Evidence map›Paper›PMID 39998958›Full record

ReviewAlzheimer's & dementia : the journal of the Alzheimer's Association2025

The interaction between dysfunction of vasculature and tauopathy in Alzheimer's disease and related dementias.

Chuyao Huang, Zhenwen Wei, Ningxiang Zheng, Jingsi Yan, Jiayu Zhang, Xinyi Ye, Wei Zhao

Abstract readReview
In one paragraph

Review in Alzheimer's & dementia : the journal of the Alzheimer's Association, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Greater Motor and Nonmotor Burden at Diagnosis Is Associated With Amyloid Copathology in Parkinson's Disease.Movement disorders : official journal of the Movement Disorder Society · 2026
    Article
  2. Unveiling the procoagulant state in Alzheimer's disease: A novel PET imaging strategy.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026
    Article
  3. Emerging directions in tauopathy research.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. The interaction between dysfunction of vasculature and tauopathy in Alzheimer's disease and related dementias.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2025
    Review
  9. 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

7 authors.

Chuyao HuangScience and Technology Innovation Center, Guangzhou University of Chinese Medicine, Guangzhou, Guangdong, China.
Zhenwen WeiScience and Technology Innovation Center, Guangzhou University of Chinese Medicine, Guangzhou, Guangdong, China.
Ningxiang ZhengScience and Technology Innovation Center, Guangzhou University of Chinese Medicine, Guangzhou, Guangdong, China.
Jingsi YanScience and Technology Innovation Center, Guangzhou University of Chinese Medicine, Guangzhou, Guangdong, China.
Jiayu ZhangScience and Technology Innovation Center, Guangzhou University of Chinese Medicine, Guangzhou, Guangdong, China.
Xinyi YeScience and Technology Innovation Center, Guangzhou University of Chinese Medicine, Guangzhou, Guangdong, China.
Wei ZhaoScience and Technology Innovation Center, Guangzhou University of Chinese Medicine, Guangzhou, Guangdong, China.

Funding

Natural Science Foundation of Guangdong Province 2019A1515011299the National Natural Science Foundation of China 81973919
6 · The paper itself

Abstract

Tauopathy is one of the pathological features of Alzheimer's disease and related dementias (ADRD). At present, there have been many studies on the formation, deposition, and intercellular transmission of tau in neurons and immune cells. The vasculature is an important component of the central nervous system. This review discusses the interaction between vasculature and tau in detail from three aspects. (1) The vascular risk factors (VRFs) discussed in this review include diabetes mellitus (DM), abnormal blood pressure (BP), and hypercholesterolemia. (2) In ADRD pathology, the hyperphosphorylation and deposition of tau interact with disrupted vasculature, such as different cells (endothelial cells, smooth muscular cells, and pericytes), the blood-brain barrier (BBB), and the cerebral lymphatic system. (3) The functions of vasculature are regulated by various signaling transductions. Endothelial nitric oxide synthase/nitric oxide, calcium signaling, Rho/Rho-associated coiled-coil containing Kinase, and receptors for advanced glycation end products are discussed in this review. Our findings indicate that the prevention and treatment of vascular health may be a potential target for ADRD combination therapy. HIGHLIGHTS: Persistent VRFs increase early disruption of vascular mechanisms and are strongly associated with tau pathology in ADRD. Cell dysfunction in the vasculature causes BBB leakage and drainage incapacity of the cerebral lymphatic system, which interacts with tau pathology. Signaling molecules in the vasculature regulate vasodilation and contraction, angiogenesis, and CBF. Abnormal signaling transduction is related to tau hyperphosphorylation and deposition.

Indexed as

Alzheimer DiseaseDementiaTauopathiesAnimalsBlood-Brain BarrierHumanstau Proteinstau ProteinsAlzheimer's disease and related dementiastauopathyvasculature

Identifiers

PMID39998958
PMCPMC11854360

What OpenQuestion holds

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Registered trials

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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.