Evidence map›Paper›PMID 39915907›Full record

ReviewCNS neuroscience & therapeutics2025

Advances in the Study of Necroptosis in Vascular Dementia: Focus on Blood-Brain Barrier and Neuroinflammation.

Yuemin Qiu, Lin Cheng, Yinyi Xiong, Ziying Liu, Chunxiao Shen, Liangliang Wang, Yujia Lu, Shufei Wei, Lushun Zhang, Seung Bum Yang and 1 more

Abstract readReview
In one paragraph

Review in CNS neuroscience & therapeutics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. 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

11 authors.

Yuemin QiuDepartment of Pathology, Affiliated Hospital of Jiujiang University, Jiujiang, Jiangxi, China.
Lin ChengDepartment of Pathology, Jiujiang Clinical Precision Medicine Research Center, Jiujiang, Jiangxi, China.
Yinyi XiongDepartment of Pathology, Jiujiang Clinical Precision Medicine Research Center, Jiujiang, Jiangxi, China.
Ziying LiuDepartment of Pathology, Affiliated Hospital of Jiujiang University, Jiujiang, Jiangxi, China.
Chunxiao ShenDepartment of Pathology, Affiliated Hospital of Jiujiang University, Jiujiang, Jiangxi, China.
Liangliang WangDepartment of Pathology, Affiliated Hospital of Jiujiang University, Jiujiang, Jiangxi, China.
Yujia LuDepartment of Pathology, Affiliated Hospital of Jiujiang University, Jiujiang, Jiangxi, China.
Shufei WeiDepartment of Pathology, Affiliated Hospital of Jiujiang University, Jiujiang, Jiangxi, China.
Lushun ZhangDepartment of Pathology, Affiliated Hospital of Jiujiang University, Jiujiang, Jiangxi, China.
Seung Bum YangDepartment of Medical Non-Commissioned Officer, Wonkwang Health Science University, Iksan, Republic of Korea.
Xiaorong ZhangDepartment of Pathology, Affiliated Hospital of Jiujiang University, Jiujiang, Jiangxi, China.ORCID 0009-0003-7840-5956

Funding

Foundation of Students' Platform for Innovation and Entrepreneurship Training Program 202411843024 to XRZFoundation of Students' Platform for Innovation and Entrepreneurship Training Program S202411843050 to CXSthe Administration of Traditional Chinese Medicine of Jiangxi Province 2022B1010 to LCthe Provincial Natural Science Foundation of Jiangxi Province 20224BAB206040 to XRZthe Science and Technology Project Founded by the Education Department of Jiangxi Province GJJ211812 to XRZthe Science and Technology Project Founded by the Education Department of Jiangxi Province GJJ211813 to LCthe Science and Technology Project Founded by the Education Department of Jiangxi Province GJJ2201928 to LLW
6 · The paper itself

Abstract

backgroundVascular dementia (VaD) includes a group of brain disorders that are characterized by cerebrovascular pathology.Neuroinflammation, disruption of the blood-brain barrier (BBB) permeability, white matter lesions, and neuronal loss are all significant pathological manifestations of VaD and play a key role in disease progression. Necroptosis, also known asprogrammed necrosis, is a mode of programmed cell death distinct from apoptosis and is closely associated with ischemic injury and neurodegenerative diseases. Recent studies have shown that necroptosis in VaD exacerbates BBB destruction, activates neuroinflammation, promotes neuronal loss, and severely affects VaD prognosis. RESULTS AND

conclusionsIn this review, we outline the significant roles of necroptosis and its molecular mechanisms in the pathological process of VaD, with a particular focus on the role of necroptosis in modulating neuroinflammation and exacerbating the disruption of BBB permeability in VaD, and elaborate on the molecular regulatory mechanisms and the centrally involved cells of necroptosis mediated by tumor necrosis factor-α in neuroinflammation in VaD. We also analyze the possibility and specific strategy that targeting necroptosis would help inhibit neuroinflammation and BBB destruction in VaD. With a focus on necroptosis, this study delved into its impact on the pathological changes and prognosis of VaD to provide new treatment ideas.

Indexed as

Blood-Brain BarrierDementia, VascularNecroptosisNeuroinflammatory DiseasesAnimalsHumansblood–brain barriernecroptosisneuroinflammationpathophysiologyvascular dementia

Identifiers

PMID39915907
PMCPMC11802338

What Socratic holds

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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.