Disentangling risk of progression and clinical trajectories in preclinical AD: views from the International Working Group

The IWG framework bridges biomarker research and clinical outcomes, advancing preclinical AD understanding. By distinguishing "asymptomatic at risk" from "presymptomatic AD," it fosters biomarker innovation, refines risk stratification, and promotes tailored therapeutic strategies. This framework advances the EuroPAD community's goals, emphasizing the need for individualized interventions and aligning research priorities with clinical and public health imperatives. References: 1 Dubois B, Villain N, Schneider L, et al. Alzheimer Disease as a Clinical-Biological Construct-An International Working Group Recommendation. JAMA Neurol 2024. 2 Jack CR, Andrews JS, Beach TG, et al. Revised criteria for diagnosis and staging of Alzheimer's disease: Alzheimer's Association Workgroup. Alzheimers Dement 2024; : 1-27. 3 Brookmeyer R, Abdalla N. Estimation of lifetime risks of Alzheimer's disease dementia using biomarkers for preclinical disease. Alzheimer's and Dementia 2018; 14: 981-8. 4 Ossenkoppele R, Pichet Binette A, Groot C, et al. Amyloid and tau PET-positive cognitively unimpaired individuals are at high risk for future cognitive decline. Nat Med 2022; 28: 2381-7.

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Publication Details

Journal
Alzheimer s & Dementia
Published
2025-12-01
DOI
https://doi.org/10.1002/alz70856_098966
Primary Topic
Dementia and Cognitive Impairment Research
Type
article
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article

Disentangling risk of progression and clinical trajectories in preclinical AD: views from the International Working Group

Nicolas Villain
Alzheimer s & Dementia
Dementia and Cognitive Impairment Research
article

Disentangling risk of progression and clinical trajectories in preclinical AD: views from the International Working Group

Nicolas Villain
article en

Abstract

The IWG framework bridges biomarker research and clinical outcomes, advancing preclinical AD understanding. By distinguishing "asymptomatic at risk" from "presymptomatic AD," it fosters biomarker innovation, refines risk stratification, and promotes tailored therapeutic strategies. This framework advances the EuroPAD community's goals, emphasizing the need for individualized interventions and aligning research priorities with clinical and public health imperatives. References: 1 Dubois B, Villain N, Schneider L, et al. Alzheimer Disease as a Clinical-Biological Construct-An International Working Group Recommendation. JAMA Neurol 2024. 2 Jack CR, Andrews JS, Beach TG, et al. Revised criteria for diagnosis and staging of Alzheimer's disease: Alzheimer's Association Workgroup. Alzheimers Dement 2024; : 1-27. 3 Brookmeyer R, Abdalla N. Estimation of lifetime risks of Alzheimer's disease dementia using biomarkers for preclinical disease. Alzheimer's and Dementia 2018; 14: 981-8. 4 Ossenkoppele R, Pichet Binette A, Groot C, et al. Amyloid and tau PET-positive cognitively unimpaired individuals are at high risk for future cognitive decline. Nat Med 2022; 28: 2381-7.

Alzheimer s & DementiaVol. 21(S2)
Assistance Publique – Hôpitaux de Paris (FR)
Partnerships for the goals
Openalex Percentile: Top 33%
Dementia and Cognitive Impairment Research
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