574
OpenAlexW3039674883

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.