Evidence map›Paper›PMID 41840280›Full record

ReviewAging clinical and experimental research2026

Why acetylcholinesterase inhibitors should be considered disease-modifying drugs for Alzheimer's disease?

Giovanni Zuliani, Carlo Cervellati, Marco Zuin, Gloria Brombo

Abstract readReview
In one paragraph

Review in Aging clinical and experimental research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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.

Giovanni ZulianiDepartment of Translational Medicine and for Romagna, University of Ferrara, Via Luigi Borsari, 46, Ferrara, 44124, Italy.
Carlo CervellatiDepartment of Translational Medicine and for Romagna, University of Ferrara, Via Luigi Borsari, 46, Ferrara, 44124, Italy. crvcrl@unife.it.ORCID http://orcid.org/0000-0003-4777-6300
Marco ZuinDepartment of Translational Medicine and for Romagna, University of Ferrara, Via Luigi Borsari, 46, Ferrara, 44124, Italy.
Gloria BromboDepartment of Translational Medicine and for Romagna, University of Ferrara, Via Luigi Borsari, 46, Ferrara, 44124, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Disease-modifying drugs (DMDs) are defined as treatments capable of altering the underlying course of a disease by slowing or modifying its biological progression rather than merely alleviating symptoms. In Alzheimer’s disease (AD), therapeutic options with proven disease-modifying effects remain limited, despite the recent approval of anti-amyloid monoclonal antibodies. Acetylcholinesterase inhibitors (AChEI), currently classified as symptomatic treatments, have accumulated a number of clinical and experimental evidence suggesting a broader role. Long-term clinical and observational studies indicate that AChEI are associated with slower cognitive and functional decline, reduced hippocampal atrophy, lower mortality rates, and improved behavioral and psychological symptoms of dementia. In parallel, preclinical and clinical data show that AChEI may influence multiple key pathogenic mechanisms of AD, including amyloid-β production/aggregation/toxicity, neuroinflammation, glutamatergic excitotoxicity, synaptic dysfunction, and cerebral hypoperfusion. Taken together, these findings support the view that AChEI fulfill the criteria of DMDs, and should be reconsidered as such in the complex therapeutic framework of Alzheimer’s disease.

Indexed as

Alzheimer DiseaseCholinesterase InhibitorsAmyloid beta-PeptidesAnimalsHumansAmyloid beta-PeptidesCholinesterase InhibitorsAcetylcholinesterase inhibitorsAlzheimer’s diseaseDementiaDisease-modifying drugs

Identifiers

PMID41840280
PMCPMC13032996

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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.