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Developing the ATX(N) classification for use across the Alzheimer disease continuum
Harald Hampel1, Jeffrey Cummings2, Kaj Blennow3,4
1Neurology Business Group, Eisai Inc., Woodcliff Lake, NJ, USA. harald_hampel@eisai.com.
The AT(N) system redefines Alzheimer disease (AD) using biomarkers for amyloid-β (Aβ), tau, and neurodegeneration. An evolving ATX(N) system incorporates new biomarkers for broader AD pathology assessment.
Area of Science:
- Neuroscience
- Biomarkers
- Alzheimer's Disease Research
Background:
- Alzheimer disease (AD) is shifting from a symptom-based definition to a clinical-biological construct.
- Fluid and neuroimaging biomarkers are crucial for this transformation.
- The AT(N) system categorizes AD pathophysiology using amyloid-β (Aβ), tau, and neurodegeneration markers.
Purpose of the Study:
- To describe the conceptual framework and clinical importance of the AT(N) and evolving ATX(N) systems.
- To summarize the use of these biomarker systems in AD clinical trials and practice.
- To discuss challenges and provide an outlook on the real-world application of the AT(N) system.
Main Methods:
- Review of current literature on AD biomarkers and classification systems.
- Analysis of the AT(N) and ATX(N) frameworks.
- Discussion of potential applications and challenges in clinical settings.
Main Results:
- The AT(N) system provides a biomarker-based classification of AD.
- The ATX(N) system expands this framework to include novel pathophysiological mechanisms.
- These systems offer potential for improved AD diagnosis, monitoring, and clinical trial design.
Conclusions:
- The AT(N) and ATX(N) systems represent a significant advancement in understanding and classifying Alzheimer disease.
- Further validation and standardization are needed for widespread clinical adoption.
- These biomarker frameworks hold promise for future AD clinical practice and research.
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