Evidence map›Paper›PMID 40930583›Full record

ArticleJournal of neurology, neurosurgery, and psychiatry2026

Accelerated long-term forgetting as a predictor of clinical onset in presymptomatic autosomal dominant Alzheimer's disease.

Nicholas Magill, Rachana Tank, Damien Ferguson, Duncan Alston, Antoinette O'Connor, Helen Rice, Kirsty Lu, Sebastian Crutch, Nick C Fox, Philip Sj Weston

Abstract read
In one paragraph

Article in Journal of neurology, neurosurgery, and psychiatry, 2026. 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

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

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

10 authors.

Nicholas MagillDementia Research Centre, UCL Queen Square Institute of Neurology, London, UK.
Rachana TankDementia Research Centre, UCL Queen Square Institute of Neurology, London, UK.
Damien FergusonDementia Research Centre, UCL Queen Square Institute of Neurology, London, UK.
Duncan AlstonDementia Research Centre, UCL Queen Square Institute of Neurology, London, UK.
Antoinette O'ConnorDementia Research Centre, UCL Queen Square Institute of Neurology, London, UK.
Helen RiceDementia Research Centre, UCL Queen Square Institute of Neurology, London, UK.
Kirsty LuDementia Research Centre, UCL Queen Square Institute of Neurology, London, UK.ORCID http://orcid.org/0000-0002-8416-2183
Sebastian CrutchDementia Research Centre, UCL Queen Square Institute of Neurology, London, UK.
Nick C FoxDementia Research Centre, UCL Queen Square Institute of Neurology, London, UK.
Philip Sj WestonDementia Research Centre, UCL Queen Square Institute of Neurology, London, UK philip.weston.11@ucl.ac.uk.ORCID http://orcid.org/0000-0003-1033-9916

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn Alzheimer's disease (AD), sensitive measures of cognitive decline prior to overt symptoms are urgently needed. Accelerated long-term forgetting (ALF), where new information is retained normally over conventional testing intervals but is then lost at an accelerated rate over the following days and weeks, has been identified cross-sectionally in presymptomatic autosomal dominant and sporadic AD cohorts. We aimed to assess whether ALF testing is predictive of proximity to future symptom onset.

methods20 asymptomatic autosomal dominant AD mutation carriers who performed normally on standard cognitive testing underwent ALF assessment with (1) a list, (2) a story and (3) a visual figure, with the testing of 30-min recall and 7-day recall. Participants were followed up annually for a median of 7 years and assessed each time with the Clinical Dementia Rating (CDR) scale.

results9/20 participants developed symptoms (CDR global>0) during follow-up. Those who became symptomatic had lower baseline ALF scores for both the list (progressors=30 (IQR, 30-36.4) and non-progressors=58.3 (IQR, 33-66.7), p=0.03) and story (progressors=58.8 (IQR, 44-66) and non-progressors=81.2 (IQR, 69.1-87.8), p<0.001). Story ALF (area under curve (AUC)=0.82) and list ALF (AUC=0.73) discriminated between those who did and did not develop symptoms.

conclusionsSeverity of ALF is not only associated with the presence of AD pathology but also predictive of clinical onset, identifying those at the highest risk of imminent decline. ALF testing offers promise in aiding presymptomatic trial recruitment, as a presymptomatic cognitive endpoint and potentially as a screening tool in the wider population.

Indexed as

Alzheimer DiseaseMemory DisordersAdultAgedDisease ProgressionFemaleHumansMaleMental RecallMiddle AgedNeuropsychological TestsALZHEIMER'S DISEASECOGNITIONCOGNITIVE NEUROPSYCHOLOGYDEMENTIAMEMORY

Identifiers

PMID40930583
PMCPMC13217076

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.