Evidence mapPaperPMID 41727487Full record

ReviewFrontiers in immunology2026

Metabolic control of neuroinflammation: focus on itaconate and its derivatives in CNS disorders.

Ying Wang, Shihui Liu, Weijie Zhu, Pengyu Hao, Jiacan Xu, Diqi Mai, Ran Chen, Haojie Han, Xuechen Bian, Bodong Wang

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

10 authors.

Ying Wang *Department of Neurosurgery, the 960th Hospital of PLA (General Hospital of Jinan Military Command), Jinan, Shandong, China.
Shihui Liu *Department of Neurosurgery, the 960th Hospital of PLA (General Hospital of Jinan Military Command), Jinan, Shandong, China.
Weijie Zhu *Department of Neurosurgery, the 960th Hospital of PLA (General Hospital of Jinan Military Command), Jinan, Shandong, China.
Pengyu HaoDepartment of Neurosurgery, the 960th Hospital of PLA (General Hospital of Jinan Military Command), Jinan, Shandong, China.
Jiacan XuDepartment of Neurosurgery, the 960th Hospital of PLA (General Hospital of Jinan Military Command), Jinan, Shandong, China.
Diqi MaiDepartment of Neurosurgery, the 960th Hospital of PLA (General Hospital of Jinan Military Command), Jinan, Shandong, China.
Ran ChenDepartment of Neurosurgery, the 960th Hospital of PLA (General Hospital of Jinan Military Command), Jinan, Shandong, China.
Haojie HanSchool of Clinical Medicine, Shandong Second Medical University, Weifang, Shandong, China.
Xuechen BianSchool of Clinical Medicine, Shandong Second Medical University, Weifang, Shandong, China.
Bodong WangDepartment of Neurosurgery, the 960th Hospital of PLA (General Hospital of Jinan Military Command), Jinan, Shandong, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The activation of microglia, which are the resident immune cells of the central nervous system (CNS), underpins the pathogenesis of neuroinflammatory and neurodegenerative diseases. Metabolic reprogramming has recently been recognized as a critical mechanism that regulates microglial activation because distinct activation phenotypes are tightly coupled to specific metabolic profiles that shape their functional and inflammatory responses. Accumulating evidence indicates that microglia produce itaconate through the tricarboxylic acid cycle, and itaconate and its derivatives play key antioxidant and anti-inflammatory roles. Mechanistically, itaconate has a major impact on the metabolic processes and functional state of microglia by blocking the NF-κB signaling route, activating the Nrf2 signaling pathway, and inhibiting succinate dehydrogenase synthesis as well as NLRP3 inflammatory vesicle activation. Collectively, these actions confer significant protection against CNS disorders, including ischemic stroke, Alzheimer's disease, Parkinson's disease, and cerebral hemorrhage. Furthermore, structurally optimized itaconate derivatives exhibit enhanced pharmacokinetics and bioactivity. This review highlights the pivotal role of itaconate and its derivatives in microglial regulation, explores their therapeutic potential in neurological diseases, and outlines future research directions, with the aim of providing a theoretical foundation for novel metabolic interventions.

Indexed as

Central Nervous System DiseasesMicrogliaNeuroinflammatory DiseasesSuccinatesAnimalsHumansSignal Transductionitaconic acidSuccinatescentral nervous system diseasesitaconatemetabolic controlmicroglianeuroinflammation

Identifiers

PMID41727487
PMCPMC12920200

What Socratic 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 Socratic graph.