Evidence map›Paper›PMID 40059063›Full record

ReviewCNS neuroscience & therapeutics2025

Linking Circadian Rhythms to Gut-Brain Axis Lipid Metabolism Associated With Endoplasmic Reticulum Stress in Alzheimer's Disease.

Jianhui Su, Lanyang Zhao, Runze Fu, Zhe Tang

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 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Article
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  5. 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

4 authors.

Jianhui SuSchool of Marine and Bioengineering, Yancheng Institute of Technology, Yancheng, Jiangsu, China.ORCID 0000-0003-4096-4341
Lanyang ZhaoSchool of Pharmacy, Nanjing University of Chinese Medicine, Nanjing, China.
Runze FuSchool of Marine and Bioengineering, Yancheng Institute of Technology, Yancheng, Jiangsu, China.
Zhe TangSchool of Chemistry & Chemical Engineering, Yancheng Institute of Technology, Yancheng, Jiangsu, China.ORCID 0000-0001-9111-3833

Funding

Study Abroad Scholarship Program of Jiangsu Government JS-2019-294the Talent Instruction Projects of the Yancheng Institute of Technology KJC2014015the Talent Instruction Projects of the Yancheng Institute of Technology XJ201724
6 · The paper itself

Abstract

backgroundAlzheimer's disease (AD) is characterized by a decline in cognitive, learning, and memory abilities. Neuroinflammation is associated with the spread of tau tangles in the neocortex of AD, leading to cognitive impairment. Therefore, clarifying the pathogenesis of Neuroinflammation and finding effective treatments are the crucial issues for the clinical management of AD.

methodWe systematically review the latest research on the pathogenesis and therapeutic strategies of AD in PubMed, Web of Science, and Elsevier SD.

resultIn this review, the mechanism of the effect of gut-brain axis lipid metabolism mediated by circadian rhythm on AD was discussed, and we also analysed the effects of inflammation and endoplasmic reticulum stress (ERS) induced by lipid abnormalities on intestinal mucosal barrier and neurodegeneration; furthermore, the importance of lipid homeostasis (phospholipids, fatty acids, sterol) in maintaining the functions of endoplasmic reticulum was emphasized. Meanwhile, as lipid composition affects protein conformation, the membrane phospholipids surrounding sarcoplasmic reticulum Ca

conclusionWe interpreted the mechanism of action between lipid microdomains and ER membrane proteins, reviewed the role of the new pathway of circadian rhythm, lipid metabolism, intestinal mucosa, and brain signaling in the pathogenesis of AD, and proposed strategies to prevent AD by changing the dietary lipid measures.

Indexed as

Alzheimer DiseaseBrainBrain-Gut AxisCircadian RhythmEndoplasmic Reticulum StressLipid MetabolismAnimalsHumansADcircadian rhythmERSinflammationintestinal mucosal barrierlipid homeostasis

Identifiers

PMID40059063
PMCPMC11890981

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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.