Reinventing “N” in the A/T/N framework: The case for digital

Breakthroughs in biomarkers for amyloid (A), tau (T), and neurodegeneration (N) have advanced the prospects of accurate Alzheimer's disease (AD) diagnosis. However, presence of pathology does not always translate into clinical expression and there are still clear knowledge gaps as to whether someone with AD biological indicators will lead to clinically apparent disease necessary to warrant drug treatments that carry toxicity risk. Reliance on decades-old assessment tools inhibits detection and monitoring at preclinical and early disease stages when new treatments could prove most effective. Evidence has accumulated that digital measures provide accurate detection of disease at early stages. We call for a re-evaluation of the A/T/N diagnostic framework, with digital evaluation measures complementing non-AD specific neurodegeneration markers, and even potentially replacing those non-specific to AD, to provide a clinically relevant feature critical to clinical trial advances and treatment decisions. Achieving this will only be possible if further research into novel digital evaluation tools is pursued with the same support and consideration as amyloid and tau.

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Publication Details

Journal
The Journal of Prevention of Alzheimer s Disease
Published
2025-12-01
DOI
https://doi.org/10.1016/j.tjpad.2025.100395
Primary Topic
Dementia and Cognitive Impairment Research
Type
article
Field-Weighted Citation Impact
0.00
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article

Reinventing “N” in the A/T/N framework: The case for digital

Nicholas James Ashton, Spencer Low, Zachary Popp, Rhoda Au et al.
The Journal of Prevention of Alzheimer s Disease
Dementia and Cognitive Impairment Research
article

Reinventing “N” in the A/T/N framework: The case for digital

Nicholas James Ashton, Spencer Low, Zachary Popp, Rhoda Au, Henrik Zetterberg
article en

Abstract

Breakthroughs in biomarkers for amyloid (A), tau (T), and neurodegeneration (N) have advanced the prospects of accurate Alzheimer's disease (AD) diagnosis. However, presence of pathology does not always translate into clinical expression and there are still clear knowledge gaps as to whether someone with AD biological indicators will lead to clinically apparent disease necessary to warrant drug treatments that carry toxicity risk. Reliance on decades-old assessment tools inhibits detection and monitoring at preclinical and early disease stages when new treatments could prove most effective. Evidence has accumulated that digital measures provide accurate detection of disease at early stages. We call for a re-evaluation of the A/T/N diagnostic framework, with digital evaluation measures complementing non-AD specific neurodegeneration markers, and even potentially replacing those non-specific to AD, to provide a clinically relevant feature critical to clinical trial advances and treatment decisions. Achieving this will only be possible if further research into novel digital evaluation tools is pursued with the same support and consideration as amyloid and tau.

The Journal of Prevention of Alzheimer s DiseaseVol. 13(1)
Boston University (US), Banner Health (US), UK Dementia Research Institute (GB), University College London (GB)
Openalex Percentile: Top 56%
Dementia and Cognitive Impairment Research
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