ReviewAging clinical and experimental research2026
Why acetylcholinesterase inhibitors should be considered disease-modifying drugs for Alzheimer's disease?
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.
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.
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.
Who cites it
1 citing paper in PubMed.
- Translating blood-based biomarkers into Alzheimer's disease clinical practice: screening, diagnosis, and longitudinal monitoring.Frontiers in aging neuroscience · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
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.
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Registered trials
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.