Evidence map›Paper›PMID 41009371›Full record

ArticleInternational journal of molecular sciences2025

Kinetic Model with Feedback Cycle for Age-Dependent Amyloid Beta Accumulation in Mice.

Vivian Tyng, Michael E Kellman

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

Vivian TyngDepartment of Chemistry and Biochemistry, University of Oregon, Eugene, OR 97403, USA.ORCID 0000-0001-6413-7178
Michael E KellmanDepartment of Chemistry and Biochemistry, University of Oregon, Eugene, OR 97403, USA.ORCID 0000-0002-6198-8812

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Amyloid beta (Aβ) is believed to play a key role in Alzheimer's disease (AD), whose causes, progression, diagnosis, and treatment nonetheless remain poorly understood despite decades of research. Recent studies suggest that Aβ in its various forms participates in multiple mutual feedback loops ("vicious cycles") including tauopathy, oxidative stress, inflammation, calcium dysregulation, excitotoxicity, and probably many others, eventually leading to neurodegeneration and cognitive decline. Here, as an initial quantitative step toward modeling this vast complexity, we explore a simple kinetic model of a coupled feedback vicious cycle for Aβ buildup based on literature data for Tg2576 mice. The model is used to examine the efficacy of various hypothetical therapeutic approaches, either singly or in combination, to mitigate Aβ buildup. While our computational results support the possible efficacy of combination interventions, they also suggest caution, inasmuch as clear synergy is not found. This kinetic approach highlights the essential importance of the vicious cycle of positive feedback in a quantitative model.

Indexed as

AgingAlzheimer DiseaseAmyloid beta-PeptidesModels, BiologicalAnimalsDisease Models, AnimalFeedback, PhysiologicalHumansKineticsMiceMice, TransgenicAmyloid beta-PeptidesAlzheimer’s diseaseamyloid betacombination interventionskinetic modelingpositive feedbackvicious cycle

Identifiers

PMID41009371
PMCPMC12469918

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.